Gene list
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Organism: Dictyostelium lacteum
Number of genes found: 10289
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium lacteum | ||||||||
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Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
NA | DLA_11879 | tRNA-Lys | GLQOFTK02G2F2O | tRNA | 786666 | 73 | - | 0.643836 |
NA | DLA_11890 | tRNA-Thr | GLQOFTK02IJPNF | tRNA | 36155 | 71 | + | 0.450704 |
NA | DLA_11868 | tRNA-Cys | GAOABQK02HUB3S | tRNA | 721243 | 72 | - | 0.458333 |
NA | DLA_11869 | tRNA-Met | GAOABQK02HUB3S | tRNA | 897459 | 73 | - | 0.479452 |
NA | DLA_11892 | tRNA-Thr | GLQOFTK02IJPNF | tRNA | 63940 | 71 | + | 0.450704 |
NA | DLA_11887 | tRNA-Arg | GLQOFTK02IIOHN | tRNA | 109759 | 72 | + | 0.555556 |
NA | DLA_11897 | tRNA-Trp | GLQOFTK02IRMR1 | tRNA | 196200 | 72 | + | 0.541667 |
NA | DLA_11882 | tRNA-Leu | GLQOFTK02GHM7A | tRNA | 168 | 79 | + | 0.506329 |
NA | DLA_11856 | tRNA-Asn | GAOABQK02G6SYV | tRNA | 100674 | 73 | + | 0.547945 |
NA | DLA_11896 | tRNA-Ser | GLQOFTK02IJPNF | tRNA | 275964 | 81 | + | 0.45679 |
NA | DLA_11866 | tRNA-Leu | GAOABQK02HUB3S | tRNA | 280948 | 80 | - | 0.5 |
NA | DLA_11863 | tRNA-Trp | GAOABQK02H81I9 | tRNA | 857696 | 72 | - | 0.541667 |
NA | DLA_11857 | tRNA-Leu | GAOABQK02G6SYV | tRNA | 411750 | 80 | + | 0.5 |
NA | DLA_11903 | tRNA-Leu | F4PJNLW01AQJ8S | tRNA | 45066 | 79 | + | 0.506329 |
NA | DLA_11885 | tRNA-Leu | GLQOFTK02GK2WV | tRNA | 383 | 81 | + | 0.580247 |
NA | DLA_11895 | tRNA-Ala | GLQOFTK02IJPNF | tRNA | 218462 | 96 | + | 0.427083 |
NA | DLA_11898 | tRNA-Arg | contig05409_1.exp | tRNA | 699375 | 72 | + | 0.555556 |
NA | DLA_11893 | tRNA-Asn | GLQOFTK02IJPNF | tRNA | 64059 | 73 | - | 0.547945 |
NA | DLA_11860 | tRNA-Thr | GAOABQK02H81I9 | tRNA | 107405 | 84 | + | 0.428571 |
NA | DLA_11858 | tRNA-Thr | GAOABQK02G7M1S | tRNA | 130378 | 71 | - | 0.450704 |
NA | DLA_11904 | tRNA-Thr | F4PJNLW01B0TO9 | tRNA | 205879 | 71 | - | 0.450704 |
NA | DLA_11849 | tRNA-Leu | F4PJNLW01DERRH | tRNA | 470374 | 81 | - | 0.580247 |
NA | DLA_11902 | tRNA-Gln | F4PJNLW01A00V1 | tRNA | 592539 | 72 | - | 0.402778 |
NA | DLA_11894 | tRNA-Ala | GLQOFTK02IJPNF | tRNA | 206906 | 96 | - | 0.427083 |
NA | DLA_11855 | tRNA-Ile | F4PJNLW02GJ9ZB | tRNA | 218415 | 87 | - | 0.413793 |
NA | DLA_11853 | tRNA-Met | F4PJNLW01EE5MJ | tRNA | 784643 | 73 | - | 0.479452 |
NA | DLA_11870 | tRNA-Met | GAOABQK02HUB3S | tRNA | 1027501 | 73 | - | 0.465753 |
NA | DLA_11876 | tRNA-Asn | GLQOFTK02FH5TG | tRNA | 1278271 | 73 | - | 0.547945 |
NA | DLA_11848 | tRNA-Met | F4PJNLW01DERRH | tRNA | 464982 | 74 | + | 0.472973 |
NA | DLA_11883 | tRNA-Pro | GLQOFTK02GHM7A | tRNA | 24767 | 71 | - | 0.464789 |
NA | DLA_11889 | tRNA-Ala | GLQOFTK02IJPNF | tRNA | 25192 | 96 | + | 0.427083 |
NA | DLA_11877 | tRNA-Arg | GLQOFTK02FH5TG | tRNA | 1306949 | 73 | + | 0.534247 |
NA | DLA_11878 | tRNA-Ser | GLQOFTK02FH5TG | tRNA | 1524417 | 81 | + | 0.518519 |
NA | DLA_11852 | tRNA-Leu | F4PJNLW01EE5MJ | tRNA | 138096 | 81 | + | 0.493827 |
NA | DLA_11867 | tRNA-Asn | GAOABQK02HUB3S | tRNA | 532556 | 72 | - | 0.555556 |
NA | DLA_11872 | tRNA-Glu | GAOABQK02IO52T | tRNA | 15376 | 72 | - | 0.527778 |
NA | DLA_11874 | tRNA-Asn | GAOABQK02JBK0O | tRNA | 104967 | 73 | + | 0.547945 |
NA | DLA_11886 | tRNA-Ser | GLQOFTK02IIOHN | tRNA | 4442 | 81 | - | 0.518519 |
NA | DLA_11901 | tRNA-Lys | newcontig00824_1.exp | tRNA | 45482 | 73 | + | 0.643836 |
NA | DLA_11871 | tRNA-Glu | GAOABQK02HUB3S | tRNA | 1752054 | 72 | - | 0.527778 |
NA | DLA_11865 | tRNA-Leu | GAOABQK02HUB3S | tRNA | 223719 | 80 | + | 0.5 |
NA | DLA_11859 | tRNA-Trp | GAOABQK02H81I9 | tRNA | 76 | 74 | - | 0.554054 |
NA | DLA_11891 | tRNA-Asn | GLQOFTK02IJPNF | tRNA | 36272 | 73 | - | 0.547945 |
NA | DLA_11875 | tRNA-Asn | GLQOFTK02FH5TG | tRNA | 1269858 | 73 | + | 0.547945 |
NA | DLA_11850 | tRNA-Met | F4PJNLW01DERRH | tRNA | 471589 | 74 | + | 0.472973 |
NA | DLA_11888 | tRNA-Leu | GLQOFTK02IIOHN | tRNA | 162119 | 79 | - | 0.506329 |
NA | DLA_11851 | tRNA-Leu | F4PJNLW01DERRH | tRNA | 700317 | 81 | + | 0.580247 |
NA | DLA_11873 | tRNA-Pseudo | GAOABQK02IO52T | tRNA | 408508 | 71 | + | 0.507042 |
NA | DLA_11884 | tRNA-Asn | GLQOFTK02GHM7A | tRNA | 559653 | 73 | + | 0.547945 |
NA | DLA_11864 | tRNA-Leu | GAOABQK02HUB3S | tRNA | 184949 | 80 | + | 0.5 |
NA | DLA_11861 | tRNA-Cys | GAOABQK02H81I9 | tRNA | 507849 | 72 | + | 0.458333 |
NA | DLA_11880 | tRNA-Lys | GLQOFTK02G2F2O | tRNA | 788411 | 74 | + | 0.648649 |
NA | DLA_11854 | tRNA-Ile | F4PJNLW02GJ9ZB | tRNA | 151375 | 87 | + | 0.413793 |
NA | DLA_11881 | tRNA-Val | GLQOFTK02G2F2O | tRNA | 859116 | 73 | - | 0.465753 |
NA | DLA_11899 | tRNA-Ser | contig05409_1.exp | tRNA | 702980 | 81 | + | 0.518519 |
NA | DLA_11900 | tRNA-Arg | newcontig00824_1.exp | tRNA | 1062 | 72 | - | 0.555556 |
NA | DLA_11862 | tRNA-Cys | GAOABQK02H81I9 | tRNA | 507992 | 72 | - | 0.458333 |
drnA | DLA_01047 | similar to the mammalian Dicer protein an RNase III protein that converts long dsRNA (double-stranded RNA) into siRNA (small interfering RNA) in Dictyostelium involved in RNA interference and microRNA processing | F4PJNLW01A00V1 | CDS | 697220 | 3645 | - | 0.314129 |
g1 | DLA_00002 | contig05409_1.exp | CDS | 2128 | 1590 | - | 0.326415 | |
g10 | DLA_00011 | contig05409_1.exp | CDS | 30982 | 756 | + | 0.260582 | |
g100 | DLA_00116 | contig05409_1.exp | CDS | 235258 | 1164 | + | 0.337629 | |
g1000 | DLA_01110 | F4PJNLW01A00V1 | CDS | 828964 | 1653 | - | 0.30127 | |
g10000 | DLA_11156 | GLQOFTK02JL55Q | CDS | 592492 | 2448 | + | 0.338235 | |
g10001 | DLA_11157 | GLQOFTK02JL55Q | CDS | 595114 | 501 | - | 0.257485 | |
g10002 | DLA_11159 | GLQOFTK02JL55Q | CDS | 596312 | 1206 | + | 0.292703 | |
g10003 | DLA_11160 | GLQOFTK02JL55Q | CDS | 597665 | 954 | + | 0.310273 | |
g10004 | DLA_11161 | catalyzes the reaction D-ribose 5-phosphate D-ribulose 5-phosphate | GLQOFTK02JL55Q | CDS | 598711 | 714 | - | 0.357143 |
g10005 | DLA_11162 | GLQOFTK02JL55Q | CDS | 599710 | 489 | - | 0.345603 | |
g10006 | DLA_11163 | Dictyostelium enzyme that hydrolyses O- and S-glycosyl compounds with a preference for cleaving the alpha1-6-O-fucolsyl bonds in fucosylated oligosaccharides secreted during development | GLQOFTK02JL55Q | CDS | 600382 | 1398 | + | 0.350501 |
g10007 | DLA_11164 | GLQOFTK02JL55Q | CDS | 602070 | 2064 | - | 0.320736 | |
g10008 | DLA_11165 | GLQOFTK02JL55Q | CDS | 604315 | 2010 | + | 0.30398 | |
g10009 | DLA_11166 | GLQOFTK02JL55Q | CDS | 606696 | 2004 | + | 0.305389 | |
g1001 | DLA_01111 | component of the SCF ubiquitin ligase complex the fpaB gene encodes a protein almost identical to that of fpaA differing in one amino acid only series of glycosylation reactions attaches a pentasaccharide chain to HyPro143 there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 831508 | 483 | - | 0.339545 |
g10010 | DLA_11167 | GLQOFTK02JL55Q | CDS | 609157 | 354 | - | 0.358757 | |
g10011 | DLA_11169 | GLQOFTK02JL55Q | CDS | 609655 | 216 | + | 0.282407 | |
g10012 | DLA_11170 | GLQOFTK02JL55Q | CDS | 610356 | 3012 | - | 0.324701 | |
g10013 | DLA_11172 | GLQOFTK02JL55Q | CDS | 614325 | 1347 | + | 0.35412 | |
g10014 | DLA_11173 | GLQOFTK02JL55Q | CDS | 616128 | 1047 | + | 0.274117 | |
g10015 | DLA_11174 | GLQOFTK02JL55Q | CDS | 617376 | 1914 | - | 0.30512 | |
g10016 | DLA_11176 | GLQOFTK02JL55Q | CDS | 621421 | 1446 | + | 0.275934 | |
g10017 | DLA_11177 | GLQOFTK02JL55Q | CDS | 623580 | 1080 | + | 0.342593 | |
g10018 | DLA_11178 | GLQOFTK02JL55Q | CDS | 624914 | 1509 | - | 0.341286 | |
g10019 | DLA_11180 | GLQOFTK02JL55Q | CDS | 628929 | 3315 | - | 0.35083 | |
g1002 | DLA_01112 | F4PJNLW01A00V1 | CDS | 832593 | 3108 | - | 0.361647 | |
g10020 | DLA_11181 | GLQOFTK02JL55Q | CDS | 633459 | 4599 | - | 0.337465 | |
g10021 | DLA_11183 | GLQOFTK02JL55Q | CDS | 638268 | 1044 | - | 0.331418 | |
g10022 | DLA_11184 | GLQOFTK02JL55Q | CDS | 639909 | 2118 | - | 0.315392 | |
g10023 | DLA_11185 | GLQOFTK02JL55Q | CDS | 642472 | 618 | + | 0.322006 | |
g10024 | DLA_11186 | GLQOFTK02JL55Q | CDS | 643290 | 1992 | - | 0.324799 | |
g10025 | DLA_11187 | GLQOFTK02JL55Q | CDS | 645934 | 3948 | + | 0.337133 | |
g10026 | DLA_11188 | GLQOFTK02JL55Q | CDS | 650159 | 3576 | - | 0.378915 | |
g10027 | DLA_11189 | GLQOFTK02JL55Q | CDS | 654226 | 543 | - | 0.325967 | |
g10028 | DLA_11190 | GLQOFTK02JL55Q | CDS | 655711 | 1617 | + | 0.393939 | |
g10029 | DLA_11191 | GLQOFTK02JL55Q | CDS | 657400 | 1626 | - | 0.289668 | |
g1003 | DLA_01113 | F4PJNLW01A00V1 | CDS | 836642 | 957 | + | 0.339603 | |
g10030 | DLA_11192 | ortholog of the conserved microsomal signal peptidase 25 kDa subunit the signal peptidase complex is a membrane-bound endoproteinase that removes signal peptides from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum contains two putative transmembrane domains | GLQOFTK02JL55Q | CDS | 659163 | 975 | - | 0.285128 |
g10031 | DLA_11194 | GLQOFTK02JL55Q | CDS | 661224 | 2520 | + | 0.290079 | |
g10032 | DLA_11195 | GLQOFTK02JL55Q | CDS | 663874 | 1269 | - | 0.35067 | |
g10033 | DLA_11196 | GLQOFTK02JL55Q | CDS | 665382 | 1260 | - | 0.292064 | |
g10034 | DLA_11197 | GLQOFTK02JL55Q | CDS | 666720 | 1188 | + | 0.310606 | |
g10035 | DLA_11198 | GLQOFTK02JL55Q | CDS | 668070 | 972 | - | 0.364198 | |
g10036 | DLA_11199 | GLQOFTK02JL55Q | CDS | 669230 | 1206 | + | 0.334163 | |
g10037 | DLA_11200 | GLQOFTK02JL55Q | CDS | 670673 | 543 | - | 0.366482 | |
g10038 | DLA_11201 | GLQOFTK02JL55Q | CDS | 672397 | 1170 | - | 0.326496 | |
g10039 | DLA_11202 | GLQOFTK02JL55Q | CDS | 674498 | 2307 | - | 0.316862 | |
g1004 | DLA_01114 | F4PJNLW01A00V1 | CDS | 837872 | 1662 | - | 0.342359 | |
g10040 | DLA_11203 | GLQOFTK02JL55Q | CDS | 677171 | 1089 | + | 0.292929 | |
g10041 | DLA_11204 | GLQOFTK02JL55Q | CDS | 678449 | 2382 | - | 0.304366 | |
g10042 | DLA_11205 | GLQOFTK02JL55Q | CDS | 681432 | 2313 | + | 0.335063 | |
g10043 | DLA_11206 | GLQOFTK02JL55Q | CDS | 683801 | 1260 | - | 0.281746 | |
g10044 | DLA_11207 | GLQOFTK02JL55Q | CDS | 685183 | 1239 | - | 0.297014 | |
g10045 | DLA_11208 | GLQOFTK02JL55Q | CDS | 686559 | 2217 | - | 0.30221 | |
g10046 | DLA_11209 | GLQOFTK02JL55Q | CDS | 689088 | 255 | - | 0.25098 | |
g10047 | DLA_11210 | GLQOFTK02JL55Q | CDS | 689818 | 1275 | + | 0.347451 | |
g10048 | DLA_11211 | similar to MCM6 a component of the Mcm2-7 hexameric complex that binds chromatin as a part of the pre-replicative complex | GLQOFTK02JL55Q | CDS | 691323 | 2565 | - | 0.332164 |
g10049 | DLA_11212 | GLQOFTK02JL55Q | CDS | 694033 | 1302 | - | 0.337174 | |
g1005 | DLA_01115 | F4PJNLW01A00V1 | CDS | 840089 | 1410 | - | 0.311348 | |
g10050 | DLA_11213 | GLQOFTK02JL55Q | CDS | 695729 | 1245 | + | 0.333333 | |
g10051 | DLA_11215 | GLQOFTK02JL55Q | CDS | 697642 | 1200 | + | 0.324167 | |
g10052 | DLA_11217 | GLQOFTK02JL55Q | CDS | 699576 | 810 | + | 0.322222 | |
g10053 | DLA_11218 | GLQOFTK02JL55Q | CDS | 700526 | 501 | + | 0.263473 | |
g10054 | DLA_11219 | GLQOFTK02JL55Q | CDS | 701178 | 2313 | - | 0.357112 | |
g10055 | DLA_11221 | GLQOFTK02JL55Q | CDS | 705405 | 2181 | + | 0.357634 | |
g10056 | DLA_11223 | GLQOFTK02JL55Q | CDS | 709304 | 3342 | + | 0.359964 | |
g10057 | DLA_11224 | GLQOFTK02JL55Q | CDS | 712922 | 999 | + | 0.282282 | |
g10058 | DLA_11225 | GLQOFTK02JL55Q | CDS | 714155 | 2184 | - | 0.305403 | |
g10059 | DLA_11226 | GLQOFTK02JL55Q | CDS | 717281 | 1278 | + | 0.319249 | |
g1006 | DLA_01116 | F4PJNLW01A00V1 | CDS | 841672 | 1410 | - | 0.370213 | |
g10060 | DLA_11227 | GLQOFTK02JL55Q | CDS | 719805 | 1713 | + | 0.318739 | |
g10061 | DLA_11228 | GLQOFTK02JL55Q | CDS | 722247 | 3852 | - | 0.350467 | |
g10062 | DLA_11229 | GLQOFTK02JL55Q | CDS | 726447 | 3363 | + | 0.359203 | |
g10063 | DLA_11232 | GLQOFTK02JL55Q | CDS | 730659 | 1578 | - | 0.320659 | |
g10064 | DLA_11233 | GLQOFTK02JL55Q | CDS | 732831 | 1545 | - | 0.330097 | |
g10065 | DLA_11234 | GLQOFTK02JL55Q | CDS | 734763 | 1584 | - | 0.325126 | |
g10066 | DLA_11235 | GLQOFTK02JL55Q | CDS | 736563 | 2583 | - | 0.348045 | |
g10067 | DLA_11238 | GLQOFTK02JL55Q | CDS | 741963 | 1305 | + | 0.3341 | |
g10068 | DLA_11239 | GLQOFTK02JL55Q | CDS | 744417 | 1392 | + | 0.34842 | |
g10069 | DLA_11240 | GLQOFTK02JL55Q | CDS | 746287 | 645 | + | 0.355039 | |
g1007 | DLA_01117 | F4PJNLW01A00V1 | CDS | 843560 | 7092 | + | 0.326424 | |
g10070 | DLA_11242 | GLQOFTK02JL55Q | CDS | 748079 | 768 | + | 0.334635 | |
g10071 | DLA_11243 | GLQOFTK02JL55Q | CDS | 749090 | 2811 | + | 0.336891 | |
g10072 | DLA_11244 | GLQOFTK02JL55Q | CDS | 752012 | 1119 | - | 0.316354 | |
g10073 | DLA_11246 | GLQOFTK02JL55Q | CDS | 753430 | 957 | + | 0.329154 | |
g10074 | DLA_11247 | GLQOFTK02JL55Q | CDS | 754900 | 834 | - | 0.321343 | |
g10075 | DLA_11248 | GLQOFTK02JL55Q | CDS | 756239 | 1938 | + | 0.288958 | |
g10076 | DLA_11249 | GLQOFTK02JL55Q | CDS | 758509 | 2061 | - | 0.339156 | |
g10077 | DLA_11250 | GLQOFTK02JL55Q | CDS | 761011 | 1563 | + | 0.31222 | |
g10078 | DLA_11251 | GLQOFTK02JL55Q | CDS | 762875 | 3936 | + | 0.306657 | |
g10079 | DLA_11252 | GLQOFTK02JL55Q | CDS | 766945 | 1365 | - | 0.298901 | |
g1008 | DLA_01118 | F4PJNLW01A00V1 | CDS | 851960 | 2121 | + | 0.286657 | |
g10080 | DLA_11253 | GLQOFTK02JL55Q | CDS | 768673 | 1773 | + | 0.267908 | |
g10081 | DLA_11254 | GLQOFTK02JL55Q | CDS | 770510 | 369 | - | 0.295393 | |
g10082 | DLA_11255 | GLQOFTK02JL55Q | CDS | 771164 | 1239 | + | 0.378531 | |
g10083 | DLA_11256 | GLQOFTK02JL55Q | CDS | 772850 | 1500 | - | 0.282 | |
g10084 | DLA_11258 | GLQOFTK02JL55Q | CDS | 774482 | 4122 | - | 0.309801 | |
g10085 | DLA_11845 | SKIP ortholog binds cyclophilin E (cypE) in a cyclosporin-independent manner | GLQOFTK02JL55Q | CDS | 778820 | 1680 | - | 0.332143 |
g10086 | DLA_11259 | GLQOFTK02JL55Q | CDS | 780755 | 444 | + | 0.31982 | |
g10087 | DLA_11260 | snRNP Sm family protein similar to H. sapiens LSMD1 and to S. pombe U6 snRNP-associated protein Lsm7 | GLQOFTK02JL55Q | CDS | 781503 | 276 | - | 0.304348 |
g10088 | DLA_11261 | GLQOFTK02JL55Q | CDS | 782177 | 3021 | + | 0.3095 | |
g10089 | DLA_11262 | GLQOFTK02JL55Q | CDS | 785510 | 3339 | + | 0.331836 | |
g1009 | DLA_01120 | F4PJNLW01A00V1 | CDS | 854260 | 417 | + | 0.302158 | |
g10090 | DLA_11263 | GLQOFTK02JL55Q | CDS | 789037 | 2133 | + | 0.304735 | |
g10091 | DLA_11264 | GLQOFTK02JL55Q | CDS | 791785 | 1065 | - | 0.340845 | |
g10092 | DLA_11265 | GLQOFTK02JL55Q | CDS | 793666 | 870 | + | 0.342529 | |
g10093 | DLA_11266 | GLQOFTK02JL55Q | CDS | 794594 | 2988 | - | 0.303213 | |
g10094 | DLA_11267 | GLQOFTK02JL55Q | CDS | 798272 | 1068 | - | 0.394195 | |
g10095 | DLA_11268 | GLQOFTK02JL55Q | CDS | 799586 | 1173 | + | 0.27792 | |
g10096 | DLA_11270 | GLQOFTK02JL55Q | CDS | 801591 | 2511 | - | 0.320191 | |
g10097 | DLA_11272 | GLQOFTK02JL55Q | CDS | 804918 | 2307 | - | 0.324231 | |
g10098 | DLA_11273 | GLQOFTK02JL55Q | CDS | 807491 | 1950 | - | 0.332308 | |
g10099 | DLA_11274 | GLQOFTK02JL55Q | CDS | 809838 | 792 | - | 0.280303 | |
g101 | DLA_00117 | contig05409_1.exp | CDS | 237058 | 1521 | - | 0.357659 | |
g1010 | DLA_01121 | F4PJNLW01A00V1 | CDS | 855110 | 2964 | + | 0.339406 | |
g10100 | DLA_11276 | localizes to the cell cortex binds myosin II and regulates microtubule length the cortical cytoskeleton and cytokinesis functions in the same pathway as racE to regulate these processes | GLQOFTK02JL55Q | CDS | 811197 | 741 | - | 0.368421 |
g10101 | DLA_11277 | GLQOFTK02JL55Q | CDS | 812499 | 579 | - | 0.264249 | |
g10102 | DLA_11278 | GLQOFTK02JL55Q | CDS | 813315 | 2511 | + | 0.309438 | |
g10103 | DLA_11279 | GLQOFTK02JL55Q | CDS | 815950 | 2742 | - | 0.31291 | |
g10104 | DLA_11282 | very similar to Acanthamoeba actobindin contains two actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domains | GLQOFTK02JL55Q | CDS | 820627 | 267 | - | 0.404494 |
g10105 | DLA_11283 | contains one C2H2-type zinc finger motif and 2 ankyrin repeats contains 2 predicted coiled-coil domains | GLQOFTK02JL55Q | CDS | 821463 | 2073 | + | 0.320309 |
g10106 | DLA_11284 | GLQOFTK02JL55Q | CDS | 823910 | 2478 | + | 0.307103 | |
g10107 | DLA_11285 | GLQOFTK02JL55Q | CDS | 826825 | 1434 | - | 0.340307 | |
g10108 | DLA_11286 | GLQOFTK02JL55Q | CDS | 828461 | 432 | + | 0.300926 | |
g10109 | DLA_11287 | GLQOFTK02JL55Q | CDS | 829023 | 804 | - | 0.298507 | |
g1011 | DLA_01122 | F4PJNLW01A00V1 | CDS | 858219 | 1269 | - | 0.327029 | |
g10110 | DLA_11288 | GLQOFTK02JL55Q | CDS | 830966 | 1485 | + | 0.257912 | |
g10111 | DLA_11289 | GLQOFTK02JL55Q | CDS | 832900 | 552 | - | 0.326087 | |
g10112 | DLA_11292 | GLQOFTK02JL55Q | CDS | 834981 | 1032 | - | 0.323643 | |
g10113 | DLA_11293 | hydrolyses alkylated adenine residues on DNA releasing 3-methyladenine | GLQOFTK02JL55Q | CDS | 836557 | 678 | + | 0.306785 |
g10114 | DLA_11294 | GLQOFTK02JL55Q | CDS | 837312 | 1827 | - | 0.316913 | |
g10115 | DLA_11295 | GLQOFTK02JL55Q | CDS | 839720 | 1299 | + | 0.293303 | |
g10116 | DLA_11296 | GLQOFTK02JL55Q | CDS | 841405 | 204 | - | 0.240196 | |
g10117 | DLA_11297 | GLQOFTK02JL55Q | CDS | 841822 | 2325 | - | 0.395699 | |
g10118 | DLA_11298 | GLQOFTK02JL55Q | CDS | 844355 | 3999 | - | 0.291323 | |
g10119 | DLA_11299 | GLQOFTK02JL55Q | CDS | 849428 | 8787 | - | 0.333447 | |
g1012 | DLA_01123 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | F4PJNLW01A00V1 | CDS | 859752 | 708 | - | 0.323446 |
g10120 | DLA_11300 | GLQOFTK02JL55Q | CDS | 859002 | 2712 | + | 0.327434 | |
g10121 | DLA_11301 | GLQOFTK02JL55Q | CDS | 861962 | 600 | - | 0.32 | |
g10122 | DLA_11304 | GLQOFTK02JL55Q | CDS | 863912 | 1107 | - | 0.273713 | |
g10123 | DLA_11305 | GLQOFTK02JL55Q | CDS | 865248 | 873 | + | 0.353952 | |
g10124 | DLA_11306 | similar to human DUSP19 predicted to have dual specificity toward SerThr and Tyr-containing proteins | GLQOFTK02JL55Q | CDS | 866368 | 669 | + | 0.313901 |
g10125 | DLA_11307 | GLQOFTK02JL55Q | CDS | 867265 | 675 | - | 0.287407 | |
g10126 | DLA_11308 | GLQOFTK02JL55Q | CDS | 868170 | 774 | + | 0.284238 | |
g10127 | DLA_11309 | GLQOFTK02JL55Q | CDS | 869532 | 4638 | + | 0.335058 | |
g10128 | DLA_11310 | GLQOFTK02JL55Q | CDS | 875396 | 753 | - | 0.350598 | |
g10129 | DLA_11311 | GLQOFTK02JL55Q | CDS | 876670 | 2493 | - | 0.340554 | |
g1013 | DLA_11462 | F4PJNLW01A00V1 | CDS | 860814 | 426 | + | 0.262911 | |
g10130 | DLA_11313 | GLQOFTK02JL55Q | CDS | 881212 | 1494 | + | 0.261044 | |
g10131 | DLA_11314 | GLQOFTK02JL55Q | CDS | 883525 | 1353 | - | 0.316334 | |
g10132 | DLA_11315 | GLQOFTK02JL55Q | CDS | 885256 | 1683 | + | 0.330362 | |
g10133 | DLA_11316 | GLQOFTK02JL55Q | CDS | 887095 | 1191 | - | 0.346767 | |
g10134 | DLA_11317 | GLQOFTK02JL55Q | CDS | 888637 | 783 | + | 0.386973 | |
g10135 | DLA_11318 | GLQOFTK02JL55Q | CDS | 890456 | 930 | + | 0.382796 | |
g10136 | DLA_11319 | GLQOFTK02JL55Q | CDS | 891714 | 3030 | + | 0.29703 | |
g10137 | DLA_11320 | GLQOFTK02JL55Q | CDS | 895372 | 3042 | + | 0.299145 | |
g10138 | DLA_11325 | GLQOFTK02JL55Q | CDS | 901802 | 2127 | - | 0.297132 | |
g10139 | DLA_11326 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | GLQOFTK02JL55Q | CDS | 904155 | 1899 | + | 0.319115 |
g1014 | DLA_01124 | F4PJNLW01A00V1 | CDS | 861418 | 939 | + | 0.332268 | |
g10140 | DLA_11327 | GLQOFTK02JL55Q | CDS | 906162 | 1623 | - | 0.292668 | |
g10141 | DLA_11328 | GLQOFTK02JL55Q | CDS | 908863 | 3234 | - | 0.365801 | |
g10142 | DLA_11329 | GLQOFTK02JL55Q | CDS | 913727 | 1065 | - | 0.266667 | |
g10143 | DLA_11330 | GLQOFTK02JL55Q | CDS | 914963 | 2328 | - | 0.35567 | |
g10144 | DLA_11332 | GLQOFTK02JL55Q | CDS | 918252 | 885 | - | 0.336723 | |
g10145 | DLA_11333 | GLQOFTK02JL55Q | CDS | 919471 | 735 | + | 0.306122 | |
g10146 | DLA_11334 | GLQOFTK02JL55Q | CDS | 920491 | 651 | + | 0.305684 | |
g10147 | DLA_11336 | GLQOFTK02JL55Q | CDS | 921786 | 1029 | - | 0.301263 | |
g10148 | DLA_11337 | GLQOFTK02JL55Q | CDS | 923441 | 1344 | + | 0.343006 | |
g10149 | DLA_11339 | GLQOFTK02JL55Q | CDS | 926847 | 1572 | + | 0.302799 | |
g1015 | DLA_01125 | F4PJNLW01A00V1 | CDS | 862685 | 960 | + | 0.291667 | |
g10150 | DLA_11340 | GLQOFTK02JL55Q | CDS | 928972 | 1500 | + | 0.344667 | |
g10151 | DLA_11341 | GLQOFTK02JL55Q | CDS | 930897 | 1131 | - | 0.300619 | |
g10152 | DLA_11342 | GLQOFTK02JL55Q | CDS | 932336 | 3042 | + | 0.32643 | |
g10153 | DLA_11343 | GLQOFTK02JL55Q | CDS | 935780 | 219 | - | 0.356164 | |
g10154 | DLA_11344 | GLQOFTK02JL55Q | CDS | 936163 | 1962 | + | 0.284913 | |
g10155 | DLA_11345 | GLQOFTK02JL55Q | CDS | 938270 | 675 | - | 0.308148 | |
g10156 | DLA_11346 | GLQOFTK02JL55Q | CDS | 940227 | 1674 | - | 0.314815 | |
g10157 | DLA_11347 | GLQOFTK02JL55Q | CDS | 942082 | 684 | + | 0.336257 | |
g10158 | DLA_11348 | GLQOFTK02JL55Q | CDS | 943182 | 702 | - | 0.259259 | |
g10159 | DLA_11349 | GLQOFTK02JL55Q | CDS | 944120 | 1290 | + | 0.378295 | |
g1016 | DLA_01126 | F4PJNLW01A00V1 | CDS | 864333 | 840 | + | 0.29881 | |
g10160 | DLA_11350 | GLQOFTK02JL55Q | CDS | 945476 | 504 | - | 0.228175 | |
g10161 | DLA_11351 | GLQOFTK02JL55Q | CDS | 946168 | 1590 | + | 0.348428 | |
g10162 | DLA_11352 | GLQOFTK02JL55Q | CDS | 948272 | 594 | + | 0.383838 | |
g10163 | DLA_11353 | GLQOFTK02JL55Q | CDS | 949197 | 3930 | + | 0.312214 | |
g10164 | DLA_11355 | GLQOFTK02JL55Q | CDS | 953671 | 1683 | + | 0.341652 | |
g10165 | DLA_11356 | GLQOFTK02JL55Q | CDS | 955499 | 1314 | - | 0.256469 | |
g10166 | DLA_11357 | GLQOFTK02JL55Q | CDS | 957238 | 1272 | + | 0.341981 | |
g10167 | DLA_11359 | GLQOFTK02JL55Q | CDS | 959371 | 207 | + | 0.246377 | |
g10168 | DLA_11360 | GLQOFTK02JL55Q | CDS | 959777 | 3450 | - | 0.308116 | |
g10169 | DLA_11361 | GLQOFTK02JL55Q | CDS | 963978 | 1605 | + | 0.378816 | |
g1017 | DLA_01127 | F4PJNLW01A00V1 | CDS | 865535 | 759 | - | 0.280632 | |
g10170 | DLA_11362 | GLQOFTK02JL55Q | CDS | 965973 | 9987 | + | 0.323521 | |
g10171 | DLA_11363 | GLQOFTK02JL55Q | CDS | 976343 | 1542 | - | 0.268482 | |
g10172 | DLA_11364 | GLQOFTK02JL55Q | CDS | 978154 | 1128 | + | 0.332447 | |
g10173 | DLA_11366 | GLQOFTK02JL55Q | CDS | 980702 | 4050 | + | 0.339012 | |
g10174 | DLA_11367 | GLQOFTK02JL55Q | CDS | 986141 | 1815 | + | 0.238567 | |
g10175 | DLA_11368 | GLQOFTK02JL55Q | CDS | 988280 | 2964 | + | 0.354251 | |
g10176 | DLA_11369 | GLQOFTK02JL55Q | CDS | 991684 | 984 | + | 0.275407 | |
g10177 | DLA_11370 | GLQOFTK02JL55Q | CDS | 992999 | 1572 | - | 0.318702 | |
g10178 | DLA_11371 | GLQOFTK02JL55Q | CDS | 996997 | 1014 | + | 0.253452 | |
g10179 | DLA_11372 | GLQOFTK02JL55Q | CDS | 998083 | 14211 | - | 0.308071 | |
g1018 | DLA_01128 | F4PJNLW01A00V1 | CDS | 866619 | 570 | + | 0.294737 | |
g10180 | DLA_11373 | GLQOFTK02JL55Q | CDS | 1013097 | 1041 | + | 0.24976 | |
g10181 | DLA_11374 | GLQOFTK02JL55Q | CDS | 1014209 | 3405 | - | 0.311894 | |
g10182 | DLA_11376 | GLQOFTK02JL55Q | CDS | 1018236 | 1665 | + | 0.303303 | |
g10183 | DLA_11378 | expressed in pstAO cells and in upper cup during culmination there is a second copy of this gene | GLQOFTK02JL55Q | CDS | 1020326 | 567 | + | 0.280423 |
g10184 | DLA_11379 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) there is a second copy of this gene | GLQOFTK02JL55Q | CDS | 1021400 | 1650 | + | 0.330909 |
g10185 | DLA_11846 | GLQOFTK02JL55Q | CDS | 1023323 | 447 | - | 0.277405 | |
g10186 | DLA_11380 | GLQOFTK02JL55Q | CDS | 1023908 | 1938 | - | 0.309598 | |
g10187 | DLA_11381 | GLQOFTK02JL55Q | CDS | 1026091 | 3936 | - | 0.302083 | |
g10188 | DLA_11383 | catalyzes the reaction ATP glycerone ADP glycerone phosphate | GLQOFTK02JL55Q | CDS | 1030200 | 3105 | - | 0.318519 |
g10189 | DLA_11384 | GLQOFTK02JQRL3 | CDS | 55 | 1617 | + | 0.324057 | |
g1019 | DLA_01129 | F4PJNLW01A00V1 | CDS | 867408 | 1245 | - | 0.349398 | |
g10190 | DLA_11385 | GLQOFTK02JQRL3 | CDS | 2009 | 6036 | - | 0.295891 | |
g10191 | DLA_11387 | GLQOFTK02JQRL3 | CDS | 8609 | 1716 | - | 0.285548 | |
g10192 | DLA_11388 | GLQOFTK02JQRL3 | CDS | 10939 | 1215 | + | 0.260082 | |
g10193 | DLA_11389 | GLQOFTK02JQRL3 | CDS | 12450 | 2151 | - | 0.30451 | |
g10194 | DLA_11390 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | GLQOFTK02JQRL3 | CDS | 15160 | 462 | + | 0.329004 |
g10195 | DLA_11391 | GLQOFTK02JQRL3 | CDS | 15957 | 1710 | + | 0.254971 | |
g10196 | DLA_11392 | GLQOFTK02JQRL3 | CDS | 18629 | 1596 | + | 0.325815 | |
g10197 | DLA_11393 | newcontig00824_1.exp | CDS | 83 | 423 | + | 0.260047 | |
g10198 | DLA_11394 | newcontig00824_1.exp | CDS | 2122 | 1557 | - | 0.263969 | |
g10199 | DLA_11395 | newcontig00824_1.exp | CDS | 4059 | 462 | - | 0.222944 | |
g102 | DLA_00118 | contig05409_1.exp | CDS | 238802 | 3519 | + | 0.318841 | |
g1020 | DLA_01130 | F4PJNLW01A00V1 | CDS | 868852 | 1428 | - | 0.279412 | |
g10200 | DLA_11396 | newcontig00824_1.exp | CDS | 4832 | 1998 | + | 0.303303 | |
g10201 | DLA_11397 | newcontig00824_1.exp | CDS | 6901 | 1347 | - | 0.316258 | |
g10202 | DLA_11398 | newcontig00824_1.exp | CDS | 8881 | 1854 | + | 0.343581 | |
g10203 | DLA_11399 | newcontig00824_1.exp | CDS | 11812 | 297 | + | 0.363636 | |
g10204 | DLA_11400 | putative metalloprotease of the peptidase M41 family which belong to a larger family of zinc metalloproteases includes the cell division protein FtsH | newcontig00824_1.exp | CDS | 12363 | 2196 | - | 0.306466 |
g10205 | DLA_11401 | newcontig00824_1.exp | CDS | 14727 | 1668 | - | 0.285372 | |
g10206 | DLA_11402 | newcontig00824_1.exp | CDS | 16718 | 1275 | - | 0.316078 | |
g10207 | DLA_11404 | newcontig00824_1.exp | CDS | 18754 | 1011 | + | 0.327399 | |
g10208 | DLA_11405 | newcontig00824_1.exp | CDS | 20258 | 936 | + | 0.306624 | |
g10209 | DLA_11406 | newcontig00824_1.exp | CDS | 21406 | 1950 | - | 0.316923 | |
g1021 | DLA_01132 | F4PJNLW01A00V1 | CDS | 871920 | 336 | + | 0.297619 | |
g10210 | DLA_11407 | newcontig00824_1.exp | CDS | 23809 | 1209 | + | 0.303557 | |
g10211 | DLA_11408 | similar to mammalian cullin 1 and 2 (CUL1 CUL2) involved in ubiquitin-mediated protein degradation regulates prestalk cell differentiation in Dictyostelium | newcontig00824_1.exp | CDS | 25375 | 2202 | + | 0.294278 |
g10212 | DLA_11409 | newcontig00824_1.exp | CDS | 29176 | 2220 | + | 0.342342 | |
g10213 | DLA_11410 | fatty acid synthases catalyze the formation of long-chain fatty acids from acetyl-CoA malonyl-CoA and NADPH. This multifunctional protein has several catalytic activities and an acyl carrier protein | newcontig00824_1.exp | CDS | 32357 | 6813 | - | 0.266549 |
g10214 | DLA_11411 | newcontig00824_1.exp | CDS | 40522 | 4515 | - | 0.337763 | |
g10215 | DLA_11847 | newcontig00824_1.exp | CDS | 45798 | 267 | + | 0.378277 | |
g10216 | DLA_11412 | newcontig00824_1.exp | CDS | 46631 | 1050 | + | 0.290476 | |
g10217 | DLA_11413 | newcontig00824_1.exp | CDS | 47805 | 1284 | - | 0.274143 | |
g10218 | DLA_11414 | newcontig00824_1.exp | CDS | 49521 | 582 | + | 0.268041 | |
g10219 | DLA_11415 | newcontig00824_1.exp | CDS | 50122 | 2034 | - | 0.213864 | |
g1022 | DLA_01133 | F4PJNLW01A00V1 | CDS | 872330 | 942 | - | 0.276008 | |
g10220 | DLA_11416 | newcontig00824_1.exp | CDS | 52538 | 1158 | + | 0.294473 | |
g10221 | DLA_11417 | ortholog of the human KCNMA1 a potassium channel activated by both membrane depolarization and increase in cytosolic Ca(2) that mediates export of K() defects in the gene cause generalized epilepsy and paroxysmal dyskinesia (GEPD) | newcontig00824_1.exp | CDS | 53719 | 3399 | - | 0.280965 |
g10222 | DLA_11418 | AGC group AKT family protein serinethreonine kinase similar to other metazoan AktPKB including an N-terminal PH domain homologous kinase and C-terminal regulatory domains and phosphorylation sites required for AktPKB activation | newcontig00824_1.exp | CDS | 58027 | 1758 | + | 0.306598 |
g10223 | DLA_11419 | newcontig00824_1.exp | CDS | 60160 | 948 | + | 0.24789 | |
g10224 | DLA_11420 | newcontig00824_1.exp | CDS | 61236 | 1065 | + | 0.280751 | |
g10225 | DLA_11421 | newcontig00824_1.exp | CDS | 62426 | 591 | - | 0.302876 | |
g10226 | DLA_11422 | newcontig00824_1.exp | CDS | 63366 | 618 | + | 0.250809 | |
g10227 | DLA_11423 | newcontig00824_1.exp | CDS | 64289 | 3288 | - | 0.314173 | |
g10228 | DLA_11424 | CAZy family GT49 similar to vertebrate acetylglucosaminyltransferase-like protein (LARGE) essential for development | newcontig00824_1.exp | CDS | 68463 | 1332 | + | 0.288288 |
g10229 | DLA_11425 | newcontig00824_1.exp | CDS | 69897 | 2085 | - | 0.31271 | |
g1023 | DLA_01134 | F4PJNLW01A00V1 | CDS | 874184 | 2289 | + | 0.367409 | |
g10230 | DLA_11426 | catalyzes the reaction oxaloacetate L-glutamate L-aspartate | newcontig00824_1.exp | CDS | 73044 | 1311 | - | 0.361556 |
g10231 | DLA_11427 | newcontig02545_1.r1.exp | CDS | 217 | 1074 | + | 0.350093 | |
g10232 | DLA_11428 | newcontig02545_1.r1.exp | CDS | 3620 | 2904 | + | 0.485193 | |
g1024 | DLA_01135 | F4PJNLW01A00V1 | CDS | 876685 | 699 | - | 0.273248 | |
g1025 | DLA_01136 | F4PJNLW01A00V1 | CDS | 877773 | 198 | + | 0.333333 | |
g1026 | DLA_01137 | F4PJNLW01A00V1 | CDS | 878684 | 1566 | - | 0.323755 | |
g1027 | DLA_01138 | F4PJNLW01A00V1 | CDS | 880585 | 786 | + | 0.321883 | |
g1028 | DLA_01139 | F4PJNLW01A00V1 | CDS | 881450 | 2721 | - | 0.314958 | |
g1029 | DLA_01140 | F4PJNLW01A00V1 | CDS | 884584 | 1035 | - | 0.320773 | |
g103 | DLA_00119 | contig05409_1.exp | CDS | 242822 | 5874 | - | 0.31665 | |
g1030 | DLA_01141 | F4PJNLW01A00V1 | CDS | 885963 | 1764 | - | 0.328231 | |
g1031 | DLA_01142 | F4PJNLW01A00V1 | CDS | 888152 | 1965 | - | 0.347074 | |
g1032 | DLA_01143 | F4PJNLW01A00V1 | CDS | 891067 | 2724 | - | 0.318282 | |
g1033 | DLA_01144 | F4PJNLW01A00V1 | CDS | 893896 | 1710 | + | 0.307602 | |
g1034 | DLA_01145 | F4PJNLW01A00V1 | CDS | 895823 | 378 | + | 0.314815 | |
g1035 | DLA_01146 | F4PJNLW01A00V1 | CDS | 896334 | 2064 | + | 0.35126 | |
g1036 | DLA_01147 | F4PJNLW01A00V1 | CDS | 898949 | 288 | + | 0.298611 | |
g1037 | DLA_01148 | F4PJNLW01A00V1 | CDS | 899630 | 510 | + | 0.309804 | |
g1038 | DLA_01149 | F4PJNLW01A00V1 | CDS | 900466 | 948 | + | 0.295359 | |
g1039 | DLA_11463 | F4PJNLW01A00V1 | CDS | 901570 | 1158 | - | 0.351468 | |
g104 | DLA_00121 | similarity to Xenopus F8A1 protein human Factor VIII intron 22 protein | contig05409_1.exp | CDS | 249883 | 1014 | + | 0.284024 |
g1040 | DLA_01150 | F4PJNLW01A00V1 | CDS | 904204 | 1107 | - | 0.31617 | |
g1041 | DLA_01151 | F4PJNLW01A00V1 | CDS | 908661 | 2589 | + | 0.3708 | |
g1042 | DLA_01152 | F4PJNLW01A00V1 | CDS | 911579 | 402 | - | 0.283582 | |
g1043 | DLA_01153 | F4PJNLW01A00V1 | CDS | 912269 | 1566 | + | 0.323116 | |
g1044 | DLA_01154 | F4PJNLW01A00V1 | CDS | 914257 | 897 | + | 0.391304 | |
g1045 | DLA_01155 | F4PJNLW01A00V1 | CDS | 915420 | 5451 | - | 0.335168 | |
g1046 | DLA_01156 | F4PJNLW01A00V1 | CDS | 921345 | 7026 | + | 0.322516 | |
g1047 | DLA_01157 | F4PJNLW01A00V1 | CDS | 928640 | 3351 | + | 0.314235 | |
g1048 | DLA_01158 | F4PJNLW01A00V1 | CDS | 932557 | 279 | + | 0.290323 | |
g1049 | DLA_01159 | F4PJNLW01A00V1 | CDS | 933048 | 1425 | - | 0.334035 | |
g105 | DLA_00122 | contig05409_1.exp | CDS | 251701 | 1341 | + | 0.314691 | |
g1050 | DLA_01160 | F4PJNLW01A00V1 | CDS | 934640 | 2652 | - | 0.347285 | |
g1051 | DLA_01161 | F4PJNLW01A00V1 | CDS | 937679 | 1728 | - | 0.32581 | |
g1052 | DLA_01162 | F4PJNLW01A00V1 | CDS | 940052 | 603 | - | 0.273632 | |
g1053 | DLA_01163 | F4PJNLW01A00V1 | CDS | 940984 | 1425 | - | 0.263158 | |
g1054 | DLA_01164 | F4PJNLW01A00V1 | CDS | 942832 | 1635 | - | 0.327829 | |
g1055 | DLA_01165 | F4PJNLW01A00V1 | CDS | 945624 | 1398 | + | 0.329041 | |
g1056 | DLA_01166 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | F4PJNLW01A00V1 | CDS | 947178 | 1215 | - | 0.365432 |
g1057 | DLA_01167 | F4PJNLW01A00V1 | CDS | 948652 | 1140 | + | 0.338596 | |
g1058 | DLA_01168 | F4PJNLW01A00V1 | CDS | 950617 | 2925 | + | 0.367863 | |
g1059 | DLA_01169 | F4PJNLW01A00V1 | CDS | 953771 | 1434 | - | 0.297071 | |
g106 | DLA_00123 | contig05409_1.exp | CDS | 253530 | 249 | - | 0.341365 | |
g1060 | DLA_11464 | F4PJNLW01A00V1 | CDS | 955280 | 339 | + | 0.286136 | |
g1061 | DLA_01170 | F4PJNLW01A00V1 | CDS | 956070 | 2178 | - | 0.374196 | |
g1062 | DLA_11465 | F4PJNLW01A00V1 | CDS | 959402 | 456 | - | 0.258772 | |
g1063 | DLA_01171 | F4PJNLW01A00V1 | CDS | 960216 | 393 | + | 0.318066 | |
g1064 | DLA_01172 | F4PJNLW01A00V1 | CDS | 961082 | 1116 | - | 0.329749 | |
g1065 | DLA_01173 | F4PJNLW01A00V1 | CDS | 962636 | 1800 | - | 0.364444 | |
g1066 | DLA_01174 | F4PJNLW01A00V1 | CDS | 965085 | 1551 | + | 0.317215 | |
g1067 | DLA_01175 | F4PJNLW01A00V1 | CDS | 966915 | 1383 | - | 0.339118 | |
g1068 | DLA_01176 | F4PJNLW01A00V1 | CDS | 968608 | 1041 | - | 0.335255 | |
g1069 | DLA_01177 | F4PJNLW01A00V1 | CDS | 970180 | 2199 | + | 0.313324 | |
g107 | DLA_00124 | contig05409_1.exp | CDS | 254278 | 780 | + | 0.265385 | |
g1070 | DLA_01178 | F4PJNLW01A00V1 | CDS | 972478 | 1959 | - | 0.335375 | |
g1071 | DLA_01179 | F4PJNLW01A00V1 | CDS | 974717 | 912 | + | 0.253289 | |
g1072 | DLA_01180 | F4PJNLW01A00V1 | CDS | 975804 | 453 | - | 0.379691 | |
g1073 | DLA_01182 | F4PJNLW01A00V1 | CDS | 977295 | 519 | - | 0.319846 | |
g1074 | DLA_01183 | F4PJNLW01A00V1 | CDS | 979121 | 1500 | - | 0.281333 | |
g1075 | DLA_01184 | F4PJNLW01A00V1 | CDS | 981106 | 906 | - | 0.343267 | |
g1076 | DLA_01186 | F4PJNLW01A00V1 | CDS | 983053 | 1326 | - | 0.306938 | |
g1077 | DLA_01188 | F4PJNLW01A00V1 | CDS | 985347 | 3480 | + | 0.310345 | |
g1078 | DLA_01190 | F4PJNLW01A00V1 | CDS | 989493 | 1569 | + | 0.342894 | |
g1079 | DLA_01192 | F4PJNLW01A00V1 | CDS | 991088 | 3372 | - | 0.283511 | |
g108 | DLA_00125 | contig05409_1.exp | CDS | 255185 | 1959 | - | 0.28535 | |
g1080 | DLA_11466 | F4PJNLW01A00V1 | CDS | 995012 | 1251 | + | 0.297362 | |
g1081 | DLA_01193 | F4PJNLW01A00V1 | CDS | 997311 | 3690 | + | 0.325745 | |
g1082 | DLA_11467 | F4PJNLW01A00V1 | CDS | 1001283 | 936 | + | 0.311966 | |
g1083 | DLA_11468 | F4PJNLW01A00V1 | CDS | 1002670 | 2007 | + | 0.284504 | |
g1084 | DLA_01194 | F4PJNLW01A00V1 | CDS | 1005316 | 3210 | + | 0.350779 | |
g1085 | DLA_01195 | catalyzes the reaction CDP-choline 12-diacylglycerol CMP a phosphatidylcholine most similar to plant genes REMI mutant forms aberrant fruiting bodies see | F4PJNLW01A00V1 | CDS | 1008714 | 1191 | + | 0.311503 |
g1086 | DLA_01197 | F4PJNLW01A00V1 | CDS | 1010803 | 579 | + | 0.279793 | |
g1087 | DLA_01198 | F4PJNLW01A00V1 | CDS | 1011517 | 1935 | + | 0.327649 | |
g1088 | DLA_01200 | F4PJNLW01A00V1 | CDS | 1013662 | 2727 | - | 0.302164 | |
g1089 | DLA_01201 | F4PJNLW01A00V1 | CDS | 1020294 | 3582 | + | 0.357063 | |
g109 | DLA_00127 | contig05409_1.exp | CDS | 257764 | 1800 | + | 0.276111 | |
g1090 | DLA_01202 | F4PJNLW01A00V1 | CDS | 1024145 | 489 | - | 0.327198 | |
g1091 | DLA_01205 | F4PJNLW01A00V1 | CDS | 1025608 | 480 | - | 0.408333 | |
g1092 | DLA_01206 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | F4PJNLW01A00V1 | CDS | 1027088 | 912 | + | 0.357456 |
g1093 | DLA_01208 | F4PJNLW01A00V1 | CDS | 1029214 | 396 | - | 0.30303 | |
g1094 | DLA_01210 | F4PJNLW01A00V1 | CDS | 1030016 | 585 | - | 0.382906 | |
g1095 | DLA_01211 | F4PJNLW01A00V1 | CDS | 1031188 | 1548 | + | 0.319767 | |
g1096 | DLA_01212 | F4PJNLW01A00V1 | CDS | 1033053 | 825 | + | 0.293333 | |
g1097 | DLA_01213 | F4PJNLW01A00V1 | CDS | 1034101 | 2148 | - | 0.366853 | |
g1098 | DLA_01214 | F4PJNLW01A00V1 | CDS | 1036723 | 1620 | - | 0.331481 | |
g1099 | DLA_01215 | F4PJNLW01A00V1 | CDS | 1038454 | 1191 | - | 0.345088 | |
g11 | DLA_00012 | contig05409_1.exp | CDS | 31937 | 660 | - | 0.301515 | |
g110 | DLA_00128 | contig05409_1.exp | CDS | 259639 | 1668 | - | 0.326739 | |
g1100 | DLA_01216 | F4PJNLW01A00V1 | CDS | 1040176 | 4545 | + | 0.345215 | |
g1101 | DLA_01217 | F4PJNLW01A00V1 | CDS | 1044962 | 4236 | + | 0.333333 | |
g1102 | DLA_01218 | F4PJNLW01A00V1 | CDS | 1049434 | 4431 | + | 0.331302 | |
g1103 | DLA_01219 | F4PJNLW01A00V1 | CDS | 1054121 | 1938 | - | 0.389061 | |
g1104 | DLA_01220 | catalyzes the reaction: 3-hydroxy-2-methylpropanoyl-CoA H2O CoA 3-hydroxy-2-methylpropanoate ortholog of the mammalian HIBCH enzyme | F4PJNLW01A00V1 | CDS | 1056585 | 1152 | - | 0.358507 |
g1105 | DLA_01221 | F4PJNLW01A00V1 | CDS | 1057888 | 1659 | + | 0.306811 | |
g1106 | DLA_01222 | F4PJNLW01A00V1 | CDS | 1059567 | 6933 | - | 0.300303 | |
g1107 | DLA_01224 | F4PJNLW01A00V1 | CDS | 1068083 | 6939 | - | 0.300331 | |
g1108 | DLA_01225 | F4PJNLW01A00V1 | CDS | 1075598 | 1473 | - | 0.285132 | |
g1109 | DLA_01226 | F4PJNLW01A00V1 | CDS | 1077570 | 1770 | + | 0.389266 | |
g111 | DLA_00129 | conserved in D. purpureum and P. pallidum contains 12 putative transmembrane domains C-terminal region similar to new-glue protein | contig05409_1.exp | CDS | 261669 | 2127 | - | 0.35402 |
g1110 | DLA_01227 | F4PJNLW01A00V1 | CDS | 1079405 | 1206 | - | 0.290216 | |
g1111 | DLA_01228 | F4PJNLW01A00V1 | CDS | 1080787 | 1110 | + | 0.311712 | |
g1112 | DLA_01229 | F4PJNLW01A00V1 | CDS | 1082234 | 2250 | - | 0.354222 | |
g1113 | DLA_01230 | F4PJNLW01A00V1 | CDS | 1086396 | 2109 | - | 0.308677 | |
g1114 | DLA_01231 | F4PJNLW01A00V1 | CDS | 1089808 | 2295 | + | 0.346405 | |
g1115 | DLA_01232 | F4PJNLW01A00V1 | CDS | 1092890 | 2142 | + | 0.332866 | |
g1116 | DLA_01233 | conserved protein of unknown function contains a putative signal peptide followed by a transmembrane domain | F4PJNLW01A00V1 | CDS | 1095509 | 222 | + | 0.396396 |
g1117 | DLA_01234 | F4PJNLW01A00V1 | CDS | 1096028 | 4542 | + | 0.337957 | |
g1118 | DLA_01235 | F4PJNLW01A00V1 | CDS | 1100695 | 1263 | - | 0.32304 | |
g1119 | DLA_01237 | F4PJNLW01A00V1 | CDS | 1102872 | 1176 | - | 0.320578 | |
g112 | DLA_00131 | contig05409_1.exp | CDS | 264691 | 3153 | + | 0.333333 | |
g1120 | DLA_01238 | F4PJNLW01A00V1 | CDS | 1105141 | 2157 | + | 0.364395 | |
g1121 | DLA_01239 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | F4PJNLW01A00V1 | CDS | 1108058 | 729 | + | 0.348422 |
g1122 | DLA_01240 | similar to D. purpureum protein contains one coiled-coil domain | F4PJNLW01A00V1 | CDS | 1109132 | 489 | - | 0.259714 |
g1123 | DLA_01241 | non-catalytic subunit of the AMP-activated protein kinase (AMPK) complex contains two CBS domains | F4PJNLW01A00V1 | CDS | 1109956 | 1629 | + | 0.333947 |
g1124 | DLA_01242 | F4PJNLW01A00V1 | CDS | 1111675 | 2160 | - | 0.307407 | |
g1125 | DLA_01243 | F4PJNLW01A00V1 | CDS | 1114056 | 4023 | - | 0.333333 | |
g1126 | DLA_11469 | F4PJNLW01A00V1 | CDS | 1118348 | 3996 | - | 0.318569 | |
g1127 | DLA_01244 | F4PJNLW01A00V1 | CDS | 1122642 | 4023 | - | 0.34079 | |
g1128 | DLA_01245 | F4PJNLW01A00V1 | CDS | 1127299 | 963 | - | 0.34891 | |
g1129 | DLA_01246 | F4PJNLW01A00V1 | CDS | 1128887 | 1311 | + | 0.334859 | |
g113 | DLA_00132 | contig05409_1.exp | CDS | 268227 | 543 | - | 0.289134 | |
g1130 | DLA_01247 | F4PJNLW01A00V1 | CDS | 1130542 | 1641 | + | 0.393053 | |
g1131 | DLA_01248 | F4PJNLW01A00V1 | CDS | 1132598 | 1683 | + | 0.382056 | |
g1132 | DLA_01249 | F4PJNLW01A00V1 | CDS | 1134624 | 1155 | + | 0.333333 | |
g1133 | DLA_01250 | F4PJNLW01A00V1 | CDS | 1135865 | 2100 | + | 0.345238 | |
g1134 | DLA_01251 | similar to the esterase encoded by | F4PJNLW01A00V1 | CDS | 1138000 | 1065 | - | 0.323005 |
g1135 | DLA_01252 | F4PJNLW01A00V1 | CDS | 1139362 | 1332 | - | 0.36036 | |
g1136 | DLA_01253 | F4PJNLW01A00V1 | CDS | 1141153 | 1866 | + | 0.338692 | |
g1137 | DLA_01255 | F4PJNLW01A00V1 | CDS | 1143780 | 1638 | + | 0.310745 | |
g1138 | DLA_01256 | F4PJNLW01A00V1 | CDS | 1145631 | 4023 | - | 0.323391 | |
g1139 | DLA_01257 | F4PJNLW01A00V1 | CDS | 1149950 | 1407 | - | 0.366027 | |
g114 | DLA_00133 | contig05409_1.exp | CDS | 269373 | 2523 | + | 0.328181 | |
g1140 | DLA_01258 | superoxide dismutase of the SOD1 family expressed at constant levels throughout the life cycle and upregulated upon oxidative stress enriched in prespore cells | F4PJNLW01A00V1 | CDS | 1151652 | 459 | - | 0.407407 |
g1141 | DLA_01259 | F4PJNLW01A00V1 | CDS | 1152403 | 1476 | - | 0.402439 | |
g1142 | DLA_01260 | homolog of mammalian Rab GDP dissociation inhibitor alpha forms a soluble complex with Rab proteins thereby preventing exchange of GDP for GTP | F4PJNLW01A00V1 | CDS | 1154536 | 1356 | + | 0.377581 |
g1143 | DLA_01261 | bifunctional enolase-phosphatase that cleaves the substrates 23-diketo-5-methylthio-1-phosphopentane and 2-hydroxy-3-keto-5-methylthio-1-phosphopentene | F4PJNLW01A00V1 | CDS | 1156181 | 801 | + | 0.330836 |
g1144 | DLA_01262 | F4PJNLW01A00V1 | CDS | 1157028 | 3807 | - | 0.353297 | |
g1145 | DLA_01263 | F4PJNLW01A00V1 | CDS | 1161441 | 261 | + | 0.398467 | |
g1146 | DLA_01264 | F4PJNLW01A00V1 | CDS | 1161847 | 1629 | - | 0.300184 | |
g1147 | DLA_01265 | F4PJNLW01A00V1 | CDS | 1163534 | 1497 | + | 0.281897 | |
g1148 | DLA_01266 | F4PJNLW01A00V1 | CDS | 1165064 | 1224 | - | 0.295752 | |
g1149 | DLA_01267 | F4PJNLW01A00V1 | CDS | 1167153 | 6837 | + | 0.346204 | |
g115 | DLA_00134 | contig05409_1.exp | CDS | 272244 | 2091 | + | 0.314682 | |
g1150 | DLA_11470 | F4PJNLW01A00V1 | CDS | 1174662 | 795 | + | 0.295597 | |
g1151 | DLA_01268 | F4PJNLW01A00V1 | CDS | 1176051 | 228 | - | 0.421053 | |
g1152 | DLA_01269 | F4PJNLW01A00V1 | CDS | 1177069 | 2502 | - | 0.323341 | |
g1153 | DLA_01270 | F4PJNLW01A00V1 | CDS | 1180005 | 4395 | - | 0.301479 | |
g1154 | DLA_01272 | F4PJNLW01A00V1 | CDS | 1185178 | 3942 | - | 0.341705 | |
g1155 | DLA_01273 | F4PJNLW01A00V1 | CDS | 1189694 | 2349 | + | 0.260962 | |
g1156 | DLA_01274 | F4PJNLW01A00V1 | CDS | 1192312 | 9372 | - | 0.330666 | |
g1157 | DLA_01275 | F4PJNLW01A00V1 | CDS | 1201874 | 1893 | - | 0.375066 | |
g1158 | DLA_01276 | F4PJNLW01A00V1 | CDS | 1204146 | 477 | + | 0.287212 | |
g1159 | DLA_01277 | F4PJNLW01A00V1 | CDS | 1205329 | 888 | - | 0.414414 | |
g116 | DLA_00136 | contig05409_1.exp | CDS | 277512 | 687 | + | 0.333333 | |
g1160 | DLA_01278 | F4PJNLW01A00V1 | CDS | 1207537 | 1776 | - | 0.377815 | |
g1161 | DLA_11471 | F4PJNLW01A00V1 | CDS | 1209647 | 3924 | - | 0.33104 | |
g1162 | DLA_01279 | F4PJNLW01A00V1 | CDS | 1214037 | 4026 | - | 0.328862 | |
g1163 | DLA_01280 | F4PJNLW01A00V1 | CDS | 1218879 | 3033 | + | 0.352456 | |
g1164 | DLA_01281 | F4PJNLW01A00V1 | CDS | 1221948 | 381 | - | 0.278215 | |
g1165 | DLA_01282 | F4PJNLW01A00V1 | CDS | 1222612 | 798 | + | 0.298246 | |
g1166 | DLA_01283 | F4PJNLW01A00V1 | CDS | 1223834 | 1074 | + | 0.296089 | |
g1167 | DLA_01284 | F4PJNLW01A00V1 | CDS | 1225330 | 4419 | - | 0.342838 | |
g1168 | DLA_01285 | F4PJNLW01A00V1 | CDS | 1231592 | 2397 | - | 0.380058 | |
g1169 | DLA_01286 | F4PJNLW01A00V1 | CDS | 1234840 | 2883 | - | 0.304544 | |
g117 | DLA_00137 | contig05409_1.exp | CDS | 279139 | 360 | + | 0.319444 | |
g1170 | DLA_01287 | C-terminus similar to Arabidopsis thaliana plant adhesion molecule 1 Drosophila melanogaster extracellular matrix adhesion protein Pollux and human rab6 GTPase activating protein GAPCENA | F4PJNLW01A00V1 | CDS | 1238303 | 1377 | + | 0.291213 |
g1171 | DLA_01288 | F4PJNLW01A00V1 | CDS | 1240312 | 1047 | - | 0.293219 | |
g1172 | DLA_01290 | F4PJNLW01A00V1 | CDS | 1243480 | 981 | + | 0.310907 | |
g1173 | DLA_01291 | F4PJNLW01A00V1 | CDS | 1244646 | 3147 | - | 0.307595 | |
g1174 | DLA_01292 | F4PJNLW01A00V1 | CDS | 1248592 | 477 | + | 0.312369 | |
g1175 | DLA_01293 | F4PJNLW01A00V1 | CDS | 1249088 | 1107 | + | 0.342367 | |
g1176 | DLA_01294 | F4PJNLW01A00V1 | CDS | 1250509 | 930 | + | 0.386021 | |
g1177 | DLA_01295 | F4PJNLW01A00V1 | CDS | 1251631 | 2424 | + | 0.314769 | |
g1178 | DLA_01296 | F4PJNLW01A00V1 | CDS | 1254097 | 3381 | - | 0.303461 | |
g1179 | DLA_01298 | F4PJNLW01A00V1 | CDS | 1258662 | 240 | + | 0.345833 | |
g118 | DLA_00139 | contig05409_1.exp | CDS | 281248 | 2517 | + | 0.309495 | |
g1180 | DLA_01299 | F4PJNLW01A00V1 | CDS | 1259286 | 897 | - | 0.362319 | |
g1181 | DLA_01300 | F4PJNLW01A00V1 | CDS | 1260850 | 1074 | - | 0.353817 | |
g1182 | DLA_01301 | F4PJNLW01A00V1 | CDS | 1264254 | 1569 | + | 0.290631 | |
g1183 | DLA_01302 | F4PJNLW01A00V1 | CDS | 1266312 | 1134 | - | 0.329806 | |
g1184 | DLA_01303 | F4PJNLW01A00V1 | CDS | 1268220 | 1251 | - | 0.366906 | |
g1185 | DLA_01304 | F4PJNLW01A00V1 | CDS | 1269820 | 4548 | + | 0.335972 | |
g1186 | DLA_01305 | F4PJNLW01A00V1 | CDS | 1274982 | 663 | + | 0.276018 | |
g1187 | DLA_01306 | F4PJNLW01A00V1 | CDS | 1275687 | 543 | - | 0.27256 | |
g1188 | DLA_01307 | F4PJNLW01A00V1 | CDS | 1276398 | 531 | - | 0.280603 | |
g1189 | DLA_01308 | F4PJNLW01A00V1 | CDS | 1277198 | 840 | + | 0.3 | |
g119 | DLA_00140 | contig05409_1.exp | CDS | 284072 | 360 | - | 0.302778 | |
g1190 | DLA_01309 | F4PJNLW01A00V1 | CDS | 1278322 | 2439 | + | 0.291923 | |
g1191 | DLA_01310 | F4PJNLW01A00V1 | CDS | 1281598 | 1455 | + | 0.320962 | |
g1192 | DLA_01311 | F4PJNLW01A00V1 | CDS | 1283081 | 1686 | - | 0.288849 | |
g1193 | DLA_01312 | F4PJNLW01A00V1 | CDS | 1285676 | 1476 | + | 0.347561 | |
g1194 | DLA_11472 | F4PJNLW01A00V1 | CDS | 1287578 | 1254 | + | 0.363636 | |
g1195 | DLA_01313 | F4PJNLW01A00V1 | CDS | 1289060 | 1809 | - | 0.297402 | |
g1196 | DLA_01314 | F4PJNLW01A00V1 | CDS | 1291700 | 1485 | + | 0.319865 | |
g1197 | DLA_01315 | F4PJNLW01A00V1 | CDS | 1293838 | 1179 | + | 0.308736 | |
g1198 | DLA_01317 | F4PJNLW01A00V1 | CDS | 1295821 | 2256 | + | 0.277926 | |
g1199 | DLA_01318 | F4PJNLW01A00V1 | CDS | 1298155 | 2430 | - | 0.310288 | |
g12 | DLA_00013 | contig05409_1.exp | CDS | 34321 | 3564 | + | 0.305556 | |
g120 | DLA_00141 | contig05409_1.exp | CDS | 284584 | 513 | + | 0.247563 | |
g1200 | DLA_01319 | F4PJNLW01A00V1 | CDS | 1300703 | 2397 | - | 0.285774 | |
g1201 | DLA_11473 | F4PJNLW01A00V1 | CDS | 1303164 | 2403 | - | 0.287973 | |
g1202 | DLA_01320 | F4PJNLW01A00V1 | CDS | 1305969 | 3759 | - | 0.3054 | |
g1203 | DLA_01321 | F4PJNLW01A00V1 | CDS | 1310522 | 621 | - | 0.380032 | |
g1204 | DLA_01322 | F4PJNLW01A00V1 | CDS | 1311871 | 774 | + | 0.316537 | |
g1205 | DLA_01323 | F4PJNLW01A00V1 | CDS | 1312839 | 1686 | - | 0.319098 | |
g1206 | DLA_01324 | F4PJNLW01A00V1 | CDS | 1314830 | 1323 | - | 0.30839 | |
g1207 | DLA_01325 | F4PJNLW01A00V1 | CDS | 1316373 | 2172 | - | 0.303867 | |
g1208 | DLA_01327 | F4PJNLW01A00V1 | CDS | 1319775 | 1596 | - | 0.285714 | |
g1209 | DLA_01329 | F4PJNLW01A00V1 | CDS | 1321589 | 1302 | - | 0.390169 | |
g121 | DLA_00142 | contig05409_1.exp | CDS | 285206 | 1227 | + | 0.323553 | |
g1210 | DLA_01330 | F4PJNLW01A00V1 | CDS | 1324138 | 3057 | - | 0.33366 | |
g1211 | DLA_01331 | F4PJNLW01A00V1 | CDS | 1328706 | 1299 | - | 0.321786 | |
g1212 | DLA_01334 | F4PJNLW01A00V1 | CDS | 1332509 | 666 | + | 0.280781 | |
g1213 | DLA_01335 | F4PJNLW01A00V1 | CDS | 1333407 | 3303 | - | 0.339691 | |
g1214 | DLA_01336 | F4PJNLW01A00V1 | CDS | 1337969 | 3510 | + | 0.335613 | |
g1215 | DLA_01337 | F4PJNLW01A00V1 | CDS | 1341753 | 5667 | - | 0.341803 | |
g1216 | DLA_01338 | F4PJNLW01A00V1 | CDS | 1347722 | 882 | - | 0.300454 | |
g1217 | DLA_01341 | F4PJNLW01A00V1 | CDS | 1349717 | 4146 | + | 0.285576 | |
g1218 | DLA_11474 | F4PJNLW01A00V1 | CDS | 1354366 | 630 | + | 0.365079 | |
g1219 | DLA_01342 | F4PJNLW01A00V1 | CDS | 1355274 | 1449 | - | 0.278813 | |
g122 | DLA_00143 | contig05409_1.exp | CDS | 286540 | 1053 | - | 0.309592 | |
g1220 | DLA_01343 | F4PJNLW01A00V1 | CDS | 1356994 | 2553 | - | 0.358402 | |
g1221 | DLA_01345 | F4PJNLW01A00V1 | CDS | 1361311 | 2187 | - | 0.34888 | |
g1222 | DLA_01346 | F4PJNLW01A00V1 | CDS | 1365312 | 1128 | + | 0.264184 | |
g1223 | DLA_01347 | F4PJNLW01A00V1 | CDS | 1366499 | 3003 | - | 0.298035 | |
g1224 | DLA_01348 | F4PJNLW01A00V1 | CDS | 1370261 | 2862 | + | 0.324249 | |
g1225 | DLA_01349 | F4PJNLW01A00V1 | CDS | 1374980 | 1335 | + | 0.301873 | |
g1226 | DLA_01350 | F4PJNLW01A00V1 | CDS | 1376663 | 435 | - | 0.416092 | |
g1227 | DLA_01351 | F4PJNLW01A00V1 | CDS | 1377733 | 1074 | - | 0.294227 | |
g1228 | DLA_01352 | F4PJNLW01A00V1 | CDS | 1379280 | 5112 | - | 0.333333 | |
g1229 | DLA_01353 | F4PJNLW01A00V1 | CDS | 1385049 | 1917 | + | 0.284298 | |
g123 | DLA_00144 | contig05409_1.exp | CDS | 287934 | 258 | - | 0.306202 | |
g1230 | DLA_01354 | F4PJNLW01A00V1 | CDS | 1387269 | 828 | + | 0.254831 | |
g1231 | DLA_01355 | F4PJNLW01A00V1 | CDS | 1389383 | 3114 | - | 0.274245 | |
g1232 | DLA_01356 | F4PJNLW01A00V1 | CDS | 1392693 | 3024 | - | 0.319775 | |
g1233 | DLA_01357 | F4PJNLW01A00V1 | CDS | 1396060 | 3738 | + | 0.266988 | |
g1234 | DLA_01358 | F4PJNLW01A00V1 | CDS | 1399984 | 1170 | + | 0.269231 | |
g1235 | DLA_11475 | F4PJNLW01A00V1 | CDS | 1401323 | 318 | - | 0.396226 | |
g1236 | DLA_01359 | protein serinethreonine kinase homologous to human Nek2 kinase involved in formation of microtubule-organizing centers (MTOCs) | F4PJNLW01A00V1 | CDS | 1401955 | 1134 | - | 0.308642 |
g1237 | DLA_01360 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H4 | F4PJNLW01A00V1 | CDS | 1403767 | 405 | + | 0.407407 |
g1238 | DLA_11476 | F4PJNLW01A00V1 | CDS | 1404591 | 942 | - | 0.323779 | |
g1239 | DLA_01361 | F4PJNLW01A00V1 | CDS | 1406049 | 3495 | - | 0.27382 | |
g124 | DLA_00145 | contig05409_1.exp | CDS | 288970 | 786 | + | 0.28117 | |
g1240 | DLA_01362 | putative Raptor protein ortholog a component of the TORC1 complex in yeasts with Lst8 and Tor does not co-immunoprecipitate with the TORC2 complex | F4PJNLW01A00V1 | CDS | 1410095 | 4344 | + | 0.350138 |
g1241 | DLA_01363 | F4PJNLW01A00V1 | CDS | 1415103 | 288 | + | 0.288194 | |
g1242 | DLA_01364 | F4PJNLW01A00V1 | CDS | 1415616 | 2718 | - | 0.278146 | |
g1243 | DLA_01365 | F4PJNLW01A00V1 | CDS | 1418602 | 504 | + | 0.257937 | |
g1244 | DLA_01366 | F4PJNLW01A00V1 | CDS | 1419396 | 3018 | + | 0.32273 | |
g1245 | DLA_01367 | F4PJNLW01A00V1 | CDS | 1422505 | 924 | - | 0.238095 | |
g1246 | DLA_01368 | F4PJNLW01A00V1 | CDS | 1424016 | 1647 | + | 0.298118 | |
g1247 | DLA_01369 | F4PJNLW01A00V1 | CDS | 1425667 | 2325 | - | 0.304086 | |
g1248 | DLA_01371 | conserved eukaryotic protein of unknown function ortholog of human SPATA20 (spermatogenesis associated 20) | F4PJNLW01A00V1 | CDS | 1428424 | 2304 | + | 0.311632 |
g1249 | DLA_01372 | similar to N-myc downstream regulated gene 1 (NDRG1) defects in NDRG1 are the cause of Charcot-Marie-Tooth disease type 4D (CMT4D) also known as hereditary motor and sensory neuropathy Lom type (HMSNL) | F4PJNLW01A00V1 | CDS | 1430927 | 1035 | - | 0.311111 |
g125 | DLA_00146 | contig05409_1.exp | CDS | 289893 | 1992 | - | 0.314257 | |
g1250 | DLA_01373 | similar to mammalian Nup54 component of the nuclear pore complex | F4PJNLW01A00V1 | CDS | 1432426 | 1329 | + | 0.327314 |
g1251 | DLA_01374 | members of this family are membrane proteins involved in long chain fatty acid elongation systems that produce 26-carbon precursors for ceramide and sphingolipid synthesis contains 7 putative transmembrane domains | F4PJNLW01A00V1 | CDS | 1434114 | 816 | + | 0.295343 |
g1252 | DLA_01375 | F4PJNLW01A00V1 | CDS | 1435351 | 843 | + | 0.301305 | |
g1253 | DLA_01376 | F4PJNLW01A00V1 | CDS | 1436456 | 330 | + | 0.381818 | |
g1254 | DLA_01377 | ortholog of human TSN DNA-binding protein that specifically recognizes consensus sequences at the breakpoint junctions in chromosomal translocations interacts with translin-associated protein X (TSNAX) | F4PJNLW01A00V1 | CDS | 1437077 | 714 | - | 0.2493 |
g1255 | DLA_01378 | F4PJNLW01A00V1 | CDS | 1438955 | 1689 | + | 0.281824 | |
g1256 | DLA_01379 | ortholog of the human CPSF2 and yeast CFT2 the 100 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs | F4PJNLW01A00V1 | CDS | 1441091 | 2268 | + | 0.307319 |
g1257 | DLA_01380 | F4PJNLW01A00V1 | CDS | 1443542 | 297 | - | 0.208754 | |
g1258 | DLA_01381 | F4PJNLW01A00V1 | CDS | 1444033 | 1494 | + | 0.281125 | |
g1259 | DLA_01382 | F4PJNLW01A00V1 | CDS | 1445702 | 1614 | - | 0.257745 | |
g126 | DLA_00147 | contig05409_1.exp | CDS | 292124 | 1776 | + | 0.315878 | |
g1260 | DLA_01383 | F4PJNLW01A00V1 | CDS | 1447566 | 1953 | - | 0.321557 | |
g1261 | DLA_01384 | F4PJNLW01A00V1 | CDS | 1450299 | 2781 | + | 0.385113 | |
g1262 | DLA_01385 | catalyzes the reaction (S)-3-(5-oxo-45-dihydro-3H-imidazol-4-yl)propanoate H2O N-formimidoyl-L-glutamate H | F4PJNLW01A00V1 | CDS | 1453545 | 1272 | + | 0.30739 |
g1263 | DLA_01386 | F4PJNLW01A00V1 | CDS | 1455017 | 978 | - | 0.282209 | |
g1264 | DLA_01388 | F4PJNLW01A00V1 | CDS | 1456550 | 3531 | + | 0.34013 | |
g1265 | DLA_01389 | belongs to a family of short proteins that includes proteins from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | F4PJNLW01A00V1 | CDS | 1460431 | 417 | - | 0.263789 |
g1266 | DLA_01390 | F4PJNLW01A00V1 | CDS | 1460970 | 1641 | + | 0.255332 | |
g1267 | DLA_01391 | F4PJNLW01A00V1 | CDS | 1462912 | 306 | - | 0.323529 | |
g1268 | DLA_01392 | F4PJNLW01A00V1 | CDS | 1463356 | 258 | - | 0.321705 | |
g1269 | DLA_01393 | F4PJNLW01A00V1 | CDS | 1463729 | 489 | - | 0.345603 | |
g127 | DLA_00148 | contig05409_1.exp | CDS | 294372 | 1056 | + | 0.329545 | |
g1270 | DLA_01395 | F4PJNLW01AQJ8S | CDS | 2 | 2664 | + | 0.265766 | |
g1271 | DLA_01396 | F4PJNLW01AQJ8S | CDS | 2795 | 2436 | - | 0.296388 | |
g1272 | DLA_11477 | F4PJNLW01AQJ8S | CDS | 6002 | 1971 | - | 0.307965 | |
g1273 | DLA_01397 | F4PJNLW01AQJ8S | CDS | 8325 | 624 | + | 0.338141 | |
g1274 | DLA_01398 | F4PJNLW01AQJ8S | CDS | 9660 | 1632 | + | 0.346814 | |
g1275 | DLA_01399 | F4PJNLW01AQJ8S | CDS | 11318 | 1299 | - | 0.287914 | |
g1276 | DLA_01400 | F4PJNLW01AQJ8S | CDS | 13128 | 1530 | - | 0.280392 | |
g1277 | DLA_01401 | F4PJNLW01AQJ8S | CDS | 15539 | 732 | + | 0.304645 | |
g1278 | DLA_01402 | F4PJNLW01AQJ8S | CDS | 16490 | 1128 | - | 0.317376 | |
g1279 | DLA_01403 | F4PJNLW01AQJ8S | CDS | 17894 | 10575 | + | 0.33078 | |
g128 | DLA_00149 | contig05409_1.exp | CDS | 295611 | 1377 | - | 0.309368 | |
g1280 | DLA_01404 | F4PJNLW01AQJ8S | CDS | 29028 | 1035 | + | 0.26087 | |
g1281 | DLA_01405 | F4PJNLW01AQJ8S | CDS | 30630 | 1047 | + | 0.30659 | |
g1282 | DLA_01406 | F4PJNLW01AQJ8S | CDS | 31744 | 1515 | - | 0.316172 | |
g1283 | DLA_01407 | F4PJNLW01AQJ8S | CDS | 34223 | 483 | + | 0.399586 | |
g1284 | DLA_01408 | F4PJNLW01AQJ8S | CDS | 35153 | 2337 | + | 0.32392 | |
g1285 | DLA_01409 | contains two EF hands very similar to Dictyostelium cbpK and cbpJ belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | F4PJNLW01AQJ8S | CDS | 37683 | 564 | + | 0.267731 |
g1286 | DLA_01410 | ortholog of Cln5 implicated in neuronal ceroid lipofuscinoses neurodegenerative disorders | F4PJNLW01AQJ8S | CDS | 38575 | 993 | + | 0.294058 |
g1287 | DLA_01411 | F4PJNLW01AQJ8S | CDS | 39766 | 495 | - | 0.262626 | |
g1288 | DLA_01412 | F4PJNLW01AQJ8S | CDS | 40617 | 462 | + | 0.296537 | |
g1289 | DLA_01413 | F4PJNLW01AQJ8S | CDS | 41380 | 936 | + | 0.299145 | |
g129 | DLA_00150 | contig05409_1.exp | CDS | 297512 | 885 | + | 0.319774 | |
g1290 | DLA_01414 | F4PJNLW01AQJ8S | CDS | 42441 | 2205 | - | 0.292517 | |
g1291 | DLA_01415 | F4PJNLW01B0TO9 | CDS | 1 | 83 | - | 0.39759 | |
g1292 | DLA_01416 | F4PJNLW01B0TO9 | CDS | 2648 | 1572 | - | 0.32888 | |
g1293 | DLA_01417 | F4PJNLW01B0TO9 | CDS | 5096 | 2721 | - | 0.309078 | |
g1294 | DLA_01418 | F4PJNLW01B0TO9 | CDS | 9018 | 1125 | + | 0.251556 | |
g1295 | DLA_01419 | F4PJNLW01B0TO9 | CDS | 10521 | 5238 | - | 0.342879 | |
g1296 | DLA_01420 | catalyzes the reaction ATP L-serine tRNASer AMP diphosphate L-seryl-tRNASer | F4PJNLW01B0TO9 | CDS | 16238 | 1449 | - | 0.309869 |
g1297 | DLA_11478 | F4PJNLW01B0TO9 | CDS | 18118 | 1587 | - | 0.327032 | |
g1298 | DLA_01421 | F4PJNLW01B0TO9 | CDS | 20012 | 498 | - | 0.317269 | |
g1299 | DLA_01423 | F4PJNLW01B0TO9 | CDS | 21081 | 1455 | - | 0.316838 | |
g13 | DLA_00015 | contig05409_1.exp | CDS | 39192 | 2106 | - | 0.353276 | |
g130 | DLA_00151 | contig05409_1.exp | CDS | 298981 | 2394 | - | 0.327485 | |
g1300 | DLA_01424 | F4PJNLW01B0TO9 | CDS | 23049 | 2097 | - | 0.322842 | |
g1301 | DLA_01425 | F4PJNLW01B0TO9 | CDS | 25300 | 834 | + | 0.229017 | |
g1302 | DLA_01426 | putative protein serinethreonine kinase the kinase domain is similar to mitogen-activated protein kinases and other STE20-like kinases stress-responsive kinase | F4PJNLW01B0TO9 | CDS | 27222 | 3570 | + | 0.333333 |
g1303 | DLA_01427 | ortholog of human SNRP70 a component of the U1 snRNP involved in mRNA splicing | F4PJNLW01B0TO9 | CDS | 31307 | 1116 | - | 0.342294 |
g1304 | DLA_01428 | F4PJNLW01B0TO9 | CDS | 32748 | 1299 | + | 0.362587 | |
g1305 | DLA_01429 | F4PJNLW01B0TO9 | CDS | 34128 | 2535 | + | 0.292308 | |
g1306 | DLA_01430 | F4PJNLW01B0TO9 | CDS | 36834 | 507 | - | 0.333333 | |
g1307 | DLA_01431 | component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) | F4PJNLW01B0TO9 | CDS | 37582 | 798 | - | 0.39599 |
g1308 | DLA_01432 | F4PJNLW01B0TO9 | CDS | 38853 | 2277 | - | 0.34036 | |
g1309 | DLA_01433 | F4PJNLW01B0TO9 | CDS | 41357 | 2292 | - | 0.323735 | |
g131 | DLA_00152 | contig05409_1.exp | CDS | 301614 | 885 | + | 0.302825 | |
g1310 | DLA_01434 | F4PJNLW01B0TO9 | CDS | 44114 | 1947 | + | 0.280431 | |
g1311 | DLA_01435 | F4PJNLW01B0TO9 | CDS | 46182 | 624 | - | 0.323718 | |
g1312 | DLA_01436 | F4PJNLW01B0TO9 | CDS | 47088 | 1335 | - | 0.260674 | |
g1313 | DLA_01437 | F4PJNLW01B0TO9 | CDS | 48608 | 2238 | + | 0.289991 | |
g1314 | DLA_01439 | F4PJNLW01B0TO9 | CDS | 51975 | 2796 | - | 0.298999 | |
g1315 | DLA_01440 | F4PJNLW01B0TO9 | CDS | 55272 | 2004 | - | 0.284431 | |
g1316 | DLA_11479 | F4PJNLW01B0TO9 | CDS | 57722 | 414 | + | 0.292271 | |
g1317 | DLA_01441 | F4PJNLW01B0TO9 | CDS | 58548 | 408 | + | 0.264706 | |
g1318 | DLA_01442 | F4PJNLW01B0TO9 | CDS | 59147 | 924 | + | 0.277056 | |
g1319 | DLA_01443 | F4PJNLW01B0TO9 | CDS | 60158 | 1917 | - | 0.337507 | |
g132 | DLA_00153 | contig05409_1.exp | CDS | 302743 | 2898 | + | 0.320566 | |
g1320 | DLA_01444 | F4PJNLW01B0TO9 | CDS | 62333 | 2799 | + | 0.287603 | |
g1321 | DLA_01445 | F4PJNLW01B0TO9 | CDS | 65460 | 1047 | + | 0.332378 | |
g1322 | DLA_01446 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | F4PJNLW01B0TO9 | CDS | 66765 | 1326 | - | 0.33635 |
g1323 | DLA_01447 | F4PJNLW01B0TO9 | CDS | 68822 | 3231 | - | 0.276695 | |
g1324 | DLA_01449 | F4PJNLW01B0TO9 | CDS | 73279 | 321 | + | 0.339564 | |
g1325 | DLA_01450 | F4PJNLW01B0TO9 | CDS | 74271 | 1605 | - | 0.286604 | |
g1326 | DLA_01452 | F4PJNLW01B0TO9 | CDS | 76843 | 4308 | + | 0.333798 | |
g1327 | DLA_01455 | F4PJNLW01B0TO9 | CDS | 82616 | 1293 | + | 0.398299 | |
g1328 | DLA_01456 | F4PJNLW01B0TO9 | CDS | 84564 | 1053 | + | 0.325736 | |
g1329 | DLA_01457 | F4PJNLW01B0TO9 | CDS | 86426 | 414 | + | 0.326087 | |
g133 | DLA_00154 | contig05409_1.exp | CDS | 306074 | 3099 | + | 0.363343 | |
g1330 | DLA_01460 | F4PJNLW01B0TO9 | CDS | 89637 | 1068 | + | 0.292135 | |
g1331 | DLA_01461 | F4PJNLW01B0TO9 | CDS | 90919 | 894 | - | 0.313199 | |
g1332 | DLA_01462 | F4PJNLW01B0TO9 | CDS | 92167 | 1032 | + | 0.300388 | |
g1333 | DLA_01463 | F4PJNLW01B0TO9 | CDS | 93373 | 3069 | - | 0.325187 | |
g1334 | DLA_01464 | F4PJNLW01B0TO9 | CDS | 97452 | 3108 | - | 0.335586 | |
g1335 | DLA_01465 | F4PJNLW01B0TO9 | CDS | 102277 | 1482 | + | 0.32726 | |
g1336 | DLA_01466 | F4PJNLW01B0TO9 | CDS | 104792 | 4062 | + | 0.339734 | |
g1337 | DLA_01467 | F4PJNLW01B0TO9 | CDS | 109233 | 1242 | + | 0.250403 | |
g1338 | DLA_01468 | F4PJNLW01B0TO9 | CDS | 110827 | 1110 | + | 0.328829 | |
g1339 | DLA_11480 | F4PJNLW01B0TO9 | CDS | 112526 | 381 | + | 0.278215 | |
g134 | DLA_00155 | contig05409_1.exp | CDS | 309545 | 1353 | - | 0.342203 | |
g1340 | DLA_01469 | F4PJNLW01B0TO9 | CDS | 113058 | 3435 | - | 0.324309 | |
g1341 | DLA_01470 | F4PJNLW01B0TO9 | CDS | 117230 | 1134 | + | 0.335097 | |
g1342 | DLA_01471 | F4PJNLW01B0TO9 | CDS | 118581 | 2379 | - | 0.332913 | |
g1343 | DLA_01472 | F4PJNLW01B0TO9 | CDS | 122449 | 4404 | + | 0.311081 | |
g1344 | DLA_01473 | F4PJNLW01B0TO9 | CDS | 127065 | 2085 | - | 0.30024 | |
g1345 | DLA_01474 | F4PJNLW01B0TO9 | CDS | 129905 | 429 | - | 0.41958 | |
g1346 | DLA_01475 | F4PJNLW01B0TO9 | CDS | 131246 | 558 | + | 0.306452 | |
g1347 | DLA_01476 | F4PJNLW01B0TO9 | CDS | 132115 | 2451 | - | 0.367197 | |
g1348 | DLA_01478 | putative protein serinethreonine kinase GSK family member of the CMGC kinase group similar to Drosophila shaggy and other glycogen synthase kinases | F4PJNLW01B0TO9 | CDS | 135859 | 1329 | - | 0.346877 |
g1349 | DLA_01479 | F4PJNLW01B0TO9 | CDS | 139727 | 2079 | + | 0.247715 | |
g135 | DLA_00156 | contig05409_1.exp | CDS | 311305 | 1410 | - | 0.36383 | |
g1350 | DLA_01480 | F4PJNLW01B0TO9 | CDS | 142358 | 2505 | - | 0.343713 | |
g1351 | DLA_01481 | F4PJNLW01B0TO9 | CDS | 145220 | 2124 | + | 0.275895 | |
g1352 | DLA_01482 | F4PJNLW01B0TO9 | CDS | 147432 | 903 | - | 0.305648 | |
g1353 | DLA_01483 | F4PJNLW01B0TO9 | CDS | 148844 | 576 | + | 0.272569 | |
g1354 | DLA_01484 | F4PJNLW01B0TO9 | CDS | 149734 | 3606 | - | 0.344981 | |
g1355 | DLA_01485 | F4PJNLW01B0TO9 | CDS | 153910 | 441 | - | 0.278912 | |
g1356 | DLA_01486 | F4PJNLW01B0TO9 | CDS | 154737 | 381 | + | 0.272966 | |
g1357 | DLA_01487 | F4PJNLW01B0TO9 | CDS | 155592 | 3951 | + | 0.370286 | |
g1358 | DLA_01488 | F4PJNLW01B0TO9 | CDS | 159821 | 1482 | + | 0.313765 | |
g1359 | DLA_01489 | F4PJNLW01B0TO9 | CDS | 162179 | 2442 | + | 0.379607 | |
g136 | DLA_00157 | contig05409_1.exp | CDS | 313401 | 3300 | + | 0.308182 | |
g1360 | DLA_01490 | F4PJNLW01B0TO9 | CDS | 164849 | 1917 | - | 0.288993 | |
g1361 | DLA_01491 | F4PJNLW01B0TO9 | CDS | 167175 | 1017 | - | 0.336283 | |
g1362 | DLA_01494 | F4PJNLW01B0TO9 | CDS | 171521 | 1596 | - | 0.358396 | |
g1363 | DLA_01495 | F4PJNLW01B0TO9 | CDS | 174884 | 1767 | + | 0.283531 | |
g1364 | DLA_01496 | F4PJNLW01B0TO9 | CDS | 176722 | 336 | - | 0.291667 | |
g1365 | DLA_01497 | F4PJNLW01B0TO9 | CDS | 177420 | 879 | + | 0.260523 | |
g1366 | DLA_01498 | F4PJNLW01B0TO9 | CDS | 178526 | 729 | - | 0.323731 | |
g1367 | DLA_01499 | ortholog of human NIF3L1 belongs to the UPF0135 (NIF3) family | F4PJNLW01B0TO9 | CDS | 179414 | 1068 | + | 0.33427 |
g1368 | DLA_01500 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | F4PJNLW01B0TO9 | CDS | 180785 | 1050 | + | 0.344762 |
g1369 | DLA_01501 | F4PJNLW01B0TO9 | CDS | 182304 | 753 | - | 0.310757 | |
g137 | DLA_00159 | contig05409_1.exp | CDS | 317672 | 6033 | + | 0.34129 | |
g1370 | DLA_01502 | component of the conserved Paf1 complex a multifunctional complex involved in histone methylation and plays a role in RNA elongation and processing | F4PJNLW01B0TO9 | CDS | 183338 | 1458 | - | 0.325789 |
g1371 | DLA_01503 | similar to human ARMC1 contains an ARM repeat ARM-repeat proteins are involved in various processes including intracellular signalling and cytoskeletal regulation | F4PJNLW01B0TO9 | CDS | 185794 | 909 | - | 0.331133 |
g1372 | DLA_01504 | F4PJNLW01B0TO9 | CDS | 187154 | 1209 | + | 0.293631 | |
g1373 | DLA_01505 | F4PJNLW01B0TO9 | CDS | 188605 | 4566 | - | 0.318003 | |
g1374 | DLA_01506 | F4PJNLW01B0TO9 | CDS | 194077 | 870 | + | 0.371264 | |
g1375 | DLA_01507 | ortholog of the human TRM61 and yeast GCD14 which catalyzes the formation of N(1)-methyladenine at position 58 (m1A58) in initiator methionyl-tRNA as a heterodimer with | F4PJNLW01B0TO9 | CDS | 195322 | 999 | - | 0.344344 |
g1376 | DLA_01508 | F4PJNLW01B0TO9 | CDS | 196432 | 1554 | + | 0.346847 | |
g1377 | DLA_01509 | F4PJNLW01B0TO9 | CDS | 198101 | 1884 | + | 0.295117 | |
g1378 | DLA_01511 | F4PJNLW01B0TO9 | CDS | 200578 | 2850 | - | 0.342807 | |
g1379 | DLA_01512 | F4PJNLW01B0TO9 | CDS | 203975 | 489 | - | 0.310838 | |
g138 | DLA_00160 | contig05409_1.exp | CDS | 323852 | 1086 | - | 0.282689 | |
g1380 | DLA_01514 | F4PJNLW01B0TO9 | CDS | 207101 | 1596 | + | 0.356516 | |
g1381 | DLA_01516 | F4PJNLW01B0TO9 | CDS | 208889 | 2067 | - | 0.253024 | |
g1382 | DLA_01517 | F4PJNLW01B0TO9 | CDS | 211173 | 438 | - | 0.326484 | |
g1383 | DLA_01518 | F4PJNLW01B0TO9 | CDS | 213267 | 231 | - | 0.324675 | |
g1384 | DLA_01519 | F4PJNLW01B0TO9 | CDS | 213764 | 1866 | - | 0.327974 | |
g1385 | DLA_01522 | F4PJNLW01B0TO9 | CDS | 216654 | 1293 | + | 0.266821 | |
g1386 | DLA_01523 | F4PJNLW01B0TO9 | CDS | 218147 | 1566 | + | 0.36143 | |
g1387 | DLA_11481 | F4PJNLW01B0TO9 | CDS | 220295 | 465 | + | 0.378495 | |
g1388 | DLA_01524 | F4PJNLW01B0TO9 | CDS | 221656 | 1332 | + | 0.293544 | |
g1389 | DLA_01525 | F4PJNLW01B0TO9 | CDS | 223167 | 1524 | + | 0.319554 | |
g139 | DLA_00161 | contig05409_1.exp | CDS | 325256 | 1395 | - | 0.314695 | |
g1390 | DLA_01526 | F4PJNLW01B0TO9 | CDS | 224832 | 1491 | + | 0.309859 | |
g1391 | DLA_01527 | F4PJNLW01B0TO9 | CDS | 226452 | 1863 | - | 0.328502 | |
g1392 | DLA_01528 | conserved peptidyl-prolyl isomerase and WD repeat-containing protein that might be involved in pre-mRNA processing peptidyl-prolyl cis-trans isomerase (PPIase) accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | F4PJNLW01B0TO9 | CDS | 229497 | 2022 | - | 0.335312 |
g1393 | DLA_01529 | catalyzes the reaction oxaloacetate L-glutamate L-aspartate | F4PJNLW01B0TO9 | CDS | 232161 | 1260 | + | 0.39127 |
g1394 | DLA_01530 | F4PJNLW01B0TO9 | CDS | 233524 | 1155 | - | 0.283117 | |
g1395 | DLA_01532 | F4PJNLW01B0TO9 | CDS | 235011 | 1656 | + | 0.277778 | |
g1396 | DLA_01533 | F4PJNLW01B0TO9 | CDS | 237574 | 1281 | + | 0.263076 | |
g1397 | DLA_01534 | F4PJNLW01B0TO9 | CDS | 239439 | 714 | - | 0.313726 | |
g1398 | DLA_01535 | ortholog of the conserved CDC45 or CDC45L protein in S. cerevisiae and S. pombe required for initiation of chromosomal DNA replication | F4PJNLW01B0TO9 | CDS | 240373 | 1866 | + | 0.311897 |
g1399 | DLA_01536 | atypical protein serinethreonine kinase contains ABC1 kinase (protein kinase-like) domain yeast ABC1 essential for the electron transfer in the BC(1) complex E.coli homolog required for ubiquinone biosynthesis | F4PJNLW01B0TO9 | CDS | 242348 | 1971 | - | 0.320142 |
g14 | DLA_00016 | contig05409_1.exp | CDS | 41701 | 774 | + | 0.29199 | |
g140 | DLA_00163 | contig05409_1.exp | CDS | 327309 | 2994 | + | 0.327321 | |
g1400 | DLA_01537 | F4PJNLW01B0TO9 | CDS | 245573 | 609 | - | 0.297209 | |
g1401 | DLA_01538 | F4PJNLW01B0TO9 | CDS | 246367 | 579 | - | 0.284974 | |
g1402 | DLA_01539 | F4PJNLW01B0TO9 | CDS | 247309 | 1005 | - | 0.340299 | |
g1403 | DLA_01540 | F4PJNLW01B0TO9 | CDS | 248661 | 771 | + | 0.367056 | |
g1404 | DLA_01541 | F4PJNLW01B0TO9 | CDS | 249679 | 669 | + | 0.31988 | |
g1405 | DLA_11482 | F4PJNLW01B0TO9 | CDS | 250482 | 1833 | - | 0.371522 | |
g1406 | DLA_01542 | F4PJNLW01B0TO9 | CDS | 252501 | 2013 | - | 0.324888 | |
g1407 | DLA_01543 | F4PJNLW01B0TO9 | CDS | 255378 | 4923 | - | 0.34288 | |
g1408 | DLA_01544 | F4PJNLW01B0TO9 | CDS | 260575 | 1464 | - | 0.383197 | |
g1409 | DLA_01545 | F4PJNLW01B0TO9 | CDS | 262242 | 1941 | + | 0.327666 | |
g141 | DLA_00164 | contig05409_1.exp | CDS | 330453 | 939 | - | 0.369542 | |
g1410 | DLA_01546 | component of the multisubunit transcription elongation factor NELF human TH1 interacts with A-Raf | F4PJNLW01B0TO9 | CDS | 264283 | 1710 | - | 0.307602 |
g1411 | DLA_01547 | F4PJNLW01B0TO9 | CDS | 266367 | 1086 | + | 0.279006 | |
g1412 | DLA_01548 | F4PJNLW01B0TO9 | CDS | 267639 | 714 | - | 0.2507 | |
g1413 | DLA_01549 | AGC group AKT family protein serinethreonine kinase similar to other metazoan AktPKB including an N-terminal PH domain homologous kinase and C-terminal regulatory domains and phosphorylation sites required for AktPKB activation | F4PJNLW01B0TO9 | CDS | 268569 | 1326 | - | 0.36727 |
g1414 | DLA_01550 | F4PJNLW01B0TO9 | CDS | 270747 | 1638 | + | 0.310745 | |
g1415 | DLA_01551 | F4PJNLW01B0TO9 | CDS | 272445 | 3360 | - | 0.285714 | |
g1416 | DLA_01553 | F4PJNLW01B0TO9 | CDS | 276262 | 1869 | + | 0.321027 | |
g1417 | DLA_01554 | F4PJNLW01B0TO9 | CDS | 278155 | 1620 | - | 0.312963 | |
g1418 | DLA_01555 | F4PJNLW01B0TO9 | CDS | 280229 | 2391 | + | 0.323296 | |
g1419 | DLA_01556 | fatty acid synthases catalyze the formation of long-chain fatty acids from acetyl-CoA malonyl-CoA and NADPH multifunctional protein with several catalytic activities and an acyl carrier protein enriched in gametes | F4PJNLW01B0TO9 | CDS | 283876 | 7014 | + | 0.329199 |
g142 | DLA_00165 | contig05409_1.exp | CDS | 332861 | 1857 | + | 0.325256 | |
g1420 | DLA_01557 | F4PJNLW01B0TO9 | CDS | 291336 | 1098 | + | 0.318761 | |
g1421 | DLA_01558 | F4PJNLW01B0TO9 | CDS | 292442 | 2073 | - | 0.2904 | |
g1422 | DLA_01559 | F4PJNLW01B0TO9 | CDS | 295022 | 765 | + | 0.287582 | |
g1423 | DLA_01560 | delta subunit of the coatomer complex involved in intracellular protein transport ortholog of human ARCN1 (COPD) | F4PJNLW01B0TO9 | CDS | 296122 | 1557 | - | 0.374438 |
g1424 | DLA_01561 | F4PJNLW01B0TO9 | CDS | 298162 | 1635 | + | 0.307034 | |
g1425 | DLA_01563 | belongs to a family of short proteins that includes proteins from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | F4PJNLW01B0TO9 | CDS | 301816 | 390 | - | 0.287179 |
g1426 | DLA_01564 | F4PJNLW01B0TO9 | CDS | 302361 | 1191 | + | 0.29555 | |
g1427 | DLA_01565 | F4PJNLW01B0TO9 | CDS | 304082 | 1884 | + | 0.309448 | |
g1428 | DLA_01566 | F4PJNLW01B0TO9 | CDS | 306077 | 1953 | - | 0.296979 | |
g1429 | DLA_01568 | F4PJNLW01B0TO9 | CDS | 308393 | 876 | - | 0.308219 | |
g143 | DLA_00166 | contig05409_1.exp | CDS | 335204 | 2232 | + | 0.37052 | |
g1430 | DLA_01570 | F4PJNLW01B0TO9 | CDS | 309827 | 1125 | + | 0.327111 | |
g1431 | DLA_01571 | F4PJNLW01B0TO9 | CDS | 311263 | 1335 | - | 0.28764 | |
g1432 | DLA_01573 | F4PJNLW01B0TO9 | CDS | 313828 | 4137 | + | 0.323664 | |
g1433 | DLA_01574 | F4PJNLW01B0TO9 | CDS | 318154 | 2289 | + | 0.294015 | |
g1434 | DLA_01575 | F4PJNLW01B0TO9 | CDS | 320553 | 1359 | + | 0.290655 | |
g1435 | DLA_01577 | belongs to the metallophosphoesterase superfamily similar to human PAPL (Ironzinc purple acid phosphatase-like protein) contains a predicted signal peptide | F4PJNLW01B0TO9 | CDS | 323050 | 3855 | - | 0.323735 |
g1436 | DLA_01578 | F4PJNLW01B0TO9 | CDS | 328700 | 1422 | + | 0.30872 | |
g1437 | DLA_01579 | F4PJNLW01B0TO9 | CDS | 330329 | 1296 | - | 0.310957 | |
g1438 | DLA_01580 | F4PJNLW01B0TO9 | CDS | 332197 | 2361 | + | 0.322321 | |
g1439 | DLA_01581 | F4PJNLW01B0TO9 | CDS | 334837 | 3507 | - | 0.358711 | |
g144 | DLA_00167 | contig05409_1.exp | CDS | 337749 | 2379 | - | 0.349306 | |
g1440 | DLA_01582 | F4PJNLW01B0TO9 | CDS | 339269 | 396 | - | 0.318182 | |
g1441 | DLA_01583 | F4PJNLW01B0TO9 | CDS | 339799 | 954 | + | 0.353249 | |
g1442 | DLA_01584 | F4PJNLW01B0TO9 | CDS | 341817 | 1674 | + | 0.305257 | |
g1443 | DLA_01586 | F4PJNLW01B0TO9 | CDS | 344464 | 1218 | + | 0.307061 | |
g1444 | DLA_01588 | F4PJNLW01B0TO9 | CDS | 346492 | 5829 | - | 0.36713 | |
g1445 | DLA_01589 | delta subunit of the central stalk of mitochondrial F1F0 ATP synthase the enzyme complex responsible for ATP synthesis | F4PJNLW01B0TO9 | CDS | 352891 | 522 | - | 0.35249 |
g1446 | DLA_01590 | F4PJNLW01B0TO9 | CDS | 353534 | 1419 | - | 0.262861 | |
g1447 | DLA_01591 | F4PJNLW01B0TO9 | CDS | 355198 | 1014 | + | 0.29783 | |
g1448 | DLA_01592 | F4PJNLW01B0TO9 | CDS | 356262 | 3189 | - | 0.288492 | |
g1449 | DLA_01593 | F4PJNLW01B0TO9 | CDS | 359947 | 2133 | - | 0.339428 | |
g145 | DLA_00169 | contig05409_1.exp | CDS | 342380 | 2388 | + | 0.319514 | |
g1450 | DLA_01594 | F4PJNLW01B0TO9 | CDS | 362413 | 2190 | - | 0.324201 | |
g1451 | DLA_01595 | F4PJNLW01B0TO9 | CDS | 365031 | 2124 | - | 0.34887 | |
g1452 | DLA_11483 | F4PJNLW01B0TO9 | CDS | 367593 | 1818 | - | 0.363586 | |
g1453 | DLA_01596 | F4PJNLW01B0TO9 | CDS | 370676 | 2817 | + | 0.376997 | |
g1454 | DLA_01597 | F4PJNLW01B0TO9 | CDS | 373793 | 624 | - | 0.291667 | |
g1455 | DLA_01598 | F4PJNLW01B0TO9 | CDS | 374921 | 1086 | + | 0.303867 | |
g1456 | DLA_01599 | F4PJNLW01B0TO9 | CDS | 376074 | 1890 | - | 0.346561 | |
g1457 | DLA_01600 | F4PJNLW01B0TO9 | CDS | 378823 | 483 | - | 0.397516 | |
g1458 | DLA_01601 | F4PJNLW01B0TO9 | CDS | 379732 | 1368 | - | 0.31652 | |
g1459 | DLA_01602 | F4PJNLW01B0TO9 | CDS | 381522 | 1641 | + | 0.289458 | |
g146 | DLA_00170 | contig05409_1.exp | CDS | 344785 | 1284 | - | 0.281153 | |
g1460 | DLA_01603 | F4PJNLW01B0TO9 | CDS | 383354 | 1617 | - | 0.31107 | |
g1461 | DLA_11484 | F4PJNLW01B0TO9 | CDS | 385114 | 279 | - | 0.27957 | |
g1462 | DLA_11485 | F4PJNLW01B0TO9 | CDS | 385583 | 492 | - | 0.304878 | |
g1463 | DLA_01604 | F4PJNLW01B0TO9 | CDS | 386653 | 912 | + | 0.266447 | |
g1464 | DLA_01606 | F4PJNLW01B0TO9 | CDS | 388319 | 1674 | - | 0.310036 | |
g1465 | DLA_01607 | F4PJNLW01B0TO9 | CDS | 390640 | 243 | + | 0.403292 | |
g1466 | DLA_01608 | F4PJNLW01B0TO9 | CDS | 391174 | 1743 | - | 0.300057 | |
g1467 | DLA_01610 | F4PJNLW01B0TO9 | CDS | 394869 | 909 | - | 0.308031 | |
g1468 | DLA_01611 | F4PJNLW01B0TO9 | CDS | 396166 | 822 | - | 0.324818 | |
g1469 | DLA_01612 | F4PJNLW01B0TO9 | CDS | 397454 | 366 | + | 0.29235 | |
g147 | DLA_00171 | contig05409_1.exp | CDS | 347403 | 2679 | + | 0.335946 | |
g1470 | DLA_01613 | F4PJNLW01B0TO9 | CDS | 398063 | 729 | - | 0.33059 | |
g1471 | DLA_01614 | F4PJNLW01B0TO9 | CDS | 399083 | 1476 | - | 0.338076 | |
g1472 | DLA_01615 | F4PJNLW01B0TO9 | CDS | 401728 | 1458 | - | 0.342936 | |
g1473 | DLA_01616 | F4PJNLW01B0TO9 | CDS | 403459 | 1506 | - | 0.34927 | |
g1474 | DLA_01617 | F4PJNLW01B0TO9 | CDS | 405669 | 1662 | - | 0.299639 | |
g1475 | DLA_01618 | F4PJNLW01B0TO9 | CDS | 407789 | 1218 | - | 0.309524 | |
g1476 | DLA_01619 | F4PJNLW01B0TO9 | CDS | 409759 | 729 | + | 0.337449 | |
g1477 | DLA_01620 | F4PJNLW01B0TO9 | CDS | 410546 | 2724 | - | 0.310206 | |
g1478 | DLA_01621 | F4PJNLW01B0TO9 | CDS | 413566 | 1383 | + | 0.352856 | |
g1479 | DLA_01622 | F4PJNLW01B0TO9 | CDS | 415221 | 1218 | + | 0.297209 | |
g148 | DLA_00172 | contig05409_1.exp | CDS | 350870 | 408 | + | 0.335784 | |
g1480 | DLA_01623 | F4PJNLW01B0TO9 | CDS | 416635 | 726 | - | 0.347107 | |
g1481 | DLA_01624 | F4PJNLW01B0TO9 | CDS | 417621 | 2877 | - | 0.316997 | |
g1482 | DLA_01625 | F4PJNLW01B0TO9 | CDS | 420914 | 1470 | + | 0.314286 | |
g1483 | DLA_01627 | F4PJNLW01B0TO9 | CDS | 423305 | 627 | - | 0.341308 | |
g1484 | DLA_01628 | F4PJNLW01B0TO9 | CDS | 425017 | 2556 | + | 0.373631 | |
g1485 | DLA_01629 | F4PJNLW01B0TO9 | CDS | 428096 | 4086 | + | 0.331865 | |
g1486 | DLA_01630 | F4PJNLW01B0TO9 | CDS | 432853 | 795 | + | 0.310692 | |
g1487 | DLA_01631 | F4PJNLW01B0TO9 | CDS | 433658 | 3039 | - | 0.300428 | |
g1488 | DLA_01632 | F4PJNLW01B0TO9 | CDS | 437271 | 1383 | + | 0.291396 | |
g1489 | DLA_01633 | F4PJNLW01B0TO9 | CDS | 438685 | 711 | - | 0.331927 | |
g149 | DLA_00173 | contig05409_1.exp | CDS | 351638 | 1389 | + | 0.321094 | |
g1490 | DLA_01635 | F4PJNLW01B0TO9 | CDS | 441697 | 753 | + | 0.240372 | |
g1491 | DLA_01636 | F4PJNLW01B0TO9 | CDS | 442594 | 1791 | - | 0.383026 | |
g1492 | DLA_01637 | F4PJNLW01B0TO9 | CDS | 444525 | 342 | - | 0.263158 | |
g1493 | DLA_01638 | F4PJNLW01B0TO9 | CDS | 445215 | 936 | + | 0.356838 | |
g1494 | DLA_01639 | F4PJNLW01B0TO9 | CDS | 446288 | 1923 | - | 0.315133 | |
g1495 | DLA_01640 | F4PJNLW01B0TO9 | CDS | 451782 | 1440 | + | 0.317361 | |
g1496 | DLA_01642 | F4PJNLW01B0TO9 | CDS | 455309 | 1668 | - | 0.302158 | |
g1497 | DLA_01643 | putative ortholog of the conserved chromatin assembly factor 1 (CAF1) subunit Bbr bNote:b Do not confuse this gene with | F4PJNLW01B0TO9 | CDS | 457292 | 741 | + | 0.31309 |
g1498 | DLA_01644 | F4PJNLW01B0TO9 | CDS | 458124 | 1008 | + | 0.310516 | |
g1499 | DLA_01645 | F4PJNLW01B0TO9 | CDS | 459162 | 1059 | - | 0.305949 | |
g15 | DLA_00017 | contig05409_1.exp | CDS | 42605 | 690 | - | 0.291304 | |
g150 | DLA_00175 | contig05409_1.exp | CDS | 354359 | 1110 | - | 0.336937 | |
g1500 | DLA_01646 | F4PJNLW01B0TO9 | CDS | 460383 | 1551 | - | 0.284333 | |
g1501 | DLA_01647 | F4PJNLW01B0TO9 | CDS | 462589 | 213 | - | 0.352113 | |
g1502 | DLA_01648 | F4PJNLW01B0TO9 | CDS | 462859 | 1767 | - | 0.32824 | |
g1503 | DLA_01649 | member of a gene family comprising | F4PJNLW01B0TO9 | CDS | 465014 | 1401 | - | 0.324768 |
g1504 | DLA_01650 | F4PJNLW01B0TO9 | CDS | 469360 | 417 | - | 0.29976 | |
g1505 | DLA_01651 | F4PJNLW01B0TO9 | CDS | 470092 | 648 | + | 0.280864 | |
g1506 | DLA_01652 | F4PJNLW01B0TO9 | CDS | 471060 | 3273 | + | 0.327223 | |
g1507 | DLA_11486 | F4PJNLW01B0TO9 | CDS | 474766 | 3195 | + | 0.3277 | |
g1508 | DLA_01653 | F4PJNLW01B0TO9 | CDS | 478494 | 369 | + | 0.341463 | |
g1509 | DLA_01654 | F4PJNLW01B0TO9 | CDS | 479169 | 300 | + | 0.316667 | |
g151 | DLA_00176 | contig05409_1.exp | CDS | 355975 | 891 | + | 0.272727 | |
g1510 | DLA_01655 | F4PJNLW01B0TO9 | CDS | 479531 | 7557 | - | 0.328702 | |
g1511 | DLA_01656 | F4PJNLW01B0TO9 | CDS | 487791 | 1650 | + | 0.39697 | |
g1512 | DLA_01657 | catalyzes the reaction ATP L-serine tRNASer AMP diphosphate L-seryl-tRNASer | F4PJNLW01B0TO9 | CDS | 489926 | 1335 | + | 0.393258 |
g1513 | DLA_01658 | conserved chaperone protein which promotes assembly of the 20S proteasome may form a dimer with psmG4 and act in concert with psmG1psmG2 | F4PJNLW01B0TO9 | CDS | 491380 | 432 | - | 0.252315 |
g1514 | DLA_01659 | F4PJNLW01B0TO9 | CDS | 492148 | 2286 | + | 0.33902 | |
g1515 | DLA_01660 | F4PJNLW01B0TO9 | CDS | 494464 | 1311 | - | 0.245614 | |
g1516 | DLA_01661 | F4PJNLW01B0TO9 | CDS | 496071 | 1734 | + | 0.307958 | |
g1517 | DLA_01662 | F4PJNLW01B0TO9 | CDS | 499112 | 363 | - | 0.363636 | |
g1518 | DLA_01663 | F4PJNLW01B0TO9 | CDS | 500043 | 3534 | + | 0.299377 | |
g1519 | DLA_01664 | F4PJNLW01B0TO9 | CDS | 503903 | 339 | - | 0.348083 | |
g152 | DLA_00177 | contains a MOZSAS-like domain (Monocytic leukemia Zinc fingerSomething About Silencing) predicted to have histone acetyltransferase activity | contig05409_1.exp | CDS | 357019 | 1254 | - | 0.349282 |
g1520 | DLA_01665 | F4PJNLW01B0TO9 | CDS | 505018 | 3645 | + | 0.298217 | |
g1521 | DLA_01666 | F4PJNLW01B0TO9 | CDS | 508951 | 339 | + | 0.351032 | |
g1522 | DLA_01667 | F4PJNLW01B0TO9 | CDS | 509429 | 636 | - | 0.283019 | |
g1523 | DLA_01669 | full transporter consisting of two ABC domains and two transmembrane domains | F4PJNLW01B0TO9 | CDS | 510429 | 5199 | - | 0.294864 |
g1524 | DLA_01671 | conserved in Dictyostelids predicted to have structural similarity to the NFT2-like superfamily (nuclear transport factor) there are two highly similar genes | F4PJNLW01B0TO9 | CDS | 516755 | 339 | + | 0.356932 |
g1525 | DLA_01672 | F4PJNLW01B0TO9 | CDS | 517274 | 1923 | + | 0.299012 | |
g1526 | DLA_01673 | F4PJNLW01B0TO9 | CDS | 519631 | 2541 | + | 0.310901 | |
g1527 | DLA_01674 | E.coli ATP-dependent DNA helicase RecQ is involved in genome maintenance similar to Bloom syndrome protein defects in BLM cause genetic instability including a high level of sister chromatid exchanges associated with a greatly increased predisposition to a wide range of cancers | F4PJNLW01B0TO9 | CDS | 522200 | 2244 | - | 0.315062 |
g1528 | DLA_01675 | F4PJNLW01B0TO9 | CDS | 524951 | 2364 | + | 0.345178 | |
g1529 | DLA_01676 | membrane ion channel activated by ATP may be involved in intracellular calcium signaling | F4PJNLW01B0TO9 | CDS | 527961 | 1122 | + | 0.33066 |
g153 | DLA_00179 | contig05409_1.exp | CDS | 358942 | 294 | - | 0.309524 | |
g1530 | DLA_01677 | F4PJNLW01B0TO9 | CDS | 529650 | 1056 | - | 0.318182 | |
g1531 | DLA_01678 | F4PJNLW01B0TO9 | CDS | 530909 | 1356 | + | 0.35767 | |
g1532 | DLA_01679 | F4PJNLW01B0TO9 | CDS | 532741 | 1728 | - | 0.325231 | |
g1533 | DLA_01680 | F4PJNLW01B0TO9 | CDS | 535602 | 1065 | + | 0.313615 | |
g1534 | DLA_01681 | ortholog of human HPS5 mutations in human HPS5 have been linked to Hermansky-Pudlak syndrome 5 contains a putative RING Zn finger there is a second copy of this gene | F4PJNLW01B0TO9 | CDS | 536782 | 4320 | - | 0.349537 |
g1535 | DLA_01683 | F4PJNLW01B0TO9 | CDS | 542491 | 1611 | + | 0.335196 | |
g1536 | DLA_01684 | F4PJNLW01B0TO9 | CDS | 544226 | 855 | - | 0.327485 | |
g1537 | DLA_01685 | F4PJNLW01B0TO9 | CDS | 545256 | 10653 | + | 0.344692 | |
g1538 | DLA_01687 | F4PJNLW01B0TO9 | CDS | 556639 | 1587 | - | 0.275362 | |
g1539 | DLA_01688 | F4PJNLW01B0TO9 | CDS | 558597 | 2556 | - | 0.331768 | |
g154 | DLA_00180 | contig05409_1.exp | CDS | 359511 | 285 | - | 0.410526 | |
g1540 | DLA_01689 | F4PJNLW01B0TO9 | CDS | 561569 | 567 | + | 0.285714 | |
g1541 | DLA_01690 | similar to mammalian EBP (and EBPL) EBP catalyzes the conversion of Delta(8)-sterols to their corresponding Delta(7)-isomers defects in hEBP cause chondrodysplasia punctata X-linked dominant type 2 a rare disorder of defective cholesterol biosynthesis | F4PJNLW01B0TO9 | CDS | 562373 | 675 | - | 0.348148 |
g1542 | DLA_11487 | F4PJNLW01B0TO9 | CDS | 563145 | 204 | + | 0.392157 | |
g1543 | DLA_01691 | F4PJNLW01B0TO9 | CDS | 564418 | 1590 | + | 0.30566 | |
g1544 | DLA_01692 | F4PJNLW01B0TO9 | CDS | 567016 | 2328 | - | 0.395619 | |
g1545 | DLA_01693 | F4PJNLW01B0TO9 | CDS | 570322 | 2535 | + | 0.3357 | |
g1546 | DLA_01694 | F4PJNLW01B0TO9 | CDS | 572998 | 1248 | - | 0.331731 | |
g1547 | DLA_01695 | F4PJNLW01B0TO9 | CDS | 574505 | 1470 | + | 0.317007 | |
g1548 | DLA_01696 | F4PJNLW01B0TO9 | CDS | 576002 | 3606 | - | 0.311425 | |
g1549 | DLA_11488 | F4PJNLW01B0TO9 | CDS | 580805 | 2460 | + | 0.387398 | |
g155 | DLA_00182 | contig05409_1.exp | CDS | 360437 | 2997 | + | 0.327661 | |
g1550 | DLA_01697 | F4PJNLW01B0TO9 | CDS | 583710 | 5862 | + | 0.360628 | |
g1551 | DLA_01698 | F4PJNLW01B0TO9 | CDS | 590472 | 1467 | - | 0.323108 | |
g1552 | DLA_01699 | F4PJNLW01B0TO9 | CDS | 592341 | 1605 | + | 0.282243 | |
g1553 | DLA_01700 | involved in pseudopod formation contains an N-terminal ADFcofilin-like actin binding domain and a c-terminal SH3 domain there is a second copy of this gene | F4PJNLW01B0TO9 | CDS | 594032 | 1341 | - | 0.370619 |
g1554 | DLA_01702 | catalyzes the reaction 4-hydroxyphenylpyruvate Osub2sub homogentisate COsub2sub there is a second copy of this gene | F4PJNLW01B0TO9 | CDS | 597042 | 1377 | + | 0.337691 |
g1555 | DLA_01703 | F4PJNLW01B0TO9 | CDS | 598580 | 1176 | - | 0.341837 | |
g1556 | DLA_01704 | F4PJNLW01B0TO9 | CDS | 599863 | 1719 | + | 0.267016 | |
g1557 | DLA_01705 | F4PJNLW01B0TO9 | CDS | 601671 | 1797 | + | 0.303283 | |
g1558 | DLA_11489 | F4PJNLW01B0TO9 | CDS | 603892 | 1677 | + | 0.297555 | |
g1559 | DLA_01706 | F4PJNLW01B0TO9 | CDS | 605631 | 1659 | - | 0.352019 | |
g156 | DLA_00183 | contig05409_1.exp | CDS | 363781 | 2511 | + | 0.3182 | |
g1560 | DLA_01708 | F4PJNLW01B0TO9 | CDS | 608428 | 2490 | - | 0.347791 | |
g1561 | DLA_01712 | F4PJNLW01B0TO9 | CDS | 613316 | 1353 | + | 0.327421 | |
g1562 | DLA_01714 | F4PJNLW01B0TO9 | CDS | 615301 | 1506 | - | 0.324037 | |
g1563 | DLA_01715 | F4PJNLW01B0TO9 | CDS | 616956 | 1179 | + | 0.332485 | |
g1564 | DLA_01716 | F4PJNLW01B0TO9 | CDS | 618733 | 624 | + | 0.301282 | |
g1565 | DLA_01717 | catalyses the endonucleolytic cleavage of apurinic or apyrimidinic sites to generate products with a 5'-phosphate there is a second copy of this gene | F4PJNLW01B0TO9 | CDS | 619613 | 828 | - | 0.317633 |
g1566 | DLA_01718 | F4PJNLW01B0TO9 | CDS | 620568 | 2382 | - | 0.288413 | |
g1567 | DLA_11490 | F4PJNLW01B0TO9 | CDS | 624423 | 1470 | + | 0.32449 | |
g1568 | DLA_01719 | F4PJNLW01B0TO9 | CDS | 626169 | 465 | + | 0.369892 | |
g1569 | DLA_01720 | F4PJNLW01B0TO9 | CDS | 626753 | 1173 | - | 0.335891 | |
g157 | DLA_00184 | contig05409_1.exp | CDS | 366449 | 225 | - | 0.235556 | |
g1570 | DLA_01721 | F4PJNLW01B0TO9 | CDS | 627998 | 1293 | + | 0.276875 | |
g1571 | DLA_01723 | F4PJNLW01B0TO9 | CDS | 629752 | 813 | - | 0.318573 | |
g1572 | DLA_01725 | peptidase M20 family zinc metallopeptidases which are glutamate carboxypeptidases contains peptidase dimerization domain | F4PJNLW01B0TO9 | CDS | 631266 | 1419 | - | 0.338971 |
g1573 | DLA_01726 | F4PJNLW01B0TO9 | CDS | 633140 | 1266 | - | 0.332543 | |
g1574 | DLA_01727 | F4PJNLW01B0TO9 | CDS | 634780 | 1782 | + | 0.289562 | |
g1575 | DLA_01728 | F4PJNLW01B0TO9 | CDS | 636612 | 1809 | - | 0.33665 | |
g1576 | DLA_01729 | F4PJNLW01B0TO9 | CDS | 638697 | 363 | + | 0.38843 | |
g1577 | DLA_01730 | F4PJNLW01B0TO9 | CDS | 639088 | 2331 | - | 0.322608 | |
g1578 | DLA_01731 | F4PJNLW01B0TO9 | CDS | 642429 | 1569 | - | 0.32441 | |
g1579 | DLA_01732 | catalyzes the first of three steps required to remove two C-4 methyl groups from an intermediate in ergosterol biosynthesis almost identical to the neighboring gene | F4PJNLW01B0TO9 | CDS | 644709 | 894 | + | 0.322148 |
g158 | DLA_00185 | contig05409_1.exp | CDS | 367394 | 1173 | + | 0.363171 | |
g1580 | DLA_01734 | F4PJNLW01B0TO9 | CDS | 647003 | 1200 | + | 0.348333 | |
g1581 | DLA_01735 | F4PJNLW01B0TO9 | CDS | 648615 | 3222 | + | 0.321539 | |
g1582 | DLA_01736 | F4PJNLW01B0TO9 | CDS | 652123 | 447 | - | 0.319911 | |
g1583 | DLA_01737 | F4PJNLW01B0TO9 | CDS | 652664 | 1623 | + | 0.265558 | |
g1584 | DLA_01738 | F4PJNLW01B0TO9 | CDS | 654498 | 450 | + | 0.306667 | |
g1585 | DLA_01739 | P-type ATPase (E1-E2) ortholog of human ATP9B and yeast NEO1 which is involved in transport from the Golgi to the ER | F4PJNLW01B0TO9 | CDS | 655356 | 3540 | - | 0.35 |
g1586 | DLA_01740 | F4PJNLW01B0TO9 | CDS | 659962 | 2082 | + | 0.300672 | |
g1587 | DLA_01741 | matches PFAM HMM for SPB_interacting (spindle pole body) protein similar to D.purpureum protein | F4PJNLW01B0TO9 | CDS | 662175 | 2247 | - | 0.321317 |
g1588 | DLA_01742 | catalyzes the reaction fructose-16-bisphosphate dihydroxy-acetone-phosphate D-glyceraldehyde-3-phosphate expressed in pstAB cells and in upper cup during culmination | F4PJNLW01B0TO9 | CDS | 664814 | 1080 | - | 0.393519 |
g1589 | DLA_01743 | F4PJNLW01B0TO9 | CDS | 666284 | 258 | + | 0.248062 | |
g159 | DLA_11433 | contig05409_1.exp | CDS | 368849 | 1725 | - | 0.293913 | |
g1590 | DLA_01744 | F4PJNLW01B0TO9 | CDS | 666768 | 1059 | - | 0.341832 | |
g1591 | DLA_01745 | F4PJNLW01B0TO9 | CDS | 668508 | 2676 | + | 0.351644 | |
g1592 | DLA_01746 | F4PJNLW01B0TO9 | CDS | 671489 | 2886 | - | 0.35447 | |
g1593 | DLA_11491 | F4PJNLW01B0TO9 | CDS | 675531 | 1932 | + | 0.280538 | |
g1594 | DLA_01747 | similar to metazoan LVT proteins whose function is unknown | F4PJNLW01B0TO9 | CDS | 678546 | 1479 | + | 0.317106 |
g1595 | DLA_01748 | F4PJNLW01B0TO9 | CDS | 680127 | 3024 | - | 0.295966 | |
g1596 | DLA_01749 | F4PJNLW01B0TO9 | CDS | 683326 | 1902 | - | 0.32387 | |
g1597 | DLA_01750 | F4PJNLW01B0TO9 | CDS | 685525 | 3492 | + | 0.302978 | |
g1598 | DLA_11492 | F4PJNLW01B0TO9 | CDS | 689319 | 204 | - | 0.29902 | |
g1599 | DLA_01751 | F4PJNLW01B0TO9 | CDS | 690315 | 3513 | + | 0.30259 | |
g16 | DLA_00018 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages induced by Legionella pneumophila infection | contig05409_1.exp | CDS | 43817 | 1428 | + | 0.341036 |
g160 | DLA_00186 | contig05409_1.exp | CDS | 370867 | 660 | - | 0.327273 | |
g1600 | DLA_01752 | F4PJNLW01B0TO9 | CDS | 695073 | 3495 | + | 0.302432 | |
g1601 | DLA_01753 | F4PJNLW01B0TO9 | CDS | 699663 | 1779 | + | 0.304666 | |
g1602 | DLA_01754 | F4PJNLW01B0TO9 | CDS | 701660 | 627 | + | 0.334928 | |
g1603 | DLA_01755 | F4PJNLW01B0TO9 | CDS | 702848 | 1662 | - | 0.305656 | |
g1604 | DLA_01756 | F4PJNLW01B0TO9 | CDS | 704668 | 921 | + | 0.320304 | |
g1605 | DLA_01757 | F4PJNLW01B0TO9 | CDS | 705678 | 1500 | + | 0.284 | |
g1606 | DLA_01758 | F4PJNLW01B0TO9 | CDS | 707303 | 1743 | - | 0.327022 | |
g1607 | DLA_11493 | F4PJNLW01B0TO9 | CDS | 710358 | 2919 | - | 0.328537 | |
g1608 | DLA_01759 | F4PJNLW01B0TO9 | CDS | 714595 | 1008 | + | 0.259921 | |
g1609 | DLA_01761 | F4PJNLW01B0TO9 | CDS | 716039 | 1155 | + | 0.299567 | |
g161 | DLA_00187 | contig05409_1.exp | CDS | 372159 | 957 | + | 0.266458 | |
g1610 | DLA_01763 | catalyzes the release of an N-terminal dipeptide from a peptide comprising four or more residues with broad specificity highly selective for Arg-Arg-2-naphthylamide at pH 9.2 there is a second copy of this gene | F4PJNLW01B0TO9 | CDS | 718084 | 2076 | - | 0.354046 |
g1611 | DLA_01764 | F4PJNLW01B0TO9 | CDS | 720522 | 630 | + | 0.311111 | |
g1612 | DLA_01765 | F4PJNLW01B0TO9 | CDS | 721439 | 594 | - | 0.318182 | |
g1613 | DLA_01766 | F4PJNLW01B0TO9 | CDS | 722504 | 225 | + | 0.351111 | |
g1614 | DLA_01767 | F4PJNLW01B0TO9 | CDS | 723057 | 1686 | - | 0.298932 | |
g1615 | DLA_01768 | F4PJNLW01B0TO9 | CDS | 725594 | 261 | + | 0.394636 | |
g1616 | DLA_01769 | F4PJNLW01B0TO9 | CDS | 726181 | 822 | + | 0.318735 | |
g1617 | DLA_01770 | F4PJNLW01B0TO9 | CDS | 727144 | 2151 | - | 0.294747 | |
g1618 | DLA_01772 | F4PJNLW01B0TO9 | CDS | 729828 | 1833 | - | 0.333879 | |
g1619 | DLA_01773 | F4PJNLW01B0TO9 | CDS | 731731 | 1278 | - | 0.313772 | |
g162 | DLA_00188 | contig05409_1.exp | CDS | 376542 | 1929 | + | 0.369103 | |
g1620 | DLA_01774 | F4PJNLW01B0TO9 | CDS | 733106 | 1431 | + | 0.280224 | |
g1621 | DLA_01775 | F4PJNLW01B0TO9 | CDS | 734695 | 1488 | + | 0.275538 | |
g1622 | DLA_01776 | F4PJNLW01B0TO9 | CDS | 736554 | 1275 | - | 0.329412 | |
g1623 | DLA_01778 | F4PJNLW01B0TO9 | CDS | 738936 | 1107 | + | 0.31075 | |
g1624 | DLA_01779 | F4PJNLW01B0TO9 | CDS | 740189 | 1752 | - | 0.358447 | |
g1625 | DLA_01780 | F4PJNLW01B0TO9 | CDS | 742277 | 1383 | - | 0.276211 | |
g1626 | DLA_01781 | F4PJNLW01B0TO9 | CDS | 743949 | 3192 | - | 0.343672 | |
g1627 | DLA_01782 | F4PJNLW01B0TO9 | CDS | 748314 | 951 | + | 0.315457 | |
g1628 | DLA_01783 | F4PJNLW01B0TO9 | CDS | 749626 | 2001 | - | 0.302849 | |
g1629 | DLA_01784 | F4PJNLW01B0TO9 | CDS | 753361 | 1098 | + | 0.384335 | |
g163 | DLA_00189 | contig05409_1.exp | CDS | 378660 | 2967 | - | 0.356589 | |
g1630 | DLA_01785 | F4PJNLW01B0TO9 | CDS | 755318 | 930 | + | 0.280645 | |
g1631 | DLA_01786 | F4PJNLW01B0TO9 | CDS | 756478 | 1416 | - | 0.286017 | |
g1632 | DLA_01787 | F4PJNLW01B0TO9 | CDS | 758257 | 1695 | + | 0.284366 | |
g1633 | DLA_01788 | F4PJNLW01B0TO9 | CDS | 760049 | 1659 | + | 0.295961 | |
g1634 | DLA_01789 | F4PJNLW01B0TO9 | CDS | 762018 | 2343 | - | 0.332053 | |
g1635 | DLA_01790 | F4PJNLW01B0TO9 | CDS | 765011 | 3840 | - | 0.359635 | |
g1636 | DLA_01791 | F4PJNLW01B0TO9 | CDS | 769374 | 1098 | + | 0.332423 | |
g1637 | DLA_01792 | F4PJNLW01B0TO9 | CDS | 772256 | 618 | - | 0.283172 | |
g1638 | DLA_01793 | F4PJNLW01B0TO9 | CDS | 773866 | 2073 | + | 0.291848 | |
g1639 | DLA_01794 | F4PJNLW01B0TO9 | CDS | 776136 | 1245 | + | 0.293173 | |
g164 | DLA_00190 | contig05409_1.exp | CDS | 382213 | 3225 | - | 0.325271 | |
g1640 | DLA_01795 | F4PJNLW01B0TO9 | CDS | 777633 | 1689 | - | 0.316163 | |
g1641 | DLA_01796 | F4PJNLW01B0TO9 | CDS | 779780 | 981 | + | 0.277268 | |
g1642 | DLA_01797 | F4PJNLW01B0TO9 | CDS | 780943 | 801 | - | 0.299625 | |
g1643 | DLA_01798 | F4PJNLW01B0TO9 | CDS | 782389 | 1941 | - | 0.277692 | |
g1644 | DLA_01799 | F4PJNLW01B0TO9 | CDS | 784630 | 1236 | + | 0.258091 | |
g1645 | DLA_01801 | has similarity to G-protein-coupled receptors predicted to have 7 transmembrane domains and a putative signal peptide | F4PJNLW01B0TO9 | CDS | 786804 | 1755 | + | 0.310541 |
g1646 | DLA_11494 | F4PJNLW01B0TO9 | CDS | 789076 | 1209 | + | 0.304384 | |
g1647 | DLA_01802 | F4PJNLW01B0TO9 | CDS | 790679 | 855 | - | 0.271345 | |
g1648 | DLA_01803 | F4PJNLW01B0TO9 | CDS | 791726 | 1998 | - | 0.32983 | |
g1649 | DLA_01804 | F4PJNLW01B0TO9 | CDS | 793976 | 384 | + | 0.244792 | |
g165 | DLA_00191 | contig05409_1.exp | CDS | 386865 | 3975 | + | 0.314969 | |
g1650 | DLA_01805 | F4PJNLW01B0TO9 | CDS | 794777 | 7773 | - | 0.318667 | |
g1651 | DLA_01808 | F4PJNLW01B0TO9 | CDS | 805203 | 3450 | + | 0.305797 | |
g1652 | DLA_01809 | F4PJNLW01B0TO9 | CDS | 809222 | 2733 | + | 0.283205 | |
g1653 | DLA_01810 | F4PJNLW01B0TO9 | CDS | 812101 | 3480 | - | 0.308333 | |
g1654 | DLA_01811 | F4PJNLW01B0TO9 | CDS | 815992 | 1170 | + | 0.326496 | |
g1655 | DLA_01812 | highly similar to acetyl-CoA synthetase which condenses acetate and CoA to acetyl-coA | F4PJNLW01B0TO9 | CDS | 817231 | 2109 | - | 0.336178 |
g1656 | DLA_01813 | F4PJNLW01B0TO9 | CDS | 819803 | 1875 | + | 0.326933 | |
g1657 | DLA_01814 | F4PJNLW01B0TO9 | CDS | 822011 | 1614 | - | 0.35316 | |
g1658 | DLA_01815 | F4PJNLW01B0TO9 | CDS | 824502 | 2334 | + | 0.325621 | |
g1659 | DLA_01816 | F4PJNLW01B0TO9 | CDS | 826940 | 1296 | - | 0.280093 | |
g166 | DLA_00193 | contig05409_1.exp | CDS | 392153 | 2205 | + | 0.350567 | |
g1660 | DLA_01817 | F4PJNLW01B0TO9 | CDS | 829466 | 1077 | + | 0.31662 | |
g1661 | DLA_11495 | F4PJNLW01B0TO9 | CDS | 831113 | 1374 | + | 0.263464 | |
g1662 | DLA_01818 | belongs to the metallophosphoesterase superfamily similar to A. thaliana PAP6 (purple acid phosphatase) contains a predicted signal peptide and putative C-terminal transmembrane domain | F4PJNLW01B0TO9 | CDS | 832815 | 1392 | + | 0.341236 |
g1663 | DLA_01819 | F4PJNLW01B0TO9 | CDS | 834291 | 1074 | - | 0.280261 | |
g1664 | DLA_01820 | F4PJNLW01B0TO9 | CDS | 835697 | 6819 | + | 0.307816 | |
g1665 | DLA_01821 | F4PJNLW01B0TO9 | CDS | 842624 | 606 | - | 0.293729 | |
g1666 | DLA_01822 | F4PJNLW01B0TO9 | CDS | 843431 | 1962 | + | 0.332314 | |
g1667 | DLA_01823 | F4PJNLW01B0TO9 | CDS | 845570 | 945 | - | 0.349206 | |
g1668 | DLA_01824 | F4PJNLW01B0TO9 | CDS | 846981 | 2520 | + | 0.289286 | |
g1669 | DLA_01825 | F4PJNLW01B0TO9 | CDS | 849641 | 1386 | + | 0.34127 | |
g167 | DLA_00194 | contig05409_1.exp | CDS | 394449 | 402 | - | 0.335821 | |
g1670 | DLA_01826 | F4PJNLW01B0TO9 | CDS | 851222 | 2280 | + | 0.257456 | |
g1671 | DLA_01827 | F4PJNLW01B0TO9 | CDS | 854682 | 3390 | + | 0.281416 | |
g1672 | DLA_01828 | F4PJNLW01B0TO9 | CDS | 858633 | 3912 | + | 0.319785 | |
g1673 | DLA_01829 | F4PJNLW01B0TO9 | CDS | 864215 | 2370 | + | 0.274684 | |
g1674 | DLA_01830 | F4PJNLW01B0TO9 | CDS | 866775 | 1389 | + | 0.327574 | |
g1675 | DLA_01831 | F4PJNLW01B0TO9 | CDS | 868402 | 1809 | + | 0.304588 | |
g1676 | DLA_01832 | Ortholog of metazoan myotrophin (MTPN) which might be involved in cerebellar morphogenesis and cardiac hypertrophy contains 2 ankyrin repeats | F4PJNLW01B0TO9 | CDS | 870602 | 360 | - | 0.347222 |
g1677 | DLA_01833 | F4PJNLW01B0TO9 | CDS | 871260 | 1281 | + | 0.326308 | |
g1678 | DLA_01834 | F4PJNLW01B0TO9 | CDS | 872573 | 1410 | - | 0.268085 | |
g1679 | DLA_01835 | F4PJNLW01B0TO9 | CDS | 874248 | 378 | + | 0.404762 | |
g168 | DLA_00195 | contig05409_1.exp | CDS | 395458 | 324 | + | 0.345679 | |
g1680 | DLA_01836 | F4PJNLW01B0TO9 | CDS | 875169 | 1017 | + | 0.291052 | |
g1681 | DLA_01840 | F4PJNLW01B0TO9 | CDS | 878000 | 420 | + | 0.352381 | |
g1682 | DLA_01841 | F4PJNLW01B0TO9 | CDS | 878850 | 864 | - | 0.277778 | |
g1683 | DLA_01843 | F4PJNLW01B0TO9 | CDS | 880002 | 4254 | + | 0.293371 | |
g1684 | DLA_01844 | F4PJNLW01B0TO9 | CDS | 885796 | 1860 | - | 0.306452 | |
g1685 | DLA_01845 | distant relative of CAZy family GT14 similar to xylosyltransferase | F4PJNLW01B0TO9 | CDS | 888187 | 1422 | + | 0.266526 |
g1686 | DLA_01846 | F4PJNLW01B0TO9 | CDS | 889929 | 7662 | - | 0.346254 | |
g1687 | DLA_01847 | F4PJNLW01B0TO9 | CDS | 898275 | 1617 | - | 0.35807 | |
g1688 | DLA_01848 | F4PJNLW01B0TO9 | CDS | 900052 | 207 | - | 0.236715 | |
g1689 | DLA_01849 | F4PJNLW01B0TO9 | CDS | 900663 | 1614 | + | 0.335192 | |
g169 | DLA_00196 | contig05409_1.exp | CDS | 395851 | 1716 | - | 0.30303 | |
g1690 | DLA_01850 | F4PJNLW01B0TO9 | CDS | 903564 | 1080 | + | 0.350926 | |
g1691 | DLA_01851 | F4PJNLW01B0TO9 | CDS | 905167 | 3105 | - | 0.335266 | |
g1692 | DLA_01852 | F4PJNLW01B0TO9 | CDS | 908516 | 1131 | + | 0.331565 | |
g1693 | DLA_01853 | F4PJNLW01B0TO9 | CDS | 909794 | 879 | - | 0.316268 | |
g1694 | DLA_01855 | F4PJNLW01B0TO9 | CDS | 911905 | 2013 | + | 0.34774 | |
g1695 | DLA_01856 | F4PJNLW01B0TO9 | CDS | 914358 | 1602 | + | 0.277154 | |
g1696 | DLA_11496 | F4PJNLW01B0TO9 | CDS | 916179 | 804 | - | 0.287313 | |
g1697 | DLA_01857 | F4PJNLW01B0TO9 | CDS | 918129 | 1437 | - | 0.347251 | |
g1698 | DLA_01858 | F4PJNLW01B0TO9 | CDS | 920783 | 915 | + | 0.315847 | |
g1699 | DLA_01859 | F4PJNLW01B0TO9 | CDS | 921944 | 2484 | - | 0.336957 | |
g17 | DLA_00019 | contig05409_1.exp | CDS | 45374 | 1470 | - | 0.293878 | |
g170 | DLA_00197 | contig05409_1.exp | CDS | 398230 | 1329 | - | 0.319037 | |
g1700 | DLA_01860 | F4PJNLW01B0TO9 | CDS | 924680 | 4245 | - | 0.345112 | |
g1701 | DLA_01861 | putative protein serinethreonine kinase belongs to the PAKL subfamily of protein kinases the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | F4PJNLW01B0TO9 | CDS | 929551 | 2454 | + | 0.332926 |
g1702 | DLA_01862 | F4PJNLW01B0TO9 | CDS | 932524 | 2376 | + | 0.305976 | |
g1703 | DLA_01863 | F4PJNLW01B0TO9 | CDS | 935176 | 3039 | + | 0.299112 | |
g1704 | DLA_01864 | F4PJNLW01B0TO9 | CDS | 938443 | 750 | + | 0.304 | |
g1705 | DLA_01865 | similar to human L antigen family member 3 (LAGE3)brbr bCommunity annotation:b DDB G0274491 codes for a small protein with significant similarities to | F4PJNLW01B0TO9 | CDS | 939329 | 306 | - | 0.267974 |
g1706 | DLA_01866 | F4PJNLW01B0TO9 | CDS | 939836 | 1410 | + | 0.261702 | |
g1707 | DLA_01867 | F4PJNLW01B0TO9 | CDS | 941539 | 414 | - | 0.304348 | |
g1708 | DLA_01868 | F4PJNLW01B0TO9 | CDS | 942191 | 438 | + | 0.315068 | |
g1709 | DLA_01869 | F4PJNLW01B0TO9 | CDS | 943115 | 1722 | + | 0.332753 | |
g171 | DLA_00198 | contig05409_1.exp | CDS | 400765 | 612 | - | 0.292484 | |
g1710 | DLA_01870 | F4PJNLW01B0TO9 | CDS | 945057 | 2793 | - | 0.31758 | |
g1711 | DLA_01871 | F4PJNLW01B0TO9 | CDS | 948167 | 1227 | + | 0.286879 | |
g1712 | DLA_01872 | ceramidase bearing more similarity with neural and alkaline ceramidases however pH optimum of the enzyme is 3 | F4PJNLW01B0TO9 | CDS | 949683 | 2130 | - | 0.389202 |
g1713 | DLA_01873 | ortholog of the human SLC25A3 and S. cerevisiae MIR1 which transports inorganic phosphate from the cytosol to the mitochondrion matrix brbr bCommunity annotation:b Overview of the | F4PJNLW01B0TO9 | CDS | 952851 | 912 | + | 0.421053 |
g1714 | DLA_01874 | F4PJNLW01B0TO9 | CDS | 955159 | 930 | - | 0.315054 | |
g1715 | DLA_01875 | F4PJNLW01B0TO9 | CDS | 958125 | 1182 | + | 0.299492 | |
g1716 | DLA_01876 | F4PJNLW01B0TO9 | CDS | 959478 | 1047 | - | 0.319007 | |
g1717 | DLA_01878 | F4PJNLW01B0TO9 | CDS | 961187 | 1968 | - | 0.307419 | |
g1718 | DLA_01881 | F4PJNLW01B0TO9 | CDS | 964762 | 2145 | + | 0.334732 | |
g1719 | DLA_01882 | F4PJNLW01B0TO9 | CDS | 967249 | 1395 | + | 0.343369 | |
g172 | DLA_00199 | contig05409_1.exp | CDS | 401809 | 738 | - | 0.306233 | |
g1720 | DLA_01883 | F4PJNLW01B0TO9 | CDS | 969312 | 3540 | + | 0.320904 | |
g1721 | DLA_01884 | belongs to the NCDKar3 subfamily predicted to play a role in mitosis | F4PJNLW01B0TO9 | CDS | 973147 | 2172 | + | 0.328729 |
g1722 | DLA_01885 | F4PJNLW01B0TO9 | CDS | 975522 | 1338 | - | 0.278774 | |
g1723 | DLA_01886 | F4PJNLW01B0TO9 | CDS | 977252 | 597 | + | 0.370184 | |
g1724 | DLA_01887 | F4PJNLW01B0TO9 | CDS | 978487 | 2199 | + | 0.27467 | |
g1725 | DLA_01889 | F4PJNLW01B0TO9 | CDS | 982370 | 1437 | - | 0.269311 | |
g1726 | DLA_01890 | F4PJNLW01B0TO9 | CDS | 985121 | 1002 | - | 0.276447 | |
g1727 | DLA_01891 | F4PJNLW01B0TO9 | CDS | 986419 | 1284 | + | 0.275701 | |
g1728 | DLA_01892 | F4PJNLW01B0TO9 | CDS | 988245 | 3060 | + | 0.32451 | |
g1729 | DLA_01893 | F4PJNLW01B0TO9 | CDS | 991488 | 3117 | + | 0.283927 | |
g173 | DLA_00200 | contig05409_1.exp | CDS | 403470 | 3306 | - | 0.301573 | |
g1730 | DLA_01895 | F4PJNLW01B0TO9 | CDS | 994905 | 1500 | + | 0.282 | |
g1731 | DLA_01896 | F4PJNLW01B0TO9 | CDS | 996867 | 1242 | + | 0.283414 | |
g1732 | DLA_01897 | F4PJNLW01B0TO9 | CDS | 998157 | 792 | - | 0.338384 | |
g1733 | DLA_01898 | F4PJNLW01B0TO9 | CDS | 999629 | 4656 | - | 0.320662 | |
g1734 | DLA_01899 | F4PJNLW01B0TO9 | CDS | 1004895 | 2139 | - | 0.322113 | |
g1735 | DLA_01900 | F4PJNLW01B0TO9 | CDS | 1008318 | 1452 | - | 0.409091 | |
g1736 | DLA_01901 | F4PJNLW01B0TO9 | CDS | 1010513 | 852 | + | 0.381455 | |
g1737 | DLA_01902 | F4PJNLW01B0TO9 | CDS | 1011607 | 1668 | + | 0.340528 | |
g1738 | DLA_01903 | F4PJNLW01B0TO9 | CDS | 1013501 | 1476 | + | 0.313008 | |
g1739 | DLA_01904 | F4PJNLW01B0TO9 | CDS | 1015738 | 1482 | + | 0.394737 | |
g174 | DLA_11434 | contig05409_1.exp | CDS | 407386 | 507 | - | 0.321499 | |
g1740 | DLA_01905 | F4PJNLW01B0TO9 | CDS | 1017531 | 1290 | + | 0.29845 | |
g1741 | DLA_01906 | F4PJNLW01B0TO9 | CDS | 1019327 | 789 | + | 0.342205 | |
g1742 | DLA_01907 | F4PJNLW01B0TO9 | CDS | 1020557 | 978 | - | 0.322086 | |
g1743 | DLA_01908 | F4PJNLW01B0TO9 | CDS | 1022240 | 714 | + | 0.259104 | |
g1744 | DLA_11497 | F4PJNLW01B0TO9 | CDS | 1023243 | 624 | + | 0.325321 | |
g1745 | DLA_11498 | F4PJNLW01B0TO9 | CDS | 1024453 | 1953 | + | 0.25192 | |
g1746 | DLA_01909 | F4PJNLW01B0TO9 | CDS | 1027298 | 2163 | + | 0.254276 | |
g1747 | DLA_01911 | conserved protein in ciliates and plants contains 9 predicted transmembrane domains including one signal peptide there is an almost identical D. discoideum protein | F4PJNLW01B3KKL | CDS | 284 | 1464 | - | 0.360656 |
g1748 | DLA_01912 | F4PJNLW01B3KKL | CDS | 2451 | 279 | + | 0.250896 | |
g1749 | DLA_01913 | F4PJNLW01B3KKL | CDS | 2956 | 603 | - | 0.363184 | |
g175 | DLA_00201 | contig05409_1.exp | CDS | 408600 | 1632 | - | 0.271446 | |
g1750 | DLA_01914 | F4PJNLW01B3KKL | CDS | 4755 | 654 | + | 0.270642 | |
g1751 | DLA_01915 | belongs to a superfamily of metalloenzymes induced by Legionella pneumophila infection | F4PJNLW01B3KKL | CDS | 5796 | 1023 | + | 0.297165 |
g1752 | DLA_01916 | F4PJNLW01B3KKL | CDS | 6890 | 723 | - | 0.35823 | |
g1753 | DLA_01917 | belongs to the thiolase family similar to human ACAA1 | F4PJNLW01B3KKL | CDS | 7999 | 1212 | + | 0.344059 |
g1754 | DLA_01918 | very similar to D. purpureum protein | F4PJNLW01B3KKL | CDS | 9279 | 1200 | - | 0.243333 |
g1755 | DLA_01919 | F4PJNLW01BNQ9D | CDS | 2 | 1744 | - | 0.30906 | |
g1756 | DLA_01920 | F4PJNLW01BNQ9D | CDS | 2025 | 2088 | - | 0.305556 | |
g1757 | DLA_11499 | F4PJNLW01BNQ9D | CDS | 5154 | 582 | + | 0.364261 | |
g1758 | DLA_01921 | F4PJNLW01BNQ9D | CDS | 6241 | 993 | + | 0.298087 | |
g1759 | DLA_01922 | F4PJNLW01BNQ9D | CDS | 7478 | 1449 | - | 0.334714 | |
g176 | DLA_00202 | contig05409_1.exp | CDS | 410427 | 1590 | - | 0.266667 | |
g1760 | DLA_01923 | F4PJNLW01BNQ9D | CDS | 9137 | 1083 | + | 0.288089 | |
g1761 | DLA_01924 | F4PJNLW01BNQ9D | CDS | 10588 | 876 | + | 0.292237 | |
g1762 | DLA_01925 | F4PJNLW01BNQ9D | CDS | 13923 | 1590 | + | 0.337107 | |
g1763 | DLA_01928 | F4PJNLW01C9MXC | CDS | 710 | 2199 | - | 0.273306 | |
g1764 | DLA_01929 | subunit of TFIID and SAGA complexes involved in RNA polymerase II transcription initiation and in chromatin modification | F4PJNLW01C9MXC | CDS | 3083 | 1080 | - | 0.317593 |
g1765 | DLA_01930 | catalyzes the reaction ATP L-threonine tRNAThr AMP diphosphate L-threonyl-tRNAThr | F4PJNLW01C9MXC | CDS | 4269 | 2040 | + | 0.290686 |
g1766 | DLA_01931 | F4PJNLW01C9MXC | CDS | 6391 | 2385 | - | 0.334172 | |
g1767 | DLA_01932 | F4PJNLW01C9MXC | CDS | 9034 | 879 | - | 0.275313 | |
g1768 | DLA_01933 | F4PJNLW01C9MXC | CDS | 10304 | 1443 | - | 0.289674 | |
g1769 | DLA_01934 | F4PJNLW01C9MXC | CDS | 11985 | 1290 | - | 0.260465 | |
g177 | DLA_00204 | contig05409_1.exp | CDS | 413350 | 1287 | + | 0.370629 | |
g1770 | DLA_01935 | F4PJNLW01C9MXC | CDS | 13897 | 1848 | - | 0.330087 | |
g1771 | DLA_11500 | F4PJNLW01C9MXC | CDS | 17042 | 615 | - | 0.263415 | |
g1772 | DLA_01936 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) shift of Dictyostelium cells from the proliferative to differentiated state highly expressed during the early stage of differentiation | F4PJNLW01C9MXC | CDS | 18046 | 642 | + | 0.334891 |
g1773 | DLA_01937 | F4PJNLW01C9MXC | CDS | 19053 | 1956 | + | 0.294479 | |
g1774 | DLA_11501 | F4PJNLW01C9MXC | CDS | 21178 | 228 | + | 0.385965 | |
g1775 | DLA_01938 | F4PJNLW01C9MXC | CDS | 21759 | 1452 | - | 0.280303 | |
g1776 | DLA_01939 | F4PJNLW01C9MXC | CDS | 24206 | 2010 | + | 0.277114 | |
g1777 | DLA_01941 | F4PJNLW01C9MXC | CDS | 26936 | 1194 | + | 0.29732 | |
g1778 | DLA_01942 | F4PJNLW01C9MXC | CDS | 28299 | 4908 | + | 0.282192 | |
g1779 | DLA_01943 | F4PJNLW01C9MXC | CDS | 33505 | 555 | + | 0.30991 | |
g178 | DLA_00205 | contig05409_1.exp | CDS | 414878 | 573 | - | 0.321117 | |
g1780 | DLA_01944 | F4PJNLW01C9MXC | CDS | 34098 | 1746 | - | 0.310997 | |
g1781 | DLA_11502 | F4PJNLW01C9MXC | CDS | 36125 | 1458 | - | 0.260631 | |
g1782 | DLA_01945 | F4PJNLW01C9MXC | CDS | 37704 | 2319 | + | 0.224666 | |
g1783 | DLA_01946 | F4PJNLW01C9MXC | CDS | 40201 | 1185 | - | 0.274262 | |
g1784 | DLA_01947 | nuclear protein and ortholog of yeast SNF12 and human SMARCD1 that are involved in chromatin remodeling there is a second copy of this gene | F4PJNLW01C9MXC | CDS | 41999 | 1413 | - | 0.322718 |
g1785 | DLA_01948 | F4PJNLW01C9MXC | CDS | 44015 | 2481 | + | 0.289802 | |
g1786 | DLA_01949 | F4PJNLW01C9MXC | CDS | 46872 | 1125 | - | 0.408 | |
g1787 | DLA_01950 | F4PJNLW01C9MXC | CDS | 48306 | 4320 | - | 0.303241 | |
g1788 | DLA_01951 | F4PJNLW01C9MXC | CDS | 53172 | 2823 | - | 0.331208 | |
g1789 | DLA_01952 | F4PJNLW01C9MXC | CDS | 56290 | 3264 | - | 0.279105 | |
g179 | DLA_00206 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | contig05409_1.exp | CDS | 416763 | 405 | + | 0.323457 |
g1790 | DLA_01953 | F4PJNLW01C9MXC | CDS | 59749 | 2139 | - | 0.320243 | |
g1791 | DLA_01954 | F4PJNLW01C9MXC | CDS | 62319 | 540 | - | 0.294444 | |
g1792 | DLA_11503 | F4PJNLW01C9MXC | CDS | 63360 | 441 | + | 0.267574 | |
g1793 | DLA_01955 | F4PJNLW01C9MXC | CDS | 63946 | 1053 | + | 0.283951 | |
g1794 | DLA_01957 | F4PJNLW01C9MXC | CDS | 67445 | 2940 | + | 0.339796 | |
g1795 | DLA_01958 | F4PJNLW01C9MXC | CDS | 70975 | 4878 | + | 0.356294 | |
g1796 | DLA_01959 | F4PJNLW01C9MXC | CDS | 76311 | 1953 | + | 0.322069 | |
g1797 | DLA_11504 | F4PJNLW01C9MXC | CDS | 78990 | 1482 | + | 0.261134 | |
g1798 | DLA_01960 | F4PJNLW01C9MXC | CDS | 80753 | 1065 | + | 0.277934 | |
g1799 | DLA_01961 | F4PJNLW01C9MXC | CDS | 81880 | 1875 | - | 0.3136 | |
g18 | DLA_00020 | contig05409_1.exp | CDS | 47066 | 1050 | + | 0.28381 | |
g180 | DLA_00207 | contig05409_1.exp | CDS | 417343 | 1845 | - | 0.337127 | |
g1800 | DLA_01963 | F4PJNLW01C9MXC | CDS | 84992 | 1206 | + | 0.262852 | |
g1801 | DLA_01964 | F4PJNLW01C9MXC | CDS | 86554 | 222 | - | 0.31982 | |
g1802 | DLA_01965 | F4PJNLW01C9MXC | CDS | 87099 | 4065 | - | 0.360394 | |
g1803 | DLA_01966 | F4PJNLW01C9MXC | CDS | 91412 | 3108 | - | 0.307272 | |
g1804 | DLA_11505 | F4PJNLW01C9MXC | CDS | 95206 | 1290 | - | 0.306202 | |
g1805 | DLA_01967 | F4PJNLW01C9MXC | CDS | 97515 | 2994 | + | 0.320975 | |
g1806 | DLA_01968 | F4PJNLW01C9MXC | CDS | 100646 | 1767 | + | 0.315224 | |
g1807 | DLA_01969 | F4PJNLW01C9MXC | CDS | 102764 | 1542 | + | 0.31323 | |
g1808 | DLA_01970 | F4PJNLW01C9MXC | CDS | 104447 | 1215 | - | 0.426337 | |
g1809 | DLA_01971 | F4PJNLW01C9MXC | CDS | 106252 | 2175 | + | 0.291494 | |
g181 | DLA_00208 | contig05409_1.exp | CDS | 419599 | 1677 | - | 0.359571 | |
g1810 | DLA_01972 | F4PJNLW01C9MXC | CDS | 109044 | 1554 | + | 0.273488 | |
g1811 | DLA_01973 | F4PJNLW01C9MXC | CDS | 112954 | 2076 | + | 0.305877 | |
g1812 | DLA_01975 | F4PJNLW01C9MXC | CDS | 115378 | 465 | - | 0.352688 | |
g1813 | DLA_01977 | F4PJNLW01C9MXC | CDS | 118291 | 1677 | + | 0.320215 | |
g1814 | DLA_01978 | F4PJNLW01C9MXC | CDS | 120975 | 3483 | - | 0.369796 | |
g1815 | DLA_01979 | F4PJNLW01C9MXC | CDS | 125202 | 3534 | + | 0.352292 | |
g1816 | DLA_01980 | F4PJNLW01C9MXC | CDS | 129365 | 891 | + | 0.280584 | |
g1817 | DLA_01981 | F4PJNLW01C9MXC | CDS | 130548 | 492 | - | 0.373984 | |
g1818 | DLA_01983 | F4PJNLW01C9MXC | CDS | 132212 | 1503 | + | 0.383234 | |
g1819 | DLA_01984 | F4PJNLW01C9MXC | CDS | 134212 | 2448 | + | 0.33415 | |
g182 | DLA_11435 | contig05409_1.exp | CDS | 421430 | 255 | - | 0.329412 | |
g1820 | DLA_11506 | F4PJNLW01C9MXC | CDS | 137442 | 387 | + | 0.366925 | |
g1821 | DLA_01985 | F4PJNLW01C9MXC | CDS | 137834 | 468 | - | 0.380342 | |
g1822 | DLA_01986 | F4PJNLW01C9MXC | CDS | 138699 | 1353 | - | 0.325203 | |
g1823 | DLA_01987 | F4PJNLW01C9MXC | CDS | 140606 | 600 | + | 0.268333 | |
g1824 | DLA_01989 | F4PJNLW01C9MXC | CDS | 141969 | 2637 | + | 0.332196 | |
g1825 | DLA_01990 | F4PJNLW01C9MXC | CDS | 144679 | 3279 | - | 0.331199 | |
g1826 | DLA_01991 | F4PJNLW01C9MXC | CDS | 148527 | 828 | - | 0.350242 | |
g1827 | DLA_01992 | F4PJNLW01C9MXC | CDS | 149644 | 2388 | - | 0.316164 | |
g1828 | DLA_01993 | F4PJNLW01C9MXC | CDS | 152107 | 2079 | - | 0.367484 | |
g1829 | DLA_01994 | F4PJNLW01C9MXC | CDS | 156500 | 594 | + | 0.228956 | |
g183 | DLA_00209 | contig05409_1.exp | CDS | 422224 | 501 | - | 0.253493 | |
g1830 | DLA_01995 | F4PJNLW01C9MXC | CDS | 157349 | 327 | - | 0.259939 | |
g1831 | DLA_01996 | F4PJNLW01C9MXC | CDS | 158585 | 909 | - | 0.29593 | |
g1832 | DLA_01997 | F4PJNLW01C9MXC | CDS | 159811 | 879 | - | 0.318544 | |
g1833 | DLA_01998 | F4PJNLW01C9MXC | CDS | 161915 | 1767 | + | 0.367855 | |
g1834 | DLA_01999 | F4PJNLW01C9MXC | CDS | 163994 | 660 | - | 0.424242 | |
g1835 | DLA_02000 | F4PJNLW01C9MXC | CDS | 165281 | 996 | + | 0.331325 | |
g1836 | DLA_02001 | F4PJNLW01C9MXC | CDS | 166645 | 267 | + | 0.307116 | |
g1837 | DLA_11507 | F4PJNLW01C9MXC | CDS | 167429 | 1632 | + | 0.307598 | |
g1838 | DLA_02002 | F4PJNLW01C9MXC | CDS | 169554 | 1647 | + | 0.342441 | |
g1839 | DLA_02003 | F4PJNLW01C9MXC | CDS | 171536 | 1776 | + | 0.345721 | |
g184 | DLA_11436 | contig05409_1.exp | CDS | 423677 | 402 | + | 0.383085 | |
g1840 | DLA_02006 | F4PJNLW01C9MXC | CDS | 176166 | 2433 | + | 0.345664 | |
g1841 | DLA_02007 | F4PJNLW01C9MXC | CDS | 178723 | 420 | - | 0.304762 | |
g1842 | DLA_02008 | F4PJNLW01C9MXC | CDS | 179384 | 2259 | + | 0.325365 | |
g1843 | DLA_02009 | F4PJNLW01C9MXC | CDS | 182189 | 813 | - | 0.445264 | |
g1844 | DLA_02014 | full transporter consisting of two ABC domains and two transmembrane domains | F4PJNLW01CH19P | CDS | 2590 | 4947 | - | 0.321609 |
g1845 | DLA_02015 | F4PJNLW01CH19P | CDS | 8186 | 732 | - | 0.312842 | |
g1846 | DLA_11508 | F4PJNLW01CH19P | CDS | 8980 | 213 | + | 0.248826 | |
g1847 | DLA_02016 | F4PJNLW01CH19P | CDS | 9505 | 672 | - | 0.31994 | |
g1848 | DLA_02017 | F4PJNLW01CH19P | CDS | 12434 | 3180 | + | 0.308176 | |
g1849 | DLA_02018 | F4PJNLW01CH19P | CDS | 15834 | 1911 | - | 0.338566 | |
g185 | DLA_00210 | contig05409_1.exp | CDS | 425058 | 3720 | + | 0.335753 | |
g1850 | DLA_02020 | F4PJNLW01CH19P | CDS | 18467 | 3444 | + | 0.315621 | |
g1851 | DLA_11509 | F4PJNLW01CH19P | CDS | 24205 | 876 | + | 0.319635 | |
g1852 | DLA_02021 | F4PJNLW01CH19P | CDS | 25167 | 483 | - | 0.287785 | |
g1853 | DLA_02022 | F4PJNLW01CH19P | CDS | 26171 | 4767 | - | 0.309419 | |
g1854 | DLA_02023 | F4PJNLW01CH19P | CDS | 31327 | 468 | - | 0.324786 | |
g1855 | DLA_11510 | F4PJNLW01CH19P | CDS | 31886 | 687 | - | 0.244541 | |
g1856 | DLA_02024 | F4PJNLW01CH19P | CDS | 32755 | 1194 | + | 0.275544 | |
g1857 | DLA_02026 | F4PJNLW01CH19P | CDS | 34078 | 1398 | - | 0.270386 | |
g1858 | DLA_02027 | F4PJNLW01CH19P | CDS | 35595 | 846 | + | 0.258865 | |
g1859 | DLA_02028 | F4PJNLW01CH19P | CDS | 36774 | 231 | + | 0.324675 | |
g186 | DLA_00211 | contig05409_1.exp | CDS | 429574 | 264 | - | 0.325758 | |
g1860 | DLA_02029 | F4PJNLW01CH19P | CDS | 37360 | 261 | - | 0.233716 | |
g1861 | DLA_02030 | F4PJNLW01CH19P | CDS | 37756 | 1650 | - | 0.355758 | |
g1862 | DLA_02033 | F4PJNLW01CH19P | CDS | 43706 | 1032 | + | 0.313953 | |
g1863 | DLA_02034 | F4PJNLW01CH19P | CDS | 45242 | 4554 | + | 0.343654 | |
g1864 | DLA_02035 | F4PJNLW01CH19P | CDS | 50139 | 597 | + | 0.266332 | |
g1865 | DLA_02036 | F4PJNLW01CH19P | CDS | 51000 | 1329 | + | 0.352144 | |
g1866 | DLA_02037 | F4PJNLW01CH19P | CDS | 53025 | 1191 | - | 0.326616 | |
g1867 | DLA_02038 | F4PJNLW01CH19P | CDS | 55096 | 714 | - | 0.277311 | |
g1868 | DLA_02039 | F4PJNLW01CH19P | CDS | 56146 | 1254 | + | 0.320574 | |
g1869 | DLA_02040 | F4PJNLW01CH19P | CDS | 58761 | 1749 | + | 0.340194 | |
g187 | DLA_00212 | catalyzes the reaction squalene AH2 O2 (S)-squalene-23-epoxide A H2O catalyzes the first oxygenation step in sterol biosynthesis | contig05409_1.exp | CDS | 430221 | 1401 | + | 0.384011 |
g1870 | DLA_02041 | F4PJNLW01CH19P | CDS | 61010 | 759 | - | 0.345191 | |
g1871 | DLA_02042 | F4PJNLW01CH19P | CDS | 62059 | 498 | - | 0.333333 | |
g1872 | DLA_02043 | F4PJNLW01CH19P | CDS | 63148 | 1011 | - | 0.297725 | |
g1873 | DLA_02044 | F4PJNLW01CH19P | CDS | 64785 | 1932 | + | 0.312629 | |
g1874 | DLA_11511 | F4PJNLW01CH19P | CDS | 67031 | 1629 | - | 0.298343 | |
g1875 | DLA_02045 | F4PJNLW01CH19P | CDS | 69162 | 1590 | - | 0.286792 | |
g1876 | DLA_11512 | F4PJNLW01CH19P | CDS | 73112 | 285 | - | 0.301754 | |
g1877 | DLA_02046 | F4PJNLW01CH19P | CDS | 73654 | 1206 | + | 0.335821 | |
g1878 | DLA_02048 | F4PJNLW01CH19P | CDS | 75505 | 588 | - | 0.319728 | |
g1879 | DLA_02049 | F4PJNLW01CH19P | CDS | 77173 | 441 | - | 0.276644 | |
g188 | DLA_00213 | contig05409_1.exp | CDS | 431852 | 564 | + | 0.296099 | |
g1880 | DLA_02051 | F4PJNLW01CH19P | CDS | 79980 | 1767 | - | 0.297114 | |
g1881 | DLA_02053 | F4PJNLW01CH19P | CDS | 82497 | 2958 | + | 0.289047 | |
g1882 | DLA_02054 | F4PJNLW01CH19P | CDS | 85535 | 510 | - | 0.356863 | |
g1883 | DLA_02055 | contains a C-terminal Bicoid-interacting 3 domain which occurs in methyltransferases that modify RNA-binding proteins has similarity to mammalian 7SK snRNA methylphosphate capping enzyme | F4PJNLW01CH19P | CDS | 86495 | 1107 | - | 0.264679 |
g1884 | DLA_02056 | F4PJNLW01CH19P | CDS | 87735 | 1626 | - | 0.305658 | |
g1885 | DLA_02057 | F4PJNLW01CH19P | CDS | 89614 | 960 | - | 0.313542 | |
g1886 | DLA_02058 | F4PJNLW01CH19P | CDS | 90672 | 1686 | - | 0.332147 | |
g1887 | DLA_02059 | F4PJNLW01CH19P | CDS | 93765 | 615 | + | 0.339837 | |
g1888 | DLA_02060 | F4PJNLW01CH19P | CDS | 94574 | 1068 | - | 0.264981 | |
g1889 | DLA_02061 | F4PJNLW01CH19P | CDS | 96374 | 2988 | - | 0.351406 | |
g189 | DLA_00214 | contig05409_1.exp | CDS | 432803 | 429 | - | 0.368298 | |
g1890 | DLA_02063 | F4PJNLW01DERRH | CDS | 1797 | 1434 | + | 0.304742 | |
g1891 | DLA_02064 | F4PJNLW01DERRH | CDS | 3464 | 780 | - | 0.288462 | |
g1892 | DLA_02065 | F4PJNLW01DERRH | CDS | 4546 | 333 | + | 0.333333 | |
g1893 | DLA_02066 | F4PJNLW01DERRH | CDS | 5098 | 639 | - | 0.311424 | |
g1894 | DLA_02067 | F4PJNLW01DERRH | CDS | 6069 | 1905 | - | 0.333858 | |
g1895 | DLA_02068 | F4PJNLW01DERRH | CDS | 10749 | 903 | + | 0.275748 | |
g1896 | DLA_02069 | F4PJNLW01DERRH | CDS | 12214 | 1836 | - | 0.323529 | |
g1897 | DLA_02070 | F4PJNLW01DERRH | CDS | 14426 | 570 | - | 0.305263 | |
g1898 | DLA_11513 | F4PJNLW01DERRH | CDS | 15159 | 2400 | + | 0.26375 | |
g1899 | DLA_02071 | F4PJNLW01DERRH | CDS | 18285 | 1749 | + | 0.280732 | |
g19 | DLA_00021 | contig05409_1.exp | CDS | 48189 | 1287 | - | 0.301476 | |
g190 | DLA_00215 | contig05409_1.exp | CDS | 434388 | 1557 | + | 0.296724 | |
g1900 | DLA_02072 | F4PJNLW01DERRH | CDS | 20262 | 1929 | + | 0.352514 | |
g1901 | DLA_02073 | F4PJNLW01DERRH | CDS | 22421 | 669 | - | 0.331839 | |
g1902 | DLA_02074 | F4PJNLW01DERRH | CDS | 23450 | 1236 | + | 0.251618 | |
g1903 | DLA_02076 | F4PJNLW01DERRH | CDS | 25871 | 8265 | - | 0.285057 | |
g1904 | DLA_02078 | F4PJNLW01DERRH | CDS | 34658 | 1374 | + | 0.372635 | |
g1905 | DLA_02079 | F4PJNLW01DERRH | CDS | 36362 | 2904 | - | 0.276859 | |
g1906 | DLA_02081 | F4PJNLW01DERRH | CDS | 40982 | 4380 | - | 0.364612 | |
g1907 | DLA_02082 | F4PJNLW01DERRH | CDS | 46237 | 3225 | - | 0.326202 | |
g1908 | DLA_11514 | F4PJNLW01DERRH | CDS | 49735 | 1839 | - | 0.334421 | |
g1909 | DLA_02083 | F4PJNLW01DERRH | CDS | 52075 | 2175 | - | 0.308506 | |
g191 | DLA_00216 | contig05409_1.exp | CDS | 436598 | 381 | - | 0.293963 | |
g1910 | DLA_02084 | F4PJNLW01DERRH | CDS | 55904 | 642 | - | 0.397196 | |
g1911 | DLA_02085 | F4PJNLW01DERRH | CDS | 56949 | 2706 | - | 0.388766 | |
g1912 | DLA_02086 | F4PJNLW01DERRH | CDS | 61634 | 3099 | + | 0.324621 | |
g1913 | DLA_02087 | F4PJNLW01DERRH | CDS | 64798 | 3456 | - | 0.286748 | |
g1914 | DLA_02088 | F4PJNLW01DERRH | CDS | 68847 | 306 | - | 0.303922 | |
g1915 | DLA_02089 | F4PJNLW01DERRH | CDS | 69678 | 4797 | + | 0.317699 | |
g1916 | DLA_02093 | F4PJNLW01DERRH | CDS | 77939 | 3597 | - | 0.310537 | |
g1917 | DLA_02094 | F4PJNLW01DERRH | CDS | 81728 | 816 | + | 0.275735 | |
g1918 | DLA_02095 | F4PJNLW01DERRH | CDS | 83164 | 1044 | + | 0.346743 | |
g1919 | DLA_02096 | F4PJNLW01DERRH | CDS | 84617 | 855 | - | 0.252632 | |
g192 | DLA_00217 | contig05409_1.exp | CDS | 439001 | 417 | - | 0.345324 | |
g1920 | DLA_02097 | F4PJNLW01DERRH | CDS | 85823 | 933 | - | 0.229368 | |
g1921 | DLA_02099 | F4PJNLW01DERRH | CDS | 87436 | 1557 | - | 0.337829 | |
g1922 | DLA_02101 | F4PJNLW01DERRH | CDS | 91978 | 1263 | - | 0.370546 | |
g1923 | DLA_02102 | one of two orthologs of NPC1 (with | F4PJNLW01DERRH | CDS | 93350 | 2724 | - | 0.374816 |
g1924 | DLA_02104 | F4PJNLW01DERRH | CDS | 97466 | 2316 | + | 0.316926 | |
g1925 | DLA_02105 | F4PJNLW01DERRH | CDS | 100080 | 795 | + | 0.299371 | |
g1926 | DLA_02106 | contains an actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domain near its N-terminus and a C-terminal SH3 (src Homology-3) domain predicted to have an N-terminal signal peptide | F4PJNLW01DERRH | CDS | 101536 | 459 | + | 0.490196 |
g1927 | DLA_11515 | F4PJNLW01DERRH | CDS | 102175 | 390 | - | 0.220513 | |
g1928 | DLA_02107 | F4PJNLW01DERRH | CDS | 102834 | 969 | - | 0.316821 | |
g1929 | DLA_02108 | F4PJNLW01DERRH | CDS | 107389 | 3471 | - | 0.273984 | |
g193 | DLA_00218 | contig05409_1.exp | CDS | 442800 | 11571 | - | 0.347593 | |
g1930 | DLA_02112 | F4PJNLW01DERRH | CDS | 114657 | 1644 | + | 0.340024 | |
g1931 | DLA_02113 | highly similar to SCY1 family kinases does not contain the consensus sequences required for kinase function however the SCY1 family encodes highly conserved non-canonical kinases that are believed to function | F4PJNLW01DERRH | CDS | 116363 | 2886 | - | 0.310464 |
g1932 | DLA_02114 | F4PJNLW01DERRH | CDS | 119843 | 1809 | + | 0.368712 | |
g1933 | DLA_02115 | F4PJNLW01DERRH | CDS | 122277 | 882 | + | 0.291383 | |
g1934 | DLA_02116 | F4PJNLW01DERRH | CDS | 123238 | 1344 | - | 0.294643 | |
g1935 | DLA_02117 | F4PJNLW01DERRH | CDS | 124838 | 2322 | - | 0.314384 | |
g1936 | DLA_02118 | F4PJNLW01DERRH | CDS | 127209 | 291 | - | 0.24055 | |
g1937 | DLA_02119 | F4PJNLW01DERRH | CDS | 129167 | 1641 | + | 0.303474 | |
g1938 | DLA_02120 | F4PJNLW01DERRH | CDS | 131132 | 1833 | + | 0.287507 | |
g1939 | DLA_02122 | F4PJNLW01DERRH | CDS | 136550 | 1689 | + | 0.292481 | |
g194 | DLA_00219 | contig05409_1.exp | CDS | 455380 | 3327 | + | 0.327322 | |
g1940 | DLA_02123 | F4PJNLW01DERRH | CDS | 138515 | 3516 | + | 0.292947 | |
g1941 | DLA_02124 | F4PJNLW01DERRH | CDS | 142381 | 3621 | - | 0.266777 | |
g1942 | DLA_02125 | F4PJNLW01DERRH | CDS | 146376 | 1869 | + | 0.310861 | |
g1943 | DLA_02126 | F4PJNLW01DERRH | CDS | 148360 | 1062 | - | 0.295669 | |
g1944 | DLA_02128 | F4PJNLW01DERRH | CDS | 149745 | 2712 | - | 0.344027 | |
g1945 | DLA_02129 | F4PJNLW01DERRH | CDS | 152805 | 1011 | - | 0.339268 | |
g1946 | DLA_02130 | F4PJNLW01DERRH | CDS | 153959 | 1074 | + | 0.295158 | |
g1947 | DLA_02131 | F4PJNLW01DERRH | CDS | 155626 | 243 | - | 0.279835 | |
g1948 | DLA_02132 | F4PJNLW01DERRH | CDS | 156534 | 2022 | - | 0.29723 | |
g1949 | DLA_02133 | F4PJNLW01DERRH | CDS | 159521 | 561 | - | 0.322638 | |
g195 | DLA_00220 | contig05409_1.exp | CDS | 458972 | 381 | - | 0.228346 | |
g1950 | DLA_02134 | F4PJNLW01DERRH | CDS | 160510 | 714 | + | 0.29972 | |
g1951 | DLA_02135 | F4PJNLW01DERRH | CDS | 161510 | 582 | + | 0.300687 | |
g1952 | DLA_02137 | conserved component of the mitochondrial intermembrane space forms a complex with Timm10 which mediates insertion of hydrophobic proteins at the inner membrane. | F4PJNLW01DERRH | CDS | 163079 | 237 | + | 0.265823 |
g1953 | DLA_02138 | ortholog of peroxin 2 required for peroxisome biogenesis contains two putative transmembrane domains mutations in human homolog cause a variety of peroxisomal disorders | F4PJNLW01DERRH | CDS | 163546 | 1275 | - | 0.300392 |
g1954 | DLA_02139 | F4PJNLW01DERRH | CDS | 165377 | 1248 | + | 0.34375 | |
g1955 | DLA_02140 | contains one DnaJ N-terminal domain and one MYND-type zinc finger domain contains 8 putative transmembrane domains | F4PJNLW01DERRH | CDS | 166725 | 1617 | - | 0.301793 |
g1956 | DLA_02142 | F4PJNLW01DERRH | CDS | 168968 | 1653 | + | 0.275862 | |
g1957 | DLA_02145 | F4PJNLW01DERRH | CDS | 173983 | 1689 | - | 0.275311 | |
g1958 | DLA_02146 | F4PJNLW01DERRH | CDS | 175887 | 1626 | - | 0.367159 | |
g1959 | DLA_02147 | F4PJNLW01DERRH | CDS | 177999 | 4176 | - | 0.288793 | |
g196 | DLA_00221 | contig05409_1.exp | CDS | 459568 | 2538 | - | 0.353428 | |
g1960 | DLA_02150 | F4PJNLW01DERRH | CDS | 183486 | 3339 | - | 0.279125 | |
g1961 | DLA_02151 | F4PJNLW01DERRH | CDS | 187104 | 1758 | - | 0.29124 | |
g1962 | DLA_02152 | F4PJNLW01DERRH | CDS | 189117 | 3288 | + | 0.296533 | |
g1963 | DLA_02153 | F4PJNLW01DERRH | CDS | 192709 | 459 | + | 0.328976 | |
g1964 | DLA_02154 | F4PJNLW01DERRH | CDS | 193309 | 1461 | + | 0.347707 | |
g1965 | DLA_02155 | F4PJNLW01DERRH | CDS | 195195 | 207 | + | 0.304348 | |
g1966 | DLA_02157 | F4PJNLW01DERRH | CDS | 196610 | 1953 | + | 0.322581 | |
g1967 | DLA_02158 | F4PJNLW01DERRH | CDS | 199507 | 432 | + | 0.351852 | |
g1968 | DLA_11516 | F4PJNLW01DERRH | CDS | 200464 | 243 | + | 0.27572 | |
g1969 | DLA_02159 | F4PJNLW01DERRH | CDS | 202025 | 1911 | + | 0.308739 | |
g197 | DLA_00222 | contig05409_1.exp | CDS | 462586 | 2604 | - | 0.357143 | |
g1970 | DLA_02160 | F4PJNLW01DERRH | CDS | 204259 | 3408 | - | 0.294014 | |
g1971 | DLA_02161 | F4PJNLW01DERRH | CDS | 207894 | 3372 | - | 0.31465 | |
g1972 | DLA_02162 | F4PJNLW01DERRH | CDS | 211574 | 3309 | + | 0.289211 | |
g1973 | DLA_02163 | F4PJNLW01DERRH | CDS | 215110 | 1011 | - | 0.327399 | |
g1974 | DLA_02164 | F4PJNLW01DERRH | CDS | 216781 | 324 | + | 0.305556 | |
g1975 | DLA_02165 | F4PJNLW01DERRH | CDS | 217239 | 4539 | - | 0.315488 | |
g1976 | DLA_02166 | F4PJNLW01DERRH | CDS | 222365 | 723 | - | 0.305671 | |
g1977 | DLA_02167 | catalyzes the reaction N-D-ribosylpurine Hsub2subO purine D-ribose | F4PJNLW01DERRH | CDS | 223179 | 1755 | - | 0.366382 |
g1978 | DLA_02169 | F4PJNLW01DERRH | CDS | 225983 | 1635 | - | 0.329664 | |
g1979 | DLA_02170 | F4PJNLW01DERRH | CDS | 227916 | 966 | + | 0.282609 | |
g198 | DLA_00223 | contig05409_1.exp | CDS | 465626 | 1779 | - | 0.362563 | |
g1980 | DLA_02171 | F4PJNLW01DERRH | CDS | 229005 | 2184 | - | 0.270604 | |
g1981 | DLA_02173 | F4PJNLW01DERRH | CDS | 232435 | 1050 | - | 0.412381 | |
g1982 | DLA_02174 | catalyzes the reaction isocitrate glyoxylate succinate | F4PJNLW01DERRH | CDS | 234194 | 1425 | - | 0.399298 |
g1983 | DLA_02175 | putative ortholog of H. sapiens CNOT3 and S. cerevisiae NOT3 component of the CCR4-NOT transcription complex | F4PJNLW01DERRH | CDS | 236457 | 2127 | + | 0.341326 |
g1984 | DLA_02177 | F4PJNLW01DERRH | CDS | 239607 | 1878 | + | 0.290735 | |
g1985 | DLA_02178 | putative RNA helicase contains an RWD domain (RING finger and WD repeat) | F4PJNLW01DERRH | CDS | 241601 | 4122 | - | 0.318535 |
g1986 | DLA_02179 | F4PJNLW01DERRH | CDS | 246124 | 6699 | + | 0.286909 | |
g1987 | DLA_02181 | F4PJNLW01DERRH | CDS | 253617 | 534 | - | 0.294007 | |
g1988 | DLA_02182 | F4PJNLW01DERRH | CDS | 254588 | 2055 | + | 0.325547 | |
g1989 | DLA_02183 | F4PJNLW01DERRH | CDS | 257541 | 3534 | + | 0.338427 | |
g199 | DLA_00224 | contig05409_1.exp | CDS | 468870 | 2700 | + | 0.348148 | |
g1990 | DLA_02186 | bCommunity annotation:b DDB_G0272740 is similar to histone2a-related transcription factors of the Hap5CBFNF-Y family which bind to the subsequence CCAAT and is threefold upregulated (p3E-7) in a Dicty strain in which the retinoblastoma-like gene rblA has been disrupted (Doquang et al in preparation). Most genes associated with S-phase or mitosis are upregulated in this strain. This is is consistent with the idea that factors of the the Hap5CBFNF-Y factors are involved in cell cycle progression in Dictyostelium as they are in animal cells. Harry MacWilliams September 2009br Closer examination of the blast results suggests that this gene does NOT code for an NF-Y subunit. Real orthologs to DDB_G0272740 do seem to occur in some fungi for instance Aspergillis and Ajellomyces although there are none in budding yeast. Insects also have a protein that is much more closely related to DDB_G0272740 than it is to nfyC it is called chrac-16 and is a component of the chromatin accessibility complex | F4PJNLW01DERRH | CDS | 262371 | 483 | + | 0.335404 |
g1991 | DLA_02187 | F4PJNLW01DERRH | CDS | 263326 | 1596 | + | 0.325188 | |
g1992 | DLA_02188 | F4PJNLW01DERRH | CDS | 265721 | 1827 | - | 0.313082 | |
g1993 | DLA_02189 | F4PJNLW01DERRH | CDS | 268216 | 1248 | - | 0.289263 | |
g1994 | DLA_11517 | F4PJNLW01DERRH | CDS | 269736 | 654 | + | 0.357798 | |
g1995 | DLA_02190 | F4PJNLW01DERRH | CDS | 270589 | 4941 | + | 0.325845 | |
g1996 | DLA_02191 | F4PJNLW01DERRH | CDS | 275682 | 1665 | - | 0.293093 | |
g1997 | DLA_02192 | F4PJNLW01DERRH | CDS | 277503 | 753 | + | 0.337317 | |
g1998 | DLA_02194 | F4PJNLW01DERRH | CDS | 279280 | 1236 | + | 0.307443 | |
g1999 | DLA_02196 | F4PJNLW01DERRH | CDS | 281279 | 687 | + | 0.298399 | |
g2 | DLA_00003 | contig05409_1.exp | CDS | 4241 | 2001 | - | 0.312844 | |
g20 | DLA_00023 | contig05409_1.exp | CDS | 50205 | 1470 | + | 0.256463 | |
g200 | DLA_00225 | contig05409_1.exp | CDS | 472000 | 960 | - | 0.361458 | |
g2000 | DLA_02197 | F4PJNLW01DERRH | CDS | 282099 | 1515 | - | 0.29835 | |
g2001 | DLA_02198 | F4PJNLW01DERRH | CDS | 284469 | 3387 | + | 0.317095 | |
g2002 | DLA_02199 | F4PJNLW01DERRH | CDS | 288085 | 1767 | + | 0.263724 | |
g2003 | DLA_02200 | F4PJNLW01DERRH | CDS | 290208 | 2994 | - | 0.358717 | |
g2004 | DLA_02201 | F4PJNLW01DERRH | CDS | 293502 | 1332 | + | 0.326577 | |
g2005 | DLA_02202 | F4PJNLW01DERRH | CDS | 294910 | 1302 | - | 0.302611 | |
g2006 | DLA_02203 | F4PJNLW01DERRH | CDS | 296729 | 804 | + | 0.314677 | |
g2007 | DLA_02205 | F4PJNLW01DERRH | CDS | 298814 | 1050 | + | 0.344762 | |
g2008 | DLA_02206 | F4PJNLW01DERRH | CDS | 300035 | 450 | - | 0.268889 | |
g2009 | DLA_02207 | F4PJNLW01DERRH | CDS | 301351 | 3474 | + | 0.312032 | |
g201 | DLA_00226 | contig05409_1.exp | CDS | 474156 | 1941 | + | 0.333849 | |
g2010 | DLA_02209 | F4PJNLW01DERRH | CDS | 306235 | 708 | + | 0.324859 | |
g2011 | DLA_02210 | F4PJNLW01DERRH | CDS | 307764 | 444 | + | 0.304054 | |
g2012 | DLA_02211 | F4PJNLW01DERRH | CDS | 308652 | 2424 | - | 0.352723 | |
g2013 | DLA_02212 | F4PJNLW01DERRH | CDS | 312485 | 3036 | + | 0.325099 | |
g2014 | DLA_02213 | F4PJNLW01DERRH | CDS | 316087 | 768 | + | 0.320312 | |
g2015 | DLA_02214 | F4PJNLW01DERRH | CDS | 317437 | 816 | - | 0.308824 | |
g2016 | DLA_02215 | F4PJNLW01DERRH | CDS | 318766 | 597 | - | 0.276382 | |
g2017 | DLA_02216 | F4PJNLW01DERRH | CDS | 319983 | 1350 | - | 0.302222 | |
g2018 | DLA_02217 | F4PJNLW01DERRH | CDS | 322559 | 447 | + | 0.324385 | |
g2019 | DLA_02218 | F4PJNLW01DERRH | CDS | 323818 | 2733 | + | 0.317234 | |
g202 | DLA_00227 | contig05409_1.exp | CDS | 476159 | 1665 | - | 0.32973 | |
g2020 | DLA_02219 | F4PJNLW01DERRH | CDS | 327130 | 1305 | - | 0.400766 | |
g2021 | DLA_02220 | F4PJNLW01DERRH | CDS | 328795 | 1659 | + | 0.373116 | |
g2022 | DLA_02221 | member of the TKL (tyrosine kinase-like) group contains a galactose oxidase central domain and three Kelch motifs | F4PJNLW01DERRH | CDS | 331361 | 3084 | + | 0.336576 |
g2023 | DLA_02222 | F4PJNLW01DERRH | CDS | 334619 | 1878 | + | 0.300319 | |
g2024 | DLA_02224 | F4PJNLW01DERRH | CDS | 337619 | 435 | + | 0.296552 | |
g2025 | DLA_02225 | F4PJNLW01DERRH | CDS | 338385 | 1125 | - | 0.423111 | |
g2026 | DLA_02226 | F4PJNLW01DERRH | CDS | 339808 | 1437 | - | 0.267919 | |
g2027 | DLA_02227 | F4PJNLW01DERRH | CDS | 341499 | 1455 | + | 0.304467 | |
g2028 | DLA_02228 | F4PJNLW01DERRH | CDS | 343003 | 1557 | - | 0.270392 | |
g2029 | DLA_02229 | F4PJNLW01DERRH | CDS | 344671 | 3309 | - | 0.290118 | |
g203 | DLA_00228 | contig05409_1.exp | CDS | 478056 | 576 | - | 0.373264 | |
g2030 | DLA_02230 | F4PJNLW01DERRH | CDS | 348200 | 5121 | - | 0.285686 | |
g2031 | DLA_02232 | F4PJNLW01DERRH | CDS | 354964 | 540 | + | 0.32037 | |
g2032 | DLA_02233 | F4PJNLW01DERRH | CDS | 355650 | 960 | - | 0.311458 | |
g2033 | DLA_02234 | catalyzes the reaction L-arginine Hsub2subO L-citrulline NHsub3sub N-terminal half highly similar to bacterial argnine deiminase an amidinotransferase | F4PJNLW01DERRH | CDS | 357152 | 2469 | + | 0.356825 |
g2034 | DLA_02236 | F4PJNLW01DERRH | CDS | 360490 | 468 | - | 0.279915 | |
g2035 | DLA_02237 | F4PJNLW01DERRH | CDS | 361545 | 1866 | + | 0.369775 | |
g2036 | DLA_11518 | F4PJNLW01DERRH | CDS | 363552 | 1533 | + | 0.282453 | |
g2037 | DLA_02238 | F4PJNLW01DERRH | CDS | 365219 | 2718 | + | 0.337748 | |
g2038 | DLA_02239 | F4PJNLW01DERRH | CDS | 368836 | 2067 | + | 0.293662 | |
g2039 | DLA_02240 | F4PJNLW01DERRH | CDS | 371275 | 2832 | - | 0.289548 | |
g204 | DLA_00229 | contig05409_1.exp | CDS | 479135 | 5376 | + | 0.322359 | |
g2040 | DLA_02242 | F4PJNLW01DERRH | CDS | 374424 | 639 | + | 0.276995 | |
g2041 | DLA_02243 | F4PJNLW01DERRH | CDS | 375261 | 840 | - | 0.308333 | |
g2042 | DLA_02244 | F4PJNLW01DERRH | CDS | 376306 | 498 | + | 0.277108 | |
g2043 | DLA_02245 | F4PJNLW01DERRH | CDS | 377043 | 1224 | - | 0.360294 | |
g2044 | DLA_02246 | F4PJNLW01DERRH | CDS | 378706 | 642 | - | 0.32866 | |
g2045 | DLA_02247 | F4PJNLW01DERRH | CDS | 379847 | 510 | - | 0.307843 | |
g2046 | DLA_02248 | F4PJNLW01DERRH | CDS | 380636 | 222 | - | 0.333333 | |
g2047 | DLA_02249 | ortholog of human and S. cerevisiae SSU72 (suppressor of SUA7 protein 2) S. cerevisiae SSU72 is involved in several roles including 3' end formation of pre-mRNA and snoRNAs and dephosphorylation of RNA polymerase II the D. discoideum homolog of yeast SUA7 is | F4PJNLW01DERRH | CDS | 381616 | 564 | + | 0.326241 |
g2048 | DLA_02250 | F4PJNLW01DERRH | CDS | 382483 | 2097 | - | 0.34144 | |
g2049 | DLA_02252 | F4PJNLW01DERRH | CDS | 385220 | 5760 | + | 0.336111 | |
g205 | DLA_00230 | contig05409_1.exp | CDS | 484578 | 606 | - | 0.313531 | |
g2050 | DLA_02253 | F4PJNLW01DERRH | CDS | 391499 | 231 | - | 0.277056 | |
g2051 | DLA_02254 | F4PJNLW01DERRH | CDS | 392695 | 2034 | + | 0.314651 | |
g2052 | DLA_02256 | F4PJNLW01DERRH | CDS | 395701 | 2118 | + | 0.314448 | |
g2053 | DLA_02258 | F4PJNLW01DERRH | CDS | 398071 | 258 | - | 0.321705 | |
g2054 | DLA_02259 | F4PJNLW01DERRH | CDS | 398942 | 468 | - | 0.260684 | |
g2055 | DLA_02260 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | F4PJNLW01DERRH | CDS | 399702 | 2160 | + | 0.346296 |
g2056 | DLA_02262 | related to the Ovarian Tumour (OTU) gene of Drosophila function is unknown but conserved cysteine and histidine and possibly the aspartate residues suggests that those not yet recognized as peptidases could possess cysteine protease activity | F4PJNLW01DERRH | CDS | 402730 | 1179 | - | 0.301103 |
g2057 | DLA_02264 | F4PJNLW01DERRH | CDS | 404448 | 300 | + | 0.276667 | |
g2058 | DLA_11519 | F4PJNLW01DERRH | CDS | 404947 | 1668 | - | 0.288369 | |
g2059 | DLA_02265 | F4PJNLW01DERRH | CDS | 406893 | 1740 | - | 0.274138 | |
g206 | DLA_00231 | contig05409_1.exp | CDS | 485681 | 843 | + | 0.351127 | |
g2060 | DLA_02266 | F4PJNLW01DERRH | CDS | 408802 | 819 | + | 0.328449 | |
g2061 | DLA_02267 | F4PJNLW01DERRH | CDS | 409660 | 603 | - | 0.291874 | |
g2062 | DLA_02268 | F4PJNLW01DERRH | CDS | 410457 | 3645 | - | 0.336351 | |
g2063 | DLA_02269 | F4PJNLW01DERRH | CDS | 414494 | 3372 | + | 0.327402 | |
g2064 | DLA_02270 | F4PJNLW01DERRH | CDS | 418357 | 1044 | + | 0.283525 | |
g2065 | DLA_02271 | F4PJNLW01DERRH | CDS | 420949 | 1620 | + | 0.302469 | |
g2066 | DLA_02272 | F4PJNLW01DERRH | CDS | 422662 | 1842 | + | 0.309446 | |
g2067 | DLA_02273 | protein serinethreonine phosphatase required for chemotaxis and development suppresses the | F4PJNLW01DERRH | CDS | 424814 | 915 | - | 0.339891 |
g2068 | DLA_02274 | F4PJNLW01DERRH | CDS | 426502 | 1080 | + | 0.426852 | |
g2069 | DLA_02275 | F4PJNLW01DERRH | CDS | 427735 | 1788 | + | 0.283557 | |
g207 | DLA_00232 | contig05409_1.exp | CDS | 487515 | 480 | - | 0.335417 | |
g2070 | DLA_02276 | F4PJNLW01DERRH | CDS | 430170 | 615 | - | 0.300813 | |
g2071 | DLA_02277 | F4PJNLW01DERRH | CDS | 430969 | 1344 | + | 0.3125 | |
g2072 | DLA_02278 | F4PJNLW01DERRH | CDS | 432510 | 2199 | - | 0.330605 | |
g2073 | DLA_02279 | F4PJNLW01DERRH | CDS | 435245 | 2370 | + | 0.353165 | |
g2074 | DLA_02280 | F4PJNLW01DERRH | CDS | 438382 | 2196 | + | 0.32377 | |
g2075 | DLA_02281 | F4PJNLW01DERRH | CDS | 440861 | 1632 | + | 0.292279 | |
g2076 | DLA_02282 | F4PJNLW01DERRH | CDS | 442717 | 1791 | + | 0.340034 | |
g2077 | DLA_02283 | F4PJNLW01DERRH | CDS | 444991 | 1725 | + | 0.243478 | |
g2078 | DLA_02284 | F4PJNLW01DERRH | CDS | 447118 | 1227 | - | 0.264059 | |
g2079 | DLA_02285 | F4PJNLW01DERRH | CDS | 448612 | 651 | + | 0.245776 | |
g208 | DLA_00233 | contig05409_1.exp | CDS | 488194 | 669 | - | 0.349776 | |
g2080 | DLA_02286 | F4PJNLW01DERRH | CDS | 449787 | 2118 | - | 0.315864 | |
g2081 | DLA_02287 | F4PJNLW01DERRH | CDS | 453019 | 774 | - | 0.316537 | |
g2082 | DLA_02288 | F4PJNLW01DERRH | CDS | 454042 | 1833 | + | 0.368249 | |
g2083 | DLA_02289 | F4PJNLW01DERRH | CDS | 455944 | 621 | - | 0.193237 | |
g2084 | DLA_02290 | F4PJNLW01DERRH | CDS | 457305 | 642 | + | 0.306854 | |
g2085 | DLA_02292 | F4PJNLW01DERRH | CDS | 458988 | 906 | - | 0.30574 | |
g2086 | DLA_02293 | F4PJNLW01DERRH | CDS | 460223 | 216 | + | 0.25463 | |
g2087 | DLA_02294 | ortholog of human FA2H S. cerevisiae SCS7 contains a cytochrome b5 heme-binding domain and 4 predicted transmembrane domains | F4PJNLW01DERRH | CDS | 460608 | 1053 | - | 0.297246 |
g2088 | DLA_02295 | very similar to acyl-coenzyme A oxidases but lacks the full domain | F4PJNLW01DERRH | CDS | 462405 | 2049 | + | 0.312347 |
g2089 | DLA_02298 | F4PJNLW01DERRH | CDS | 465875 | 1908 | - | 0.361111 | |
g209 | DLA_00234 | contig05409_1.exp | CDS | 489310 | 1308 | + | 0.332569 | |
g2090 | DLA_02304 | F4PJNLW01DERRH | CDS | 472123 | 201 | - | 0.293532 | |
g2091 | DLA_02305 | F4PJNLW01DERRH | CDS | 473996 | 1182 | - | 0.37225 | |
g2092 | DLA_02306 | F4PJNLW01DERRH | CDS | 476826 | 1020 | + | 0.290196 | |
g2093 | DLA_02307 | F4PJNLW01DERRH | CDS | 477952 | 1251 | - | 0.286171 | |
g2094 | DLA_11520 | F4PJNLW01DERRH | CDS | 479507 | 1053 | - | 0.226971 | |
g2095 | DLA_02309 | F4PJNLW01DERRH | CDS | 480929 | 2331 | + | 0.265551 | |
g2096 | DLA_02310 | F4PJNLW01DERRH | CDS | 483304 | 1515 | - | 0.285149 | |
g2097 | DLA_02311 | F4PJNLW01DERRH | CDS | 485150 | 924 | + | 0.262987 | |
g2098 | DLA_02312 | F4PJNLW01DERRH | CDS | 486095 | 2109 | - | 0.26221 | |
g2099 | DLA_02313 | F4PJNLW01DERRH | CDS | 488478 | 1860 | + | 0.327419 | |
g21 | DLA_00024 | contig05409_1.exp | CDS | 51750 | 4119 | - | 0.312212 | |
g210 | DLA_00235 | contig05409_1.exp | CDS | 490745 | 477 | - | 0.278826 | |
g2100 | DLA_02314 | F4PJNLW01DERRH | CDS | 490482 | 948 | + | 0.317511 | |
g2101 | DLA_02315 | F4PJNLW01DERRH | CDS | 491620 | 300 | - | 0.24 | |
g2102 | DLA_02316 | AGC group AKT family protein serinethreonine kinase similar to other metazoan AktPKB including an N-terminal PH domain homologous kinase and C-terminal regulatory domains and phosphorylation sites required for AktPKB activation | F4PJNLW01DERRH | CDS | 492601 | 1605 | + | 0.316511 |
g2103 | DLA_02317 | F4PJNLW01DERRH | CDS | 494755 | 1548 | + | 0.273256 | |
g2104 | DLA_02318 | F4PJNLW01DERRH | CDS | 496452 | 873 | - | 0.296678 | |
g2105 | DLA_02319 | F4PJNLW01DERRH | CDS | 497752 | 2889 | + | 0.283143 | |
g2106 | DLA_02321 | F4PJNLW01DERRH | CDS | 501586 | 2130 | + | 0.320188 | |
g2107 | DLA_02322 | F4PJNLW01DERRH | CDS | 504619 | 3096 | + | 0.320413 | |
g2108 | DLA_02323 | F4PJNLW01DERRH | CDS | 508296 | 5091 | + | 0.310941 | |
g2109 | DLA_02324 | F4PJNLW01DERRH | CDS | 514197 | 3657 | - | 0.283292 | |
g211 | DLA_00236 | contig05409_1.exp | CDS | 491684 | 1548 | + | 0.307494 | |
g2110 | DLA_02325 | F4PJNLW01DERRH | CDS | 517999 | 3723 | - | 0.288746 | |
g2111 | DLA_02326 | contains the metal-dependent phosphohydrolase HD region similar to the H. sapiens SAM domain and HD domain-containing protein 1 (SAMHD1) but lacking the N-terminal SAM domain | F4PJNLW01DERRH | CDS | 522253 | 1446 | + | 0.313278 |
g2112 | DLA_02327 | F4PJNLW01DERRH | CDS | 523842 | 1416 | - | 0.251412 | |
g2113 | DLA_02328 | F4PJNLW01DERRH | CDS | 525869 | 1803 | + | 0.297837 | |
g2114 | DLA_02329 | F4PJNLW01DERRH | CDS | 527970 | 375 | - | 0.253333 | |
g2115 | DLA_02330 | F4PJNLW01DERRH | CDS | 529004 | 1323 | - | 0.378685 | |
g2116 | DLA_02331 | F4PJNLW01DERRH | CDS | 531195 | 5007 | + | 0.317955 | |
g2117 | DLA_02332 | F4PJNLW01DERRH | CDS | 536660 | 2052 | + | 0.352339 | |
g2118 | DLA_02333 | F4PJNLW01DERRH | CDS | 538893 | 2685 | - | 0.356425 | |
g2119 | DLA_02334 | F4PJNLW01DERRH | CDS | 542855 | 219 | - | 0.347032 | |
g212 | DLA_00237 | contig05409_1.exp | CDS | 493532 | 759 | - | 0.267457 | |
g2120 | DLA_02335 | F4PJNLW01DERRH | CDS | 543480 | 240 | + | 0.258333 | |
g2121 | DLA_02336 | F4PJNLW01DERRH | CDS | 543900 | 4401 | - | 0.329016 | |
g2122 | DLA_02337 | F4PJNLW01DERRH | CDS | 550631 | 336 | - | 0.303571 | |
g2123 | DLA_02338 | F4PJNLW01DERRH | CDS | 551075 | 1446 | + | 0.325726 | |
g2124 | DLA_02339 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases there is a second copy of this gene | F4PJNLW01DERRH | CDS | 552865 | 1164 | - | 0.34622 |
g2125 | DLA_02340 | F4PJNLW01DERRH | CDS | 554500 | 3648 | + | 0.302357 | |
g2126 | DLA_02341 | similar to budding yeast Sar1 a 21 kDa GTP- binding protein involved in vesicular transport between the endoplasmic reticulum and the Golgi | F4PJNLW01DERRH | CDS | 558311 | 570 | - | 0.342105 |
g2127 | DLA_02342 | F4PJNLW01DERRH | CDS | 559738 | 1632 | + | 0.293505 | |
g2128 | DLA_02343 | F4PJNLW01DERRH | CDS | 561494 | 1683 | + | 0.299465 | |
g2129 | DLA_02344 | F4PJNLW01DERRH | CDS | 563367 | 951 | + | 0.298633 | |
g213 | DLA_00238 | contig05409_1.exp | CDS | 494802 | 1380 | + | 0.344203 | |
g2130 | DLA_02345 | F4PJNLW01DERRH | CDS | 564709 | 1395 | - | 0.277419 | |
g2131 | DLA_02346 | F4PJNLW01DERRH | CDS | 568066 | 1404 | + | 0.318376 | |
g2132 | DLA_02347 | F4PJNLW01DERRH | CDS | 569759 | 1056 | - | 0.347538 | |
g2133 | DLA_02348 | F4PJNLW01DERRH | CDS | 571287 | 1404 | + | 0.312678 | |
g2134 | DLA_02350 | F4PJNLW01DERRH | CDS | 573091 | 1656 | - | 0.30314 | |
g2135 | DLA_02351 | F4PJNLW01DERRH | CDS | 577253 | 1275 | - | 0.376471 | |
g2136 | DLA_02352 | contains one RF-1 domain similar to human ICT1 (immature colon carcinoma transcript 1 protein) | F4PJNLW01DERRH | CDS | 578788 | 441 | + | 0.306122 |
g2137 | DLA_02353 | F4PJNLW01DERRH | CDS | 579554 | 396 | - | 0.330808 | |
g2138 | DLA_11521 | F4PJNLW01DERRH | CDS | 580992 | 225 | - | 0.324444 | |
g2139 | DLA_02354 | F4PJNLW01DERRH | CDS | 581485 | 393 | - | 0.300254 | |
g214 | DLA_00239 | contig05409_1.exp | CDS | 496650 | 1584 | + | 0.328283 | |
g2140 | DLA_02355 | F4PJNLW01DERRH | CDS | 582450 | 618 | + | 0.338188 | |
g2141 | DLA_02356 | F4PJNLW01DERRH | CDS | 583991 | 2916 | + | 0.326475 | |
g2142 | DLA_02357 | F4PJNLW01DERRH | CDS | 587571 | 909 | - | 0.354235 | |
g2143 | DLA_02358 | F4PJNLW01DERRH | CDS | 588974 | 1461 | + | 0.310746 | |
g2144 | DLA_02359 | component of the Dictyostelium Arp2Arp3 complex contributes to DdPPK2 activity also described as member of the polyphosphate kinase PPK3 family | F4PJNLW01DERRH | CDS | 591126 | 1176 | + | 0.366497 |
g2145 | DLA_02360 | F4PJNLW01DERRH | CDS | 593350 | 1875 | + | 0.3248 | |
g2146 | DLA_02361 | F4PJNLW01DERRH | CDS | 595738 | 756 | - | 0.328042 | |
g2147 | DLA_02362 | F4PJNLW01DERRH | CDS | 596905 | 744 | + | 0.307796 | |
g2148 | DLA_02363 | F4PJNLW01DERRH | CDS | 598124 | 2364 | + | 0.340102 | |
g2149 | DLA_02364 | F4PJNLW01DERRH | CDS | 601400 | 1248 | + | 0.339744 | |
g215 | DLA_11437 | contig05409_1.exp | CDS | 498601 | 1371 | + | 0.318745 | |
g2150 | DLA_02365 | F4PJNLW01DERRH | CDS | 603155 | 1260 | + | 0.34127 | |
g2151 | DLA_02366 | F4PJNLW01DERRH | CDS | 604902 | 573 | + | 0.356021 | |
g2152 | DLA_02367 | F4PJNLW01DERRH | CDS | 605747 | 2016 | - | 0.364087 | |
g2153 | DLA_02368 | F4PJNLW01DERRH | CDS | 608208 | 7680 | + | 0.327214 | |
g2154 | DLA_02370 | F4PJNLW01DERRH | CDS | 615978 | 4080 | - | 0.318873 | |
g2155 | DLA_02371 | F4PJNLW01DERRH | CDS | 620452 | 1353 | - | 0.329638 | |
g2156 | DLA_02373 | F4PJNLW01DERRH | CDS | 622765 | 1491 | + | 0.348089 | |
g2157 | DLA_02374 | F4PJNLW01DERRH | CDS | 624718 | 477 | + | 0.29979 | |
g2158 | DLA_02375 | F4PJNLW01DERRH | CDS | 625530 | 2805 | + | 0.335472 | |
g2159 | DLA_02376 | F4PJNLW01DERRH | CDS | 628678 | 1065 | + | 0.335211 | |
g216 | DLA_00240 | contig05409_1.exp | CDS | 500740 | 1035 | + | 0.317874 | |
g2160 | DLA_02377 | F4PJNLW01DERRH | CDS | 630088 | 1296 | + | 0.3125 | |
g2161 | DLA_02378 | 34 kDa subunit of heterodimeric actin capping protein cap3234 32 kDa subunit is encoded by acpA contributes to the dynactin complex | F4PJNLW01DERRH | CDS | 632199 | 846 | + | 0.369976 |
g2162 | DLA_02380 | member of the AGC kinase group similar to kinase domains of NDR (nuclear Dbf2-related) and MAST (microtubule-associated serinethreonine kinase) | F4PJNLW01DERRH | CDS | 633835 | 4887 | + | 0.331492 |
g2163 | DLA_02381 | F4PJNLW01DERRH | CDS | 639639 | 3507 | + | 0.278871 | |
g2164 | DLA_02383 | F4PJNLW01DERRH | CDS | 643513 | 528 | + | 0.320076 | |
g2165 | DLA_02384 | F4PJNLW01DERRH | CDS | 644315 | 945 | - | 0.326984 | |
g2166 | DLA_02385 | F4PJNLW01DERRH | CDS | 646165 | 1683 | + | 0.286393 | |
g2167 | DLA_02386 | F4PJNLW01DERRH | CDS | 648072 | 1086 | + | 0.333333 | |
g2168 | DLA_02388 | F4PJNLW01DERRH | CDS | 650583 | 1488 | + | 0.30578 | |
g2169 | DLA_02389 | F4PJNLW01DERRH | CDS | 652174 | 966 | - | 0.354037 | |
g217 | DLA_00241 | contig05409_1.exp | CDS | 501969 | 1797 | + | 0.304953 | |
g2170 | DLA_02390 | F4PJNLW01DERRH | CDS | 654784 | 2079 | + | 0.334776 | |
g2171 | DLA_02391 | F4PJNLW01DERRH | CDS | 657051 | 1575 | - | 0.345397 | |
g2172 | DLA_02392 | F4PJNLW01DERRH | CDS | 658997 | 1602 | + | 0.32834 | |
g2173 | DLA_02393 | F4PJNLW01DERRH | CDS | 660867 | 1635 | + | 0.310703 | |
g2174 | DLA_02394 | F4PJNLW01DERRH | CDS | 662630 | 2847 | - | 0.336495 | |
g2175 | DLA_02395 | F4PJNLW01DERRH | CDS | 665801 | 1602 | + | 0.303371 | |
g2176 | DLA_02396 | F4PJNLW01DERRH | CDS | 667623 | 1647 | + | 0.313904 | |
g2177 | DLA_02397 | F4PJNLW01DERRH | CDS | 669543 | 573 | - | 0.369983 | |
g2178 | DLA_02398 | F4PJNLW01DERRH | CDS | 670836 | 1455 | + | 0.314777 | |
g2179 | DLA_02399 | F4PJNLW01DERRH | CDS | 672767 | 447 | + | 0.313199 | |
g218 | DLA_00242 | contig05409_1.exp | CDS | 504449 | 207 | + | 0.362319 | |
g2180 | DLA_02400 | F4PJNLW01DERRH | CDS | 673694 | 2010 | + | 0.31791 | |
g2181 | DLA_02401 | F4PJNLW01DERRH | CDS | 675835 | 1575 | + | 0.290159 | |
g2182 | DLA_02402 | F4PJNLW01DERRH | CDS | 677448 | 1251 | - | 0.272582 | |
g2183 | DLA_02403 | F4PJNLW01DERRH | CDS | 679196 | 3123 | - | 0.361191 | |
g2184 | DLA_02404 | F4PJNLW01DERRH | CDS | 682692 | 837 | + | 0.293907 | |
g2185 | DLA_02405 | F4PJNLW01DERRH | CDS | 683706 | 2817 | + | 0.265886 | |
g2186 | DLA_02407 | F4PJNLW01DERRH | CDS | 686710 | 1143 | - | 0.300962 | |
g2187 | DLA_02408 | F4PJNLW01DERRH | CDS | 688219 | 978 | - | 0.311861 | |
g2188 | DLA_02409 | F4PJNLW01DERRH | CDS | 689648 | 390 | + | 0.330769 | |
g2189 | DLA_02410 | F4PJNLW01DERRH | CDS | 690191 | 645 | - | 0.268217 | |
g219 | DLA_00243 | conserved low molecular weight phosphotyrosine protein phosphatase acts on tyrosine phosphorylated proteins low-MW aryl phosphates and natural and synthetic acyl phosphates | contig05409_1.exp | CDS | 504881 | 534 | + | 0.299625 |
g2190 | DLA_02411 | similar to human ZDHHC16 (zinc finger DHHC domain-containing protein 16) contains 4 putative transmembrane domains | F4PJNLW01DERRH | CDS | 691057 | 996 | + | 0.264056 |
g2191 | DLA_02412 | F4PJNLW01DERRH | CDS | 692195 | 1149 | - | 0.280244 | |
g2192 | DLA_02413 | F4PJNLW01DERRH | CDS | 693649 | 1407 | - | 0.267946 | |
g2193 | DLA_02414 | F4PJNLW01DERRH | CDS | 696290 | 1455 | - | 0.292783 | |
g2194 | DLA_02415 | F4PJNLW01DERRH | CDS | 698259 | 1287 | + | 0.305361 | |
g2195 | DLA_02416 | F4PJNLW01DERRH | CDS | 700714 | 226 | + | 0.358407 | |
g2196 | DLA_02417 | F4PJNLW01DL4V0 | CDS | 286 | 2565 | + | 0.292788 | |
g2197 | DLA_02418 | F4PJNLW01DL4V0 | CDS | 3136 | 921 | - | 0.324647 | |
g2198 | DLA_02419 | F4PJNLW01DL4V0 | CDS | 4582 | 1329 | + | 0.315275 | |
g2199 | DLA_02420 | F4PJNLW01DL4V0 | CDS | 6082 | 801 | - | 0.265918 | |
g22 | DLA_00026 | contig05409_1.exp | CDS | 56708 | 2028 | + | 0.324951 | |
g220 | DLA_00244 | contig05409_1.exp | CDS | 505581 | 492 | - | 0.367886 | |
g2200 | DLA_02421 | F4PJNLW01DL4V0 | CDS | 7218 | 888 | + | 0.25 | |
g2201 | DLA_02422 | F4PJNLW01DL4V0 | CDS | 8281 | 1506 | + | 0.282869 | |
g2202 | DLA_02423 | F4PJNLW01DL4V0 | CDS | 10016 | 492 | - | 0.27439 | |
g2203 | DLA_02424 | F4PJNLW01DL4V0 | CDS | 11101 | 2979 | + | 0.302115 | |
g2204 | DLA_02425 | F4PJNLW01DL4V0 | CDS | 14892 | 489 | - | 0.267894 | |
g2205 | DLA_02427 | F4PJNLW01DL4V0 | CDS | 16269 | 894 | - | 0.314318 | |
g2206 | DLA_02429 | F4PJNLW01EE5MJ | CDS | 154 | 1812 | + | 0.312362 | |
g2207 | DLA_02432 | F4PJNLW01EE5MJ | CDS | 5435 | 1047 | - | 0.30277 | |
g2208 | DLA_02433 | F4PJNLW01EE5MJ | CDS | 7786 | 3030 | + | 0.29934 | |
g2209 | DLA_02434 | F4PJNLW01EE5MJ | CDS | 11521 | 4248 | - | 0.305085 | |
g221 | DLA_00245 | contig05409_1.exp | CDS | 506395 | 1575 | + | 0.32127 | |
g2210 | DLA_02435 | F4PJNLW01EE5MJ | CDS | 15976 | 4845 | - | 0.31806 | |
g2211 | DLA_02436 | F4PJNLW01EE5MJ | CDS | 21053 | 4320 | - | 0.290509 | |
g2212 | DLA_02437 | F4PJNLW01EE5MJ | CDS | 25737 | 4242 | - | 0.303866 | |
g2213 | DLA_02438 | F4PJNLW01EE5MJ | CDS | 30323 | 546 | - | 0.31685 | |
g2214 | DLA_02439 | F4PJNLW01EE5MJ | CDS | 31062 | 2133 | - | 0.311299 | |
g2215 | DLA_02440 | F4PJNLW01EE5MJ | CDS | 33600 | 810 | + | 0.328395 | |
g2216 | DLA_02442 | F4PJNLW01EE5MJ | CDS | 37107 | 2034 | + | 0.345133 | |
g2217 | DLA_02443 | F4PJNLW01EE5MJ | CDS | 39460 | 954 | + | 0.316562 | |
g2218 | DLA_02444 | F4PJNLW01EE5MJ | CDS | 40852 | 1836 | - | 0.328431 | |
g2219 | DLA_02446 | very similar to the mammalian glucosidase II subunit beta also known as protein kinase C substrate 80K-H which catalyzes the sequential removal of two alpha-13-linked glucose residues in the second step of N-linked oligosaccharide processing also similar to yeast GTB1 defects in human PRKCSH are a cause of polycystic liver disease (PCLD) | F4PJNLW01EE5MJ | CDS | 44405 | 1395 | + | 0.326882 |
g222 | DLA_00246 | contig05409_1.exp | CDS | 508105 | 1119 | + | 0.297587 | |
g2220 | DLA_02447 | F4PJNLW01EE5MJ | CDS | 46366 | 828 | - | 0.373188 | |
g2221 | DLA_02448 | F4PJNLW01EE5MJ | CDS | 48223 | 651 | + | 0.298003 | |
g2222 | DLA_02449 | F4PJNLW01EE5MJ | CDS | 49018 | 1320 | - | 0.368182 | |
g2223 | DLA_02450 | F4PJNLW01EE5MJ | CDS | 50619 | 546 | - | 0.300366 | |
g2224 | DLA_02451 | F4PJNLW01EE5MJ | CDS | 51431 | 1824 | + | 0.302632 | |
g2225 | DLA_02452 | F4PJNLW01EE5MJ | CDS | 53523 | 2505 | - | 0.295409 | |
g2226 | DLA_02456 | F4PJNLW01EE5MJ | CDS | 57774 | 1611 | - | 0.371819 | |
g2227 | DLA_02457 | F4PJNLW01EE5MJ | CDS | 59569 | 825 | + | 0.321212 | |
g2228 | DLA_02458 | in S. cerevisiae essential for the fidelity of chromosome transmission and component of the RFC complexbrbr bCommunity annotation:b CTF18 ( | F4PJNLW01EE5MJ | CDS | 60463 | 2562 | - | 0.323575 |
g2229 | DLA_02460 | F4PJNLW01EE5MJ | CDS | 64137 | 1395 | + | 0.32043 | |
g223 | DLA_00249 | contig05409_1.exp | CDS | 512213 | 2949 | + | 0.2706 | |
g2230 | DLA_02462 | F4PJNLW01EE5MJ | CDS | 66467 | 2622 | - | 0.31312 | |
g2231 | DLA_02463 | F4PJNLW01EE5MJ | CDS | 69546 | 1530 | + | 0.347712 | |
g2232 | DLA_02464 | F4PJNLW01EE5MJ | CDS | 71463 | 1431 | + | 0.415793 | |
g2233 | DLA_02465 | F4PJNLW01EE5MJ | CDS | 73342 | 2217 | + | 0.28507 | |
g2234 | DLA_02466 | F4PJNLW01EE5MJ | CDS | 76241 | 747 | - | 0.344043 | |
g2235 | DLA_02469 | F4PJNLW01EE5MJ | CDS | 78419 | 2289 | - | 0.351682 | |
g2236 | DLA_02470 | F4PJNLW01EE5MJ | CDS | 81014 | 1212 | + | 0.285479 | |
g2237 | DLA_02471 | F4PJNLW01EE5MJ | CDS | 82403 | 3486 | - | 0.335341 | |
g2238 | DLA_02472 | F4PJNLW01EE5MJ | CDS | 86819 | 1212 | - | 0.306931 | |
g2239 | DLA_02473 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | F4PJNLW01EE5MJ | CDS | 89204 | 498 | + | 0.359438 |
g224 | DLA_00250 | contig05409_1.exp | CDS | 515467 | 3195 | + | 0.320814 | |
g2240 | DLA_02474 | F4PJNLW01EE5MJ | CDS | 90599 | 333 | + | 0.375375 | |
g2241 | DLA_02475 | F4PJNLW01EE5MJ | CDS | 91269 | 729 | - | 0.322359 | |
g2242 | DLA_02476 | F4PJNLW01EE5MJ | CDS | 92490 | 585 | + | 0.305983 | |
g2243 | DLA_02477 | F4PJNLW01EE5MJ | CDS | 93131 | 2730 | - | 0.335897 | |
g2244 | DLA_02481 | F4PJNLW01EE5MJ | CDS | 99352 | 2415 | - | 0.342443 | |
g2245 | DLA_02482 | F4PJNLW01EE5MJ | CDS | 102051 | 534 | - | 0.397004 | |
g2246 | DLA_02483 | F4PJNLW01EE5MJ | CDS | 103357 | 627 | + | 0.414673 | |
g2247 | DLA_02484 | catalyzes the reaction alpha-D-mannose 1-phosphate D-mannose 6-phosphate | F4PJNLW01EE5MJ | CDS | 104560 | 741 | + | 0.306343 |
g2248 | DLA_02485 | F4PJNLW01EE5MJ | CDS | 105506 | 1389 | - | 0.362131 | |
g2249 | DLA_02486 | F4PJNLW01EE5MJ | CDS | 107128 | 1710 | - | 0.380702 | |
g225 | DLA_00251 | contig05409_1.exp | CDS | 518732 | 1461 | - | 0.325804 | |
g2250 | DLA_02487 | F4PJNLW01EE5MJ | CDS | 109186 | 201 | - | 0.238806 | |
g2251 | DLA_02488 | F4PJNLW01EE5MJ | CDS | 109636 | 4569 | + | 0.33968 | |
g2252 | DLA_02489 | F4PJNLW01EE5MJ | CDS | 115007 | 2484 | - | 0.293076 | |
g2253 | DLA_11522 | F4PJNLW01EE5MJ | CDS | 117818 | 1245 | + | 0.324498 | |
g2254 | DLA_02490 | F4PJNLW01EE5MJ | CDS | 120402 | 1422 | + | 0.291842 | |
g2255 | DLA_02491 | F4PJNLW01EE5MJ | CDS | 122005 | 1104 | - | 0.320652 | |
g2256 | DLA_11523 | F4PJNLW01EE5MJ | CDS | 123438 | 1152 | - | 0.333333 | |
g2257 | DLA_02492 | F4PJNLW01EE5MJ | CDS | 124939 | 1149 | - | 0.37772 | |
g2258 | DLA_02493 | F4PJNLW01EE5MJ | CDS | 127130 | 4536 | + | 0.309965 | |
g2259 | DLA_02494 | F4PJNLW01EE5MJ | CDS | 131950 | 5448 | - | 0.324706 | |
g226 | DLA_00252 | contig05409_1.exp | CDS | 520501 | 1173 | + | 0.30861 | |
g2260 | DLA_02495 | F4PJNLW01EE5MJ | CDS | 138880 | 2247 | - | 0.365821 | |
g2261 | DLA_02496 | F4PJNLW01EE5MJ | CDS | 141455 | 6441 | - | 0.334886 | |
g2262 | DLA_02497 | F4PJNLW01EE5MJ | CDS | 148989 | 6384 | + | 0.350877 | |
g2263 | DLA_02499 | F4PJNLW01EE5MJ | CDS | 157099 | 1092 | + | 0.311355 | |
g2264 | DLA_02500 | F4PJNLW01EE5MJ | CDS | 158741 | 1872 | - | 0.313034 | |
g2265 | DLA_02501 | F4PJNLW01EE5MJ | CDS | 161286 | 4029 | + | 0.315215 | |
g2266 | DLA_02502 | F4PJNLW01EE5MJ | CDS | 165514 | 1254 | - | 0.389952 | |
g2267 | DLA_02503 | F4PJNLW01EE5MJ | CDS | 167375 | 2418 | - | 0.330438 | |
g2268 | DLA_02504 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | F4PJNLW01EE5MJ | CDS | 170057 | 2556 | - | 0.330595 |
g2269 | DLA_02508 | F4PJNLW01EE5MJ | CDS | 174693 | 1038 | + | 0.266859 | |
g227 | DLA_00253 | contig05409_1.exp | CDS | 521712 | 639 | - | 0.28169 | |
g2270 | DLA_02509 | F4PJNLW01EE5MJ | CDS | 176088 | 1011 | - | 0.292779 | |
g2271 | DLA_02510 | catalyzes the reaction succinate ubiquinone fumarate ubiquinol cytochrome b560 subunit contains 2 transmembrane domains | F4PJNLW01EE5MJ | CDS | 177446 | 597 | + | 0.351759 |
g2272 | DLA_02511 | F4PJNLW01EE5MJ | CDS | 178455 | 1602 | - | 0.314607 | |
g2273 | DLA_02513 | F4PJNLW01EE5MJ | CDS | 181437 | 918 | - | 0.339869 | |
g2274 | DLA_02514 | similar to ubiquitin in the N-terminal region contains one von Willebrand factor (vWF) type A domain | F4PJNLW01EE5MJ | CDS | 182810 | 1980 | - | 0.322222 |
g2275 | DLA_02515 | F4PJNLW01EE5MJ | CDS | 184989 | 2679 | - | 0.329601 | |
g2276 | DLA_02517 | F4PJNLW01EE5MJ | CDS | 187796 | 369 | + | 0.289973 | |
g2277 | DLA_02519 | F4PJNLW01EE5MJ | CDS | 188812 | 960 | + | 0.309375 | |
g2278 | DLA_02520 | F4PJNLW01EE5MJ | CDS | 190279 | 1485 | + | 0.297643 | |
g2279 | DLA_02521 | F4PJNLW01EE5MJ | CDS | 192285 | 1467 | + | 0.306748 | |
g228 | DLA_00254 | contig05409_1.exp | CDS | 522967 | 534 | + | 0.430712 | |
g2280 | DLA_02522 | F4PJNLW01EE5MJ | CDS | 194409 | 1344 | + | 0.306548 | |
g2281 | DLA_02523 | F4PJNLW01EE5MJ | CDS | 195831 | 1731 | + | 0.302137 | |
g2282 | DLA_02524 | F4PJNLW01EE5MJ | CDS | 198242 | 2193 | - | 0.336981 | |
g2283 | DLA_02525 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | F4PJNLW01EE5MJ | CDS | 200780 | 1800 | + | 0.306667 |
g2284 | DLA_02526 | F4PJNLW01EE5MJ | CDS | 202874 | 3267 | - | 0.373125 | |
g2285 | DLA_02527 | F4PJNLW01EE5MJ | CDS | 207745 | 1950 | - | 0.38359 | |
g2286 | DLA_02528 | F4PJNLW01EE5MJ | CDS | 210161 | 1857 | - | 0.283791 | |
g2287 | DLA_11524 | F4PJNLW01EE5MJ | CDS | 212292 | 267 | + | 0.307116 | |
g2288 | DLA_02529 | F4PJNLW01EE5MJ | CDS | 212854 | 930 | - | 0.337634 | |
g2289 | DLA_02531 | F4PJNLW01EE5MJ | CDS | 214852 | 5394 | + | 0.342047 | |
g229 | DLA_00256 | contig05409_1.exp | CDS | 524048 | 294 | + | 0.29932 | |
g2290 | DLA_02532 | F4PJNLW01EE5MJ | CDS | 220604 | 456 | + | 0.342105 | |
g2291 | DLA_02533 | F4PJNLW01EE5MJ | CDS | 221235 | 4041 | + | 0.309329 | |
g2292 | DLA_02534 | F4PJNLW01EE5MJ | CDS | 225419 | 1422 | - | 0.362166 | |
g2293 | DLA_02535 | F4PJNLW01EE5MJ | CDS | 227311 | 2112 | + | 0.309186 | |
g2294 | DLA_02536 | F4PJNLW01EE5MJ | CDS | 229541 | 363 | - | 0.272727 | |
g2295 | DLA_02537 | F4PJNLW01EE5MJ | CDS | 230488 | 1137 | + | 0.282322 | |
g2296 | DLA_02538 | F4PJNLW01EE5MJ | CDS | 231917 | 831 | - | 0.305656 | |
g2297 | DLA_02539 | homolog of human SLC35B4 S. cerevisiae YEA4 contains 9 putative transmembrane domains | F4PJNLW01EE5MJ | CDS | 233195 | 1620 | + | 0.271605 |
g2298 | DLA_02541 | F4PJNLW01EE5MJ | CDS | 235127 | 4590 | - | 0.325272 | |
g2299 | DLA_02542 | F4PJNLW01EE5MJ | CDS | 240220 | 2424 | + | 0.304043 | |
g23 | DLA_00027 | contig05409_1.exp | CDS | 59383 | 1641 | - | 0.33638 | |
g230 | DLA_00257 | contig05409_1.exp | CDS | 527002 | 1392 | + | 0.35704 | |
g2300 | DLA_02543 | F4PJNLW01EE5MJ | CDS | 242888 | 2571 | + | 0.317775 | |
g2301 | DLA_02544 | F4PJNLW01EE5MJ | CDS | 245689 | 2445 | + | 0.345603 | |
g2302 | DLA_02545 | F4PJNLW01EE5MJ | CDS | 248576 | 1083 | - | 0.322253 | |
g2303 | DLA_02546 | F4PJNLW01EE5MJ | CDS | 250911 | 1335 | + | 0.322097 | |
g2304 | DLA_02547 | F4PJNLW01EE5MJ | CDS | 252570 | 3954 | + | 0.262013 | |
g2305 | DLA_02548 | F4PJNLW01EE5MJ | CDS | 256752 | 3549 | - | 0.31051 | |
g2306 | DLA_02550 | F4PJNLW01EE5MJ | CDS | 260902 | 897 | - | 0.338907 | |
g2307 | DLA_11525 | F4PJNLW01EE5MJ | CDS | 262147 | 885 | - | 0.310734 | |
g2308 | DLA_02551 | F4PJNLW01EE5MJ | CDS | 263249 | 1152 | + | 0.305556 | |
g2309 | DLA_02552 | F4PJNLW01EE5MJ | CDS | 264490 | 1134 | - | 0.29806 | |
g231 | DLA_00258 | contig05409_1.exp | CDS | 528688 | 3471 | + | 0.332181 | |
g2310 | DLA_02553 | F4PJNLW01EE5MJ | CDS | 265738 | 1455 | - | 0.287285 | |
g2311 | DLA_02555 | F4PJNLW01EE5MJ | CDS | 267824 | 2103 | + | 0.309082 | |
g2312 | DLA_02556 | F4PJNLW01EE5MJ | CDS | 270520 | 1629 | - | 0.304481 | |
g2313 | DLA_02557 | F4PJNLW01EE5MJ | CDS | 273651 | 1254 | + | 0.358852 | |
g2314 | DLA_02558 | F4PJNLW01EE5MJ | CDS | 275444 | 555 | - | 0.245045 | |
g2315 | DLA_02559 | F4PJNLW01EE5MJ | CDS | 276235 | 741 | + | 0.300945 | |
g2316 | DLA_02561 | F4PJNLW01EE5MJ | CDS | 277899 | 348 | - | 0.241379 | |
g2317 | DLA_02562 | F4PJNLW01EE5MJ | CDS | 278398 | 1965 | - | 0.354198 | |
g2318 | DLA_02563 | F4PJNLW01EE5MJ | CDS | 280458 | 603 | + | 0.268657 | |
g2319 | DLA_02564 | bifunctional enzyme that catalyzes the reactions Nsup10sup-formyl-Hsub4subF AICAR tetrahydrofolate phosphoribosyl-formamido-carboxamide and phosphoribosyl-formamido-carboxamide IMP Hsub2subO expressed in prespore cells | F4PJNLW01EE5MJ | CDS | 281676 | 1587 | + | 0.361689 |
g232 | DLA_00259 | contig05409_1.exp | CDS | 532316 | 264 | + | 0.30303 | |
g2320 | DLA_02566 | F4PJNLW01EE5MJ | CDS | 284500 | 1374 | - | 0.36754 | |
g2321 | DLA_02567 | F4PJNLW01EE5MJ | CDS | 286080 | 1269 | - | 0.287628 | |
g2322 | DLA_02568 | F4PJNLW01EE5MJ | CDS | 287875 | 1101 | + | 0.369664 | |
g2323 | DLA_02569 | F4PJNLW01EE5MJ | CDS | 289151 | 3285 | - | 0.327549 | |
g2324 | DLA_02570 | F4PJNLW01EE5MJ | CDS | 292896 | 543 | - | 0.360958 | |
g2325 | DLA_02571 | F4PJNLW01EE5MJ | CDS | 294226 | 1146 | + | 0.399651 | |
g2326 | DLA_02573 | F4PJNLW01EE5MJ | CDS | 296326 | 2718 | - | 0.336277 | |
g2327 | DLA_02574 | F4PJNLW01EE5MJ | CDS | 299310 | 1146 | + | 0.356021 | |
g2328 | DLA_02575 | similar to human TMEM144 contains 10 predicted transmembrane domains | F4PJNLW01EE5MJ | CDS | 300819 | 1098 | - | 0.351548 |
g2329 | DLA_02576 | F4PJNLW01EE5MJ | CDS | 302604 | 1479 | + | 0.369844 | |
g233 | DLA_00260 | contig05409_1.exp | CDS | 532716 | 2115 | - | 0.329078 | |
g2330 | DLA_02577 | F4PJNLW01EE5MJ | CDS | 304268 | 1359 | + | 0.292862 | |
g2331 | DLA_02578 | F4PJNLW01EE5MJ | CDS | 306650 | 234 | + | 0.324786 | |
g2332 | DLA_02579 | F4PJNLW01EE5MJ | CDS | 308501 | 2493 | + | 0.30365 | |
g2333 | DLA_02580 | F4PJNLW01EE5MJ | CDS | 311170 | 1512 | - | 0.39418 | |
g2334 | DLA_02581 | F4PJNLW01EE5MJ | CDS | 313047 | 876 | + | 0.284247 | |
g2335 | DLA_02583 | F4PJNLW01EE5MJ | CDS | 315011 | 810 | - | 0.311111 | |
g2336 | DLA_02584 | F4PJNLW01EE5MJ | CDS | 316180 | 1230 | - | 0.321138 | |
g2337 | DLA_02585 | F4PJNLW01EE5MJ | CDS | 317569 | 1173 | - | 0.384484 | |
g2338 | DLA_02588 | F4PJNLW01EE5MJ | CDS | 321261 | 813 | - | 0.367774 | |
g2339 | DLA_02589 | F4PJNLW01EE5MJ | CDS | 322533 | 963 | + | 0.330218 | |
g234 | DLA_00261 | contig05409_1.exp | CDS | 535283 | 1473 | - | 0.308893 | |
g2340 | DLA_02590 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | F4PJNLW01EE5MJ | CDS | 323676 | 885 | + | 0.281356 |
g2341 | DLA_02591 | F4PJNLW01EE5MJ | CDS | 324958 | 2022 | - | 0.300198 | |
g2342 | DLA_02594 | F4PJNLW01EE5MJ | CDS | 327477 | 2202 | + | 0.343778 | |
g2343 | DLA_11526 | F4PJNLW01EE5MJ | CDS | 329858 | 801 | - | 0.324594 | |
g2344 | DLA_02595 | F4PJNLW01EE5MJ | CDS | 330963 | 870 | - | 0.344828 | |
g2345 | DLA_02596 | F4PJNLW01EE5MJ | CDS | 332082 | 2229 | + | 0.32795 | |
g2346 | DLA_11527 | F4PJNLW01EE5MJ | CDS | 334523 | 477 | - | 0.408805 | |
g2347 | DLA_02597 | F4PJNLW01EE5MJ | CDS | 335037 | 1137 | - | 0.310466 | |
g2348 | DLA_02598 | F4PJNLW01EE5MJ | CDS | 336903 | 2295 | - | 0.342484 | |
g2349 | DLA_02599 | F4PJNLW01EE5MJ | CDS | 339679 | 1890 | + | 0.356614 | |
g235 | DLA_00262 | contig05409_1.exp | CDS | 536892 | 1434 | + | 0.285914 | |
g2350 | DLA_02600 | F4PJNLW01EE5MJ | CDS | 341646 | 693 | - | 0.290043 | |
g2351 | DLA_02601 | F4PJNLW01EE5MJ | CDS | 343120 | 753 | + | 0.318725 | |
g2352 | DLA_02602 | F4PJNLW01EE5MJ | CDS | 343941 | 1917 | - | 0.34168 | |
g2353 | DLA_02603 | F4PJNLW01EE5MJ | CDS | 346036 | 1038 | - | 0.330443 | |
g2354 | DLA_02604 | F4PJNLW01EE5MJ | CDS | 347562 | 1611 | + | 0.359404 | |
g2355 | DLA_02605 | F4PJNLW01EE5MJ | CDS | 349403 | 1944 | + | 0.297839 | |
g2356 | DLA_02606 | F4PJNLW01EE5MJ | CDS | 351662 | 2148 | - | 0.3473 | |
g2357 | DLA_02607 | F4PJNLW01EE5MJ | CDS | 354640 | 645 | - | 0.339535 | |
g2358 | DLA_02608 | F4PJNLW01EE5MJ | CDS | 356045 | 1539 | + | 0.359324 | |
g2359 | DLA_02609 | F4PJNLW01EE5MJ | CDS | 357944 | 339 | - | 0.312684 | |
g236 | DLA_00263 | contig05409_1.exp | CDS | 538358 | 1656 | - | 0.301932 | |
g2360 | DLA_02610 | F4PJNLW01EE5MJ | CDS | 358341 | 906 | + | 0.307947 | |
g2361 | DLA_02611 | F4PJNLW01EE5MJ | CDS | 359488 | 1440 | + | 0.297917 | |
g2362 | DLA_02612 | F4PJNLW01EE5MJ | CDS | 361585 | 2547 | + | 0.299176 | |
g2363 | DLA_02613 | F4PJNLW01EE5MJ | CDS | 364580 | 621 | - | 0.289855 | |
g2364 | DLA_02614 | F4PJNLW01EE5MJ | CDS | 365601 | 5229 | - | 0.347676 | |
g2365 | DLA_02615 | catalyzes the reaction ATP ethanolamine ADP O-phosphoethanolamine | F4PJNLW01EE5MJ | CDS | 371747 | 1074 | + | 0.290503 |
g2366 | DLA_02616 | F4PJNLW01EE5MJ | CDS | 373247 | 591 | + | 0.279188 | |
g2367 | DLA_02618 | F4PJNLW01EE5MJ | CDS | 373941 | 1221 | - | 0.328419 | |
g2368 | DLA_02619 | F4PJNLW01EE5MJ | CDS | 375408 | 1371 | - | 0.408461 | |
g2369 | DLA_02621 | F4PJNLW01EE5MJ | CDS | 377325 | 1002 | - | 0.291417 | |
g237 | DLA_00264 | contig05409_1.exp | CDS | 540310 | 1800 | - | 0.360556 | |
g2370 | DLA_02622 | F4PJNLW01EE5MJ | CDS | 378817 | 768 | + | 0.291667 | |
g2371 | DLA_02623 | F4PJNLW01EE5MJ | CDS | 379741 | 2967 | - | 0.296933 | |
g2372 | DLA_02625 | F4PJNLW01EE5MJ | CDS | 383687 | 2985 | - | 0.307873 | |
g2373 | DLA_02627 | F4PJNLW01EE5MJ | CDS | 387997 | 471 | + | 0.292994 | |
g2374 | DLA_02628 | F4PJNLW01EE5MJ | CDS | 390127 | 1431 | + | 0.297694 | |
g2375 | DLA_02629 | F4PJNLW01EE5MJ | CDS | 392072 | 1374 | - | 0.315138 | |
g2376 | DLA_02630 | F4PJNLW01EE5MJ | CDS | 394228 | 465 | + | 0.288172 | |
g2377 | DLA_02631 | member of the alpha-actininspectrin superfamily dimerizes with cortexillin I involved in cytokinesis and development and associates with the actin cytoskeleton | F4PJNLW01EE5MJ | CDS | 395523 | 1353 | - | 0.36881 |
g2378 | DLA_02632 | F4PJNLW01EE5MJ | CDS | 397210 | 1104 | - | 0.274457 | |
g2379 | DLA_02633 | F4PJNLW01EE5MJ | CDS | 398493 | 1431 | - | 0.360587 | |
g238 | DLA_00265 | contig05409_1.exp | CDS | 543001 | 5781 | + | 0.337485 | |
g2380 | DLA_02635 | F4PJNLW01EE5MJ | CDS | 401669 | 4497 | + | 0.381143 | |
g2381 | DLA_02636 | F4PJNLW01EE5MJ | CDS | 406795 | 3672 | + | 0.353214 | |
g2382 | DLA_02637 | F4PJNLW01EE5MJ | CDS | 410668 | 450 | - | 0.313333 | |
g2383 | DLA_02638 | F4PJNLW01EE5MJ | CDS | 411622 | 3039 | + | 0.348799 | |
g2384 | DLA_02639 | F4PJNLW01EE5MJ | CDS | 415069 | 1365 | - | 0.315751 | |
g2385 | DLA_02640 | catalytic subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase | F4PJNLW01EE5MJ | CDS | 416797 | 1710 | + | 0.330994 |
g2386 | DLA_02641 | F4PJNLW01EE5MJ | CDS | 419950 | 1467 | + | 0.408316 | |
g2387 | DLA_02642 | F4PJNLW01EE5MJ | CDS | 421773 | 1086 | - | 0.316759 | |
g2388 | DLA_02643 | F4PJNLW01EE5MJ | CDS | 423201 | 1062 | + | 0.339925 | |
g2389 | DLA_02644 | F4PJNLW01EE5MJ | CDS | 424427 | 822 | - | 0.343066 | |
g239 | DLA_00266 | contig05409_1.exp | CDS | 549282 | 381 | + | 0.293963 | |
g2390 | DLA_02645 | homolog of human SLC35C1 (GDP-fucose transporter 1) defects in human SLC35C1 are the cause of leukocyte adhesion deficiency type II contains 10 putative transmembrane domains | F4PJNLW01EE5MJ | CDS | 425446 | 1080 | - | 0.308333 |
g2391 | DLA_02646 | F4PJNLW01EE5MJ | CDS | 427191 | 471 | + | 0.392781 | |
g2392 | DLA_02647 | F4PJNLW01EE5MJ | CDS | 427686 | 870 | - | 0.293103 | |
g2393 | DLA_02648 | subunit of the splicing factor SF3B required for spliceosome assembly belongs to the SF3b10 (splicing factor 3B 10 kDa subunit) family | F4PJNLW01EE5MJ | CDS | 428837 | 285 | + | 0.34386 |
g2394 | DLA_02649 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | F4PJNLW01EE5MJ | CDS | 429301 | 1893 | - | 0.364501 |
g2395 | DLA_02650 | F4PJNLW01EE5MJ | CDS | 432099 | 2643 | - | 0.331063 | |
g2396 | DLA_02652 | F4PJNLW01EE5MJ | CDS | 436038 | 390 | - | 0.294872 | |
g2397 | DLA_02654 | F4PJNLW01EE5MJ | CDS | 437395 | 1938 | - | 0.325593 | |
g2398 | DLA_02657 | F4PJNLW01EE5MJ | CDS | 440849 | 750 | + | 0.293333 | |
g2399 | DLA_02658 | F4PJNLW01EE5MJ | CDS | 441816 | 1785 | - | 0.347339 | |
g24 | DLA_00028 | contig05409_1.exp | CDS | 61377 | 3906 | - | 0.323605 | |
g240 | DLA_00267 | contig05409_1.exp | CDS | 549811 | 813 | + | 0.289053 | |
g2400 | DLA_11528 | F4PJNLW01EE5MJ | CDS | 443870 | 609 | - | 0.326765 | |
g2401 | DLA_02659 | F4PJNLW01EE5MJ | CDS | 445106 | 1449 | - | 0.434783 | |
g2402 | DLA_02660 | F4PJNLW01EE5MJ | CDS | 446810 | 2196 | - | 0.32969 | |
g2403 | DLA_02661 | F4PJNLW01EE5MJ | CDS | 449307 | 336 | + | 0.25 | |
g2404 | DLA_02662 | F4PJNLW01EE5MJ | CDS | 450030 | 423 | - | 0.394799 | |
g2405 | DLA_02663 | F4PJNLW01EE5MJ | CDS | 450963 | 1677 | + | 0.294574 | |
g2406 | DLA_02664 | F4PJNLW01EE5MJ | CDS | 452756 | 450 | - | 0.306667 | |
g2407 | DLA_02665 | F4PJNLW01EE5MJ | CDS | 453401 | 4122 | - | 0.34983 | |
g2408 | DLA_02668 | F4PJNLW01EE5MJ | CDS | 458284 | 3003 | + | 0.330003 | |
g2409 | DLA_02669 | F4PJNLW01EE5MJ | CDS | 462028 | 5133 | + | 0.337619 | |
g241 | DLA_00268 | contig05409_1.exp | CDS | 550759 | 1434 | - | 0.324268 | |
g2410 | DLA_02670 | TFIID subunit involved in RNA polymerase II transcription initiation | F4PJNLW01EE5MJ | CDS | 467525 | 1728 | + | 0.311343 |
g2411 | DLA_02671 | F4PJNLW01EE5MJ | CDS | 469324 | 723 | - | 0.290456 | |
g2412 | DLA_02672 | full transporter consisting of two ABC domains and two transmembrane domains there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 470340 | 4365 | - | 0.376174 |
g2413 | DLA_02674 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub expressed in pstAB cells and in upper cup during culmination | F4PJNLW01EE5MJ | CDS | 475903 | 1905 | - | 0.342782 |
g2414 | DLA_02675 | catalyzes the reaction: acyl-CoA 12-diacylglycerol CoA triacylglycerol similar to mammalian DGAT1 contains 9 predicted transmembrane domains | F4PJNLW01EE5MJ | CDS | 478140 | 1689 | + | 0.328005 |
g2415 | DLA_02676 | contains 3 zinc-binding LIM domains LIM domains are found in proteins with differing functions including gene expression and cytoskeleton organisation and development | F4PJNLW01EE5MJ | CDS | 480213 | 552 | - | 0.342391 |
g2416 | DLA_02677 | contains a N-terminal uridine kinase domaine domain and a C-terminal adenylate cyclase domain like the UdkC protein and other plant proteins | F4PJNLW01EE5MJ | CDS | 480988 | 1494 | + | 0.323963 |
g2417 | DLA_02678 | catalyzes the reaction isocitrate NAD 2-oxoglutarate CO2 NADH | F4PJNLW01EE5MJ | CDS | 482810 | 1047 | - | 0.372493 |
g2418 | DLA_02679 | F4PJNLW01EE5MJ | CDS | 484352 | 1005 | + | 0.342289 | |
g2419 | DLA_02680 | F4PJNLW01EE5MJ | CDS | 485473 | 1023 | - | 0.309873 | |
g242 | DLA_00269 | contig05409_1.exp | CDS | 552351 | 1014 | + | 0.381657 | |
g2420 | DLA_02681 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages induced by Legionella pneumophila infection | F4PJNLW01EE5MJ | CDS | 486833 | 1524 | + | 0.370735 |
g2421 | DLA_02682 | F4PJNLW01EE5MJ | CDS | 488927 | 750 | - | 0.325333 | |
g2422 | DLA_02683 | F4PJNLW01EE5MJ | CDS | 490169 | 492 | - | 0.284553 | |
g2423 | DLA_02684 | F4PJNLW01EE5MJ | CDS | 490736 | 3402 | + | 0.289242 | |
g2424 | DLA_02685 | F4PJNLW01EE5MJ | CDS | 494455 | 1422 | - | 0.415612 | |
g2425 | DLA_02686 | F4PJNLW01EE5MJ | CDS | 497320 | 1461 | + | 0.381246 | |
g2426 | DLA_02687 | F4PJNLW01EE5MJ | CDS | 499115 | 4104 | + | 0.34308 | |
g2427 | DLA_02690 | F4PJNLW01EE5MJ | CDS | 506870 | 1776 | + | 0.310248 | |
g2428 | DLA_02691 | F4PJNLW01EE5MJ | CDS | 508852 | 2733 | + | 0.320161 | |
g2429 | DLA_02692 | F4PJNLW01EE5MJ | CDS | 512012 | 333 | - | 0.324324 | |
g243 | DLA_00270 | contig05409_1.exp | CDS | 554322 | 879 | - | 0.29124 | |
g2430 | DLA_02693 | F4PJNLW01EE5MJ | CDS | 512515 | 1812 | + | 0.351545 | |
g2431 | DLA_02694 | F4PJNLW01EE5MJ | CDS | 514560 | 2319 | - | 0.351013 | |
g2432 | DLA_02697 | F4PJNLW01EE5MJ | CDS | 519322 | 3981 | + | 0.373524 | |
g2433 | DLA_02698 | F4PJNLW01EE5MJ | CDS | 523589 | 1584 | + | 0.275884 | |
g2434 | DLA_02699 | F4PJNLW01EE5MJ | CDS | 525262 | 972 | + | 0.337449 | |
g2435 | DLA_02700 | F4PJNLW01EE5MJ | CDS | 526323 | 1653 | - | 0.304295 | |
g2436 | DLA_02701 | F4PJNLW01EE5MJ | CDS | 528190 | 2787 | - | 0.311446 | |
g2437 | DLA_02702 | F4PJNLW01EE5MJ | CDS | 531535 | 972 | - | 0.269547 | |
g2438 | DLA_02703 | F4PJNLW01EE5MJ | CDS | 532795 | 498 | + | 0.25502 | |
g2439 | DLA_02704 | F4PJNLW01EE5MJ | CDS | 533451 | 2232 | - | 0.338262 | |
g244 | DLA_00271 | contig05409_1.exp | CDS | 555630 | 1065 | - | 0.380282 | |
g2440 | DLA_02705 | F4PJNLW01EE5MJ | CDS | 535762 | 1254 | - | 0.313397 | |
g2441 | DLA_02706 | F4PJNLW01EE5MJ | CDS | 538396 | 1752 | - | 0.376142 | |
g2442 | DLA_02708 | F4PJNLW01EE5MJ | CDS | 540537 | 732 | + | 0.331967 | |
g2443 | DLA_02710 | F4PJNLW01EE5MJ | CDS | 542134 | 1761 | - | 0.329358 | |
g2444 | DLA_02712 | F4PJNLW01EE5MJ | CDS | 544525 | 2784 | + | 0.336566 | |
g2445 | DLA_02715 | F4PJNLW01EE5MJ | CDS | 549691 | 1638 | - | 0.263126 | |
g2446 | DLA_02716 | F4PJNLW01EE5MJ | CDS | 551853 | 2004 | + | 0.271956 | |
g2447 | DLA_02717 | F4PJNLW01EE5MJ | CDS | 554514 | 1056 | + | 0.316288 | |
g2448 | DLA_02718 | F4PJNLW01EE5MJ | CDS | 555757 | 1047 | - | 0.321872 | |
g2449 | DLA_02719 | F4PJNLW01EE5MJ | CDS | 557376 | 7473 | + | 0.372006 | |
g245 | DLA_00272 | contig05409_1.exp | CDS | 557093 | 1836 | - | 0.283769 | |
g2450 | DLA_02720 | F4PJNLW01EE5MJ | CDS | 565066 | 2763 | + | 0.338762 | |
g2451 | DLA_02721 | F4PJNLW01EE5MJ | CDS | 568245 | 2721 | - | 0.334803 | |
g2452 | DLA_02722 | F4PJNLW01EE5MJ | CDS | 572857 | 1359 | - | 0.296542 | |
g2453 | DLA_02723 | F4PJNLW01EE5MJ | CDS | 574428 | 1848 | - | 0.350649 | |
g2454 | DLA_02724 | F4PJNLW01EE5MJ | CDS | 576949 | 1017 | - | 0.311701 | |
g2455 | DLA_02725 | F4PJNLW01EE5MJ | CDS | 579082 | 2658 | - | 0.322047 | |
g2456 | DLA_11529 | F4PJNLW01EE5MJ | CDS | 582034 | 387 | - | 0.374677 | |
g2457 | DLA_02726 | F4PJNLW01EE5MJ | CDS | 582875 | 5502 | - | 0.321156 | |
g2458 | DLA_02727 | F4PJNLW01EE5MJ | CDS | 588955 | 3414 | - | 0.347393 | |
g2459 | DLA_02728 | F4PJNLW01EE5MJ | CDS | 593887 | 2484 | + | 0.324477 | |
g246 | DLA_00273 | contig05409_1.exp | CDS | 559447 | 2865 | + | 0.37103 | |
g2460 | DLA_02729 | F4PJNLW01EE5MJ | CDS | 597268 | 1272 | - | 0.316824 | |
g2461 | DLA_02730 | F4PJNLW01EE5MJ | CDS | 598939 | 1338 | + | 0.289985 | |
g2462 | DLA_02731 | ortholog of the Prp19 protein in mammals a nuclear matrix protein protein that plays a role in DNA double-strand break repair in S. cerevisiae and in S. pombe a RNA splicing factor and a ubiquitin-protein ligase contains 6 WD-40 repeats and an N-terminal U-box motif | F4PJNLW01EE5MJ | CDS | 600513 | 1497 | - | 0.370073 |
g2463 | DLA_02732 | F4PJNLW01EE5MJ | CDS | 602542 | 888 | + | 0.275901 | |
g2464 | DLA_02733 | F4PJNLW01EE5MJ | CDS | 603644 | 5577 | - | 0.337637 | |
g2465 | DLA_02735 | F4PJNLW01EE5MJ | CDS | 610087 | 1056 | - | 0.356061 | |
g2466 | DLA_02736 | F4PJNLW01EE5MJ | CDS | 611396 | 2547 | + | 0.328229 | |
g2467 | DLA_02737 | F4PJNLW01EE5MJ | CDS | 614224 | 2649 | + | 0.348056 | |
g2468 | DLA_02738 | F4PJNLW01EE5MJ | CDS | 617381 | 840 | - | 0.264286 | |
g2469 | DLA_02740 | F4PJNLW01EE5MJ | CDS | 619141 | 1839 | + | 0.353453 | |
g247 | DLA_00274 | contig05409_1.exp | CDS | 562762 | 1740 | - | 0.314943 | |
g2470 | DLA_02741 | subunit 4 of the conserved replication complex GINS which is essential for initiation of DNA replication in X. laevis | F4PJNLW01EE5MJ | CDS | 621318 | 597 | - | 0.247906 |
g2471 | DLA_02742 | F4PJNLW01EE5MJ | CDS | 622198 | 1227 | + | 0.277099 | |
g2472 | DLA_02743 | F4PJNLW01EE5MJ | CDS | 623570 | 633 | + | 0.257504 | |
g2473 | DLA_02744 | F4PJNLW01EE5MJ | CDS | 624351 | 3513 | + | 0.317108 | |
g2474 | DLA_02745 | F4PJNLW01EE5MJ | CDS | 627998 | 1914 | - | 0.323929 | |
g2475 | DLA_02746 | F4PJNLW01EE5MJ | CDS | 630181 | 2235 | + | 0.332438 | |
g2476 | DLA_02747 | F4PJNLW01EE5MJ | CDS | 633838 | 2796 | + | 0.311516 | |
g2477 | DLA_02748 | F4PJNLW01EE5MJ | CDS | 637138 | 1848 | - | 0.33171 | |
g2478 | DLA_02749 | F4PJNLW01EE5MJ | CDS | 639638 | 564 | - | 0.319149 | |
g2479 | DLA_02750 | F4PJNLW01EE5MJ | CDS | 640671 | 258 | - | 0.27907 | |
g248 | DLA_00275 | contig05409_1.exp | CDS | 564707 | 588 | - | 0.336735 | |
g2480 | DLA_02751 | F4PJNLW01EE5MJ | CDS | 641186 | 1014 | + | 0.324458 | |
g2481 | DLA_02752 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | F4PJNLW01EE5MJ | CDS | 642626 | 11559 | + | 0.33541 |
g2482 | DLA_02753 | F4PJNLW01EE5MJ | CDS | 654387 | 5724 | - | 0.332809 | |
g2483 | DLA_02754 | F4PJNLW01EE5MJ | CDS | 660861 | 1974 | - | 0.295339 | |
g2484 | DLA_02755 | F4PJNLW01EE5MJ | CDS | 663291 | 963 | + | 0.266874 | |
g2485 | DLA_02756 | F4PJNLW01EE5MJ | CDS | 664548 | 966 | + | 0.442029 | |
g2486 | DLA_02757 | F4PJNLW01EE5MJ | CDS | 665749 | 648 | + | 0.376543 | |
g2487 | DLA_02758 | F4PJNLW01EE5MJ | CDS | 666600 | 420 | - | 0.330952 | |
g2488 | DLA_02759 | F4PJNLW01EE5MJ | CDS | 667342 | 6816 | + | 0.359008 | |
g2489 | DLA_02760 | F4PJNLW01EE5MJ | CDS | 674351 | 555 | - | 0.263063 | |
g249 | DLA_00277 | contig05409_1.exp | CDS | 566249 | 3003 | - | 0.330669 | |
g2490 | DLA_02761 | F4PJNLW01EE5MJ | CDS | 675292 | 3822 | + | 0.343799 | |
g2491 | DLA_02762 | F4PJNLW01EE5MJ | CDS | 680144 | 1761 | + | 0.334469 | |
g2492 | DLA_02763 | F4PJNLW01EE5MJ | CDS | 681946 | 621 | - | 0.275362 | |
g2493 | DLA_02764 | F4PJNLW01EE5MJ | CDS | 682829 | 612 | - | 0.263072 | |
g2494 | DLA_02766 | F4PJNLW01EE5MJ | CDS | 683815 | 1683 | - | 0.314914 | |
g2495 | DLA_02767 | F4PJNLW01EE5MJ | CDS | 685824 | 1446 | + | 0.375519 | |
g2496 | DLA_02768 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | F4PJNLW01EE5MJ | CDS | 687331 | 2985 | - | 0.344389 |
g2497 | DLA_02769 | F4PJNLW01EE5MJ | CDS | 690595 | 297 | + | 0.296296 | |
g2498 | DLA_02770 | F4PJNLW01EE5MJ | CDS | 691045 | 969 | - | 0.298246 | |
g2499 | DLA_02771 | F4PJNLW01EE5MJ | CDS | 692274 | 1284 | + | 0.332555 | |
g25 | DLA_00029 | contig05409_1.exp | CDS | 66655 | 3291 | + | 0.366758 | |
g250 | DLA_00278 | contig05409_1.exp | CDS | 569644 | 1920 | + | 0.340104 | |
g2500 | DLA_02772 | F4PJNLW01EE5MJ | CDS | 693787 | 798 | - | 0.303258 | |
g2501 | DLA_02773 | F4PJNLW01EE5MJ | CDS | 695125 | 1632 | - | 0.315564 | |
g2502 | DLA_02774 | F4PJNLW01EE5MJ | CDS | 697422 | 1587 | + | 0.293006 | |
g2503 | DLA_02776 | F4PJNLW01EE5MJ | CDS | 699156 | 999 | - | 0.286286 | |
g2504 | DLA_02777 | F4PJNLW01EE5MJ | CDS | 700257 | 1089 | + | 0.315886 | |
g2505 | DLA_02778 | F4PJNLW01EE5MJ | CDS | 701735 | 1137 | + | 0.326297 | |
g2506 | DLA_02779 | F4PJNLW01EE5MJ | CDS | 703198 | 1284 | - | 0.358255 | |
g2507 | DLA_02780 | F4PJNLW01EE5MJ | CDS | 704784 | 1113 | - | 0.322552 | |
g2508 | DLA_02781 | F4PJNLW01EE5MJ | CDS | 706288 | 2118 | + | 0.352691 | |
g2509 | DLA_02782 | F4PJNLW01EE5MJ | CDS | 708861 | 1593 | - | 0.29818 | |
g251 | DLA_00279 | contig05409_1.exp | CDS | 571713 | 933 | + | 0.352626 | |
g2510 | DLA_02783 | F4PJNLW01EE5MJ | CDS | 710638 | 1659 | - | 0.283303 | |
g2511 | DLA_02785 | F4PJNLW01EE5MJ | CDS | 713149 | 4359 | + | 0.332416 | |
g2512 | DLA_02786 | F4PJNLW01EE5MJ | CDS | 717933 | 1389 | + | 0.349892 | |
g2513 | DLA_02787 | F4PJNLW01EE5MJ | CDS | 719586 | 828 | - | 0.345411 | |
g2514 | DLA_02788 | F4PJNLW01EE5MJ | CDS | 721035 | 2421 | + | 0.327551 | |
g2515 | DLA_02789 | F4PJNLW01EE5MJ | CDS | 724167 | 387 | + | 0.268734 | |
g2516 | DLA_02790 | F4PJNLW01EE5MJ | CDS | 724995 | 1611 | + | 0.340161 | |
g2517 | DLA_02791 | F4PJNLW01EE5MJ | CDS | 726759 | 1041 | + | 0.295869 | |
g2518 | DLA_02792 | F4PJNLW01EE5MJ | CDS | 727968 | 2568 | - | 0.315031 | |
g2519 | DLA_02793 | F4PJNLW01EE5MJ | CDS | 730885 | 1683 | + | 0.289958 | |
g252 | DLA_00280 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR WD40 and protein kinase domains | contig05409_1.exp | CDS | 572926 | 8451 | - | 0.357236 |
g2520 | DLA_02794 | F4PJNLW01EE5MJ | CDS | 732818 | 813 | - | 0.341943 | |
g2521 | DLA_02795 | F4PJNLW01EE5MJ | CDS | 734003 | 3651 | - | 0.326212 | |
g2522 | DLA_02796 | F4PJNLW01EE5MJ | CDS | 737876 | 1452 | - | 0.302342 | |
g2523 | DLA_02797 | F4PJNLW01EE5MJ | CDS | 739700 | 3531 | - | 0.323138 | |
g2524 | DLA_02798 | F4PJNLW01EE5MJ | CDS | 743917 | 831 | - | 0.320096 | |
g2525 | DLA_02799 | F4PJNLW01EE5MJ | CDS | 745500 | 744 | + | 0.349462 | |
g2526 | DLA_02800 | F4PJNLW01EE5MJ | CDS | 746832 | 1137 | + | 0.307828 | |
g2527 | DLA_02801 | F4PJNLW01EE5MJ | CDS | 748256 | 2673 | + | 0.354284 | |
g2528 | DLA_02802 | ortholog of the human DHX9 that unwinds double-stranded DNA and RNA in a 3' to 5' direction | F4PJNLW01EE5MJ | CDS | 751371 | 4032 | - | 0.312252 |
g2529 | DLA_02803 | F4PJNLW01EE5MJ | CDS | 755693 | 927 | - | 0.283711 | |
g253 | DLA_00281 | contig05409_1.exp | CDS | 583999 | 981 | + | 0.307849 | |
g2530 | DLA_02804 | F4PJNLW01EE5MJ | CDS | 756724 | 1689 | + | 0.28656 | |
g2531 | DLA_02805 | F4PJNLW01EE5MJ | CDS | 758432 | 1533 | - | 0.306588 | |
g2532 | DLA_02806 | F4PJNLW01EE5MJ | CDS | 760271 | 447 | - | 0.261745 | |
g2533 | DLA_02807 | F4PJNLW01EE5MJ | CDS | 760964 | 339 | + | 0.227139 | |
g2534 | DLA_02808 | F4PJNLW01EE5MJ | CDS | 761715 | 4392 | - | 0.346084 | |
g2535 | DLA_02809 | F4PJNLW01EE5MJ | CDS | 767285 | 1239 | + | 0.274415 | |
g2536 | DLA_02810 | F4PJNLW01EE5MJ | CDS | 768921 | 1665 | - | 0.332132 | |
g2537 | DLA_02811 | F4PJNLW01EE5MJ | CDS | 770710 | 1575 | + | 0.363175 | |
g2538 | DLA_02812 | F4PJNLW01EE5MJ | CDS | 772707 | 996 | + | 0.331325 | |
g2539 | DLA_02813 | F4PJNLW01EE5MJ | CDS | 774560 | 1326 | - | 0.273002 | |
g254 | DLA_00282 | contig05409_1.exp | CDS | 585130 | 792 | - | 0.294192 | |
g2540 | DLA_02814 | F4PJNLW01EE5MJ | CDS | 776978 | 2097 | + | 0.304244 | |
g2541 | DLA_02815 | F4PJNLW01EE5MJ | CDS | 779152 | 1344 | - | 0.338542 | |
g2542 | DLA_02816 | F4PJNLW01EE5MJ | CDS | 781075 | 2442 | + | 0.285831 | |
g2543 | DLA_02817 | F4PJNLW01EE5MJ | CDS | 784926 | 1428 | + | 0.362045 | |
g2544 | DLA_02821 | highly conserved protein interacts with TATA binding protein (TBP) and with the SCF (Skp1-Cul1-F-box) ubiquitin ligase complex | F4PJNLW01EE5MJ | CDS | 788159 | 3693 | - | 0.315732 |
g2545 | DLA_02822 | catalyzes the reaction ATP L-histidine tRNAHis AMP diphosphate L-histidyl-tRNAHis | F4PJNLW01EE5MJ | CDS | 792242 | 1569 | - | 0.312938 |
g2546 | DLA_02823 | F4PJNLW01EE5MJ | CDS | 794069 | 3654 | - | 0.315545 | |
g2547 | DLA_02824 | F4PJNLW01EE5MJ | CDS | 798262 | 1302 | - | 0.300307 | |
g2548 | DLA_02825 | F4PJNLW01EE5MJ | CDS | 803547 | 1668 | + | 0.395084 | |
g2549 | DLA_02826 | F4PJNLW01EE5MJ | CDS | 806057 | 1491 | + | 0.327968 | |
g255 | DLA_00283 | contig05409_1.exp | CDS | 586348 | 3684 | - | 0.336591 | |
g2550 | DLA_02827 | F4PJNLW01EE5MJ | CDS | 807819 | 1671 | - | 0.308797 | |
g2551 | DLA_02829 | F4PJNLW01EE5MJ | CDS | 810255 | 2385 | - | 0.307338 | |
g2552 | DLA_02830 | F4PJNLW01EE5MJ | CDS | 813504 | 555 | - | 0.295496 | |
g2553 | DLA_02831 | F4PJNLW01EE5MJ | CDS | 815035 | 1290 | - | 0.347287 | |
g2554 | DLA_02832 | F4PJNLW01EE5MJ | CDS | 816913 | 1428 | - | 0.334734 | |
g2555 | DLA_02833 | F4PJNLW01EE5MJ | CDS | 819149 | 828 | + | 0.365942 | |
g2556 | DLA_02834 | F4PJNLW01EE5MJ | CDS | 820222 | 621 | + | 0.294686 | |
g2557 | DLA_02835 | F4PJNLW01EE5MJ | CDS | 821312 | 303 | - | 0.313531 | |
g2558 | DLA_02836 | F4PJNLW01EE5MJ | CDS | 821803 | 708 | - | 0.303672 | |
g2559 | DLA_02840 | F4PJNLW01EE5MJ | CDS | 823472 | 318 | - | 0.305031 | |
g256 | DLA_11438 | putative ortholog of H. sapiens transducin beta-like 2 (TBL2) deleted in patients with Williams-Beuren syndrome (WBS) | contig05409_1.exp | CDS | 590685 | 1350 | - | 0.287407 |
g2560 | DLA_02841 | F4PJNLW01EE5MJ | CDS | 824531 | 777 | - | 0.311454 | |
g2561 | DLA_02843 | F4PJNLW01EE5MJ | CDS | 827504 | 351 | + | 0.270655 | |
g2562 | DLA_02844 | F4PJNLW01EE5MJ | CDS | 827942 | 3414 | - | 0.345636 | |
g2563 | DLA_02846 | F4PJNLW01EE5MJ | CDS | 831991 | 3546 | - | 0.295262 | |
g2564 | DLA_02847 | F4PJNLW01EE5MJ | CDS | 836147 | 1173 | - | 0.310315 | |
g2565 | DLA_02848 | F4PJNLW01EE5MJ | CDS | 837770 | 2082 | - | 0.306436 | |
g2566 | DLA_02849 | F4PJNLW01EE5MJ | CDS | 840278 | 3147 | - | 0.31109 | |
g2567 | DLA_02851 | F4PJNLW01EE5MJ | CDS | 843820 | 2844 | - | 0.300281 | |
g2568 | DLA_02852 | F4PJNLW01EE5MJ | CDS | 846859 | 660 | + | 0.321212 | |
g2569 | DLA_02853 | F4PJNLW01EE5MJ | CDS | 847624 | 3453 | - | 0.32812 | |
g257 | DLA_00284 | contig05409_1.exp | CDS | 592341 | 4653 | - | 0.344724 | |
g2570 | DLA_02854 | contains one putative transmembrane domain similar to D. purpureum protein | F4PJNLW01EE5MJ | CDS | 851806 | 2226 | + | 0.320305 |
g2571 | DLA_02855 | F4PJNLW01EE5MJ | CDS | 854469 | 1170 | + | 0.323932 | |
g2572 | DLA_02856 | F4PJNLW01EE5MJ | CDS | 855747 | 1704 | + | 0.316901 | |
g2573 | DLA_02857 | contains a putative Like-Sm (Lsm) domain possible homolog of LSM12 | F4PJNLW01EE5MJ | CDS | 857550 | 537 | - | 0.3054 |
g2574 | DLA_02858 | catalyzes the reaction GDP-L-fucose NADP GDP-4-dehydro-6-deoxy-D-mannose NADPH H | F4PJNLW01EE5MJ | CDS | 858491 | 948 | + | 0.341772 |
g2575 | DLA_02859 | F4PJNLW01EE5MJ | CDS | 859900 | 1149 | - | 0.326371 | |
g2576 | DLA_02860 | F4PJNLW01EE5MJ | CDS | 861531 | 1191 | + | 0.313182 | |
g2577 | DLA_11530 | F4PJNLW01EE5MJ | CDS | 863338 | 726 | + | 0.330579 | |
g2578 | DLA_02861 | F4PJNLW01EE5MJ | CDS | 864104 | 2604 | - | 0.320276 | |
g2579 | DLA_02862 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein similar to the H. sapiens POR protein that is defect in adrenal hyperplasia variant type (AHV) a syndrome with disordered steroidogenesis | F4PJNLW01EE5MJ | CDS | 866908 | 1932 | - | 0.371636 |
g258 | DLA_00285 | contig05409_1.exp | CDS | 597300 | 225 | + | 0.262222 | |
g2580 | DLA_02863 | ortholog of CLN2TPP1 contains a predicted signal peptide enriched in prespore cells | F4PJNLW01EE5MJ | CDS | 869289 | 1596 | - | 0.390977 |
g2581 | DLA_02864 | F4PJNLW01EE5MJ | CDS | 871672 | 1962 | + | 0.392457 | |
g2582 | DLA_02865 | belongs to the acyltransferase superfamily contains 2 predicted transmembrane domains | F4PJNLW01EE5MJ | CDS | 874026 | 1086 | - | 0.331492 |
g2583 | DLA_02866 | F4PJNLW01EE5MJ | CDS | 875987 | 948 | - | 0.295359 | |
g2584 | DLA_02867 | F4PJNLW01EE5MJ | CDS | 877359 | 1086 | - | 0.298343 | |
g2585 | DLA_02868 | F4PJNLW01EE5MJ | CDS | 878837 | 1809 | - | 0.328911 | |
g2586 | DLA_02869 | F4PJNLW01EE5MJ | CDS | 880997 | 1695 | + | 0.315634 | |
g2587 | DLA_11531 | F4PJNLW01EE5MJ | CDS | 882745 | 3390 | - | 0.314159 | |
g2588 | DLA_02870 | F4PJNLW01EE5MJ | CDS | 886645 | 5736 | - | 0.339435 | |
g2589 | DLA_02871 | F4PJNLW01EE5MJ | CDS | 893127 | 1461 | + | 0.27447 | |
g259 | DLA_00286 | contig05409_1.exp | CDS | 598011 | 1737 | - | 0.340818 | |
g2590 | DLA_02873 | F4PJNLW01EE5MJ | CDS | 896635 | 1440 | + | 0.272917 | |
g2591 | DLA_02874 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | F4PJNLW01EE5MJ | CDS | 898216 | 14703 | - | 0.327484 |
g2592 | DLA_02875 | F4PJNLW01EE5MJ | CDS | 913386 | 1989 | + | 0.293615 | |
g2593 | DLA_02876 | F4PJNLW01EE5MJ | CDS | 915521 | 2775 | - | 0.338378 | |
g2594 | DLA_02877 | F4PJNLW01EE5MJ | CDS | 918769 | 3492 | + | 0.340779 | |
g2595 | DLA_02878 | F4PJNLW01EE5MJ | CDS | 922352 | 609 | - | 0.321839 | |
g2596 | DLA_02879 | F4PJNLW01EE5MJ | CDS | 923135 | 2952 | + | 0.315041 | |
g2597 | DLA_02880 | F4PJNLW01EE5MJ | CDS | 926238 | 558 | + | 0.317204 | |
g2598 | DLA_02883 | F4PJNLW01EE5MJ | CDS | 929105 | 1083 | + | 0.351801 | |
g2599 | DLA_02884 | F4PJNLW01EE5MJ | CDS | 930398 | 1143 | + | 0.31671 | |
g26 | DLA_00031 | contig05409_1.exp | CDS | 70155 | 735 | - | 0.338776 | |
g260 | DLA_00288 | contig05409_1.exp | CDS | 600848 | 1137 | - | 0.289358 | |
g2600 | DLA_02885 | catalyzes the reaction AMP pyrophosphate PRPP adenine in nucleoside salvage pathways | F4PJNLW01EE5MJ | CDS | 932083 | 597 | - | 0.341709 |
g2601 | DLA_02886 | F4PJNLW01EE5MJ | CDS | 933002 | 534 | + | 0.28839 | |
g2602 | DLA_02887 | F4PJNLW01EE5MJ | CDS | 934016 | 3438 | - | 0.357475 | |
g2603 | DLA_02888 | F4PJNLW01EE5MJ | CDS | 938672 | 708 | - | 0.351695 | |
g2604 | DLA_02889 | ortholog of the mammalian GTPBP3 and S. cerevisiae MSS1 GTPases responsible for the 5-carboxymethylaminomethyl modification of the wobble uridine base in mitochondrial tRNAs | F4PJNLW01EE5MJ | CDS | 939609 | 1605 | - | 0.321495 |
g2605 | DLA_02890 | contains six kelch repeats which are known to be involved in various biological processes | F4PJNLW01EE5MJ | CDS | 941357 | 1224 | - | 0.343954 |
g2606 | DLA_02891 | contains Sec23Sec24 zinc finger trunk and helical domains yeast Sec23Sec24 is a component of COPII (coat protein complex II) involved in ER to Golgi transport | F4PJNLW01EE5MJ | CDS | 943766 | 2277 | + | 0.317523 |
g2607 | DLA_02893 | F4PJNLW01EE5MJ | CDS | 946211 | 1323 | + | 0.357521 | |
g2608 | DLA_02894 | F4PJNLW01EE5MJ | CDS | 947771 | 1821 | - | 0.319055 | |
g2609 | DLA_02895 | F4PJNLW01EE5MJ | CDS | 949884 | 711 | + | 0.309423 | |
g261 | DLA_00289 | contig05409_1.exp | CDS | 602682 | 2556 | + | 0.354069 | |
g2610 | DLA_02896 | F4PJNLW01EE5MJ | CDS | 951271 | 549 | - | 0.315118 | |
g2611 | DLA_02897 | F4PJNLW01EE5MJ | CDS | 952213 | 2286 | + | 0.306649 | |
g2612 | DLA_02898 | F4PJNLW01EE5MJ | CDS | 954839 | 1068 | - | 0.308989 | |
g2613 | DLA_11532 | F4PJNLW01EE5MJ | CDS | 956438 | 558 | - | 0.299283 | |
g2614 | DLA_02899 | conserved from bacteria to plants to alveolata contains 10 predicted transmembrane domains | F4PJNLW01EE5MJ | CDS | 957651 | 1221 | - | 0.325143 |
g2615 | DLA_02902 | similar to bacterial endo-14-beta-glucanase expressed in pstAO cells | F4PJNLW01EE5MJ | CDS | 960317 | 1725 | + | 0.361739 |
g2616 | DLA_02903 | F4PJNLW01EE5MJ | CDS | 962934 | 1245 | + | 0.330924 | |
g2617 | DLA_02905 | F4PJNLW01EE5MJ | CDS | 964648 | 1923 | - | 0.368175 | |
g2618 | DLA_02906 | F4PJNLW01EE5MJ | CDS | 967215 | 1188 | + | 0.285354 | |
g2619 | DLA_02907 | F4PJNLW01EE5MJ | CDS | 968642 | 354 | + | 0.276836 | |
g262 | DLA_00290 | contig05409_1.exp | CDS | 605877 | 1869 | + | 0.305511 | |
g2620 | DLA_02908 | F4PJNLW01EE5MJ | CDS | 969208 | 3174 | - | 0.333018 | |
g2621 | DLA_02909 | F4PJNLW01EE5MJ | CDS | 973377 | 288 | + | 0.315972 | |
g2622 | DLA_02910 | F4PJNLW01EE5MJ | CDS | 973891 | 2289 | - | 0.328965 | |
g2623 | DLA_02911 | F4PJNLW01EE5MJ | CDS | 976541 | 699 | + | 0.32475 | |
g2624 | DLA_02912 | F4PJNLW01EE5MJ | CDS | 977594 | 636 | + | 0.34434 | |
g2625 | DLA_02913 | F4PJNLW01EE5MJ | CDS | 978386 | 1458 | + | 0.391632 | |
g2626 | DLA_02914 | F4PJNLW01EE5MJ | CDS | 980007 | 2058 | + | 0.3207 | |
g2627 | DLA_02915 | F4PJNLW01EE5MJ | CDS | 982387 | 687 | - | 0.326055 | |
g2628 | DLA_02916 | F4PJNLW01EE5MJ | CDS | 983803 | 1734 | + | 0.318916 | |
g2629 | DLA_02917 | F4PJNLW01EE5MJ | CDS | 985681 | 558 | - | 0.290323 | |
g263 | DLA_00291 | contig05409_1.exp | CDS | 608171 | 2115 | - | 0.297872 | |
g2630 | DLA_02918 | F4PJNLW01EE5MJ | CDS | 986682 | 1068 | + | 0.425094 | |
g2631 | DLA_02920 | F4PJNLW01EE5MJ | CDS | 987952 | 834 | + | 0.303357 | |
g2632 | DLA_02921 | F4PJNLW01EE5MJ | CDS | 989364 | 1104 | + | 0.336957 | |
g2633 | DLA_02923 | F4PJNLW01EE5MJ | CDS | 993468 | 3117 | + | 0.336221 | |
g2634 | DLA_02924 | F4PJNLW01EE5MJ | CDS | 997192 | 1437 | - | 0.268615 | |
g2635 | DLA_02925 | F4PJNLW01EE5MJ | CDS | 998892 | 1449 | + | 0.348516 | |
g2636 | DLA_02926 | F4PJNLW01EE5MJ | CDS | 1000811 | 2118 | - | 0.344193 | |
g2637 | DLA_11533 | F4PJNLW01EE5MJ | CDS | 1004492 | 969 | + | 0.302374 | |
g2638 | DLA_02927 | F4PJNLW01EE5MJ | CDS | 1005629 | 1932 | - | 0.321429 | |
g2639 | DLA_02928 | F4PJNLW01EE5MJ | CDS | 1007985 | 1662 | + | 0.299639 | |
g264 | DLA_00292 | contig05409_1.exp | CDS | 611002 | 1161 | - | 0.29888 | |
g2640 | DLA_02929 | F4PJNLW01EE5MJ | CDS | 1009683 | 1953 | - | 0.303635 | |
g2641 | DLA_02930 | F4PJNLW01EE5MJ | CDS | 1013205 | 1566 | + | 0.298851 | |
g2642 | DLA_02933 | colocalizes with clathrin spots suggesting involvement in endocytosis does not localize to pseudopods in wild type in SCAR depleted mutants WASP replaces the functions of SCAR and localizes to pseudopods | F4PJNLW01EE5MJ | CDS | 1015460 | 1269 | + | 0.405831 |
g2643 | DLA_02934 | F4PJNLW01EE5MJ | CDS | 1016942 | 1704 | + | 0.2723 | |
g2644 | DLA_02935 | F4PJNLW01EE5MJ | CDS | 1019362 | 948 | + | 0.280591 | |
g2645 | DLA_02936 | ortholog of the H. sapiens L2HGDH which when defective causes L-2-hydroxyglutaric aciduria-a rare autosomal recessive disorder | F4PJNLW01EE5MJ | CDS | 1020371 | 1296 | - | 0.330247 |
g2646 | DLA_02937 | F4PJNLW01EE5MJ | CDS | 1022156 | 1284 | + | 0.35514 | |
g2647 | DLA_02938 | F4PJNLW01EE5MJ | CDS | 1023584 | 2526 | - | 0.300871 | |
g2648 | DLA_02939 | wealky similar to acid ceramidase which catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine | F4PJNLW01EE5MJ | CDS | 1026651 | 1278 | + | 0.356025 |
g2649 | DLA_02940 | F4PJNLW01EE5MJ | CDS | 1028129 | 6285 | + | 0.322832 | |
g265 | DLA_00293 | contig05409_1.exp | CDS | 613034 | 1332 | + | 0.293544 | |
g2650 | DLA_02941 | F4PJNLW01EE5MJ | CDS | 1034745 | 1086 | - | 0.347145 | |
g2651 | DLA_02942 | F4PJNLW01EE5MJ | CDS | 1035977 | 888 | - | 0.414414 | |
g2652 | DLA_02944 | F4PJNLW01EE5MJ | CDS | 1037367 | 2694 | - | 0.308463 | |
g2653 | DLA_02945 | F4PJNLW01EE5MJ | CDS | 1040175 | 618 | - | 0.326861 | |
g2654 | DLA_02946 | F4PJNLW01EE5MJ | CDS | 1041294 | 681 | + | 0.309838 | |
g2655 | DLA_02947 | similar to human HSBP1 HSBP1 is a negative regulator of the heat shock response there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 1042211 | 306 | + | 0.281046 |
g2656 | DLA_02948 | F4PJNLW01EE5MJ | CDS | 1042739 | 1278 | - | 0.311424 | |
g2657 | DLA_02949 | F4PJNLW01EE5MJ | CDS | 1044784 | 1410 | - | 0.338298 | |
g2658 | DLA_02950 | similar to human PDAP1 (PDGFA-associated protein 1) there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 1046830 | 597 | + | 0.356784 |
g2659 | DLA_02951 | similar to the mammalian Hypoxia up-regulated protein 1 (HYOU1) a protein that plays a role in cytoprotective cellular mechanisms triggered by oxygen deprivation there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 1047513 | 2721 | - | 0.336641 |
g266 | DLA_00294 | contig05409_1.exp | CDS | 614693 | 2682 | - | 0.302013 | |
g2660 | DLA_02952 | F4PJNLW01EE5MJ | CDS | 1050672 | 2481 | - | 0.310762 | |
g2661 | DLA_02954 | belongs to the short chain dehydrogenasesreductases family ortholog of human HSD17B10 which is involved in mitochondrial tRNA maturation and by interacting with intracellular amyloid-beta may contribute to the neuronal dysfunction associated with Alzheimer disease | F4PJNLW01EE5MJ | CDS | 1053508 | 780 | + | 0.384615 |
g2662 | DLA_02955 | F4PJNLW01EE5MJ | CDS | 1054406 | 618 | - | 0.313916 | |
g2663 | DLA_02956 | F4PJNLW01EE5MJ | CDS | 1055224 | 1890 | - | 0.325397 | |
g2664 | DLA_02957 | F4PJNLW01EE5MJ | CDS | 1057419 | 3426 | - | 0.345593 | |
g2665 | DLA_02958 | F4PJNLW01EE5MJ | CDS | 1061283 | 4632 | + | 0.360751 | |
g2666 | DLA_02959 | F4PJNLW01EE5MJ | CDS | 1066576 | 1845 | + | 0.339295 | |
g2667 | DLA_02960 | catalyzes the reduction of sphinganine to 3-dehydrosphinganine in glycosphingolipid metabolism there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 1068664 | 1044 | - | 0.319923 |
g2668 | DLA_02961 | F4PJNLW01EE5MJ | CDS | 1070320 | 777 | + | 0.328185 | |
g2669 | DLA_02962 | F4PJNLW01EE5MJ | CDS | 1071253 | 3879 | - | 0.364527 | |
g267 | DLA_00295 | contig05409_1.exp | CDS | 618353 | 1266 | - | 0.28594 | |
g2670 | DLA_02963 | F4PJNLW01EE5MJ | CDS | 1076247 | 225 | + | 0.324444 | |
g2671 | DLA_02964 | F4PJNLW01EE5MJ | CDS | 1076687 | 1122 | - | 0.34492 | |
g2672 | DLA_02965 | F4PJNLW01EE5MJ | CDS | 1078535 | 3300 | + | 0.35697 | |
g2673 | DLA_02966 | F4PJNLW01EE5MJ | CDS | 1082165 | 1071 | - | 0.3324 | |
g2674 | DLA_02967 | F4PJNLW01EE5MJ | CDS | 1083851 | 354 | + | 0.285311 | |
g2675 | DLA_02968 | F4PJNLW01EE5MJ | CDS | 1084369 | 1584 | - | 0.315025 | |
g2676 | DLA_02970 | F4PJNLW01EE5MJ | CDS | 1086402 | 1746 | - | 0.256586 | |
g2677 | DLA_02972 | F4PJNLW01EE5MJ | CDS | 1089833 | 405 | + | 0.34321 | |
g2678 | DLA_02974 | F4PJNLW01EE5MJ | CDS | 1090682 | 1731 | - | 0.257077 | |
g2679 | DLA_02975 | F4PJNLW01EE5MJ | CDS | 1094434 | 1740 | + | 0.256897 | |
g268 | DLA_00298 | contig05409_1.exp | CDS | 621251 | 1761 | + | 0.35548 | |
g2680 | DLA_02976 | belongs to the MCAKKif2 subfamily contains 1 SAM domain predicted to play a role in mitosis | F4PJNLW01EE5MJ | CDS | 1096365 | 3057 | + | 0.342493 |
g2681 | DLA_02977 | F4PJNLW01EE5MJ | CDS | 1100171 | 1548 | - | 0.289406 | |
g2682 | DLA_02978 | F4PJNLW01EE5MJ | CDS | 1101852 | 648 | - | 0.322531 | |
g2683 | DLA_02979 | F4PJNLW01EE5MJ | CDS | 1102678 | 996 | - | 0.341365 | |
g2684 | DLA_02980 | F4PJNLW01EE5MJ | CDS | 1104230 | 873 | + | 0.315006 | |
g2685 | DLA_11534 | F4PJNLW01EE5MJ | CDS | 1105164 | 399 | - | 0.305764 | |
g2686 | DLA_02981 | F4PJNLW01EE5MJ | CDS | 1106577 | 735 | - | 0.315646 | |
g2687 | DLA_02982 | F4PJNLW01EE5MJ | CDS | 1107434 | 2595 | - | 0.322158 | |
g2688 | DLA_02983 | F4PJNLW01EE5MJ | CDS | 1110499 | 987 | + | 0.256332 | |
g2689 | DLA_02984 | F4PJNLW01EE5MJ | CDS | 1111560 | 1422 | - | 0.274262 | |
g269 | DLA_00299 | contig05409_1.exp | CDS | 623235 | 2199 | + | 0.289677 | |
g2690 | DLA_02985 | F4PJNLW01EE5MJ | CDS | 1113660 | 1383 | + | 0.326103 | |
g2691 | DLA_02986 | F4PJNLW01EE5MJ | CDS | 1115334 | 1575 | - | 0.335238 | |
g2692 | DLA_02987 | F4PJNLW01EE5MJ | CDS | 1117694 | 1050 | + | 0.345714 | |
g2693 | DLA_02988 | F4PJNLW01EE5MJ | CDS | 1119035 | 1752 | - | 0.311073 | |
g2694 | DLA_11535 | F4PJNLW01EE5MJ | CDS | 1121026 | 1623 | - | 0.316081 | |
g2695 | DLA_02989 | F4PJNLW01EE5MJ | CDS | 1123189 | 1227 | + | 0.308883 | |
g2696 | DLA_02990 | F4PJNLW01EE5MJ | CDS | 1124736 | 1419 | + | 0.275546 | |
g2697 | DLA_02991 | F4PJNLW01EE5MJ | CDS | 1127162 | 1287 | + | 0.34965 | |
g2698 | DLA_02992 | F4PJNLW01EE5MJ | CDS | 1128734 | 1071 | + | 0.286648 | |
g2699 | DLA_02993 | regulatory subunit 2 of the protein serinethreonine phosphatase 4 PPC4 ( | F4PJNLW01EE5MJ | CDS | 1129951 | 798 | + | 0.302005 |
g27 | DLA_00032 | contig05409_1.exp | CDS | 71158 | 3114 | - | 0.312139 | |
g270 | DLA_00300 | contig05409_1.exp | CDS | 625941 | 2418 | + | 0.35732 | |
g2700 | DLA_02994 | F4PJNLW01EE5MJ | CDS | 1131119 | 945 | + | 0.277249 | |
g2701 | DLA_02995 | F4PJNLW01EE5MJ | CDS | 1132168 | 750 | - | 0.357333 | |
g2702 | DLA_02996 | F4PJNLW01EE5MJ | CDS | 1133112 | 1554 | + | 0.29408 | |
g2703 | DLA_02997 | F4PJNLW01EE5MJ | CDS | 1135019 | 1623 | + | 0.340727 | |
g2704 | DLA_02998 | F4PJNLW01EE5MJ | CDS | 1136943 | 1596 | + | 0.282581 | |
g2705 | DLA_02999 | F4PJNLW01EE5MJ | CDS | 1138608 | 2625 | - | 0.299429 | |
g2706 | DLA_03000 | F4PJNLW01EE5MJ | CDS | 1141772 | 873 | + | 0.317297 | |
g2707 | DLA_03001 | F4PJNLW01EE5MJ | CDS | 1142690 | 738 | - | 0.319783 | |
g2708 | DLA_03003 | endoplasmic reticulum receptor for the KDEL signal sequence of proteins resident in the endoplasmic reticulum believed to cycle between the cis side of the Golgi apparatus and the ER | F4PJNLW01EE5MJ | CDS | 1143920 | 663 | + | 0.266968 |
g2709 | DLA_03004 | F4PJNLW01EE5MJ | CDS | 1144961 | 318 | - | 0.289308 | |
g271 | DLA_00301 | contig05409_1.exp | CDS | 628909 | 1554 | + | 0.348777 | |
g2710 | DLA_03006 | F4PJNLW01EE5MJ | CDS | 1146469 | 1509 | - | 0.348575 | |
g2711 | DLA_03007 | F4PJNLW01EE5MJ | CDS | 1148480 | 1926 | + | 0.286085 | |
g2712 | DLA_03008 | F4PJNLW01EE5MJ | CDS | 1150620 | 1479 | - | 0.338742 | |
g2713 | DLA_03009 | F4PJNLW01EE5MJ | CDS | 1152979 | 1371 | + | 0.28884 | |
g2714 | DLA_03010 | F4PJNLW01EE5MJ | CDS | 1154444 | 4911 | - | 0.321116 | |
g2715 | DLA_03011 | F4PJNLW01EE5MJ | CDS | 1160692 | 624 | - | 0.299679 | |
g2716 | DLA_03012 | F4PJNLW01EE5MJ | CDS | 1161711 | 456 | - | 0.333333 | |
g2717 | DLA_03013 | F4PJNLW01EE5MJ | CDS | 1162905 | 4197 | + | 0.340481 | |
g2718 | DLA_03014 | F4PJNLW01EE5MJ | CDS | 1167232 | 900 | - | 0.27 | |
g2719 | DLA_03015 | F4PJNLW01EE5MJ | CDS | 1168470 | 1383 | + | 0.361533 | |
g272 | DLA_00302 | contig05409_1.exp | CDS | 631415 | 1266 | + | 0.338863 | |
g2720 | DLA_03016 | F4PJNLW01EE5MJ | CDS | 1170267 | 1944 | + | 0.314815 | |
g2721 | DLA_03017 | F4PJNLW01EE5MJ | CDS | 1172536 | 321 | - | 0.29595 | |
g2722 | DLA_03018 | F4PJNLW01EE5MJ | CDS | 1173334 | 7125 | + | 0.278456 | |
g2723 | DLA_03019 | F4PJNLW01EE5MJ | CDS | 1180703 | 774 | - | 0.276486 | |
g2724 | DLA_03020 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | F4PJNLW01EE5MJ | CDS | 1181808 | 477 | + | 0.333333 |
g2725 | DLA_11536 | F4PJNLW01EE5MJ | CDS | 1182673 | 393 | + | 0.348601 | |
g2726 | DLA_03021 | F4PJNLW01EE5MJ | CDS | 1183360 | 573 | + | 0.209424 | |
g2727 | DLA_03022 | F4PJNLW01EE5MJ | CDS | 1183977 | 1803 | - | 0.298392 | |
g2728 | DLA_03023 | F4PJNLW01EE5MJ | CDS | 1186112 | 7353 | - | 0.300286 | |
g2729 | DLA_03024 | F4PJNLW01EE5MJ | CDS | 1194441 | 1767 | + | 0.348048 | |
g273 | DLA_00303 | contig05409_1.exp | CDS | 632735 | 792 | - | 0.299242 | |
g2730 | DLA_03025 | F4PJNLW01EE5MJ | CDS | 1196433 | 2709 | + | 0.287929 | |
g2731 | DLA_03026 | F4PJNLW01EE5MJ | CDS | 1199446 | 831 | + | 0.262335 | |
g2732 | DLA_03027 | F4PJNLW01EE5MJ | CDS | 1200415 | 2052 | - | 0.263158 | |
g2733 | DLA_03028 | F4PJNLW01EE5MJ | CDS | 1203141 | 2085 | - | 0.267146 | |
g2734 | DLA_03029 | F4PJNLW01EE5MJ | CDS | 1205355 | 546 | + | 0.305861 | |
g2735 | DLA_03030 | F4PJNLW01EE5MJ | CDS | 1206039 | 4062 | - | 0.28582 | |
g2736 | DLA_03032 | F4PJNLW01EE5MJ | CDS | 1210577 | 453 | - | 0.293598 | |
g2737 | DLA_03033 | F4PJNLW01EE5MJ | CDS | 1211230 | 1098 | + | 0.295082 | |
g2738 | DLA_03034 | F4PJNLW01EE5MJ | CDS | 1212538 | 609 | - | 0.341544 | |
g2739 | DLA_03035 | F4PJNLW01EE5MJ | CDS | 1213710 | 1593 | + | 0.338983 | |
g274 | DLA_00304 | contig05409_1.exp | CDS | 633807 | 3063 | + | 0.320601 | |
g2740 | DLA_03036 | F4PJNLW01EE5MJ | CDS | 1215730 | 2028 | + | 0.354537 | |
g2741 | DLA_03037 | F4PJNLW01EE5MJ | CDS | 1218082 | 477 | + | 0.264151 | |
g2742 | DLA_03038 | F4PJNLW01EE5MJ | CDS | 1218792 | 1533 | + | 0.296151 | |
g2743 | DLA_03039 | F4PJNLW01EE5MJ | CDS | 1220955 | 1596 | + | 0.323308 | |
g2744 | DLA_03040 | F4PJNLW01EE5MJ | CDS | 1222843 | 381 | - | 0.272966 | |
g2745 | DLA_03041 | F4PJNLW02G7WH6 | CDS | 1 | 83 | - | 0.385542 | |
g2746 | DLA_11537 | F4PJNLW02G7WH6 | CDS | 1527 | 1446 | - | 0.329184 | |
g2747 | DLA_03042 | F4PJNLW02G7WH6 | CDS | 3354 | 1992 | - | 0.291667 | |
g2748 | DLA_03043 | F4PJNLW02G7WH6 | CDS | 5567 | 957 | + | 0.290491 | |
g2749 | DLA_03044 | F4PJNLW02G7WH6 | CDS | 6773 | 924 | + | 0.270563 | |
g275 | DLA_00305 | contig05409_1.exp | CDS | 637009 | 627 | - | 0.30622 | |
g2750 | DLA_03045 | F4PJNLW02G7WH6 | CDS | 8506 | 1951 | + | 0.307535 | |
g2751 | DLA_03046 | F4PJNLW02GJ9ZB | CDS | 228 | 2283 | + | 0.238721 | |
g2752 | DLA_03047 | F4PJNLW02GJ9ZB | CDS | 3449 | 1461 | + | 0.312799 | |
g2753 | DLA_03048 | similar to human Zinc finger SWIM domain-containing protein 7 a regulator of homologous recombination in eukaryotic cells | F4PJNLW02GJ9ZB | CDS | 5191 | 495 | - | 0.252525 |
g2754 | DLA_03049 | F4PJNLW02GJ9ZB | CDS | 6108 | 684 | + | 0.263158 | |
g2755 | DLA_03050 | F4PJNLW02GJ9ZB | CDS | 7002 | 1566 | - | 0.355045 | |
g2756 | DLA_03051 | F4PJNLW02GJ9ZB | CDS | 8930 | 291 | - | 0.243986 | |
g2757 | DLA_03052 | F4PJNLW02GJ9ZB | CDS | 9649 | 435 | - | 0.273563 | |
g2758 | DLA_03053 | F4PJNLW02GJ9ZB | CDS | 10329 | 1521 | + | 0.335963 | |
g2759 | DLA_03054 | F4PJNLW02GJ9ZB | CDS | 12246 | 297 | - | 0.333333 | |
g276 | DLA_00306 | contig05409_1.exp | CDS | 638305 | 1236 | + | 0.326052 | |
g2760 | DLA_03055 | F4PJNLW02GJ9ZB | CDS | 12747 | 3666 | - | 0.321877 | |
g2761 | DLA_03058 | F4PJNLW02GJ9ZB | CDS | 19279 | 2277 | + | 0.347826 | |
g2762 | DLA_03059 | F4PJNLW02GJ9ZB | CDS | 21863 | 822 | - | 0.341849 | |
g2763 | DLA_03061 | F4PJNLW02GJ9ZB | CDS | 23701 | 594 | - | 0.338384 | |
g2764 | DLA_03062 | F4PJNLW02GJ9ZB | CDS | 25142 | 687 | + | 0.308588 | |
g2765 | DLA_03064 | F4PJNLW02GJ9ZB | CDS | 26317 | 3153 | + | 0.338091 | |
g2766 | DLA_03065 | F4PJNLW02GJ9ZB | CDS | 29735 | 1536 | - | 0.283203 | |
g2767 | DLA_11538 | F4PJNLW02GJ9ZB | CDS | 31330 | 1614 | - | 0.260223 | |
g2768 | DLA_03066 | F4PJNLW02GJ9ZB | CDS | 33140 | 1542 | - | 0.28275 | |
g2769 | DLA_03067 | ortholog of human HPS4 mutations in human HPS4 have been linked to Hermansky-Pudlak syndrome 4 | F4PJNLW02GJ9ZB | CDS | 34989 | 1446 | - | 0.291148 |
g277 | DLA_00307 | contig05409_1.exp | CDS | 639887 | 1617 | - | 0.367965 | |
g2770 | DLA_03068 | F4PJNLW02GJ9ZB | CDS | 37062 | 987 | + | 0.281662 | |
g2771 | DLA_03069 | F4PJNLW02GJ9ZB | CDS | 38713 | 2556 | - | 0.353678 | |
g2772 | DLA_11539 | F4PJNLW02GJ9ZB | CDS | 41747 | 1527 | - | 0.330714 | |
g2773 | DLA_03070 | F4PJNLW02GJ9ZB | CDS | 43416 | 1755 | + | 0.274644 | |
g2774 | DLA_03071 | F4PJNLW02GJ9ZB | CDS | 45194 | 1554 | - | 0.331403 | |
g2775 | DLA_03072 | similar to discoidin I almost identical to its downstream gene DD7-1 | F4PJNLW02GJ9ZB | CDS | 47030 | 870 | - | 0.389655 |
g2776 | DLA_03073 | F4PJNLW02GJ9ZB | CDS | 48650 | 3747 | - | 0.363491 | |
g2777 | DLA_03074 | F4PJNLW02GJ9ZB | CDS | 52496 | 1779 | + | 0.284992 | |
g2778 | DLA_03075 | F4PJNLW02GJ9ZB | CDS | 54726 | 792 | + | 0.315657 | |
g2779 | DLA_03076 | F4PJNLW02GJ9ZB | CDS | 56201 | 2220 | - | 0.340991 | |
g278 | DLA_00308 | contig05409_1.exp | CDS | 641944 | 711 | + | 0.331927 | |
g2780 | DLA_03077 | F4PJNLW02GJ9ZB | CDS | 58668 | 438 | + | 0.299087 | |
g2781 | DLA_03079 | F4PJNLW02GJ9ZB | CDS | 60206 | 1170 | - | 0.296581 | |
g2782 | DLA_03080 | F4PJNLW02GJ9ZB | CDS | 61746 | 327 | + | 0.351682 | |
g2783 | DLA_03081 | F4PJNLW02GJ9ZB | CDS | 62489 | 273 | - | 0.241758 | |
g2784 | DLA_03082 | F4PJNLW02GJ9ZB | CDS | 63078 | 1443 | + | 0.305613 | |
g2785 | DLA_03083 | F4PJNLW02GJ9ZB | CDS | 64788 | 1737 | - | 0.299367 | |
g2786 | DLA_03085 | F4PJNLW02GJ9ZB | CDS | 67097 | 867 | + | 0.320646 | |
g2787 | DLA_03086 | F4PJNLW02GJ9ZB | CDS | 68053 | 234 | - | 0.247863 | |
g2788 | DLA_11540 | F4PJNLW02GJ9ZB | CDS | 68575 | 477 | - | 0.283019 | |
g2789 | DLA_03087 | F4PJNLW02GJ9ZB | CDS | 69598 | 1650 | + | 0.295758 | |
g279 | DLA_00309 | contig05409_1.exp | CDS | 642788 | 738 | + | 0.345528 | |
g2790 | DLA_03088 | F4PJNLW02GJ9ZB | CDS | 71309 | 5259 | - | 0.301578 | |
g2791 | DLA_03089 | F4PJNLW02GJ9ZB | CDS | 77075 | 306 | + | 0.27451 | |
g2792 | DLA_03090 | F4PJNLW02GJ9ZB | CDS | 77740 | 1314 | - | 0.303653 | |
g2793 | DLA_03093 | F4PJNLW02GJ9ZB | CDS | 79952 | 564 | - | 0.352837 | |
g2794 | DLA_03094 | F4PJNLW02GJ9ZB | CDS | 81109 | 1848 | + | 0.261364 | |
g2795 | DLA_03095 | F4PJNLW02GJ9ZB | CDS | 83052 | 1323 | - | 0.250945 | |
g2796 | DLA_03096 | F4PJNLW02GJ9ZB | CDS | 84683 | 393 | + | 0.256997 | |
g2797 | DLA_03097 | F4PJNLW02GJ9ZB | CDS | 85137 | 2370 | - | 0.337975 | |
g2798 | DLA_03099 | F4PJNLW02GJ9ZB | CDS | 88631 | 795 | + | 0.237736 | |
g2799 | DLA_03100 | F4PJNLW02GJ9ZB | CDS | 89678 | 1719 | - | 0.399069 | |
g28 | DLA_11429 | contig05409_1.exp | CDS | 74373 | 1581 | - | 0.285262 | |
g280 | DLA_00310 | contig05409_1.exp | CDS | 644143 | 1581 | + | 0.320683 | |
g2800 | DLA_03101 | F4PJNLW02GJ9ZB | CDS | 92375 | 900 | + | 0.372222 | |
g2801 | DLA_03102 | F4PJNLW02GJ9ZB | CDS | 93421 | 645 | + | 0.296124 | |
g2802 | DLA_03103 | F4PJNLW02GJ9ZB | CDS | 94819 | 1356 | - | 0.309735 | |
g2803 | DLA_03104 | ortholog of the mammalian geranylgeranyl diphosphate synthase 1 includes the enzymes dimethylallyltransferase (EC 2.5.1.1) geranyltranstransferase (EC 2.5.1.10) and farnesyltranstransferase (EC 2.5.1.29) | F4PJNLW02GJ9ZB | CDS | 96933 | 894 | + | 0.290828 |
g2804 | DLA_03105 | F4PJNLW02GJ9ZB | CDS | 97996 | 1242 | - | 0.34219 | |
g2805 | DLA_03106 | F4PJNLW02GJ9ZB | CDS | 99567 | 8028 | - | 0.309791 | |
g2806 | DLA_03107 | class I (unconventiona) myosin component of actin-based molecular motor | F4PJNLW02GJ9ZB | CDS | 108769 | 3240 | + | 0.400926 |
g2807 | DLA_03108 | F4PJNLW02GJ9ZB | CDS | 112664 | 924 | + | 0.314935 | |
g2808 | DLA_03109 | F4PJNLW02GJ9ZB | CDS | 113811 | 1383 | - | 0.344902 | |
g2809 | DLA_03110 | F4PJNLW02GJ9ZB | CDS | 115532 | 1767 | + | 0.286361 | |
g281 | DLA_00311 | contig05409_1.exp | CDS | 645976 | 2772 | - | 0.306277 | |
g2810 | DLA_03111 | putative metalloprotease of the peptidase M41 family which belong to a larger family of zinc metalloproteases includes the cell division protein FtsH | F4PJNLW02GJ9ZB | CDS | 117563 | 1668 | + | 0.342926 |
g2811 | DLA_11541 | F4PJNLW02GJ9ZB | CDS | 119251 | 372 | + | 0.33871 | |
g2812 | DLA_03112 | F4PJNLW02GJ9ZB | CDS | 120467 | 2079 | + | 0.343434 | |
g2813 | DLA_03113 | F4PJNLW02GJ9ZB | CDS | 122654 | 1593 | - | 0.402385 | |
g2814 | DLA_03114 | F4PJNLW02GJ9ZB | CDS | 124717 | 1752 | - | 0.285388 | |
g2815 | DLA_03115 | putative ortholog of H. sapiens AATF apoptosis-antagonizing transcription factorbrbr bCommunity annotation:b DDB_G0270496 shows extensive similarities with the | F4PJNLW02GJ9ZB | CDS | 126566 | 1449 | + | 0.287095 |
g2816 | DLA_03116 | similar to eukaryotic translation initiation factor 4A isoform 2 | F4PJNLW02GJ9ZB | CDS | 129122 | 1155 | + | 0.386147 |
g2817 | DLA_03117 | F4PJNLW02GJ9ZB | CDS | 130769 | 1206 | + | 0.303483 | |
g2818 | DLA_03118 | E. coli ATP-dependent DNA helicase RecQ is involved in genome maintenance this is the ortholog of the H. sapiens Werner syndrome protein defects in WRN cause the premature onset of multiple age-related disorders | F4PJNLW02GJ9ZB | CDS | 132381 | 2568 | + | 0.279595 |
g2819 | DLA_03119 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide | F4PJNLW02GJ9ZB | CDS | 135346 | 642 | + | 0.38785 |
g282 | DLA_00312 | contig05409_1.exp | CDS | 649460 | 1122 | - | 0.374332 | |
g2820 | DLA_03120 | F4PJNLW02GJ9ZB | CDS | 136367 | 480 | - | 0.2625 | |
g2821 | DLA_03124 | F4PJNLW02GJ9ZB | CDS | 139171 | 1548 | + | 0.278424 | |
g2822 | DLA_03125 | F4PJNLW02GJ9ZB | CDS | 140838 | 1908 | - | 0.243711 | |
g2823 | DLA_03126 | F4PJNLW02GJ9ZB | CDS | 143581 | 2193 | - | 0.321021 | |
g2824 | DLA_03127 | F4PJNLW02GJ9ZB | CDS | 146833 | 2541 | - | 0.245179 | |
g2825 | DLA_03128 | similar to CDK1 and CDK2 cell cycle CAK (CDK-activating kinase) kinases predicted to activate SG2 cyclins cyclin A B and D | F4PJNLW02GJ9ZB | CDS | 150193 | 900 | + | 0.331111 |
g2826 | DLA_03129 | F4PJNLW02GJ9ZB | CDS | 151535 | 948 | + | 0.375527 | |
g2827 | DLA_03130 | F4PJNLW02GJ9ZB | CDS | 153292 | 1029 | - | 0.275996 | |
g2828 | DLA_03131 | F4PJNLW02GJ9ZB | CDS | 154793 | 1191 | + | 0.315701 | |
g2829 | DLA_03132 | F4PJNLW02GJ9ZB | CDS | 156068 | 498 | - | 0.162651 | |
g283 | DLA_00313 | contig05409_1.exp | CDS | 651193 | 612 | - | 0.315359 | |
g2830 | DLA_03133 | F4PJNLW02GJ9ZB | CDS | 156718 | 2268 | - | 0.243386 | |
g2831 | DLA_03134 | F4PJNLW02GJ9ZB | CDS | 159108 | 2223 | - | 0.234368 | |
g2832 | DLA_03135 | F4PJNLW02GJ9ZB | CDS | 161521 | 1932 | - | 0.297101 | |
g2833 | DLA_03136 | F4PJNLW02GJ9ZB | CDS | 163936 | 2019 | - | 0.330857 | |
g2834 | DLA_03137 | F4PJNLW02GJ9ZB | CDS | 166213 | 3015 | - | 0.328027 | |
g2835 | DLA_03138 | F4PJNLW02GJ9ZB | CDS | 169414 | 1224 | - | 0.291667 | |
g2836 | DLA_03139 | F4PJNLW02GJ9ZB | CDS | 170832 | 585 | - | 0.290598 | |
g2837 | DLA_03140 | similar to Dna2 a DNA replication factor required for Okazaki fragment processing and involved in DNA repair pathways | F4PJNLW02GJ9ZB | CDS | 172310 | 4101 | - | 0.292855 |
g2838 | DLA_03141 | F4PJNLW02GJ9ZB | CDS | 176752 | 1095 | + | 0.313242 | |
g2839 | DLA_03143 | F4PJNLW02GJ9ZB | CDS | 179820 | 957 | + | 0.273772 | |
g284 | DLA_00314 | contig05409_1.exp | CDS | 652127 | 3645 | + | 0.322908 | |
g2840 | DLA_03144 | F4PJNLW02GJ9ZB | CDS | 180828 | 3843 | - | 0.282332 | |
g2841 | DLA_03146 | F4PJNLW02GJ9ZB | CDS | 185247 | 4974 | - | 0.268999 | |
g2842 | DLA_03148 | F4PJNLW02GJ9ZB | CDS | 190712 | 3003 | - | 0.33633 | |
g2843 | DLA_03149 | F4PJNLW02GJ9ZB | CDS | 194193 | 1374 | - | 0.291121 | |
g2844 | DLA_03150 | CAZy family GT4 catalyzes N-linked mannosylation | F4PJNLW02GJ9ZB | CDS | 195869 | 1299 | - | 0.321016 |
g2845 | DLA_03151 | F4PJNLW02GJ9ZB | CDS | 197599 | 3150 | + | 0.292064 | |
g2846 | DLA_03152 | F4PJNLW02GJ9ZB | CDS | 200786 | 735 | - | 0.180952 | |
g2847 | DLA_03153 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | F4PJNLW02GJ9ZB | CDS | 202165 | 441 | + | 0.331066 |
g2848 | DLA_03154 | F4PJNLW02GJ9ZB | CDS | 203261 | 1839 | + | 0.334965 | |
g2849 | DLA_03155 | F4PJNLW02GJ9ZB | CDS | 205177 | 552 | - | 0.266304 | |
g285 | DLA_00315 | contig05409_1.exp | CDS | 656889 | 1608 | + | 0.28607 | |
g2850 | DLA_03156 | involved in regulation of inositol (145) trisphosphate levels | F4PJNLW02GJ9ZB | CDS | 205856 | 2190 | + | 0.310502 |
g2851 | DLA_03157 | F4PJNLW02GJ9ZB | CDS | 208126 | 2085 | - | 0.305516 | |
g2852 | DLA_03159 | F4PJNLW02GJ9ZB | CDS | 211423 | 1239 | - | 0.268765 | |
g2853 | DLA_03160 | F4PJNLW02GJ9ZB | CDS | 213172 | 4545 | + | 0.256106 | |
g2854 | DLA_03161 | F4PJNLW02GJ9ZB | CDS | 219535 | 1602 | + | 0.300874 | |
g2855 | DLA_03163 | F4PJNLW02GJ9ZB | CDS | 222488 | 4947 | + | 0.258945 | |
g2856 | DLA_03164 | F4PJNLW02GJ9ZB | CDS | 227560 | 543 | - | 0.287293 | |
g2857 | DLA_11542 | similar to eukaryotic initiation factor 4A isoform 3 | F4PJNLW02GJ9ZB | CDS | 228496 | 1212 | + | 0.319307 |
g2858 | DLA_03165 | F4PJNLW02GJ9ZB | CDS | 230121 | 3357 | + | 0.309503 | |
g2859 | DLA_03166 | catalyzes the reaction GTP succinate CoA GDP phosphate succinyl-CoA | F4PJNLW02GJ9ZB | CDS | 233884 | 1269 | + | 0.351458 |
g286 | DLA_00316 | contig05409_1.exp | CDS | 658614 | 336 | + | 0.318452 | |
g2860 | DLA_03167 | F4PJNLW02GJ9ZB | CDS | 235329 | 1605 | + | 0.284112 | |
g2861 | DLA_03168 | component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) | F4PJNLW02GJ9ZB | CDS | 237020 | 1530 | - | 0.39085 |
g2862 | DLA_03171 | F4PJNLW02GJ9ZB | CDS | 240592 | 1371 | - | 0.383662 | |
g2863 | DLA_03172 | F4PJNLW02GJ9ZB | CDS | 242485 | 5940 | - | 0.295791 | |
g2864 | DLA_03174 | F4PJNLW02GJ9ZB | CDS | 249581 | 2211 | - | 0.333786 | |
g2865 | DLA_03175 | F4PJNLW02GJ9ZB | CDS | 253374 | 2625 | - | 0.358476 | |
g2866 | DLA_03176 | F4PJNLW02GJ9ZB | CDS | 256321 | 867 | + | 0.334487 | |
g2867 | DLA_03177 | F4PJNLW02GJ9ZB | CDS | 257382 | 2595 | - | 0.274759 | |
g2868 | DLA_03178 | F4PJNLW02GJ9ZB | CDS | 260513 | 1386 | + | 0.365079 | |
g2869 | DLA_03179 | F4PJNLW02GJ9ZB | CDS | 261980 | 741 | - | 0.291498 | |
g287 | DLA_00317 | contig05409_1.exp | CDS | 659718 | 4656 | + | 0.348797 | |
g2870 | DLA_03181 | catalyzes the reaction ATP HCOsub3subsup-sup propionyl-CoA ADP phosphate D-methylmalonyl-CoA | F4PJNLW02GJ9ZB | CDS | 264109 | 2022 | - | 0.37636 |
g2871 | DLA_03182 | F4PJNLW02GJ9ZB | CDS | 266560 | 510 | + | 0.235294 | |
g2872 | DLA_03183 | F4PJNLW02GJ9ZB | CDS | 267425 | 897 | - | 0.344482 | |
g2873 | DLA_03184 | F4PJNLW02GJ9ZB | CDS | 268779 | 864 | + | 0.280093 | |
g2874 | DLA_03185 | F4PJNLW02GJ9ZB | CDS | 270085 | 927 | - | 0.316073 | |
g2875 | DLA_03186 | F4PJNLW02GJ9ZB | CDS | 271124 | 3012 | - | 0.299801 | |
g2876 | DLA_03188 | F4PJNLW02GJ9ZB | CDS | 274842 | 2049 | - | 0.243533 | |
g2877 | DLA_03189 | F4PJNLW02HBBIY | CDS | 1 | 1128 | - | 0.196809 | |
g2878 | DLA_03190 | F4PJNLW02HBBIY | CDS | 1676 | 813 | + | 0.403444 | |
g2879 | DLA_03191 | F4PJNLW02HBBIY | CDS | 3696 | 846 | + | 0.329787 | |
g288 | DLA_00318 | contig05409_1.exp | CDS | 664886 | 2070 | - | 0.323671 | |
g2880 | DLA_03192 | F4PJNLW02HBBIY | CDS | 4701 | 1035 | - | 0.27343 | |
g2881 | DLA_03193 | F4PJNLW02HBBIY | CDS | 6961 | 1041 | + | 0.361191 | |
g2882 | DLA_03194 | F4PJNLW02HBBIY | CDS | 8492 | 3045 | - | 0.336617 | |
g2883 | DLA_03195 | F4PJNLW02HBBIY | CDS | 12011 | 2160 | - | 0.350926 | |
g2884 | DLA_03196 | F4PJNLW02HBBIY | CDS | 14506 | 1686 | + | 0.314947 | |
g2885 | DLA_03197 | F4PJNLW02HBBIY | CDS | 16207 | 1767 | - | 0.317487 | |
g2886 | DLA_03199 | F4PJNLW02HBBIY | CDS | 18214 | 3558 | + | 0.298482 | |
g2887 | DLA_03200 | ortholog of bacterial Mgsup2sup transporter mgtA contains eight transmembrane domains | F4PJNLW02HBBIY | CDS | 22158 | 2820 | - | 0.375532 |
g2888 | DLA_03202 | F4PJNLW02HBBIY | CDS | 26108 | 1389 | + | 0.314615 | |
g2889 | DLA_03203 | F4PJNLW02HBBIY | CDS | 27596 | 7104 | - | 0.352055 | |
g289 | DLA_00320 | contig05409_1.exp | CDS | 668785 | 627 | + | 0.317384 | |
g2890 | DLA_03204 | F4PJNLW02HBBIY | CDS | 35274 | 3366 | - | 0.369578 | |
g2891 | DLA_03205 | F4PJNLW02HBBIY | CDS | 40341 | 816 | - | 0.28799 | |
g2892 | DLA_03206 | F4PJNLW02HBBIY | CDS | 41930 | 3438 | + | 0.322862 | |
g2893 | DLA_03207 | F4PJNLW02HBBIY | CDS | 45769 | 627 | - | 0.349282 | |
g2894 | DLA_03209 | F4PJNLW02HBBIY | CDS | 47744 | 780 | + | 0.317949 | |
g2895 | DLA_03210 | F4PJNLW02HBBIY | CDS | 48699 | 2763 | - | 0.364821 | |
g2896 | DLA_03211 | F4PJNLW02HBBIY | CDS | 51888 | 222 | + | 0.315315 | |
g2897 | DLA_03212 | ortholog of S. pombe Cwf15 and S. cerevisiae Cwc15 thought to be non-essential components of an mRNA splicing complex there is a second copy of this gene | F4PJNLW02HBBIY | CDS | 52262 | 696 | + | 0.29454 |
g2898 | DLA_03213 | F4PJNLW02HBBIY | CDS | 53086 | 351 | - | 0.2849 | |
g2899 | DLA_03214 | F4PJNLW02HBBIY | CDS | 53522 | 957 | + | 0.290491 | |
g29 | DLA_00033 | contig05409_1.exp | CDS | 76038 | 801 | + | 0.254682 | |
g290 | DLA_00321 | contig05409_1.exp | CDS | 670186 | 2427 | - | 0.271117 | |
g2900 | DLA_03215 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | F4PJNLW02HBBIY | CDS | 55334 | 3594 | + | 0.378687 |
g2901 | DLA_03216 | F4PJNLW02HBBIY | CDS | 59139 | 2268 | - | 0.334215 | |
g2902 | DLA_03217 | F4PJNLW02HBBIY | CDS | 63032 | 2532 | + | 0.329779 | |
g2903 | DLA_03218 | F4PJNLW02HBBIY | CDS | 65746 | 1101 | + | 0.318801 | |
g2904 | DLA_03219 | F4PJNLW02HBBIY | CDS | 67277 | 885 | + | 0.273446 | |
g2905 | DLA_11543 | F4PJNLW02HBBIY | CDS | 68331 | 1203 | - | 0.285952 | |
g2906 | DLA_03221 | F4PJNLW02HBBIY | CDS | 69761 | 2688 | - | 0.316964 | |
g2907 | DLA_03222 | catalyzes the reaction ATP L-glutamate ammonia ADP phosphate L-glutamine | F4PJNLW02HBBIY | CDS | 72788 | 1494 | + | 0.314592 |
g2908 | DLA_03223 | F4PJNLW02HBBIY | CDS | 74419 | 1467 | + | 0.314928 | |
g2909 | DLA_03225 | highly similar to | F4PJNLW02HBBIY | CDS | 76710 | 738 | + | 0.296748 |
g291 | DLA_00322 | contig05409_1.exp | CDS | 673007 | 2217 | - | 0.348218 | |
g2910 | DLA_03226 | F4PJNLW02HBBIY | CDS | 77827 | 1074 | - | 0.356611 | |
g2911 | DLA_03227 | F4PJNLW02HBBIY | CDS | 79177 | 3573 | - | 0.302267 | |
g2912 | DLA_03228 | F4PJNLW02HBBIY | CDS | 83035 | 1992 | + | 0.299197 | |
g2913 | DLA_11544 | F4PJNLW02HBBIY | CDS | 85078 | 1683 | + | 0.299465 | |
g2914 | DLA_03229 | F4PJNLW02HBBIY | CDS | 87106 | 285 | + | 0.319298 | |
g2915 | DLA_03230 | F4PJNLW02HBBIY | CDS | 87970 | 3300 | + | 0.36303 | |
g2916 | DLA_03231 | F4PJNLW02HBBIY | CDS | 91551 | 771 | + | 0.286641 | |
g2917 | DLA_03233 | F4PJNLW02HBBIY | CDS | 92444 | 381 | + | 0.228346 | |
g2918 | DLA_11545 | F4PJNLW02HBBIY | CDS | 92943 | 429 | + | 0.249417 | |
g2919 | DLA_03234 | F4PJNLW02HBBIY | CDS | 93924 | 1290 | - | 0.343411 | |
g292 | DLA_00324 | contig05409_1.exp | CDS | 676113 | 1521 | + | 0.293886 | |
g2920 | DLA_03235 | F4PJNLW02HBBIY | CDS | 95713 | 1701 | + | 0.309818 | |
g2921 | DLA_03236 | F4PJNLW02HBBIY | CDS | 97770 | 1467 | - | 0.334015 | |
g2922 | DLA_03237 | F4PJNLW02HBBIY | CDS | 100288 | 2214 | + | 0.337398 | |
g2923 | DLA_03238 | F4PJNLW02HBBIY | CDS | 102679 | 810 | + | 0.318519 | |
g2924 | DLA_03239 | F4PJNLW02HBBIY | CDS | 103863 | 957 | - | 0.345873 | |
g2925 | DLA_03240 | F4PJNLW02HBBIY | CDS | 104969 | 810 | - | 0.324691 | |
g2926 | DLA_03241 | F4PJNLW02HBBIY | CDS | 106620 | 1935 | - | 0.355039 | |
g2927 | DLA_03242 | F4PJNLW02HBBIY | CDS | 108985 | 1764 | - | 0.3322 | |
g2928 | DLA_03243 | F4PJNLW02HBBIY | CDS | 112022 | 666 | - | 0.292793 | |
g2929 | DLA_03244 | F4PJNLW02HBBIY | CDS | 113092 | 1488 | + | 0.341398 | |
g293 | DLA_00325 | contig05409_1.exp | CDS | 677866 | 867 | - | 0.297578 | |
g2930 | DLA_03245 | F4PJNLW02HBBIY | CDS | 114871 | 1320 | - | 0.346212 | |
g2931 | DLA_03246 | F4PJNLW02HBBIY | CDS | 116483 | 801 | + | 0.360799 | |
g2932 | DLA_03247 | F4PJNLW02HBBIY | CDS | 117536 | 645 | - | 0.344186 | |
g2933 | DLA_03248 | F4PJNLW02HBBIY | CDS | 118459 | 1113 | + | 0.338724 | |
g2934 | DLA_03250 | F4PJNLW02HBBIY | CDS | 121491 | 3333 | - | 0.357336 | |
g2935 | DLA_03251 | F4PJNLW02HBBIY | CDS | 125268 | 1197 | - | 0.350877 | |
g2936 | DLA_03252 | F4PJNLW02HBBIY | CDS | 127044 | 2301 | + | 0.333768 | |
g2937 | DLA_03255 | F4PJNLW02HBBIY | CDS | 130695 | 675 | + | 0.266667 | |
g2938 | DLA_03256 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | F4PJNLW02HBBIY | CDS | 131742 | 747 | - | 0.337349 |
g2939 | DLA_03257 | F4PJNLW02HBBIY | CDS | 132940 | 597 | - | 0.363484 | |
g294 | DLA_00326 | contig05409_1.exp | CDS | 679029 | 933 | + | 0.350482 | |
g2940 | DLA_03258 | F4PJNLW02HBBIY | CDS | 134547 | 1719 | + | 0.314136 | |
g2941 | DLA_03259 | F4PJNLW02HBBIY | CDS | 136651 | 1407 | + | 0.327647 | |
g2942 | DLA_03260 | F4PJNLW02HBBIY | CDS | 138381 | 11952 | + | 0.347808 | |
g2943 | DLA_03261 | F4PJNLW02HBBIY | CDS | 150620 | 855 | + | 0.329825 | |
g2944 | DLA_03262 | F4PJNLW02HBBIY | CDS | 151698 | 1647 | - | 0.35337 | |
g2945 | DLA_03263 | F4PJNLW02HBBIY | CDS | 154101 | 447 | - | 0.308725 | |
g2946 | DLA_03264 | F4PJNLW02HBBIY | CDS | 154894 | 1431 | - | 0.328442 | |
g2947 | DLA_03265 | F4PJNLW02HBBIY | CDS | 156764 | 1272 | + | 0.305818 | |
g2948 | DLA_03266 | F4PJNLW02HBBIY | CDS | 158076 | 1917 | - | 0.314032 | |
g2949 | DLA_03267 | F4PJNLW02HBBIY | CDS | 160267 | 1491 | - | 0.279007 | |
g295 | DLA_00327 | contig05409_1.exp | CDS | 680157 | 1872 | + | 0.293803 | |
g2950 | DLA_03269 | F4PJNLW02HBBIY | CDS | 162758 | 798 | - | 0.330827 | |
g2951 | DLA_03270 | F4PJNLW02HBBIY | CDS | 163762 | 3789 | - | 0.301135 | |
g2952 | DLA_03272 | F4PJNLW02HBBIY | CDS | 168271 | 2685 | + | 0.296834 | |
g2953 | DLA_03273 | F4PJNLW02HBBIY | CDS | 172175 | 3267 | + | 0.295378 | |
g2954 | DLA_03275 | F4PJNLW02HBBIY | CDS | 176262 | 3339 | + | 0.300689 | |
g2955 | DLA_03276 | F4PJNLW02HBBIY | CDS | 179680 | 3546 | - | 0.302876 | |
g2956 | DLA_03277 | F4PJNLW02HBBIY | CDS | 183626 | 1581 | + | 0.376977 | |
g2957 | DLA_03278 | F4PJNLW02HBBIY | CDS | 185474 | 1140 | + | 0.277193 | |
g2958 | DLA_03279 | F4PJNLW02HBBIY | CDS | 186711 | 555 | - | 0.313514 | |
g2959 | DLA_03280 | F4PJNLW02HBBIY | CDS | 187466 | 3477 | - | 0.311763 | |
g296 | DLA_00329 | contig05409_1.exp | CDS | 683075 | 867 | - | 0.299885 | |
g2960 | DLA_03281 | F4PJNLW02HBBIY | CDS | 191999 | 420 | - | 0.304762 | |
g2961 | DLA_03282 | F4PJNLW02HBBIY | CDS | 192513 | 1218 | + | 0.305419 | |
g2962 | DLA_03283 | F4PJNLW02HBBIY | CDS | 193854 | 1845 | - | 0.278591 | |
g2963 | DLA_03284 | F4PJNLW02HBBIY | CDS | 195774 | 1503 | - | 0.283433 | |
g2964 | DLA_03285 | F4PJNLW02HBBIY | CDS | 197662 | 273 | - | 0.278388 | |
g2965 | DLA_03286 | highly conserved protein involved in GPI biosynthesis forms a complex with DPM1 and DPM3 regulates the biosynthesis of dolichol-phosphate-mannose there is a second copy of this gene | F4PJNLW02HBBIY | CDS | 198281 | 237 | - | 0.270042 |
g2966 | DLA_03287 | F4PJNLW02HBBIY | CDS | 198743 | 561 | - | 0.304813 | |
g2967 | DLA_03288 | F4PJNLW02HBBIY | CDS | 199659 | 1515 | + | 0.368977 | |
g2968 | DLA_03289 | F4PJNLW02HBBIY | CDS | 201439 | 1026 | - | 0.359649 | |
g2969 | DLA_03290 | F4PJNLW02HBBIY | CDS | 202920 | 1443 | + | 0.309078 | |
g297 | DLA_00330 | contig05409_1.exp | CDS | 685317 | 1479 | - | 0.382015 | |
g2970 | DLA_11546 | F4PJNLW02HBBIY | CDS | 204489 | 1734 | + | 0.325836 | |
g2971 | DLA_03291 | F4PJNLW02HBBIY | CDS | 206822 | 2460 | + | 0.34878 | |
g2972 | DLA_03292 | F4PJNLW02HBBIY | CDS | 209684 | 3564 | + | 0.300224 | |
g2973 | DLA_03294 | F4PJNLW02HBBIY | CDS | 215030 | 2130 | - | 0.290141 | |
g2974 | DLA_03295 | F4PJNLW02HBBIY | CDS | 217672 | 3483 | + | 0.294574 | |
g2975 | DLA_03296 | F4PJNLW02HBBIY | CDS | 221443 | 357 | + | 0.235294 | |
g2976 | DLA_03297 | F4PJNLW02HBBIY | CDS | 223069 | 1848 | + | 0.356061 | |
g2977 | DLA_03298 | F4PJNLW02HBBIY | CDS | 225129 | 2649 | + | 0.326161 | |
g2978 | DLA_03299 | F4PJNLW02HBBIY | CDS | 227899 | 1155 | + | 0.349784 | |
g2979 | DLA_03300 | F4PJNLW02HBBIY | CDS | 229722 | 1140 | - | 0.372807 | |
g298 | DLA_00331 | contig05409_1.exp | CDS | 687372 | 711 | + | 0.209564 | |
g2980 | DLA_03301 | F4PJNLW02HBBIY | CDS | 232173 | 2199 | - | 0.34925 | |
g2981 | DLA_11547 | F4PJNLW02HBBIY | CDS | 235008 | 246 | - | 0.300813 | |
g2982 | DLA_03302 | F4PJNLW02HBBIY | CDS | 235556 | 1293 | + | 0.311678 | |
g2983 | DLA_03303 | F4PJNLW02HBBIY | CDS | 236901 | 2343 | - | 0.33248 | |
g2984 | DLA_03304 | F4PJNLW02HBBIY | CDS | 240134 | 2109 | + | 0.293504 | |
g2985 | DLA_03305 | similar to discoidin I almost identical to its downstream gene DD7-1 | F4PJNLW02HBBIY | CDS | 242385 | 789 | - | 0.338403 |
g2986 | DLA_03306 | F4PJNLW02HBBIY | CDS | 244490 | 204 | + | 0.284314 | |
g2987 | DLA_03308 | F4PJNLW02HBBIY | CDS | 245603 | 216 | + | 0.324074 | |
g2988 | DLA_03310 | F4PJNLW02HBBIY | CDS | 247385 | 1254 | + | 0.359649 | |
g2989 | DLA_03311 | F4PJNLW02HBBIY | CDS | 248817 | 558 | + | 0.356631 | |
g299 | DLA_00332 | contig05409_1.exp | CDS | 688249 | 450 | + | 0.286667 | |
g2990 | DLA_03312 | F4PJNLW02HBBIY | CDS | 249623 | 546 | - | 0.31685 | |
g2991 | DLA_03313 | F4PJNLW02HBBIY | CDS | 251475 | 2058 | - | 0.327502 | |
g2992 | DLA_03314 | F4PJNLW02HBBIY | CDS | 253881 | 1785 | - | 0.329412 | |
g2993 | DLA_03315 | F4PJNLW02HBBIY | CDS | 255934 | 1698 | + | 0.3298 | |
g2994 | DLA_03316 | F4PJNLW02HBBIY | CDS | 257882 | 1578 | + | 0.291508 | |
g2995 | DLA_03317 | F4PJNLW02HBBIY | CDS | 259572 | 1311 | - | 0.315789 | |
g2996 | DLA_03318 | F4PJNLW02HBBIY | CDS | 260957 | 1767 | + | 0.301641 | |
g2997 | DLA_03319 | F4PJNLW02HBBIY | CDS | 262896 | 1476 | + | 0.365854 | |
g2998 | DLA_03320 | F4PJNLW02HBBIY | CDS | 264643 | 3888 | + | 0.345679 | |
g2999 | DLA_03321 | F4PJNLW02HBBIY | CDS | 269400 | 1704 | + | 0.330399 | |
g3 | DLA_00004 | contig05409_1.exp | CDS | 7120 | 1737 | + | 0.329879 | |
g30 | DLA_00034 | composed of approx. 35 copies of a 24-amino-acid cysteine-rich repeat expression is decreased in | contig05409_1.exp | CDS | 77119 | 2190 | - | 0.376712 |
g300 | DLA_00333 | contig05409_1.exp | CDS | 689049 | 615 | + | 0.291057 | |
g3000 | DLA_03322 | F4PJNLW02HBBIY | CDS | 271712 | 870 | - | 0.333333 | |
g3001 | DLA_03323 | F4PJNLW02HBBIY | CDS | 272950 | 927 | - | 0.372168 | |
g3002 | DLA_03325 | F4PJNLW02HBBIY | CDS | 274576 | 726 | + | 0.330579 | |
g3003 | DLA_03326 | F4PJNLW02HBBIY | CDS | 275354 | 981 | - | 0.308868 | |
g3004 | DLA_03327 | F4PJNLW02HBBIY | CDS | 276608 | 1248 | - | 0.373397 | |
g3005 | DLA_03329 | catalyzes the release of N-terminal amino acids preferentially methionine from peptides and arylamides | F4PJNLW02HBBIY | CDS | 278456 | 2310 | - | 0.337662 |
g3006 | DLA_03331 | F4PJNLW02HBBIY | CDS | 281279 | 723 | + | 0.31397 | |
g3007 | DLA_03332 | F4PJNLW02HBBIY | CDS | 282024 | 3378 | - | 0.328005 | |
g3008 | DLA_11548 | F4PJNLW02HBBIY | CDS | 285549 | 3285 | - | 0.333333 | |
g3009 | DLA_03333 | F4PJNLW02HBBIY | CDS | 288988 | 4692 | - | 0.372336 | |
g301 | DLA_00334 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | contig05409_1.exp | CDS | 690602 | 2142 | + | 0.337068 |
g3010 | DLA_03334 | F4PJNLW02HBBIY | CDS | 294258 | 1596 | - | 0.368421 | |
g3011 | DLA_03335 | F4PJNLW02HBBIY | CDS | 296520 | 444 | - | 0.346847 | |
g3012 | DLA_03336 | F4PJNLW02HBBIY | CDS | 299440 | 1821 | + | 0.299286 | |
g3013 | DLA_03337 | F4PJNLW02HBBIY | CDS | 301738 | 1665 | + | 0.312913 | |
g3014 | DLA_03338 | F4PJNLW02HBBIY | CDS | 303758 | 909 | + | 0.325633 | |
g3015 | DLA_03340 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 19 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | F4PJNLW02HBBIY | CDS | 306780 | 1032 | + | 0.310078 |
g3016 | DLA_03341 | F4PJNLW02HBBIY | CDS | 308155 | 3942 | - | 0.345003 | |
g3017 | DLA_03342 | F4PJNLW02HBBIY | CDS | 313180 | 2661 | + | 0.346486 | |
g3018 | DLA_03343 | F4PJNLW02HBBIY | CDS | 316072 | 1266 | - | 0.279621 | |
g3019 | DLA_03345 | F4PJNLW02HBBIY | CDS | 318594 | 1884 | + | 0.333864 | |
g302 | DLA_00335 | contig05409_1.exp | CDS | 693895 | 2262 | + | 0.276304 | |
g3020 | DLA_03346 | F4PJNLW02HBBIY | CDS | 320856 | 540 | - | 0.32037 | |
g3021 | DLA_03347 | F4PJNLW02HBBIY | CDS | 321833 | 1110 | + | 0.341441 | |
g3022 | DLA_03348 | F4PJNLW02HBBIY | CDS | 323292 | 1377 | - | 0.299201 | |
g3023 | DLA_03349 | F4PJNLW02HBBIY | CDS | 324992 | 1083 | + | 0.319483 | |
g3024 | DLA_03350 | F4PJNLW02HBBIY | CDS | 326127 | 2319 | - | 0.355326 | |
g3025 | DLA_03351 | F4PJNLW02HBBIY | CDS | 328584 | 741 | - | 0.306343 | |
g3026 | DLA_03353 | F4PJNLW02HBBIY | CDS | 329890 | 1920 | + | 0.311458 | |
g3027 | DLA_03354 | F4PJNLW02HBBIY | CDS | 333049 | 246 | + | 0.365854 | |
g3028 | DLA_03355 | F4PJNLW02HBBIY | CDS | 333797 | 1293 | - | 0.348028 | |
g3029 | DLA_11549 | F4PJNLW02HBBIY | CDS | 335500 | 3363 | + | 0.282783 | |
g303 | DLA_00336 | contig05409_1.exp | CDS | 696740 | 2211 | + | 0.289462 | |
g3030 | DLA_03356 | F4PJNLW02HBBIY | CDS | 339256 | 1587 | + | 0.320731 | |
g3031 | DLA_03357 | F4PJNLW02HBBIY | CDS | 341053 | 8295 | + | 0.332007 | |
g3032 | DLA_03359 | F4PJNLW02HBBIY | CDS | 350089 | 4194 | + | 0.330949 | |
g3033 | DLA_03360 | F4PJNLW02HBBIY | CDS | 354483 | 3060 | - | 0.35 | |
g3034 | DLA_03361 | F4PJNLW02HBBIY | CDS | 357878 | 2271 | - | 0.369441 | |
g3035 | DLA_03362 | F4PJNLW02HBBIY | CDS | 361414 | 2673 | + | 0.34306 | |
g3036 | DLA_11550 | member of the same super family as valosin-containing protein (VCP) and CDC48brbr bCommunity annotation:b DDB G0272777 appears to be the Dicty-specific AAA-ATPase related cdc48 (cdcD) in Dicty and other organisms. When | F4PJNLW02HBBIY | CDS | 364335 | 2112 | - | 0.304451 |
g3037 | DLA_03363 | F4PJNLW02HBBIY | CDS | 366615 | 2451 | - | 0.339861 | |
g3038 | DLA_03364 | F4PJNLW02HBBIY | CDS | 369340 | 360 | + | 0.438889 | |
g3039 | DLA_03365 | F4PJNLW02HBBIY | CDS | 371781 | 1038 | + | 0.315992 | |
g304 | DLA_00337 | contig05409_1.exp | CDS | 699933 | 834 | + | 0.320144 | |
g3040 | DLA_03366 | F4PJNLW02HBBIY | CDS | 373624 | 423 | + | 0.390071 | |
g3041 | DLA_03367 | F4PJNLW02HBBIY | CDS | 374233 | 792 | - | 0.289141 | |
g3042 | DLA_03368 | F4PJNLW02HBBIY | CDS | 375236 | 1740 | - | 0.384483 | |
g3043 | DLA_03369 | F4PJNLW02HBBIY | CDS | 378053 | 4266 | - | 0.339897 | |
g3044 | DLA_11551 | F4PJNLW02HBBIY | CDS | 382889 | 1017 | - | 0.368732 | |
g3045 | DLA_03370 | F4PJNLW02HBBIY | CDS | 384208 | 672 | - | 0.33631 | |
g3046 | DLA_03371 | similar to human AOAH (acyloxyacyl hydrolase) removes the secondary (acyloxyacyl-linked) fatty acyl chains from the lipid A region of bacterial lipopolysaccharides contains a predicted signal peptide contains 1 saposin B-type domain | F4PJNLW02HBBIY | CDS | 385311 | 1701 | + | 0.37037 |
g3047 | DLA_03372 | F4PJNLW02HBBIY | CDS | 387662 | 687 | + | 0.286754 | |
g3048 | DLA_03373 | F4PJNLW02HBBIY | CDS | 389543 | 651 | + | 0.256528 | |
g3049 | DLA_03374 | F4PJNLW02HBBIY | CDS | 390309 | 1293 | + | 0.246713 | |
g305 | DLA_00339 | contig05409_1.exp | CDS | 703213 | 699 | + | 0.353362 | |
g3050 | DLA_03375 | F4PJNLW02HBBIY | CDS | 392087 | 2382 | + | 0.253149 | |
g3051 | DLA_03376 | F4PJNLW02HBBIY | CDS | 394666 | 4044 | - | 0.3227 | |
g3052 | DLA_03377 | F4PJNLW02HBBIY | CDS | 399288 | 1779 | + | 0.323777 | |
g3053 | DLA_03380 | F4PJNLW02HBBIY | CDS | 402551 | 813 | + | 0.335793 | |
g3054 | DLA_03381 | F4PJNLW02HBBIY | CDS | 404265 | 2835 | - | 0.325926 | |
g3055 | DLA_03382 | F4PJNLW02HBBIY | CDS | 407808 | 4188 | + | 0.317813 | |
g3056 | DLA_03383 | F4PJNLW02HBBIY | CDS | 412070 | 1302 | - | 0.281106 | |
g3057 | DLA_03384 | F4PJNLW02HBBIY | CDS | 413497 | 1506 | - | 0.282205 | |
g3058 | DLA_03385 | induced by Legionella pneumophila infection similar to D. purpureum protein | F4PJNLW02HBBIY | CDS | 415281 | 642 | - | 0.344237 |
g3059 | DLA_03386 | F4PJNLW02HBBIY | CDS | 416453 | 1569 | + | 0.305927 | |
g306 | DLA_00340 | contig05409_1.exp | CDS | 705125 | 4287 | - | 0.284581 | |
g3060 | DLA_03387 | F4PJNLW02HBBIY | CDS | 418335 | 3711 | - | 0.306656 | |
g3061 | DLA_03388 | F4PJNLW02HBBIY | CDS | 422744 | 2760 | + | 0.350362 | |
g3062 | DLA_03389 | F4PJNLW02HBBIY | CDS | 426110 | 330 | - | 0.309091 | |
g3063 | DLA_03390 | F4PJNLW02HBBIY | CDS | 426670 | 852 | - | 0.327465 | |
g3064 | DLA_03391 | F4PJNLW02HBBIY | CDS | 428002 | 354 | - | 0.313559 | |
g3065 | DLA_03392 | F4PJNLW02HBBIY | CDS | 428730 | 1320 | + | 0.306061 | |
g3066 | DLA_03393 | F4PJNLW02HBBIY | CDS | 430102 | 1008 | - | 0.293651 | |
g3067 | DLA_03395 | F4PJNLW02HBBIY | CDS | 432501 | 1332 | - | 0.311562 | |
g3068 | DLA_03396 | F4PJNLW02HBBIY | CDS | 434716 | 969 | - | 0.343653 | |
g3069 | DLA_03397 | F4PJNLW02HBBIY | CDS | 435823 | 1455 | - | 0.294158 | |
g307 | DLA_00342 | similar to histidine ammonia-lyase which catalyzes the reaction L-histidine urocanate NHsub3sub there is a second copy of this gene | contig05409_1.exp | CDS | 709746 | 1596 | - | 0.305138 |
g3070 | DLA_03398 | F4PJNLW02HBBIY | CDS | 437562 | 297 | + | 0.30303 | |
g3071 | DLA_03399 | F4PJNLW02HBBIY | CDS | 438003 | 1629 | - | 0.302026 | |
g3072 | DLA_03400 | F4PJNLW02HBBIY | CDS | 439894 | 1020 | + | 0.330392 | |
g3073 | DLA_03401 | F4PJNLW02HBBIY | CDS | 441018 | 2130 | - | 0.258685 | |
g3074 | DLA_03403 | F4PJNLW02HBBIY | CDS | 444040 | 2112 | - | 0.256629 | |
g3075 | DLA_03404 | F4PJNLW02HBBIY | CDS | 446462 | 1188 | - | 0.258418 | |
g3076 | DLA_03405 | F4PJNLW02HBBIY | CDS | 449301 | 333 | + | 0.336336 | |
g3077 | DLA_03407 | F4PJNLW02HBBIY | CDS | 449674 | 2418 | + | 0.310587 | |
g3078 | DLA_03408 | F4PJNLW02HBBIY | CDS | 452790 | 471 | + | 0.343949 | |
g3079 | DLA_03411 | F4PJNLW02HBBIY | CDS | 454956 | 579 | + | 0.279793 | |
g308 | DLA_00344 | contig05409_1.exp | CDS | 712042 | 3285 | + | 0.23379 | |
g3080 | DLA_03412 | F4PJNLW02HBBIY | CDS | 455828 | 2091 | - | 0.360115 | |
g3081 | DLA_03413 | F4PJNLW02HBBIY | CDS | 458825 | 2091 | + | 0.361549 | |
g3082 | DLA_03414 | F4PJNLW02HBBIY | CDS | 461231 | 2265 | + | 0.342605 | |
g3083 | DLA_03415 | F4PJNLW02HBBIY | CDS | 463904 | 1506 | - | 0.355246 | |
g3084 | DLA_03416 | F4PJNLW02HBBIY | CDS | 465938 | 792 | + | 0.284091 | |
g3085 | DLA_03417 | F4PJNLW02HBBIY | CDS | 467255 | 213 | + | 0.295775 | |
g3086 | DLA_03418 | F4PJNLW02HBBIY | CDS | 467710 | 1548 | - | 0.357235 | |
g3087 | DLA_11552 | F4PJNLW02HBBIY | CDS | 470168 | 672 | - | 0.453869 | |
g3088 | DLA_03419 | F4PJNLW02HBBIY | CDS | 471362 | 375 | - | 0.301333 | |
g3089 | DLA_03420 | F4PJNLW02HBBIY | CDS | 471910 | 2058 | - | 0.335277 | |
g309 | DLA_00345 | contig05409_1.exp | CDS | 715521 | 858 | - | 0.296037 | |
g3090 | DLA_03421 | ortholog of S. cerevisiae MAK16 and mammalian RBM13 inyeast an essential nuclear protein constituent of 66S pre-ribosomal particles | F4PJNLW02HBBIY | CDS | 475160 | 987 | - | 0.298886 |
g3091 | DLA_03422 | F4PJNLW02HBBIY | CDS | 476540 | 492 | + | 0.29065 | |
g3092 | DLA_03423 | F4PJNLW02HBBIY | CDS | 477700 | 1311 | - | 0.292906 | |
g3093 | DLA_03424 | F4PJNLW02HBBIY | CDS | 479562 | 468 | + | 0.292735 | |
g3094 | DLA_03426 | F4PJNLW02HBBIY | CDS | 480552 | 2499 | - | 0.392957 | |
g3095 | DLA_03427 | ortholog of mammalian NCPB1 and yeast STO1 large subunit of the heterodimeric cap binding complex involved in mediating U snRNA export from the nucleus | F4PJNLW02HBBIY | CDS | 483896 | 2184 | - | 0.320513 |
g3096 | DLA_03428 | ortholog of the mammalian kin17 protein a zinc finger nuclear protein | F4PJNLW02HBBIY | CDS | 486757 | 1194 | + | 0.306533 |
g3097 | DLA_03429 | F4PJNLW02HBBIY | CDS | 488683 | 621 | + | 0.344605 | |
g3098 | DLA_03430 | F4PJNLW02HBBIY | CDS | 490348 | 459 | + | 0.283224 | |
g3099 | DLA_03431 | hydrolyses D-fructose 16-bisphosphate to D-fructose 6-phosphate and phosphate (EC 3.1.3.11) | F4PJNLW02HBBIY | CDS | 491079 | 1017 | - | 0.347099 |
g31 | DLA_00035 | contig05409_1.exp | CDS | 80479 | 372 | + | 0.266129 | |
g310 | DLA_00346 | contig05409_1.exp | CDS | 716527 | 5658 | + | 0.347649 | |
g3100 | DLA_03432 | F4PJNLW02HBBIY | CDS | 492640 | 2343 | + | 0.279129 | |
g3101 | DLA_03433 | catalyzes the reaction ATP L-histidine tRNAHis AMP diphosphate L-histidyl-tRNAHis similar to bacterial histidine-tRNA ligase | F4PJNLW02HBBIY | CDS | 495146 | 1371 | - | 0.297593 |
g3102 | DLA_03434 | F4PJNLW02HBBIY | CDS | 496733 | 1002 | + | 0.258483 | |
g3103 | DLA_03435 | precursor of SDF-2 similar to diazepam binding inhibitor enriched in prespore cells | F4PJNLW02HBBIY | CDS | 497870 | 255 | - | 0.380392 |
g3104 | DLA_03436 | catalyzes the reaction ATP 3-methylcrotonoyl-CoA HCOsub3subsup-sup ADP phosphate 3-methylglutaconyl-CoA | F4PJNLW02HBBIY | CDS | 498605 | 3723 | - | 0.348375 |
g3105 | DLA_03438 | F4PJNLW02HBBIY | CDS | 502666 | 3060 | - | 0.319935 | |
g3106 | DLA_03439 | F4PJNLW02HBBIY | CDS | 506170 | 1254 | + | 0.283892 | |
g3107 | DLA_03440 | F4PJNLW02HBBIY | CDS | 507521 | 1179 | - | 0.283291 | |
g3108 | DLA_03441 | F4PJNLW02HBBIY | CDS | 508940 | 1194 | + | 0.292295 | |
g3109 | DLA_03442 | F4PJNLW02HBBIY | CDS | 510622 | 852 | + | 0.346244 | |
g311 | DLA_11439 | contig05409_1.exp | CDS | 722598 | 762 | + | 0.341207 | |
g3110 | DLA_03443 | F4PJNLW02HBBIY | CDS | 511690 | 2019 | + | 0.253591 | |
g3111 | DLA_03444 | F4PJNLW02HBBIY | CDS | 514355 | 1509 | + | 0.304838 | |
g3112 | DLA_03446 | F4PJNLW02HBBIY | CDS | 516374 | 1500 | - | 0.352 | |
g3113 | DLA_03447 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases there is a second copy of this gene | F4PJNLW02HBBIY | CDS | 518303 | 1077 | + | 0.287837 |
g3114 | DLA_03448 | F4PJNLW02HBBIY | CDS | 519872 | 744 | + | 0.278226 | |
g3115 | DLA_03449 | F4PJNLW02HBBIY | CDS | 520752 | 3420 | - | 0.287134 | |
g3116 | DLA_03450 | F4PJNLW02HBBIY | CDS | 525616 | 825 | + | 0.283636 | |
g3117 | DLA_03451 | F4PJNLW02HBBIY | CDS | 526519 | 1467 | + | 0.29516 | |
g3118 | DLA_03453 | F4PJNLW02HBBIY | CDS | 529123 | 660 | - | 0.286364 | |
g3119 | DLA_03454 | F4PJNLW02HBBIY | CDS | 530489 | 1473 | + | 0.306857 | |
g312 | DLA_00347 | contig05409_1.exp | CDS | 723678 | 1476 | + | 0.295393 | |
g3120 | DLA_03455 | F4PJNLW02HBBIY | CDS | 532673 | 435 | + | 0.268966 | |
g3121 | DLA_03456 | F4PJNLW02HBBIY | CDS | 533381 | 276 | - | 0.423913 | |
g3122 | DLA_03457 | F4PJNLW02HBBIY | CDS | 533964 | 1893 | - | 0.303751 | |
g3123 | DLA_03458 | interacts with the phg2 kinase pathway plays a role in the transition from growth to differentiationbr there is a second copy of this gene | F4PJNLW02HBBIY | CDS | 536188 | 936 | + | 0.316239 |
g3124 | DLA_03459 | ortholog of H. sapiens DOHH that catalyzes the hydroxylation of the N(6)-(4-aminobutyl)-L-lysine intermediate to form hypusine an essential post-translational modification only found in mature eIF5A factor the first reaction is catalyzed by Dhps there is a second copy of this gene | F4PJNLW02HBBIY | CDS | 537719 | 984 | + | 0.325203 |
g3125 | DLA_03460 | F4PJNLW02HBBIY | CDS | 538874 | 2118 | + | 0.296506 | |
g3126 | DLA_03461 | F4PJNLW02HBBIY | CDS | 541258 | 3984 | - | 0.299699 | |
g3127 | DLA_03462 | F4PJNLW02HBBIY | CDS | 546113 | 1023 | + | 0.312805 | |
g3128 | DLA_03464 | F4PJNLW02HBBIY | CDS | 548108 | 1059 | - | 0.283286 | |
g3129 | DLA_03465 | F4PJNLW02HBBIY | CDS | 549482 | 1548 | + | 0.29199 | |
g313 | DLA_00348 | contig05409_1.exp | CDS | 725171 | 978 | - | 0.264826 | |
g3130 | DLA_03466 | F4PJNLW02HBBIY | CDS | 551387 | 1626 | - | 0.263223 | |
g3131 | DLA_03468 | F4PJNLW02HBBIY | CDS | 553786 | 1002 | + | 0.307385 | |
g3132 | DLA_03470 | F4PJNLW02HBBIY | CDS | 555732 | 1137 | + | 0.254178 | |
g3133 | DLA_03471 | F4PJNLW02HBBIY | CDS | 557247 | 675 | - | 0.317037 | |
g3134 | DLA_03472 | F4PJNLW02HBBIY | CDS | 558698 | 1005 | - | 0.269652 | |
g3135 | DLA_03473 | F4PJNLW02HBBIY | CDS | 560215 | 663 | - | 0.324284 | |
g3136 | DLA_03474 | F4PJNLW02HBBIY | CDS | 561159 | 1773 | - | 0.318105 | |
g3137 | DLA_03475 | F4PJNLW02I2K04 | CDS | 54 | 2028 | - | 0.428008 | |
g3138 | DLA_03476 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | GAOABQK02FRRQV | CDS | 93 | 1956 | - | 0.314417 |
g3139 | DLA_03477 | GAOABQK02FRRQV | CDS | 3450 | 1020 | + | 0.335294 | |
g314 | DLA_00349 | contig05409_1.exp | CDS | 726372 | 732 | - | 0.338798 | |
g3140 | DLA_03478 | GAOABQK02FRRQV | CDS | 5157 | 1668 | + | 0.266787 | |
g3141 | DLA_03480 | GAOABQK02FRRQV | CDS | 7360 | 795 | - | 0.271698 | |
g3142 | DLA_03481 | GAOABQK02FRRQV | CDS | 8217 | 807 | - | 0.276332 | |
g3143 | DLA_03483 | GAOABQK02FRRQV | CDS | 10266 | 675 | - | 0.331852 | |
g3144 | DLA_03484 | GAOABQK02FRRQV | CDS | 11166 | 678 | - | 0.294985 | |
g3145 | DLA_03485 | GAOABQK02FRRQV | CDS | 12583 | 3768 | + | 0.292463 | |
g3146 | DLA_03487 | GAOABQK02FRRQV | CDS | 16869 | 3723 | - | 0.284717 | |
g3147 | DLA_03488 | GAOABQK02FRRQV | CDS | 20884 | 1053 | + | 0.273504 | |
g3148 | DLA_03490 | GAOABQK02FRRQV | CDS | 24877 | 957 | + | 0.281087 | |
g3149 | DLA_03492 | GAOABQK02FRRQV | CDS | 27276 | 1512 | + | 0.353836 | |
g315 | DLA_00350 | contig05409_1.exp | CDS | 728057 | 2577 | - | 0.327901 | |
g3150 | DLA_03493 | GAOABQK02FRRQV | CDS | 28841 | 1167 | - | 0.289632 | |
g3151 | DLA_03494 | belongs to the metallophosphoesterase superfamily similar to human PAPL (Ironzinc purple acid phosphatase-like protein) contains a predicted signal peptide | GAOABQK02FRRQV | CDS | 30548 | 1275 | + | 0.36549 |
g3152 | DLA_03495 | GAOABQK02FRRQV | CDS | 32147 | 4350 | + | 0.301839 | |
g3153 | DLA_11553 | GAOABQK02FRRQV | CDS | 36789 | 267 | - | 0.299625 | |
g3154 | DLA_03496 | GAOABQK02FRRQV | CDS | 37129 | 363 | - | 0.341598 | |
g3155 | DLA_03497 | catalyzes the reaction nicotinamide Hsub2subO nicotinate NHsub3sub | GAOABQK02FRRQV | CDS | 38469 | 618 | + | 0.299353 |
g3156 | DLA_03498 | GAOABQK02FRRQV | CDS | 39437 | 1425 | - | 0.30386 | |
g3157 | DLA_03500 | GAOABQK02FRRQV | CDS | 43650 | 1671 | - | 0.263315 | |
g3158 | DLA_03501 | GAOABQK02FRRQV | CDS | 45854 | 825 | + | 0.282424 | |
g3159 | DLA_03502 | GAOABQK02FRRQV | CDS | 48920 | 618 | - | 0.349515 | |
g316 | DLA_00351 | contig05409_1.exp | CDS | 731164 | 2238 | - | 0.382484 | |
g3160 | DLA_03503 | GAOABQK02FRRQV | CDS | 49958 | 408 | + | 0.316176 | |
g3161 | DLA_03504 | GAOABQK02FRRQV | CDS | 50723 | 534 | - | 0.294007 | |
g3162 | DLA_03506 | GAOABQK02FRRQV | CDS | 51713 | 1470 | - | 0.327891 | |
g3163 | DLA_03508 | GAOABQK02FRRQV | CDS | 55722 | 3678 | - | 0.313214 | |
g3164 | DLA_03509 | GAOABQK02FRRQV | CDS | 59809 | 3363 | + | 0.316979 | |
g3165 | DLA_03510 | GAOABQK02FRRQV | CDS | 64358 | 1059 | + | 0.27101 | |
g3166 | DLA_03511 | GAOABQK02FRRQV | CDS | 65654 | 624 | - | 0.267628 | |
g3167 | DLA_03512 | GAOABQK02FRRQV | CDS | 68017 | 324 | + | 0.305556 | |
g3168 | DLA_03513 | GAOABQK02FRRQV | CDS | 68726 | 1254 | + | 0.338118 | |
g3169 | DLA_03514 | GAOABQK02FRRQV | CDS | 70236 | 273 | - | 0.271062 | |
g317 | DLA_00353 | contig05409_1.exp | CDS | 734290 | 2256 | + | 0.299645 | |
g3170 | DLA_03515 | GAOABQK02FRRQV | CDS | 71039 | 369 | + | 0.279133 | |
g3171 | DLA_03516 | GAOABQK02FRRQV | CDS | 72428 | 3078 | + | 0.348928 | |
g3172 | DLA_03517 | GAOABQK02FRRQV | CDS | 75694 | 1617 | + | 0.28757 | |
g3173 | DLA_03518 | GAOABQK02FRRQV | CDS | 77528 | 759 | - | 0.304348 | |
g3174 | DLA_03519 | GAOABQK02FRRQV | CDS | 78462 | 2457 | - | 0.310134 | |
g3175 | DLA_03520 | GAOABQK02FRRQV | CDS | 81554 | 2970 | + | 0.26734 | |
g3176 | DLA_03521 | GAOABQK02FRRQV | CDS | 84783 | 1224 | - | 0.268791 | |
g3177 | DLA_03522 | GAOABQK02FRRQV | CDS | 86254 | 1782 | + | 0.274972 | |
g3178 | DLA_03524 | GAOABQK02FRRQV | CDS | 88457 | 1269 | + | 0.321513 | |
g3179 | DLA_03525 | GAOABQK02FRRQV | CDS | 89834 | 633 | - | 0.268562 | |
g318 | DLA_00354 | contig05409_1.exp | CDS | 736765 | 1800 | - | 0.335556 | |
g3180 | DLA_03526 | GAOABQK02FRRQV | CDS | 90944 | 1326 | + | 0.349925 | |
g3181 | DLA_03527 | GAOABQK02FRRQV | CDS | 92488 | 702 | + | 0.339031 | |
g3182 | DLA_03528 | GAOABQK02FRRQV | CDS | 93435 | 846 | + | 0.289598 | |
g3183 | DLA_03529 | GAOABQK02FRRQV | CDS | 94417 | 1041 | + | 0.338136 | |
g3184 | DLA_03530 | GAOABQK02FRRQV | CDS | 95883 | 798 | + | 0.305764 | |
g3185 | DLA_03531 | GAOABQK02FRRQV | CDS | 96846 | 912 | - | 0.369518 | |
g3186 | DLA_03532 | GAOABQK02FRRQV | CDS | 98661 | 2277 | + | 0.282389 | |
g3187 | DLA_03533 | GAOABQK02FRRQV | CDS | 101138 | 1380 | - | 0.341304 | |
g3188 | DLA_03534 | GAOABQK02FRRQV | CDS | 103284 | 2385 | + | 0.27673 | |
g3189 | DLA_03535 | GAOABQK02FRRQV | CDS | 105813 | 1647 | - | 0.32544 | |
g319 | DLA_00357 | contig05409_1.exp | CDS | 740090 | 828 | - | 0.281401 | |
g3190 | DLA_03536 | GAOABQK02FRRQV | CDS | 107515 | 249 | + | 0.277108 | |
g3191 | DLA_03537 | GAOABQK02FRRQV | CDS | 108268 | 1464 | + | 0.286885 | |
g3192 | DLA_03538 | GAOABQK02FRRQV | CDS | 109887 | 2103 | + | 0.318117 | |
g3193 | DLA_03539 | GAOABQK02FRRQV | CDS | 112303 | 3321 | - | 0.314965 | |
g3194 | DLA_03540 | GAOABQK02FRRQV | CDS | 115994 | 3666 | + | 0.318058 | |
g3195 | DLA_03541 | GAOABQK02FRRQV | CDS | 120021 | 2229 | - | 0.359354 | |
g3196 | DLA_03542 | GAOABQK02FRRQV | CDS | 122267 | 1053 | + | 0.351377 | |
g3197 | DLA_03544 | GAOABQK02FWKR3 | CDS | 1396 | 738 | + | 0.247967 | |
g3198 | DLA_03545 | GAOABQK02FWKR3 | CDS | 2249 | 4032 | - | 0.304315 | |
g3199 | DLA_03546 | GAOABQK02FWKR3 | CDS | 6603 | 1368 | - | 0.301901 | |
g32 | DLA_00036 | contig05409_1.exp | CDS | 81204 | 1857 | + | 0.287022 | |
g320 | DLA_00358 | contig05409_1.exp | CDS | 742083 | 492 | + | 0.376016 | |
g3200 | DLA_03547 | catalyzes the addition of GlcNAc (N-acetylglucosamine) to HyPro143-Skp1 (FpaAFpaB) in the cytosol | GAOABQK02FWKR3 | CDS | 8322 | 801 | + | 0.285893 |
g3201 | DLA_03548 | GAOABQK02FWKR3 | CDS | 9226 | 1002 | - | 0.419162 | |
g3202 | DLA_03549 | GAOABQK02FWKR3 | CDS | 11072 | 2175 | + | 0.310805 | |
g3203 | DLA_03550 | GAOABQK02FWKR3 | CDS | 13472 | 561 | + | 0.276292 | |
g3204 | DLA_03551 | GAOABQK02FWKR3 | CDS | 14300 | 1245 | - | 0.356627 | |
g3205 | DLA_03553 | GAOABQK02FWKR3 | CDS | 16016 | 729 | + | 0.304527 | |
g3206 | DLA_03554 | GAOABQK02FWKR3 | CDS | 17009 | 441 | - | 0.321995 | |
g3207 | DLA_03555 | GAOABQK02FWKR3 | CDS | 17848 | 1452 | - | 0.278926 | |
g3208 | DLA_03556 | GAOABQK02FWKR3 | CDS | 19703 | 825 | + | 0.287273 | |
g3209 | DLA_03557 | GAOABQK02FWKR3 | CDS | 20867 | 1314 | + | 0.266362 | |
g321 | DLA_00360 | contig05409_1.exp | CDS | 742886 | 930 | - | 0.305376 | |
g3210 | DLA_03558 | GAOABQK02FWKR3 | CDS | 22355 | 579 | - | 0.264249 | |
g3211 | DLA_03560 | GAOABQK02FWKR3 | CDS | 24327 | 2148 | + | 0.293762 | |
g3212 | DLA_03561 | GAOABQK02FWKR3 | CDS | 26890 | 1065 | - | 0.392488 | |
g3213 | DLA_03562 | GAOABQK02FWKR3 | CDS | 28424 | 321 | - | 0.29595 | |
g3214 | DLA_03563 | GAOABQK02FWKR3 | CDS | 29049 | 378 | + | 0.256614 | |
g3215 | DLA_03564 | GAOABQK02FWKR3 | CDS | 29523 | 2253 | - | 0.255215 | |
g3216 | DLA_11554 | CK2 family protein kinase a ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | GAOABQK02FWKR3 | CDS | 32017 | 1611 | - | 0.306021 |
g3217 | DLA_03565 | GAOABQK02FWKR3 | CDS | 34210 | 1734 | - | 0.313726 | |
g3218 | DLA_03566 | GAOABQK02FWKR3 | CDS | 36162 | 1374 | - | 0.259825 | |
g3219 | DLA_03567 | GAOABQK02FWKR3 | CDS | 38047 | 2856 | + | 0.267857 | |
g322 | DLA_00361 | contig05409_1.exp | CDS | 744348 | 672 | + | 0.285714 | |
g3220 | DLA_03568 | GAOABQK02FWKR3 | CDS | 41622 | 846 | - | 0.281324 | |
g3221 | DLA_03569 | GAOABQK02FWKR3 | CDS | 42770 | 1341 | + | 0.303505 | |
g3222 | DLA_03570 | GAOABQK02FWKR3 | CDS | 44196 | 4614 | - | 0.296922 | |
g3223 | DLA_03571 | GAOABQK02FWKR3 | CDS | 50096 | 2094 | + | 0.292264 | |
g3224 | DLA_03572 | GAOABQK02FWKR3 | CDS | 52412 | 1107 | - | 0.34869 | |
g3225 | DLA_03573 | GAOABQK02FWKR3 | CDS | 54643 | 1029 | + | 0.250729 | |
g3226 | DLA_03575 | GAOABQK02G6SYV | CDS | 543 | 768 | - | 0.304688 | |
g3227 | DLA_03576 | ortholog of slc25a17 a peroximal membrane protein involved in transport of solutes contains five transmembrane domains brbr bCommunity annotation:b Overview of the | GAOABQK02G6SYV | CDS | 2023 | 927 | + | 0.325782 |
g3228 | DLA_03577 | GAOABQK02G6SYV | CDS | 3253 | 1932 | - | 0.279503 | |
g3229 | DLA_03578 | GAOABQK02G6SYV | CDS | 5925 | 1269 | - | 0.371158 | |
g323 | DLA_00362 | contig05409_1.exp | CDS | 745328 | 2628 | - | 0.332572 | |
g3230 | DLA_03579 | GAOABQK02G6SYV | CDS | 8611 | 279 | - | 0.258065 | |
g3231 | DLA_03580 | GAOABQK02G6SYV | CDS | 9097 | 1371 | + | 0.302699 | |
g3232 | DLA_03581 | GAOABQK02G6SYV | CDS | 10896 | 894 | - | 0.394855 | |
g3233 | DLA_03582 | GAOABQK02G6SYV | CDS | 12303 | 1566 | - | 0.280971 | |
g3234 | DLA_11555 | GAOABQK02G6SYV | CDS | 15044 | 1494 | - | 0.27577 | |
g3235 | DLA_03583 | GAOABQK02G6SYV | CDS | 16679 | 1134 | - | 0.272487 | |
g3236 | DLA_03584 | GAOABQK02G6SYV | CDS | 18653 | 2628 | + | 0.334855 | |
g3237 | DLA_03585 | GAOABQK02G6SYV | CDS | 21634 | 1155 | - | 0.338528 | |
g3238 | DLA_03586 | GAOABQK02G6SYV | CDS | 23264 | 1053 | - | 0.31529 | |
g3239 | DLA_03587 | GAOABQK02G6SYV | CDS | 24865 | 1158 | + | 0.37133 | |
g324 | DLA_11440 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | contig05409_1.exp | CDS | 748626 | 564 | - | 0.285461 |
g3240 | DLA_03588 | GAOABQK02G6SYV | CDS | 26197 | 882 | - | 0.272109 | |
g3241 | DLA_03589 | GAOABQK02G6SYV | CDS | 27606 | 1335 | - | 0.367041 | |
g3242 | DLA_03590 | GAOABQK02G6SYV | CDS | 29665 | 1203 | + | 0.305071 | |
g3243 | DLA_03591 | GAOABQK02G6SYV | CDS | 31557 | 831 | + | 0.308063 | |
g3244 | DLA_03592 | GAOABQK02G6SYV | CDS | 32475 | 729 | - | 0.318244 | |
g3245 | DLA_03593 | GAOABQK02G6SYV | CDS | 33456 | 1323 | - | 0.292517 | |
g3246 | DLA_03595 | GAOABQK02G6SYV | CDS | 35631 | 5286 | - | 0.315929 | |
g3247 | DLA_03596 | GAOABQK02G6SYV | CDS | 41870 | 576 | + | 0.347222 | |
g3248 | DLA_03597 | GAOABQK02G6SYV | CDS | 42729 | 2463 | + | 0.298011 | |
g3249 | DLA_03598 | GAOABQK02G6SYV | CDS | 45405 | 987 | - | 0.288754 | |
g325 | DLA_00363 | contig05409_1.exp | CDS | 749479 | 909 | - | 0.330033 | |
g3250 | DLA_03599 | GAOABQK02G6SYV | CDS | 46486 | 2328 | - | 0.290378 | |
g3251 | DLA_03600 | GAOABQK02G6SYV | CDS | 49521 | 2328 | + | 0.293385 | |
g3252 | DLA_03602 | GAOABQK02G6SYV | CDS | 53048 | 1665 | - | 0.275676 | |
g3253 | DLA_03603 | GAOABQK02G6SYV | CDS | 55466 | 672 | - | 0.334821 | |
g3254 | DLA_11556 | GAOABQK02G6SYV | CDS | 56260 | 591 | - | 0.323181 | |
g3255 | DLA_03604 | GAOABQK02G6SYV | CDS | 57713 | 1089 | - | 0.33517 | |
g3256 | DLA_03605 | GAOABQK02G6SYV | CDS | 59221 | 1914 | - | 0.316614 | |
g3257 | DLA_03607 | GAOABQK02G6SYV | CDS | 64445 | 1473 | + | 0.365241 | |
g3258 | DLA_03608 | GAOABQK02G6SYV | CDS | 66151 | 1023 | - | 0.30303 | |
g3259 | DLA_03609 | GAOABQK02G6SYV | CDS | 67515 | 2352 | - | 0.269558 | |
g326 | DLA_00364 | contig05409_1.exp | CDS | 750574 | 1857 | + | 0.351104 | |
g3260 | DLA_03610 | GAOABQK02G6SYV | CDS | 70432 | 1929 | + | 0.299119 | |
g3261 | DLA_03611 | GAOABQK02G6SYV | CDS | 72667 | 4257 | + | 0.327226 | |
g3262 | DLA_03612 | GAOABQK02G6SYV | CDS | 77627 | 10218 | + | 0.343805 | |
g3263 | DLA_03613 | GAOABQK02G6SYV | CDS | 88105 | 2811 | - | 0.289577 | |
g3264 | DLA_11557 | GAOABQK02G6SYV | CDS | 91033 | 2730 | - | 0.355311 | |
g3265 | DLA_03614 | GAOABQK02G6SYV | CDS | 94330 | 1947 | + | 0.334361 | |
g3266 | DLA_03615 | GAOABQK02G6SYV | CDS | 96392 | 471 | - | 0.284501 | |
g3267 | DLA_03616 | GAOABQK02G6SYV | CDS | 97173 | 2745 | - | 0.289982 | |
g3268 | DLA_03617 | GAOABQK02G6SYV | CDS | 101798 | 2007 | - | 0.344793 | |
g3269 | DLA_03618 | GAOABQK02G6SYV | CDS | 104472 | 1677 | - | 0.323792 | |
g327 | DLA_00365 | contig05409_1.exp | CDS | 752461 | 885 | - | 0.315254 | |
g3270 | DLA_03619 | GAOABQK02G6SYV | CDS | 106715 | 1842 | + | 0.337676 | |
g3271 | DLA_03620 | GAOABQK02G6SYV | CDS | 109034 | 627 | + | 0.341308 | |
g3272 | DLA_03621 | GAOABQK02G6SYV | CDS | 109928 | 1635 | + | 0.345566 | |
g3273 | DLA_03622 | GAOABQK02G6SYV | CDS | 111748 | 2454 | - | 0.350856 | |
g3274 | DLA_03623 | GAOABQK02G6SYV | CDS | 114457 | 1575 | - | 0.304127 | |
g3275 | DLA_03624 | GAOABQK02G6SYV | CDS | 116368 | 456 | - | 0.414474 | |
g3276 | DLA_03625 | GAOABQK02G6SYV | CDS | 117700 | 2319 | + | 0.29323 | |
g3277 | DLA_03627 | GAOABQK02G6SYV | CDS | 120541 | 1149 | - | 0.314186 | |
g3278 | DLA_03628 | GAOABQK02G6SYV | CDS | 122726 | 1329 | + | 0.280662 | |
g3279 | DLA_03629 | GAOABQK02G6SYV | CDS | 124198 | 534 | - | 0.294007 | |
g328 | DLA_00368 | contains a N-terminal Calponin Homology (CH) domain 3 LIM domains and 4 LIM-related domains (LRDs) | contig05409_1.exp | CDS | 756297 | 2094 | + | 0.352436 |
g3280 | DLA_03630 | GAOABQK02G6SYV | CDS | 125487 | 432 | - | 0.331019 | |
g3281 | DLA_03632 | GAOABQK02G6SYV | CDS | 126434 | 1728 | + | 0.282986 | |
g3282 | DLA_03633 | GAOABQK02G6SYV | CDS | 128412 | 1755 | + | 0.278632 | |
g3283 | DLA_03634 | GAOABQK02G6SYV | CDS | 130347 | 831 | + | 0.358604 | |
g3284 | DLA_03635 | GAOABQK02G6SYV | CDS | 131543 | 1659 | - | 0.298373 | |
g3285 | DLA_03636 | GAOABQK02G6SYV | CDS | 133610 | 1074 | - | 0.280261 | |
g3286 | DLA_03637 | GAOABQK02G6SYV | CDS | 136318 | 693 | - | 0.326118 | |
g3287 | DLA_03638 | GAOABQK02G6SYV | CDS | 137428 | 3060 | - | 0.331046 | |
g3288 | DLA_03639 | GAOABQK02G6SYV | CDS | 140737 | 3126 | - | 0.339091 | |
g3289 | DLA_03640 | GAOABQK02G6SYV | CDS | 144500 | 1566 | + | 0.387612 | |
g329 | DLA_11441 | contig05409_1.exp | CDS | 758528 | 1401 | + | 0.306924 | |
g3290 | DLA_03641 | GAOABQK02G6SYV | CDS | 146700 | 627 | - | 0.344498 | |
g3291 | DLA_03642 | GAOABQK02G6SYV | CDS | 147880 | 3057 | - | 0.336277 | |
g3292 | DLA_03644 | GAOABQK02G6SYV | CDS | 152082 | 1056 | + | 0.305871 | |
g3293 | DLA_11558 | GAOABQK02G6SYV | CDS | 153513 | 723 | + | 0.307054 | |
g3294 | DLA_03645 | GAOABQK02G6SYV | CDS | 155307 | 2265 | + | 0.314349 | |
g3295 | DLA_03646 | GAOABQK02G6SYV | CDS | 157955 | 282 | - | 0.283688 | |
g3296 | DLA_03647 | GAOABQK02G6SYV | CDS | 158561 | 1182 | + | 0.335871 | |
g3297 | DLA_03648 | MBOAT family protein membrane proteins that contains a variety of acyltransferase enzymes contains 8 predicted transmembrane domains | GAOABQK02G6SYV | CDS | 159826 | 1374 | - | 0.299854 |
g3298 | DLA_03649 | GAOABQK02G6SYV | CDS | 161683 | 453 | - | 0.337748 | |
g3299 | DLA_03650 | GAOABQK02G6SYV | CDS | 162692 | 1452 | + | 0.290634 | |
g33 | DLA_00037 | contig05409_1.exp | CDS | 83093 | 4545 | - | 0.331133 | |
g330 | DLA_00369 | contig05409_1.exp | CDS | 759972 | 1812 | + | 0.275386 | |
g3300 | DLA_03651 | GAOABQK02G6SYV | CDS | 164317 | 2496 | + | 0.323718 | |
g3301 | DLA_03652 | GAOABQK02G6SYV | CDS | 167120 | 1545 | - | 0.27767 | |
g3302 | DLA_03653 | GAOABQK02G6SYV | CDS | 168942 | 540 | - | 0.411111 | |
g3303 | DLA_03654 | GAOABQK02G6SYV | CDS | 169897 | 792 | + | 0.34596 | |
g3304 | DLA_11559 | GAOABQK02G6SYV | CDS | 170738 | 465 | - | 0.288172 | |
g3305 | DLA_03655 | GAOABQK02G6SYV | CDS | 171413 | 1791 | + | 0.400335 | |
g3306 | DLA_03656 | GAOABQK02G6SYV | CDS | 173499 | 615 | - | 0.326829 | |
g3307 | DLA_03657 | GAOABQK02G6SYV | CDS | 174459 | 1758 | + | 0.366894 | |
g3308 | DLA_03658 | GAOABQK02G6SYV | CDS | 176311 | 666 | - | 0.285285 | |
g3309 | DLA_03659 | GAOABQK02G6SYV | CDS | 177264 | 1551 | - | 0.30303 | |
g331 | DLA_00370 | contig05409_1.exp | CDS | 762135 | 621 | + | 0.312399 | |
g3310 | DLA_03661 | GAOABQK02G6SYV | CDS | 180286 | 2283 | + | 0.281647 | |
g3311 | DLA_03663 | GAOABQK02G6SYV | CDS | 182941 | 540 | - | 0.285185 | |
g3312 | DLA_03664 | GAOABQK02G6SYV | CDS | 183732 | 1002 | - | 0.322355 | |
g3313 | DLA_11560 | GAOABQK02G6SYV | CDS | 185015 | 1029 | - | 0.287658 | |
g3314 | DLA_03665 | GAOABQK02G6SYV | CDS | 186528 | 1341 | - | 0.287099 | |
g3315 | DLA_03666 | GAOABQK02G6SYV | CDS | 189425 | 4677 | + | 0.315587 | |
g3316 | DLA_03667 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GAOABQK02G6SYV | CDS | 194474 | 921 | + | 0.324647 |
g3317 | DLA_03668 | GAOABQK02G6SYV | CDS | 196045 | 3507 | + | 0.312803 | |
g3318 | DLA_03669 | GAOABQK02G6SYV | CDS | 199820 | 1020 | - | 0.297059 | |
g3319 | DLA_03670 | GAOABQK02G6SYV | CDS | 201242 | 375 | - | 0.28 | |
g332 | DLA_00371 | contig05409_1.exp | CDS | 764016 | 1917 | + | 0.305164 | |
g3320 | DLA_03671 | GAOABQK02G6SYV | CDS | 201811 | 948 | - | 0.301688 | |
g3321 | DLA_03672 | GAOABQK02G6SYV | CDS | 203062 | 3678 | - | 0.366504 | |
g3322 | DLA_03673 | GAOABQK02G6SYV | CDS | 207498 | 4548 | + | 0.348505 | |
g3323 | DLA_03674 | GAOABQK02G6SYV | CDS | 212409 | 1938 | + | 0.339009 | |
g3324 | DLA_03675 | GAOABQK02G6SYV | CDS | 214861 | 1596 | + | 0.3302 | |
g3325 | DLA_03676 | GAOABQK02G6SYV | CDS | 216583 | 1068 | - | 0.284644 | |
g3326 | DLA_03677 | GAOABQK02G6SYV | CDS | 218357 | 363 | + | 0.391185 | |
g3327 | DLA_03678 | GAOABQK02G6SYV | CDS | 218911 | 315 | + | 0.333333 | |
g3328 | DLA_03679 | GAOABQK02G6SYV | CDS | 219606 | 1974 | + | 0.333333 | |
g3329 | DLA_03680 | GAOABQK02G6SYV | CDS | 221699 | 456 | - | 0.29386 | |
g333 | DLA_00373 | contig05409_1.exp | CDS | 767842 | 822 | - | 0.33455 | |
g3330 | DLA_03681 | GAOABQK02G6SYV | CDS | 222332 | 384 | - | 0.356771 | |
g3331 | DLA_03682 | GAOABQK02G6SYV | CDS | 223011 | 336 | - | 0.291667 | |
g3332 | DLA_03684 | GAOABQK02G6SYV | CDS | 224313 | 591 | + | 0.306261 | |
g3333 | DLA_03685 | GAOABQK02G6SYV | CDS | 225029 | 1599 | - | 0.377736 | |
g3334 | DLA_03686 | GAOABQK02G6SYV | CDS | 227337 | 2196 | + | 0.352914 | |
g3335 | DLA_03687 | GAOABQK02G6SYV | CDS | 229973 | 1197 | + | 0.329156 | |
g3336 | DLA_03689 | GAOABQK02G6SYV | CDS | 231693 | 1032 | - | 0.304264 | |
g3337 | DLA_03691 | similar to animal and plant cystatin A3 member of the stefin cystatin family of cysteine protease inhibitors | GAOABQK02G6SYV | CDS | 233842 | 282 | - | 0.358156 |
g3338 | DLA_03692 | GAOABQK02G6SYV | CDS | 234498 | 1512 | + | 0.343915 | |
g3339 | DLA_03693 | GAOABQK02G6SYV | CDS | 236260 | 948 | - | 0.345992 | |
g334 | DLA_00374 | contig05409_1.exp | CDS | 768973 | 2394 | - | 0.327485 | |
g3340 | DLA_03694 | GAOABQK02G6SYV | CDS | 237723 | 3390 | + | 0.336283 | |
g3341 | DLA_03695 | GAOABQK02G6SYV | CDS | 241316 | 1428 | - | 0.310924 | |
g3342 | DLA_03696 | GAOABQK02G6SYV | CDS | 243409 | 648 | + | 0.341049 | |
g3343 | DLA_03698 | GAOABQK02G6SYV | CDS | 245967 | 1977 | - | 0.327769 | |
g3344 | DLA_03699 | GAOABQK02G6SYV | CDS | 250929 | 1113 | - | 0.322552 | |
g3345 | DLA_03700 | GAOABQK02G6SYV | CDS | 252694 | 1908 | - | 0.358491 | |
g3346 | DLA_03701 | GAOABQK02G6SYV | CDS | 255220 | 822 | - | 0.323601 | |
g3347 | DLA_03702 | GAOABQK02G6SYV | CDS | 257265 | 2175 | - | 0.34023 | |
g3348 | DLA_03703 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | GAOABQK02G6SYV | CDS | 259800 | 1452 | - | 0.403581 |
g3349 | DLA_03704 | GAOABQK02G6SYV | CDS | 262262 | 1518 | - | 0.395916 | |
g335 | DLA_00375 | contig05409_1.exp | CDS | 771550 | 1635 | - | 0.301529 | |
g3350 | DLA_03706 | GAOABQK02G6SYV | CDS | 264850 | 3468 | - | 0.364475 | |
g3351 | DLA_03707 | GAOABQK02G6SYV | CDS | 269181 | 2418 | + | 0.323408 | |
g3352 | DLA_03708 | GAOABQK02G6SYV | CDS | 272143 | 1062 | + | 0.283428 | |
g3353 | DLA_03709 | GAOABQK02G6SYV | CDS | 273361 | 1599 | - | 0.337711 | |
g3354 | DLA_03710 | GAOABQK02G6SYV | CDS | 276246 | 1026 | - | 0.296296 | |
g3355 | DLA_03711 | GAOABQK02G6SYV | CDS | 277710 | 1317 | + | 0.333333 | |
g3356 | DLA_03712 | GAOABQK02G6SYV | CDS | 279991 | 558 | + | 0.387097 | |
g3357 | DLA_03713 | GAOABQK02G6SYV | CDS | 282815 | 663 | + | 0.380091 | |
g3358 | DLA_03714 | GAOABQK02G6SYV | CDS | 283677 | 285 | - | 0.266667 | |
g3359 | DLA_03715 | GAOABQK02G6SYV | CDS | 284213 | 957 | + | 0.327064 | |
g336 | DLA_00377 | contig05409_1.exp | CDS | 773318 | 1272 | - | 0.358491 | |
g3360 | DLA_03716 | GAOABQK02G6SYV | CDS | 285474 | 1665 | - | 0.300901 | |
g3361 | DLA_03717 | GAOABQK02G6SYV | CDS | 287320 | 3657 | + | 0.361499 | |
g3362 | DLA_03718 | GAOABQK02G6SYV | CDS | 291195 | 753 | + | 0.337317 | |
g3363 | DLA_03719 | GAOABQK02G6SYV | CDS | 292019 | 648 | - | 0.299383 | |
g3364 | DLA_03720 | GAOABQK02G6SYV | CDS | 292920 | 825 | - | 0.335758 | |
g3365 | DLA_03721 | GAOABQK02G6SYV | CDS | 293942 | 1500 | + | 0.337333 | |
g3366 | DLA_03722 | GAOABQK02G6SYV | CDS | 295482 | 3510 | - | 0.271795 | |
g3367 | DLA_03723 | GAOABQK02G6SYV | CDS | 299947 | 1791 | + | 0.3445 | |
g3368 | DLA_03724 | GAOABQK02G6SYV | CDS | 302063 | 1557 | + | 0.398844 | |
g3369 | DLA_03725 | GAOABQK02G6SYV | CDS | 303890 | 1206 | + | 0.34743 | |
g337 | DLA_00378 | contig05409_1.exp | CDS | 775137 | 663 | + | 0.322775 | |
g3370 | DLA_03726 | GAOABQK02G6SYV | CDS | 305947 | 8409 | + | 0.31823 | |
g3371 | DLA_03727 | GAOABQK02G6SYV | CDS | 314663 | 1830 | + | 0.345902 | |
g3372 | DLA_03729 | GAOABQK02G6SYV | CDS | 316818 | 3996 | + | 0.318318 | |
g3373 | DLA_03730 | GAOABQK02G6SYV | CDS | 321485 | 342 | - | 0.423977 | |
g3374 | DLA_03731 | GAOABQK02G6SYV | CDS | 322155 | 2322 | + | 0.327304 | |
g3375 | DLA_03732 | GAOABQK02G6SYV | CDS | 324633 | 270 | - | 0.248148 | |
g3376 | DLA_03733 | GAOABQK02G6SYV | CDS | 325564 | 1002 | - | 0.339321 | |
g3377 | DLA_03734 | GAOABQK02G6SYV | CDS | 326741 | 1803 | - | 0.290072 | |
g3378 | DLA_03735 | GAOABQK02G6SYV | CDS | 328832 | 1515 | + | 0.344554 | |
g3379 | DLA_03736 | GAOABQK02G6SYV | CDS | 330798 | 1671 | + | 0.329743 | |
g338 | DLA_00379 | contig05409_1.exp | CDS | 776405 | 2091 | + | 0.290292 | |
g3380 | DLA_03737 | GAOABQK02G6SYV | CDS | 332556 | 1758 | + | 0.307167 | |
g3381 | DLA_03738 | GAOABQK02G6SYV | CDS | 334425 | 1299 | - | 0.357198 | |
g3382 | DLA_03739 | GAOABQK02G6SYV | CDS | 336613 | 1917 | + | 0.345331 | |
g3383 | DLA_03740 | GAOABQK02G6SYV | CDS | 338558 | 1890 | - | 0.336508 | |
g3384 | DLA_03742 | GAOABQK02G6SYV | CDS | 340993 | 3132 | - | 0.36143 | |
g3385 | DLA_03744 | GAOABQK02G6SYV | CDS | 344782 | 1104 | + | 0.355072 | |
g3386 | DLA_03745 | GAOABQK02G6SYV | CDS | 346298 | 1770 | + | 0.333333 | |
g3387 | DLA_03746 | GAOABQK02G6SYV | CDS | 348396 | 1593 | - | 0.357188 | |
g3388 | DLA_03747 | GAOABQK02G6SYV | CDS | 350293 | 3246 | - | 0.278805 | |
g3389 | DLA_03748 | GAOABQK02G6SYV | CDS | 353880 | 396 | + | 0.290404 | |
g339 | DLA_00380 | contig05409_1.exp | CDS | 778614 | 1128 | - | 0.338652 | |
g3390 | DLA_03749 | GAOABQK02G6SYV | CDS | 354485 | 1395 | - | 0.324731 | |
g3391 | DLA_03750 | GAOABQK02G6SYV | CDS | 355999 | 1728 | + | 0.278935 | |
g3392 | DLA_03751 | GAOABQK02G6SYV | CDS | 358236 | 1203 | - | 0.360765 | |
g3393 | DLA_03752 | GAOABQK02G6SYV | CDS | 361326 | 306 | - | 0.339869 | |
g3394 | DLA_03754 | GAOABQK02G6SYV | CDS | 361752 | 987 | - | 0.320162 | |
g3395 | DLA_03755 | GAOABQK02G6SYV | CDS | 363597 | 558 | + | 0.320789 | |
g3396 | DLA_03756 | GAOABQK02G6SYV | CDS | 364614 | 840 | - | 0.360714 | |
g3397 | DLA_03757 | GAOABQK02G6SYV | CDS | 366273 | 1212 | + | 0.35396 | |
g3398 | DLA_03758 | GAOABQK02G6SYV | CDS | 367832 | 870 | - | 0.331034 | |
g3399 | DLA_03759 | GAOABQK02G6SYV | CDS | 370033 | 2235 | + | 0.297539 | |
g34 | DLA_00038 | contig05409_1.exp | CDS | 88232 | 1248 | + | 0.290064 | |
g340 | DLA_00382 | contig05409_1.exp | CDS | 780606 | 1968 | - | 0.338415 | |
g3400 | DLA_03760 | GAOABQK02G6SYV | CDS | 372776 | 564 | - | 0.33156 | |
g3401 | DLA_03761 | GAOABQK02G6SYV | CDS | 373601 | 1809 | + | 0.342731 | |
g3402 | DLA_03762 | GAOABQK02G6SYV | CDS | 375866 | 450 | + | 0.384444 | |
g3403 | DLA_03763 | GAOABQK02G6SYV | CDS | 376413 | 1389 | - | 0.25414 | |
g3404 | DLA_03764 | GAOABQK02G6SYV | CDS | 377857 | 1104 | + | 0.286232 | |
g3405 | DLA_03766 | GAOABQK02G6SYV | CDS | 380671 | 1143 | + | 0.32021 | |
g3406 | DLA_03767 | GAOABQK02G6SYV | CDS | 382092 | 360 | - | 0.391667 | |
g3407 | DLA_03768 | GAOABQK02G6SYV | CDS | 382832 | 1020 | - | 0.278431 | |
g3408 | DLA_03769 | GAOABQK02G6SYV | CDS | 384133 | 1446 | + | 0.359613 | |
g3409 | DLA_11561 | GAOABQK02G6SYV | CDS | 385789 | 414 | + | 0.323671 | |
g341 | DLA_00383 | contig05409_1.exp | CDS | 782753 | 1023 | - | 0.333333 | |
g3410 | DLA_03770 | GAOABQK02G6SYV | CDS | 387012 | 558 | + | 0.415771 | |
g3411 | DLA_03774 | GAOABQK02G6SYV | CDS | 392468 | 333 | - | 0.321321 | |
g3412 | DLA_03775 | GAOABQK02G6SYV | CDS | 393352 | 3546 | + | 0.368302 | |
g3413 | DLA_03776 | GAOABQK02G6SYV | CDS | 397085 | 2187 | + | 0.321902 | |
g3414 | DLA_03777 | GAOABQK02G6SYV | CDS | 399763 | 2940 | + | 0.287415 | |
g3415 | DLA_03778 | GAOABQK02G6SYV | CDS | 402987 | 4983 | + | 0.314469 | |
g3416 | DLA_03779 | GAOABQK02G6SYV | CDS | 408422 | 1185 | + | 0.313924 | |
g3417 | DLA_03780 | GAOABQK02G6SYV | CDS | 409965 | 1389 | + | 0.272858 | |
g3418 | DLA_03781 | GAOABQK02G6SYV | CDS | 412054 | 3114 | - | 0.248876 | |
g3419 | DLA_03782 | GAOABQK02G6SYV | CDS | 415793 | 3216 | - | 0.277674 | |
g342 | DLA_00384 | contig05409_1.exp | CDS | 784499 | 1161 | + | 0.349699 | |
g3420 | DLA_11562 | GAOABQK02G6SYV | CDS | 419681 | 2340 | - | 0.316667 | |
g3421 | DLA_03783 | CAZy family GT24 catalyzes N-linked glucosylation REMI mutant forms aberrant fruiting bodies see | GAOABQK02G6SYV | CDS | 422763 | 4611 | - | 0.348514 |
g3422 | DLA_03784 | GAOABQK02G6SYV | CDS | 427655 | 1599 | - | 0.368355 | |
g3423 | DLA_03785 | GAOABQK02G6SYV | CDS | 430264 | 1803 | + | 0.30782 | |
g3424 | DLA_03786 | GAOABQK02G6SYV | CDS | 432345 | 1371 | - | 0.318745 | |
g3425 | DLA_03787 | GAOABQK02G6SYV | CDS | 434397 | 1398 | - | 0.309728 | |
g3426 | DLA_03788 | GAOABQK02G6SYV | CDS | 436227 | 1404 | - | 0.319088 | |
g3427 | DLA_03789 | GAOABQK02G6SYV | CDS | 438427 | 573 | - | 0.310646 | |
g3428 | DLA_03790 | GAOABQK02G6SYV | CDS | 439293 | 1437 | - | 0.312457 | |
g3429 | DLA_03791 | GAOABQK02G6SYV | CDS | 441157 | 1755 | - | 0.292877 | |
g343 | DLA_00385 | contig05409_1.exp | CDS | 786606 | 237 | + | 0.308017 | |
g3430 | DLA_03792 | GAOABQK02G6SYV | CDS | 443537 | 1035 | + | 0.374879 | |
g3431 | DLA_03793 | full transporter consisting of two ABC domains and two transmembrane domains there is a second copy of this gene | GAOABQK02G6SYV | CDS | 445089 | 4329 | - | 0.374682 |
g3432 | DLA_03794 | GAOABQK02G6SYV | CDS | 450078 | 879 | - | 0.334471 | |
g3433 | DLA_03795 | GAOABQK02G6SYV | CDS | 451406 | 1896 | + | 0.353376 | |
g3434 | DLA_03797 | GAOABQK02G6SYV | CDS | 454028 | 2922 | + | 0.356605 | |
g3435 | DLA_03798 | GAOABQK02G6SYV | CDS | 457204 | 1590 | + | 0.328302 | |
g3436 | DLA_03799 | GAOABQK02G6SYV | CDS | 458950 | 297 | - | 0.286195 | |
g3437 | DLA_03800 | GAOABQK02G6SYV | CDS | 460333 | 1611 | + | 0.299193 | |
g3438 | DLA_03802 | similar to mammalian lysophosphatidic acid acyltransferase zeta (1-acylglycerol-3-phosphate O-acyltransferase 6) contains 3 putative transmembrane domains | GAOABQK02G6SYV | CDS | 462554 | 1416 | + | 0.33404 |
g3439 | DLA_03803 | catalyzes the reaction S-adenosyl-L-methionine 1-aminocyclopropane-1-carboxylate methylthioadenosine | GAOABQK02G6SYV | CDS | 464213 | 1305 | - | 0.310345 |
g344 | DLA_00386 | contig05409_1.exp | CDS | 787271 | 429 | + | 0.379953 | |
g3440 | DLA_03804 | GAOABQK02G6SYV | CDS | 466146 | 1542 | + | 0.291829 | |
g3441 | DLA_03805 | GAOABQK02G6SYV | CDS | 467790 | 1587 | - | 0.376812 | |
g3442 | DLA_03806 | GAOABQK02G6SYV | CDS | 469637 | 1152 | + | 0.269965 | |
g3443 | DLA_03807 | similar to Ixodes scapularis U2 small nuclear ribonucleoprotein A human c10orf11 has 3 leucine-rich repeats which are involved in protein-protein interactions | GAOABQK02G6SYV | CDS | 471332 | 1266 | + | 0.331754 |
g3444 | DLA_03808 | GAOABQK02G6SYV | CDS | 472770 | 1848 | + | 0.33171 | |
g3445 | DLA_03809 | GAOABQK02G6SYV | CDS | 474745 | 1185 | - | 0.295359 | |
g3446 | DLA_03810 | GAOABQK02G6SYV | CDS | 476197 | 2400 | + | 0.371667 | |
g3447 | DLA_03812 | GAOABQK02G6SYV | CDS | 480074 | 1476 | - | 0.298781 | |
g3448 | DLA_03813 | similar to ATP-dependent RNA helicase M NAM7and to putative helicases involved in RNA maturation SEN1 human senataxin imlicated in ataxia-ocular apraxia 2 (AOA2) and amyotrophic lateral sclerosis 4 (ALS4) also belongs to this family | GAOABQK02G6SYV | CDS | 481931 | 2796 | + | 0.344778 |
g3449 | DLA_03814 | GAOABQK02G6SYV | CDS | 484945 | 633 | + | 0.339652 | |
g345 | DLA_00387 | contig05409_1.exp | CDS | 788448 | 1968 | + | 0.38313 | |
g3450 | DLA_03815 | GAOABQK02G6SYV | CDS | 485740 | 1905 | - | 0.323885 | |
g3451 | DLA_11563 | GAOABQK02G6SYV | CDS | 487823 | 1044 | - | 0.316092 | |
g3452 | DLA_11564 | GAOABQK02G6SYV | CDS | 489064 | 405 | + | 0.259259 | |
g3453 | DLA_03816 | GAOABQK02G6SYV | CDS | 489697 | 1356 | - | 0.270649 | |
g3454 | DLA_03817 | GAOABQK02G6SYV | CDS | 491404 | 699 | + | 0.320458 | |
g3455 | DLA_03818 | GAOABQK02G6SYV | CDS | 492295 | 1332 | - | 0.328078 | |
g3456 | DLA_03819 | GAOABQK02G6SYV | CDS | 494209 | 3531 | - | 0.361371 | |
g3457 | DLA_03820 | GAOABQK02G6SYV | CDS | 498275 | 1332 | + | 0.350601 | |
g3458 | DLA_03821 | GAOABQK02G6SYV | CDS | 499729 | 1557 | - | 0.31535 | |
g3459 | DLA_03822 | GAOABQK02G6SYV | CDS | 501489 | 2526 | - | 0.340063 | |
g346 | DLA_00388 | contig05409_1.exp | CDS | 790802 | 348 | + | 0.301724 | |
g3460 | DLA_03823 | GAOABQK02G6SYV | CDS | 504206 | 1911 | - | 0.339613 | |
g3461 | DLA_03824 | GAOABQK02G6SYV | CDS | 506332 | 1548 | - | 0.322997 | |
g3462 | DLA_03825 | GAOABQK02G6SYV | CDS | 508002 | 1626 | - | 0.309963 | |
g3463 | DLA_03827 | GAOABQK02G6SYV | CDS | 510061 | 291 | + | 0.381443 | |
g3464 | DLA_03828 | GAOABQK02G6SYV | CDS | 510570 | 4845 | - | 0.328173 | |
g3465 | DLA_03830 | GAOABQK02G6SYV | CDS | 515867 | 1734 | + | 0.303345 | |
g3466 | DLA_03831 | GAOABQK02G6SYV | CDS | 517711 | 768 | - | 0.290365 | |
g3467 | DLA_03832 | GAOABQK02G6SYV | CDS | 518766 | 1185 | - | 0.298734 | |
g3468 | DLA_03833 | GAOABQK02G6SYV | CDS | 520292 | 807 | + | 0.266419 | |
g3469 | DLA_03837 | GAOABQK02G6SYV | CDS | 523195 | 246 | + | 0.382114 | |
g347 | DLA_00389 | conserved protein similar to S. cerevisiae EMI5 a mitochondrial protein which is involved in meiotic-specific transcription and sporulation | contig05409_1.exp | CDS | 791218 | 396 | - | 0.262626 |
g3470 | DLA_03840 | GAOABQK02G6SYV | CDS | 525513 | 750 | + | 0.336 | |
g3471 | DLA_03841 | GAOABQK02G6SYV | CDS | 526337 | 408 | - | 0.335784 | |
g3472 | DLA_03843 | GAOABQK02G6SYV | CDS | 529185 | 837 | - | 0.295102 | |
g3473 | DLA_03845 | GAOABQK02G6SYV | CDS | 530881 | 1758 | - | 0.263367 | |
g3474 | DLA_03846 | GAOABQK02G6SYV | CDS | 533480 | 1353 | - | 0.338507 | |
g3475 | DLA_03847 | GAOABQK02G6SYV | CDS | 535135 | 6423 | - | 0.336291 | |
g3476 | DLA_03849 | cyclosporin A-sensitive peptidylprolyl cis-trans isomerase binds the SKIP ortholog snwA in a cyclosporin-independent manner | GAOABQK02G6SYV | CDS | 542218 | 504 | + | 0.333333 |
g3477 | DLA_03851 | GAOABQK02G6SYV | CDS | 543912 | 2457 | + | 0.307692 | |
g3478 | DLA_03852 | GAOABQK02G6SYV | CDS | 546677 | 672 | + | 0.303571 | |
g3479 | DLA_03854 | GAOABQK02G6SYV | CDS | 548414 | 2544 | - | 0.307783 | |
g348 | DLA_00390 | contig05409_1.exp | CDS | 791755 | 2778 | - | 0.338013 | |
g3480 | DLA_03855 | GAOABQK02G6SYV | CDS | 551057 | 1443 | - | 0.327789 | |
g3481 | DLA_03856 | GAOABQK02G6SYV | CDS | 552904 | 582 | + | 0.268041 | |
g3482 | DLA_03857 | GAOABQK02G6SYV | CDS | 553761 | 1065 | - | 0.33615 | |
g3483 | DLA_03860 | GAOABQK02G6SYV | CDS | 558283 | 2547 | - | 0.360817 | |
g3484 | DLA_03861 | GAOABQK02G6SYV | CDS | 561224 | 927 | - | 0.32794 | |
g3485 | DLA_03862 | GAOABQK02G6SYV | CDS | 562346 | 1152 | - | 0.360243 | |
g3486 | DLA_11565 | GAOABQK02G6SYV | CDS | 563782 | 966 | - | 0.318841 | |
g3487 | DLA_03863 | similar to the conserved MYO7A unconventional myosin required in Dictyostelium for phagocytosis and substrate adhesion | GAOABQK02G6SYV | CDS | 565582 | 6801 | - | 0.3573 |
g3488 | DLA_03864 | GAOABQK02G6SYV | CDS | 573471 | 1539 | - | 0.372969 | |
g3489 | DLA_03865 | GAOABQK02G6SYV | CDS | 575533 | 807 | + | 0.358116 | |
g349 | DLA_00391 | contig05409_1.exp | CDS | 795034 | 1401 | + | 0.326909 | |
g3490 | DLA_03866 | GAOABQK02G6SYV | CDS | 576546 | 942 | + | 0.29087 | |
g3491 | DLA_03867 | GAOABQK02G6SYV | CDS | 577899 | 558 | + | 0.277778 | |
g3492 | DLA_03868 | GAOABQK02G6SYV | CDS | 578793 | 1689 | - | 0.357608 | |
g3493 | DLA_03869 | GAOABQK02G6SYV | CDS | 581405 | 1251 | + | 0.331735 | |
g3494 | DLA_03871 | GAOABQK02G6SYV | CDS | 587490 | 1854 | - | 0.335491 | |
g3495 | DLA_03873 | high affinity cAMP receptor belongs to the serpentineG-protein coupled receptor family there is a second copy of this gene | GAOABQK02G6SYV | CDS | 591267 | 1197 | - | 0.319131 |
g3496 | DLA_03874 | GAOABQK02G6SYV | CDS | 593889 | 402 | + | 0.375622 | |
g3497 | DLA_03875 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family kinase activity stimulated by hyperosmolarity and heat shock there is a second copy of this gene | GAOABQK02G6SYV | CDS | 594795 | 1926 | - | 0.339564 |
g3498 | DLA_03876 | GAOABQK02G6SYV | CDS | 597512 | 1959 | + | 0.346095 | |
g3499 | DLA_03877 | GAOABQK02G6SYV | CDS | 599757 | 1542 | - | 0.328794 | |
g35 | DLA_00039 | contig05409_1.exp | CDS | 90186 | 903 | + | 0.292359 | |
g350 | DLA_00392 | contig05409_1.exp | CDS | 796582 | 2334 | - | 0.322622 | |
g3500 | DLA_03878 | GAOABQK02G6SYV | CDS | 601776 | 2961 | + | 0.321175 | |
g3501 | DLA_03879 | GAOABQK02G6SYV | CDS | 605045 | 720 | - | 0.288889 | |
g3502 | DLA_03880 | GAOABQK02G6SYV | CDS | 606627 | 1980 | + | 0.354545 | |
g3503 | DLA_03881 | GAOABQK02G6SYV | CDS | 609301 | 6957 | - | 0.323559 | |
g3504 | DLA_03883 | GAOABQK02G6SYV | CDS | 617157 | 891 | + | 0.289562 | |
g3505 | DLA_11566 | GAOABQK02G6SYV | CDS | 618488 | 891 | + | 0.310887 | |
g3506 | DLA_03884 | GAOABQK02G6SYV | CDS | 619796 | 1389 | - | 0.318934 | |
g3507 | DLA_03885 | catalyzes the reaction UMP diphosphate uracil 5-phospho-alpha-D-ribose 1-diphosphate | GAOABQK02G6SYV | CDS | 621683 | 630 | - | 0.334921 |
g3508 | DLA_03886 | GAOABQK02G6SYV | CDS | 622509 | 1536 | - | 0.324219 | |
g3509 | DLA_03887 | GAOABQK02G6SYV | CDS | 624174 | 2328 | + | 0.311856 | |
g351 | DLA_00393 | contig05409_1.exp | CDS | 799576 | 837 | + | 0.356033 | |
g3510 | DLA_03888 | GAOABQK02G6SYV | CDS | 627805 | 1086 | + | 0.274401 | |
g3511 | DLA_03889 | GAOABQK02G6SYV | CDS | 629025 | 1698 | - | 0.275618 | |
g3512 | DLA_03890 | GAOABQK02G6SYV | CDS | 631330 | 567 | - | 0.322751 | |
g3513 | DLA_03891 | GAOABQK02G6SYV | CDS | 632847 | 726 | - | 0.297521 | |
g3514 | DLA_03892 | GAOABQK02G6SYV | CDS | 633787 | 1749 | - | 0.326472 | |
g3515 | DLA_03893 | GAOABQK02G6SYV | CDS | 635732 | 858 | + | 0.306527 | |
g3516 | DLA_11567 | GAOABQK02G6SYV | CDS | 636618 | 1053 | + | 0.289649 | |
g3517 | DLA_03894 | GAOABQK02G6SYV | CDS | 637681 | 1158 | - | 0.284111 | |
g3518 | DLA_03895 | GAOABQK02G6SYV | CDS | 639274 | 3756 | + | 0.316294 | |
g3519 | DLA_03896 | GAOABQK02G6SYV | CDS | 643275 | 1059 | - | 0.276676 | |
g352 | DLA_00394 | component of the RNA polymerase III complex has similarity to H. sapiens RPC3RPC62 and S. cerevisiae RPC82 | contig05409_1.exp | CDS | 800464 | 1881 | - | 0.302499 |
g3520 | DLA_03897 | GAOABQK02G6SYV | CDS | 647761 | 2139 | + | 0.306685 | |
g3521 | DLA_03898 | conserved splice factor that is required for the first ATP-dependent step in spliceosome assembly and for the interaction of U2 snRNP with the branchpoint the human ortholog (BAT1) forms a homodimer and interacts directly with | GAOABQK02G6SYV | CDS | 650307 | 1281 | + | 0.357533 |
g3522 | DLA_03899 | 20 kDa component of the Dictyostelium Arp2Arp3 complex | GAOABQK02G6SYV | CDS | 653426 | 507 | - | 0.303748 |
g3523 | DLA_03900 | GAOABQK02G6SYV | CDS | 655071 | 240 | + | 0.270833 | |
g3524 | DLA_03901 | GAOABQK02G6SYV | CDS | 655654 | 2310 | + | 0.302164 | |
g3525 | DLA_03902 | contains 6 ankyrin repeats contains one VPS9 (vacuolar sorting protein 9) domain similar to D. purpureum protein | GAOABQK02G6SYV | CDS | 659140 | 2520 | + | 0.335317 |
g3526 | DLA_03903 | GAOABQK02G6SYV | CDS | 662138 | 1884 | + | 0.339703 | |
g3527 | DLA_03904 | putative pseudogene fragment similar to D. discoideum gene | GAOABQK02G6SYV | CDS | 664249 | 1158 | - | 0.309154 |
g3528 | DLA_03906 | belongs to the glycoside hydrolase 5 (cellulase) family 5 contains a predicted signal sequence | GAOABQK02G6SYV | CDS | 666039 | 1515 | + | 0.329373 |
g3529 | DLA_03907 | GAOABQK02G6SYV | CDS | 667658 | 600 | - | 0.311667 | |
g353 | DLA_00395 | contig05409_1.exp | CDS | 802656 | 519 | - | 0.356455 | |
g3530 | DLA_03909 | transfers a segment of a 14-alpha-D-glucan chain to a primary hydroxyl group in a similar glucan chain | GAOABQK02G6SYV | CDS | 670759 | 2049 | - | 0.348463 |
g3531 | DLA_03910 | GAOABQK02G6SYV | CDS | 673618 | 4368 | + | 0.344322 | |
g3532 | DLA_03911 | GAOABQK02G6SYV | CDS | 679161 | 1125 | + | 0.291556 | |
g3533 | DLA_03912 | GAOABQK02G6SYV | CDS | 680633 | 1791 | + | 0.339475 | |
g3534 | DLA_03913 | GAOABQK02G6SYV | CDS | 682530 | 1821 | - | 0.344316 | |
g3535 | DLA_03914 | GAOABQK02G6SYV | CDS | 684774 | 348 | - | 0.318966 | |
g3536 | DLA_03915 | GAOABQK02G6SYV | CDS | 685325 | 1365 | + | 0.335531 | |
g3537 | DLA_03916 | STE SerThr protein kinase family mitogen-activated protein kinase kinase involved in chemotaxis and early development phosphorylates the MAP kinase Erk1 (erkA) is sumoyalated by sumo and ubiquinated by mip1 | GAOABQK02G6SYV | CDS | 686979 | 1284 | - | 0.323209 |
g3538 | DLA_03917 | similar to the human JMJD6 which is required for organ differentiation during embryogenesis | GAOABQK02G6SYV | CDS | 688553 | 2643 | - | 0.341657 |
g3539 | DLA_03918 | GAOABQK02G6SYV | CDS | 691591 | 372 | + | 0.473118 | |
g354 | DLA_00396 | contig05409_1.exp | CDS | 804316 | 3354 | - | 0.320811 | |
g3540 | DLA_03919 | GAOABQK02G6SYV | CDS | 692274 | 342 | - | 0.25731 | |
g3541 | DLA_03920 | ortholog of importin 4 a nuclear transport receptor that is thought to mediate docking of the importinsubstrate complex to the nuclear pore complex | GAOABQK02G6SYV | CDS | 692880 | 3261 | - | 0.329347 |
g3542 | DLA_03921 | induced by Legionella pneumophila infection similar to D. purpureum protein | GAOABQK02G6SYV | CDS | 696701 | 645 | - | 0.372093 |
g3543 | DLA_03922 | GAOABQK02G6SYV | CDS | 697620 | 2601 | - | 0.323337 | |
g3544 | DLA_03924 | GAOABQK02G6SYV | CDS | 700456 | 2271 | - | 0.308234 | |
g3545 | DLA_03926 | has similarity to the mammalian adiponectin receptor protein 1 contains 6 predicted transmembrane domains | GAOABQK02G7M1S | CDS | 450 | 1068 | + | 0.282772 |
g3546 | DLA_03927 | GAOABQK02G7M1S | CDS | 1702 | 1749 | + | 0.291595 | |
g3547 | DLA_03928 | GAOABQK02G7M1S | CDS | 6786 | 4326 | + | 0.306519 | |
g3548 | DLA_03929 | GAOABQK02G7M1S | CDS | 11990 | 597 | + | 0.318258 | |
g3549 | DLA_03930 | GAOABQK02G7M1S | CDS | 12808 | 2847 | + | 0.334387 | |
g355 | DLA_00397 | contig05409_1.exp | CDS | 808084 | 16536 | - | 0.350448 | |
g3550 | DLA_03931 | GAOABQK02G7M1S | CDS | 15698 | 1599 | - | 0.25641 | |
g3551 | DLA_03932 | GAOABQK02G7M1S | CDS | 17613 | 1815 | + | 0.320661 | |
g3552 | DLA_11568 | GAOABQK02G7M1S | CDS | 19585 | 1572 | + | 0.28626 | |
g3553 | DLA_03933 | GAOABQK02G7M1S | CDS | 21408 | 2463 | + | 0.321965 | |
g3554 | DLA_03934 | catalyzes the reaction lipoamide pyruvate S-acetyldihydrolipoamide COsub2sub E1 beta component of pyruvate dehydrogenase complex which contains multiple copies of three enzymatic components: pyruvate dehydrogenase (E1 | GAOABQK02G7M1S | CDS | 24397 | 1086 | - | 0.364641 |
g3555 | DLA_03936 | GAOABQK02G7M1S | CDS | 26030 | 1914 | + | 0.282132 | |
g3556 | DLA_11569 | GAOABQK02G7M1S | CDS | 28255 | 1632 | + | 0.291667 | |
g3557 | DLA_03937 | GAOABQK02G7M1S | CDS | 30188 | 774 | + | 0.352713 | |
g3558 | DLA_03938 | GAOABQK02G7M1S | CDS | 31797 | 4113 | + | 0.292001 | |
g3559 | DLA_03941 | GAOABQK02G7M1S | CDS | 39882 | 4146 | - | 0.348287 | |
g356 | DLA_00398 | contig05409_1.exp | CDS | 825096 | 1860 | + | 0.310753 | |
g3560 | DLA_03942 | GAOABQK02G7M1S | CDS | 44899 | 6978 | - | 0.338062 | |
g3561 | DLA_03945 | GAOABQK02G7M1S | CDS | 55144 | 483 | - | 0.287785 | |
g3562 | DLA_03946 | GAOABQK02G7M1S | CDS | 55976 | 3279 | - | 0.300396 | |
g3563 | DLA_03947 | GAOABQK02G7M1S | CDS | 59591 | 2475 | - | 0.310707 | |
g3564 | DLA_03948 | GAOABQK02G7M1S | CDS | 62218 | 2151 | - | 0.3245 | |
g3565 | DLA_03949 | GAOABQK02G7M1S | CDS | 65770 | 963 | - | 0.330218 | |
g3566 | DLA_03950 | GAOABQK02G7M1S | CDS | 67013 | 558 | - | 0.301075 | |
g3567 | DLA_03951 | GAOABQK02G7M1S | CDS | 67898 | 3429 | + | 0.345582 | |
g3568 | DLA_03952 | GAOABQK02G7M1S | CDS | 71620 | 3717 | + | 0.312618 | |
g3569 | DLA_03953 | GAOABQK02G7M1S | CDS | 75474 | 612 | - | 0.320261 | |
g357 | DLA_00399 | contig05409_1.exp | CDS | 827116 | 696 | - | 0.251437 | |
g3570 | DLA_03954 | GAOABQK02G7M1S | CDS | 76251 | 3687 | + | 0.272851 | |
g3571 | DLA_03955 | GAOABQK02G7M1S | CDS | 80289 | 1812 | - | 0.337196 | |
g3572 | DLA_03956 | GAOABQK02G7M1S | CDS | 82888 | 726 | + | 0.269972 | |
g3573 | DLA_03957 | GAOABQK02G7M1S | CDS | 83998 | 852 | + | 0.255869 | |
g3574 | DLA_03958 | GAOABQK02G7M1S | CDS | 85058 | 909 | + | 0.271727 | |
g3575 | DLA_03959 | GAOABQK02G7M1S | CDS | 85979 | 1875 | - | 0.273067 | |
g3576 | DLA_03960 | GAOABQK02G7M1S | CDS | 88187 | 1986 | + | 0.309164 | |
g3577 | DLA_03961 | GAOABQK02G7M1S | CDS | 90544 | 2664 | + | 0.36036 | |
g3578 | DLA_03962 | GAOABQK02G7M1S | CDS | 93700 | 2844 | + | 0.360408 | |
g3579 | DLA_03963 | GAOABQK02G7M1S | CDS | 97029 | 624 | - | 0.3125 | |
g358 | DLA_00400 | contig05409_1.exp | CDS | 828334 | 1611 | - | 0.310366 | |
g3580 | DLA_03965 | GAOABQK02G7M1S | CDS | 100910 | 4380 | - | 0.364612 | |
g3581 | DLA_03966 | GAOABQK02G7M1S | CDS | 105947 | 1389 | + | 0.269258 | |
g3582 | DLA_03967 | GAOABQK02G7M1S | CDS | 107487 | 348 | - | 0.295977 | |
g3583 | DLA_03968 | GAOABQK02G7M1S | CDS | 108253 | 1482 | + | 0.32861 | |
g3584 | DLA_03969 | GAOABQK02G7M1S | CDS | 110032 | 2364 | - | 0.299492 | |
g3585 | DLA_03972 | GAOABQK02G7M1S | CDS | 117205 | 999 | - | 0.314314 | |
g3586 | DLA_03973 | GAOABQK02G7M1S | CDS | 118766 | 1617 | + | 0.321583 | |
g3587 | DLA_03974 | GAOABQK02G7M1S | CDS | 120773 | 726 | - | 0.318182 | |
g3588 | DLA_03975 | GAOABQK02G7M1S | CDS | 122669 | 888 | + | 0.292793 | |
g3589 | DLA_03976 | GAOABQK02G7M1S | CDS | 123708 | 1461 | + | 0.283368 | |
g359 | DLA_00401 | contig05409_1.exp | CDS | 830609 | 1770 | - | 0.337853 | |
g3590 | DLA_03977 | GAOABQK02G7M1S | CDS | 125271 | 510 | - | 0.288235 | |
g3591 | DLA_03978 | GAOABQK02G7M1S | CDS | 127331 | 837 | - | 0.401434 | |
g3592 | DLA_03983 | GAOABQK02G7M1S | CDS | 133452 | 3414 | - | 0.356766 | |
g3593 | DLA_03984 | GAOABQK02G7M1S | CDS | 137500 | 1347 | - | 0.30438 | |
g3594 | DLA_03985 | GAOABQK02G7M1S | CDS | 138960 | 201 | + | 0.253731 | |
g3595 | DLA_03986 | GAOABQK02G7M1S | CDS | 139601 | 444 | - | 0.324324 | |
g3596 | DLA_03987 | GAOABQK02G7M1S | CDS | 140194 | 3315 | - | 0.328808 | |
g3597 | DLA_03988 | GAOABQK02G7M1S | CDS | 144108 | 1587 | - | 0.303718 | |
g3598 | DLA_03989 | GAOABQK02G7M1S | CDS | 147803 | 1818 | + | 0.378438 | |
g3599 | DLA_03990 | GAOABQK02G7M1S | CDS | 149697 | 1500 | - | 0.238 | |
g36 | DLA_00041 | contig05409_1.exp | CDS | 91681 | 2490 | - | 0.377108 | |
g360 | DLA_00402 | contig05409_1.exp | CDS | 832845 | 675 | + | 0.355556 | |
g3600 | DLA_03991 | GAOABQK02G7M1S | CDS | 151574 | 564 | + | 0.262411 | |
g3601 | DLA_03992 | GAOABQK02G7M1S | CDS | 152251 | 1218 | + | 0.339901 | |
g3602 | DLA_03993 | GAOABQK02G7M1S | CDS | 153817 | 1245 | + | 0.286747 | |
g3603 | DLA_03994 | GAOABQK02G7M1S | CDS | 155119 | 1881 | + | 0.316853 | |
g3604 | DLA_03995 | GAOABQK02G7M1S | CDS | 157585 | 1608 | + | 0.317786 | |
g3605 | DLA_03996 | GAOABQK02G7M1S | CDS | 160354 | 216 | + | 0.268519 | |
g3606 | DLA_03997 | catalyzes the reaction R)-lactate 2 ferricytochrome c pyruvate 2 ferrocytochrome c | GAOABQK02G7M1S | CDS | 160920 | 1677 | + | 0.302922 |
g3607 | DLA_03998 | GAOABQK02G7M1S | CDS | 163405 | 3723 | + | 0.351061 | |
g3608 | DLA_03999 | GAOABQK02G7M1S | CDS | 167514 | 5022 | + | 0.324572 | |
g3609 | DLA_04000 | GAOABQK02G7M1S | CDS | 172823 | 1935 | - | 0.31938 | |
g361 | DLA_00403 | contig05409_1.exp | CDS | 833698 | 1035 | - | 0.369082 | |
g3610 | DLA_04001 | GAOABQK02G7M1S | CDS | 175123 | 4947 | - | 0.332727 | |
g3611 | DLA_04002 | GAOABQK02G7M1S | CDS | 181193 | 1065 | + | 0.294836 | |
g3612 | DLA_04003 | GAOABQK02G7M1S | CDS | 182590 | 1659 | - | 0.314045 | |
g3613 | DLA_04004 | GAOABQK02G7M1S | CDS | 184890 | 462 | + | 0.28355 | |
g3614 | DLA_04005 | GAOABQK02G7M1S | CDS | 185537 | 507 | - | 0.360947 | |
g3615 | DLA_04006 | GAOABQK02G7M1S | CDS | 186265 | 456 | - | 0.265351 | |
g3616 | DLA_04007 | GAOABQK02G7M1S | CDS | 187236 | 1224 | + | 0.335784 | |
g3617 | DLA_04010 | GAOABQK02G7M1S | CDS | 189264 | 579 | - | 0.317789 | |
g3618 | DLA_04011 | GAOABQK02G7M1S | CDS | 190496 | 729 | - | 0.33882 | |
g3619 | DLA_04012 | GAOABQK02G7M1S | CDS | 191848 | 615 | + | 0.273171 | |
g362 | DLA_00404 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) there is a second copy of this gene | contig05409_1.exp | CDS | 835030 | 828 | + | 0.328502 |
g3620 | DLA_04013 | GAOABQK02G7M1S | CDS | 192591 | 570 | - | 0.303509 | |
g3621 | DLA_04014 | GAOABQK02G7M1S | CDS | 193339 | 1047 | - | 0.310411 | |
g3622 | DLA_04015 | GAOABQK02G7M1S | CDS | 194635 | 6603 | - | 0.377707 | |
g3623 | DLA_04017 | GAOABQK02G7M1S | CDS | 202037 | 1119 | + | 0.36193 | |
g3624 | DLA_11570 | GAOABQK02G7M1S | CDS | 205556 | 618 | + | 0.276699 | |
g3625 | DLA_04018 | GAOABQK02G7M1S | CDS | 206575 | 879 | + | 0.399317 | |
g3626 | DLA_04019 | GAOABQK02G7M1S | CDS | 207704 | 888 | - | 0.35473 | |
g3627 | DLA_04020 | GAOABQK02G7M1S | CDS | 209078 | 951 | - | 0.330179 | |
g3628 | DLA_04021 | GAOABQK02G7M1S | CDS | 210418 | 1698 | - | 0.331567 | |
g3629 | DLA_04024 | GAOABQK02G7M1S | CDS | 214433 | 1974 | + | 0.377913 | |
g363 | DLA_00405 | contig05409_1.exp | CDS | 836218 | 762 | - | 0.255906 | |
g3630 | DLA_04025 | GAOABQK02G7M1S | CDS | 217291 | 2040 | - | 0.261275 | |
g3631 | DLA_04026 | GAOABQK02G7M1S | CDS | 219713 | 1872 | + | 0.346688 | |
g3632 | DLA_04027 | GAOABQK02G7M1S | CDS | 221675 | 1260 | - | 0.321429 | |
g3633 | DLA_04028 | GAOABQK02G7M1S | CDS | 224475 | 774 | + | 0.351421 | |
g3634 | DLA_04029 | GAOABQK02G7M1S | CDS | 225384 | 912 | - | 0.339912 | |
g3635 | DLA_04031 | GAOABQK02G7M1S | CDS | 227137 | 1110 | + | 0.362162 | |
g3636 | DLA_04032 | GAOABQK02G7M1S | CDS | 228574 | 939 | + | 0.338658 | |
g3637 | DLA_04033 | GAOABQK02G7M1S | CDS | 229888 | 2763 | + | 0.330076 | |
g3638 | DLA_04034 | GAOABQK02G7M1S | CDS | 232995 | 3114 | + | 0.32948 | |
g3639 | DLA_04035 | GAOABQK02G7M1S | CDS | 236433 | 3210 | + | 0.329907 | |
g364 | DLA_00406 | contig05409_1.exp | CDS | 837070 | 2592 | + | 0.255015 | |
g3640 | DLA_04036 | GAOABQK02G7M1S | CDS | 239785 | 2796 | - | 0.271102 | |
g3641 | DLA_04038 | GAOABQK02G7M1S | CDS | 243382 | 723 | + | 0.329184 | |
g3642 | DLA_04039 | GAOABQK02G7M1S | CDS | 244551 | 4338 | - | 0.345781 | |
g3643 | DLA_04040 | GAOABQK02G7M1S | CDS | 249470 | 579 | + | 0.321244 | |
g3644 | DLA_04041 | GAOABQK02G7M1S | CDS | 250249 | 3735 | - | 0.326104 | |
g3645 | DLA_04042 | GAOABQK02G7M1S | CDS | 256078 | 327 | - | 0.299694 | |
g3646 | DLA_04043 | GAOABQK02G7M1S | CDS | 256611 | 1230 | + | 0.334146 | |
g3647 | DLA_04044 | GAOABQK02G7M1S | CDS | 257955 | 1452 | - | 0.304408 | |
g3648 | DLA_04045 | GAOABQK02G7M1S | CDS | 259772 | 2646 | - | 0.309146 | |
g3649 | DLA_04046 | GAOABQK02G7M1S | CDS | 262530 | 3594 | - | 0.328603 | |
g365 | DLA_00407 | contig05409_1.exp | CDS | 839758 | 1317 | - | 0.356872 | |
g3650 | DLA_04047 | GAOABQK02G7M1S | CDS | 266514 | 666 | + | 0.364865 | |
g3651 | DLA_04048 | GAOABQK02G7M1S | CDS | 267342 | 516 | - | 0.304264 | |
g3652 | DLA_04049 | GAOABQK02G7M1S | CDS | 268969 | 1509 | - | 0.340623 | |
g3653 | DLA_04050 | highly similar to mammalian SAHH (catalyzes the hydrolysis of S-adenosyl-L-homocysteine into adenosine and homocysteine) localizes to actin rods found in spores | GAOABQK02G7M1S | CDS | 271164 | 3738 | - | 0.356073 |
g3654 | DLA_04051 | GAOABQK02G7M1S | CDS | 276008 | 3660 | - | 0.296448 | |
g3655 | DLA_11571 | GAOABQK02G7M1S | CDS | 280149 | 549 | + | 0.333333 | |
g3656 | DLA_04052 | GAOABQK02G7M1S | CDS | 281829 | 1176 | + | 0.34949 | |
g3657 | DLA_04053 | GAOABQK02G7M1S | CDS | 283237 | 1683 | + | 0.263815 | |
g3658 | DLA_11572 | GAOABQK02G7M1S | CDS | 285979 | 885 | + | 0.346893 | |
g3659 | DLA_04054 | GAOABQK02G7M1S | CDS | 287135 | 1572 | + | 0.302799 | |
g366 | DLA_00408 | contig05409_1.exp | CDS | 841728 | 696 | + | 0.313218 | |
g3660 | DLA_04055 | GAOABQK02G7M1S | CDS | 288864 | 6180 | - | 0.348706 | |
g3661 | DLA_04056 | catalyzes the conversion of delta-aminolevulinic acid to porphobilinogen the second step in heme biosynthesis | GAOABQK02G7M1S | CDS | 296588 | 1005 | + | 0.363184 |
g3662 | DLA_04057 | GAOABQK02G7M1S | CDS | 297746 | 3153 | - | 0.350143 | |
g3663 | DLA_04058 | GAOABQK02G7M1S | CDS | 301570 | 690 | - | 0.318841 | |
g3664 | DLA_04060 | GAOABQK02G7M1S | CDS | 303809 | 1908 | + | 0.343816 | |
g3665 | DLA_04061 | ortholog of integrator complex subunit 2 component of a multiprotein mediator of small nuclear RNA processing | GAOABQK02G7M1S | CDS | 306119 | 3360 | - | 0.284821 |
g3666 | DLA_04062 | GAOABQK02G7M1S | CDS | 310741 | 3696 | - | 0.291667 | |
g3667 | DLA_04063 | GAOABQK02G7M1S | CDS | 314710 | 1107 | - | 0.307136 | |
g3668 | DLA_04064 | GAOABQK02G7M1S | CDS | 316863 | 1038 | + | 0.33526 | |
g3669 | DLA_04065 | GAOABQK02G7M1S | CDS | 317956 | 2370 | + | 0.278903 | |
g367 | DLA_00409 | contig05409_1.exp | CDS | 842702 | 2277 | + | 0.348265 | |
g3670 | DLA_04066 | catalyzes the reaction ATP L-aspartate tRNAAsp AMP diphosphate L-aspartyl-tRNAAsp | GAOABQK02G7M1S | CDS | 320736 | 3195 | - | 0.342097 |
g3671 | DLA_04068 | GAOABQK02G7M1S | CDS | 326176 | 975 | + | 0.317949 | |
g3672 | DLA_04069 | catalyzes the reaction 3-phospho-hydroxypyruvate L-glutamate 2-oxoglutarate 3-phospho-serine | GAOABQK02G7M1S | CDS | 327683 | 1122 | - | 0.322638 |
g3673 | DLA_04070 | GAOABQK02G7M1S | CDS | 329319 | 1029 | + | 0.347911 | |
g3674 | DLA_04071 | GAOABQK02G7M1S | CDS | 330703 | 1125 | + | 0.424 | |
g3675 | DLA_04072 | catalyzes the reaction succinate ubiquinone fumarate ubiquinol | GAOABQK02G7M1S | CDS | 332371 | 627 | + | 0.355662 |
g3676 | DLA_04073 | GAOABQK02G7M1S | CDS | 333146 | 1035 | - | 0.30628 | |
g3677 | DLA_04074 | GAOABQK02G7M1S | CDS | 334590 | 3030 | - | 0.30099 | |
g3678 | DLA_04076 | GAOABQK02G7M1S | CDS | 339178 | 2208 | + | 0.291214 | |
g3679 | DLA_04077 | GAOABQK02G7M1S | CDS | 342331 | 696 | + | 0.326149 | |
g368 | DLA_00410 | contig05409_1.exp | CDS | 845124 | 1605 | - | 0.290966 | |
g3680 | DLA_04078 | GAOABQK02G7M1S | CDS | 343638 | 1425 | - | 0.338947 | |
g3681 | DLA_11573 | GAOABQK02G7M1S | CDS | 346778 | 1020 | + | 0.290196 | |
g3682 | DLA_04079 | GAOABQK02G7M1S | CDS | 348085 | 3858 | + | 0.29549 | |
g3683 | DLA_04080 | component of the ELL complex an RNA polymerase II transcription factor and of the ESCRT-II complex (endosomal sorting complex required for transport) | GAOABQK02G7M1S | CDS | 352180 | 495 | - | 0.268687 |
g3684 | DLA_04081 | GAOABQK02G7M1S | CDS | 352987 | 447 | + | 0.322148 | |
g3685 | DLA_04082 | GAOABQK02G7M1S | CDS | 353676 | 741 | - | 0.34143 | |
g3686 | DLA_04083 | GAOABQK02G7M1S | CDS | 354857 | 903 | + | 0.301218 | |
g3687 | DLA_04084 | similar to plant and fungi NADH dehydrogenases such as S. cerevisiae NDE1 and NDE2 the external mitochondrial NADH dehydrogenases that catalyze the oxidation of cytosolic NADH | GAOABQK02G7M1S | CDS | 355979 | 1332 | + | 0.332583 |
g3688 | DLA_04085 | GAOABQK02G7M1S | CDS | 357572 | 1707 | - | 0.357938 | |
g3689 | DLA_04086 | GAOABQK02G7M1S | CDS | 360092 | 6528 | + | 0.339614 | |
g369 | DLA_00411 | contig05409_1.exp | CDS | 847210 | 1617 | + | 0.309833 | |
g3690 | DLA_04087 | GAOABQK02G7M1S | CDS | 366763 | 1575 | - | 0.285714 | |
g3691 | DLA_04089 | GAOABQK02G7M1S | CDS | 368628 | 1068 | + | 0.339888 | |
g3692 | DLA_11574 | GAOABQK02G7M1S | CDS | 370061 | 1737 | + | 0.276914 | |
g3693 | DLA_04090 | GAOABQK02G7M1S | CDS | 372262 | 6327 | + | 0.314525 | |
g3694 | DLA_04092 | GAOABQK02G7M1S | CDS | 379842 | 1392 | + | 0.346983 | |
g3695 | DLA_04094 | GAOABQK02G7M1S | CDS | 382351 | 426 | + | 0.328638 | |
g3696 | DLA_04095 | GAOABQK02G7M1S | CDS | 382945 | 1068 | + | 0.268727 | |
g3697 | DLA_04096 | GAOABQK02G7M1S | CDS | 384274 | 2109 | + | 0.303461 | |
g3698 | DLA_04097 | GAOABQK02G7M1S | CDS | 387014 | 903 | + | 0.317829 | |
g3699 | DLA_04098 | GAOABQK02G7M1S | CDS | 388776 | 825 | + | 0.313939 | |
g37 | DLA_11430 | contig05409_1.exp | CDS | 95230 | 717 | - | 0.294282 | |
g370 | DLA_00412 | contig05409_1.exp | CDS | 849111 | 4869 | + | 0.326761 | |
g3700 | DLA_04099 | GAOABQK02G7M1S | CDS | 390242 | 204 | - | 0.338235 | |
g3701 | DLA_04102 | GAOABQK02G7M1S | CDS | 391155 | 1005 | + | 0.294527 | |
g3702 | DLA_04103 | GAOABQK02G7M1S | CDS | 394070 | 1671 | + | 0.305206 | |
g3703 | DLA_04104 | GAOABQK02G7M1S | CDS | 396022 | 1254 | + | 0.317384 | |
g3704 | DLA_04105 | GAOABQK02G7M1S | CDS | 397611 | 1419 | - | 0.359408 | |
g3705 | DLA_04106 | GAOABQK02G7M1S | CDS | 399900 | 2148 | + | 0.332868 | |
g3706 | DLA_04107 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | GAOABQK02G7M1S | CDS | 402520 | 1800 | + | 0.329444 |
g3707 | DLA_04108 | GAOABQK02G7M1S | CDS | 404677 | 912 | - | 0.26864 | |
g3708 | DLA_04109 | GAOABQK02G7M1S | CDS | 405886 | 612 | + | 0.315359 | |
g3709 | DLA_04110 | GAOABQK02G7M1S | CDS | 406536 | 1113 | - | 0.327942 | |
g371 | DLA_00413 | contig05409_1.exp | CDS | 854183 | 1509 | - | 0.309476 | |
g3710 | DLA_04111 | GAOABQK02G7M1S | CDS | 408054 | 1758 | + | 0.32992 | |
g3711 | DLA_04112 | GAOABQK02G7M1S | CDS | 410391 | 900 | + | 0.331111 | |
g3712 | DLA_04113 | GAOABQK02G7M1S | CDS | 411453 | 1245 | - | 0.355823 | |
g3713 | DLA_04114 | similar to Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) contains one SH3 (src Homology-3) domain | GAOABQK02G7M1S | CDS | 413945 | 2100 | + | 0.350952 |
g3714 | DLA_04116 | GAOABQK02G7M1S | CDS | 417046 | 2091 | - | 0.359158 | |
g3715 | DLA_04117 | elongation factor 1 alpha one of two genes coding for the same protein binds and bundles F-actin | GAOABQK02G7M1S | CDS | 420469 | 1365 | + | 0.4337 |
g3716 | DLA_04118 | GAOABQK02G7M1S | CDS | 422500 | 2340 | + | 0.341453 | |
g3717 | DLA_04119 | catalyzes the transfer of a geranyl-geranyl moiety from geranyl-geranyl pyrophosphate to both cysteines in Rab proteins with an -XXCC -XCXC and -CCXX C-terminal forms a hetero-dimer with the | GAOABQK02G7M1S | CDS | 424989 | 936 | - | 0.280983 |
g3718 | DLA_04120 | ortholog of the mediator of RNA polymerase II transcription subunit 7 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | GAOABQK02G7M1S | CDS | 426205 | 750 | + | 0.294667 |
g3719 | DLA_04121 | GAOABQK02G7M1S | CDS | 427078 | 1353 | - | 0.288987 | |
g372 | DLA_00414 | contig05409_1.exp | CDS | 855930 | 810 | + | 0.28642 | |
g3720 | DLA_04122 | GAOABQK02G7M1S | CDS | 429216 | 297 | + | 0.3367 | |
g3721 | DLA_04123 | GAOABQK02G7M1S | CDS | 430091 | 675 | + | 0.321481 | |
g3722 | DLA_04125 | GAOABQK02G7M1S | CDS | 431257 | 1086 | - | 0.341621 | |
g3723 | DLA_04126 | GAOABQK02G7M1S | CDS | 432623 | 1785 | + | 0.322129 | |
g3724 | DLA_04127 | GAOABQK02G7M1S | CDS | 435447 | 1488 | + | 0.297715 | |
g3725 | DLA_04128 | GAOABQK02G7M1S | CDS | 436959 | 2169 | - | 0.323651 | |
g3726 | DLA_04129 | catalyzes the reaction ATP L-tryptophan tRNATrp AMP diphosphate L-tryptophan-tRNAThr | GAOABQK02G7M1S | CDS | 439506 | 1212 | + | 0.364686 |
g3727 | DLA_04130 | GAOABQK02G7M1S | CDS | 440807 | 2445 | - | 0.31002 | |
g3728 | DLA_04131 | GAOABQK02G7M1S | CDS | 443716 | 3468 | - | 0.297001 | |
g3729 | DLA_04133 | GAOABQK02G7M1S | CDS | 448264 | 1008 | - | 0.291667 | |
g373 | DLA_00415 | contig05409_1.exp | CDS | 857329 | 495 | + | 0.359596 | |
g3730 | DLA_04134 | GAOABQK02G7M1S | CDS | 452000 | 471 | + | 0.343949 | |
g3731 | DLA_11575 | putative glycosyltransferase involved in GPI biosynthesis subunit of the transferase that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-N-acetylglucosamine to phosphatidylinositol (PI) | GAOABQK02G7M1S | CDS | 452536 | 507 | - | 0.254438 |
g3732 | DLA_04135 | GAOABQK02G7M1S | CDS | 453346 | 2685 | - | 0.347858 | |
g3733 | DLA_04136 | GAOABQK02G7M1S | CDS | 457369 | 2406 | + | 0.334165 | |
g3734 | DLA_04137 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | GAOABQK02G7M1S | CDS | 460239 | 579 | - | 0.336788 |
g3735 | DLA_04138 | GAOABQK02G7M1S | CDS | 461027 | 738 | - | 0.280488 | |
g3736 | DLA_04140 | GAOABQK02G7M1S | CDS | 462856 | 510 | + | 0.339216 | |
g3737 | DLA_04141 | GAOABQK02G7M1S | CDS | 463659 | 3450 | + | 0.295652 | |
g3738 | DLA_11576 | GAOABQK02G7M1S | CDS | 467418 | 894 | + | 0.302013 | |
g3739 | DLA_04142 | GAOABQK02G7M1S | CDS | 468427 | 678 | - | 0.277286 | |
g374 | DLA_00416 | contig05409_1.exp | CDS | 858035 | 360 | - | 0.261111 | |
g3740 | DLA_04143 | GAOABQK02G7M1S | CDS | 469379 | 1320 | - | 0.312879 | |
g3741 | DLA_04144 | GAOABQK02G7M1S | CDS | 471893 | 2535 | - | 0.341223 | |
g3742 | DLA_04146 | GAOABQK02G7M1S | CDS | 475143 | 780 | + | 0.341026 | |
g3743 | DLA_04147 | GAOABQK02G7M1S | CDS | 476343 | 951 | - | 0.328076 | |
g3744 | DLA_04148 | GAOABQK02G7M1S | CDS | 477898 | 1425 | + | 0.310175 | |
g3745 | DLA_04149 | conserved protein may catalyze reversible transfer reactions of coenzyme A groups from CoA-thioesters to free acids | GAOABQK02G7M1S | CDS | 479380 | 1350 | - | 0.319259 |
g3746 | DLA_04150 | GAOABQK02G7M1S | CDS | 480843 | 990 | + | 0.30101 | |
g3747 | DLA_04151 | GAOABQK02G7M1S | CDS | 482080 | 1110 | - | 0.31982 | |
g3748 | DLA_04152 | GAOABQK02G7M1S | CDS | 483553 | 1671 | - | 0.286655 | |
g3749 | DLA_04153 | GAOABQK02G7M1S | CDS | 485480 | 1737 | + | 0.284974 | |
g375 | DLA_00417 | contig05409_1.exp | CDS | 858575 | 954 | + | 0.371069 | |
g3750 | DLA_04154 | GAOABQK02G7M1S | CDS | 487367 | 6270 | + | 0.322967 | |
g3751 | DLA_04155 | GAOABQK02G7M1S | CDS | 493756 | 570 | - | 0.273684 | |
g3752 | DLA_04156 | GAOABQK02G7M1S | CDS | 494645 | 684 | + | 0.258772 | |
g3753 | DLA_04157 | GAOABQK02G7M1S | CDS | 495700 | 2271 | + | 0.326288 | |
g3754 | DLA_04158 | GAOABQK02G7M1S | CDS | 498362 | 828 | + | 0.299517 | |
g3755 | DLA_04159 | GAOABQK02G7M1S | CDS | 499607 | 927 | - | 0.274002 | |
g3756 | DLA_04160 | GAOABQK02G7M1S | CDS | 500809 | 834 | - | 0.327338 | |
g3757 | DLA_04161 | contains a SAM (and some other nucleotide) binding motif similar to bacterial and eukaryotic methyltransferases | GAOABQK02G7M1S | CDS | 501974 | 774 | + | 0.322997 |
g3758 | DLA_04163 | GAOABQK02G7M1S | CDS | 503353 | 843 | - | 0.321471 | |
g3759 | DLA_04164 | GAOABQK02G7M1S | CDS | 505124 | 729 | + | 0.315501 | |
g376 | DLA_00418 | contig05409_1.exp | CDS | 860886 | 2061 | + | 0.368268 | |
g3760 | DLA_04165 | GAOABQK02G7M1S | CDS | 506209 | 324 | + | 0.262346 | |
g3761 | DLA_04166 | GAOABQK02G7M1S | CDS | 506791 | 1362 | - | 0.35022 | |
g3762 | DLA_04167 | GAOABQK02G7M1S | CDS | 508398 | 1860 | - | 0.313441 | |
g3763 | DLA_04168 | GAOABQK02G7M1S | CDS | 510770 | 219 | - | 0.292237 | |
g3764 | DLA_04169 | GAOABQK02G7M1S | CDS | 511358 | 2334 | + | 0.323051 | |
g3765 | DLA_04170 | GAOABQK02G7M1S | CDS | 514079 | 3081 | - | 0.285297 | |
g3766 | DLA_04171 | GAOABQK02G7M1S | CDS | 518183 | 771 | - | 0.32166 | |
g3767 | DLA_04172 | GAOABQK02G7M1S | CDS | 519686 | 1815 | + | 0.35978 | |
g3768 | DLA_04173 | GAOABQK02G7M1S | CDS | 521665 | 1233 | - | 0.321979 | |
g3769 | DLA_04176 | GAOABQK02G7M1S | CDS | 524263 | 3051 | + | 0.274664 | |
g377 | DLA_00419 | contig05409_1.exp | CDS | 865945 | 2151 | + | 0.355184 | |
g3770 | DLA_04177 | GAOABQK02G7M1S | CDS | 527832 | 2493 | - | 0.382671 | |
g3771 | DLA_04178 | GAOABQK02G7M1S | CDS | 530995 | 1695 | - | 0.359292 | |
g3772 | DLA_04179 | GAOABQK02G7M1S | CDS | 533102 | 561 | + | 0.322638 | |
g3773 | DLA_04181 | GAOABQK02G7M1S | CDS | 534801 | 963 | - | 0.328141 | |
g3774 | DLA_04182 | GAOABQK02G7M1S | CDS | 536367 | 2754 | + | 0.324256 | |
g3775 | DLA_04183 | GAOABQK02G7M1S | CDS | 539353 | 522 | + | 0.293103 | |
g3776 | DLA_04184 | GAOABQK02G7M1S | CDS | 540616 | 1884 | + | 0.36518 | |
g3777 | DLA_04185 | GAOABQK02G7M1S | CDS | 542664 | 3417 | + | 0.287972 | |
g3778 | DLA_04187 | GAOABQK02G7M1S | CDS | 547597 | 1608 | - | 0.389925 | |
g3779 | DLA_04188 | GAOABQK02G7M1S | CDS | 550353 | 3459 | - | 0.298352 | |
g378 | DLA_00421 | contig05409_1.exp | CDS | 869549 | 1632 | + | 0.349877 | |
g3780 | DLA_04189 | 120 kDa F-actin binding protein also often called filamin involved in actin cytoskeleton organization motility and development enriched in prestalk cells | GAOABQK02G7M1S | CDS | 554030 | 2580 | - | 0.404264 |
g3781 | DLA_04191 | GAOABQK02G7M1S | CDS | 557831 | 1689 | + | 0.326229 | |
g3782 | DLA_04192 | GAOABQK02G7M1S | CDS | 559788 | 3381 | - | 0.359065 | |
g3783 | DLA_04195 | GAOABQK02G7M1S | CDS | 563952 | 1836 | + | 0.348039 | |
g3784 | DLA_04196 | GAOABQK02G7M1S | CDS | 566511 | 1071 | + | 0.345472 | |
g3785 | DLA_04197 | GAOABQK02G7M1S | CDS | 567949 | 3168 | - | 0.349432 | |
g3786 | DLA_04198 | GAOABQK02G7M1S | CDS | 571410 | 3756 | - | 0.390841 | |
g3787 | DLA_04199 | GAOABQK02G7M1S | CDS | 576773 | 861 | + | 0.390244 | |
g3788 | DLA_04200 | GAOABQK02G7M1S | CDS | 577819 | 1269 | - | 0.319937 | |
g3789 | DLA_04201 | GAOABQK02G7M1S | CDS | 579318 | 369 | + | 0.303523 | |
g379 | DLA_00422 | contig05409_1.exp | CDS | 871500 | 1257 | - | 0.311058 | |
g3790 | DLA_04202 | GAOABQK02G7M1S | CDS | 580096 | 5727 | + | 0.330016 | |
g3791 | DLA_04203 | GAOABQK02G7M1S | CDS | 586046 | 1668 | + | 0.374101 | |
g3792 | DLA_11577 | GAOABQK02G7M1S | CDS | 588432 | 513 | - | 0.335283 | |
g3793 | DLA_04204 | GAOABQK02G7M1S | CDS | 589579 | 453 | - | 0.320088 | |
g3794 | DLA_04205 | GAOABQK02G7M1S | CDS | 591169 | 504 | + | 0.373016 | |
g3795 | DLA_04206 | GAOABQK02G7M1S | CDS | 592107 | 861 | + | 0.360046 | |
g3796 | DLA_04207 | GAOABQK02G7M1S | CDS | 593102 | 819 | - | 0.291819 | |
g3797 | DLA_04210 | GAOABQK02G7M1S | CDS | 597633 | 2283 | + | 0.34078 | |
g3798 | DLA_04212 | GAOABQK02G7M1S | CDS | 601056 | 2631 | - | 0.333333 | |
g3799 | DLA_04213 | GAOABQK02G7M1S | CDS | 604665 | 1314 | + | 0.362253 | |
g38 | DLA_00042 | contig05409_1.exp | CDS | 96439 | 1317 | - | 0.248292 | |
g380 | DLA_00423 | contig05409_1.exp | CDS | 873747 | 381 | + | 0.333333 | |
g3800 | DLA_04215 | GAOABQK02G7M1S | CDS | 606402 | 1665 | + | 0.313514 | |
g3801 | DLA_04216 | GAOABQK02G7M1S | CDS | 608408 | 612 | - | 0.254902 | |
g3802 | DLA_04217 | GAOABQK02G7M1S | CDS | 609604 | 1872 | - | 0.307692 | |
g3803 | DLA_04218 | GAOABQK02G7M1S | CDS | 612161 | 795 | + | 0.354717 | |
g3804 | DLA_04220 | GAOABQK02G7M1S | CDS | 613921 | 1488 | - | 0.373656 | |
g3805 | DLA_11578 | GAOABQK02G7M1S | CDS | 615729 | 234 | - | 0.354701 | |
g3806 | DLA_04221 | GAOABQK02G7M1S | CDS | 616325 | 339 | - | 0.353982 | |
g3807 | DLA_04222 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | GAOABQK02G7M1S | CDS | 617133 | 4275 | - | 0.349942 |
g3808 | DLA_04223 | GAOABQK02G7M1S | CDS | 621654 | 5355 | - | 0.313912 | |
g3809 | DLA_04224 | GAOABQK02G7M1S | CDS | 628146 | 5130 | - | 0.316764 | |
g381 | DLA_00424 | contig05409_1.exp | CDS | 874529 | 1143 | - | 0.342082 | |
g3810 | DLA_04227 | GAOABQK02G7M1S | CDS | 635018 | 5355 | - | 0.314846 | |
g3811 | DLA_04228 | GAOABQK02G7M1S | CDS | 641792 | 5373 | - | 0.317513 | |
g3812 | DLA_04229 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | GAOABQK02G7M1S | CDS | 647809 | 462 | - | 0.352814 |
g3813 | DLA_04230 | GAOABQK02G7M1S | CDS | 648885 | 1185 | + | 0.314768 | |
g3814 | DLA_04231 | GAOABQK02G7M1S | CDS | 650560 | 960 | - | 0.33125 | |
g3815 | DLA_04232 | GAOABQK02G7M1S | CDS | 651853 | 2955 | - | 0.324196 | |
g3816 | DLA_04233 | GAOABQK02G7M1S | CDS | 656435 | 1044 | - | 0.304598 | |
g3817 | DLA_04234 | GAOABQK02G7M1S | CDS | 658296 | 621 | + | 0.309179 | |
g3818 | DLA_04236 | GAOABQK02G7M1S | CDS | 659824 | 384 | - | 0.289062 | |
g3819 | DLA_04237 | GAOABQK02G7M1S | CDS | 660323 | 2250 | + | 0.296 | |
g382 | DLA_00425 | contig05409_1.exp | CDS | 875815 | 552 | + | 0.251812 | |
g3820 | DLA_04238 | GAOABQK02G7M1S | CDS | 663166 | 1119 | - | 0.266309 | |
g3821 | DLA_04239 | GAOABQK02G7M1S | CDS | 664421 | 2448 | - | 0.319853 | |
g3822 | DLA_04240 | GAOABQK02G7M1S | CDS | 667131 | 873 | + | 0.28866 | |
g3823 | DLA_04241 | GAOABQK02G7M1S | CDS | 668114 | 2208 | - | 0.341033 | |
g3824 | DLA_04242 | GAOABQK02G7M1S | CDS | 671261 | 2346 | + | 0.331628 | |
g3825 | DLA_04243 | GAOABQK02G7M1S | CDS | 673690 | 447 | - | 0.272931 | |
g3826 | DLA_04244 | G-actin binding protein that is located to filopodia binds to VASP and is involved in chemotaxis | GAOABQK02G7M1S | CDS | 674853 | 378 | + | 0.386243 |
g3827 | DLA_04245 | GAOABQK02G7M1S | CDS | 675659 | 1404 | + | 0.299145 | |
g3828 | DLA_04246 | GAOABQK02G7M1S | CDS | 677269 | 744 | - | 0.337366 | |
g3829 | DLA_04247 | GAOABQK02G7M1S | CDS | 678225 | 2883 | + | 0.310441 | |
g383 | DLA_00426 | contig05409_1.exp | CDS | 877599 | 1206 | + | 0.349917 | |
g3830 | DLA_04248 | GAOABQK02G7M1S | CDS | 681315 | 441 | - | 0.321995 | |
g3831 | DLA_04249 | GAOABQK02G7M1S | CDS | 682139 | 366 | - | 0.278689 | |
g3832 | DLA_04250 | contains a BRCT domain (C-terminal domain of a breast cancer susceptibility protein) which is often found in proteins involved in cell cycle checkpoint | GAOABQK02G7M1S | CDS | 682610 | 1275 | - | 0.334902 |
g3833 | DLA_04251 | GAOABQK02G7M1S | CDS | 684370 | 4170 | + | 0.347002 | |
g3834 | DLA_04252 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | GAOABQK02G7M1S | CDS | 688757 | 1176 | - | 0.292517 |
g3835 | DLA_04253 | GAOABQK02G7M1S | CDS | 690803 | 2187 | + | 0.313672 | |
g3836 | DLA_04254 | GAOABQK02G7M1S | CDS | 693478 | 3450 | - | 0.325507 | |
g3837 | DLA_04255 | GAOABQK02G7M1S | CDS | 697436 | 480 | + | 0.360417 | |
g3838 | DLA_04256 | GAOABQK02G7M1S | CDS | 699600 | 1266 | + | 0.345972 | |
g3839 | DLA_04257 | GAOABQK02G7M1S | CDS | 701740 | 663 | - | 0.294118 | |
g384 | DLA_00427 | contig05409_1.exp | CDS | 879047 | 2526 | + | 0.342043 | |
g3840 | DLA_04258 | GAOABQK02G7M1S | CDS | 703062 | 903 | + | 0.370986 | |
g3841 | DLA_04259 | GAOABQK02G7M1S | CDS | 704299 | 624 | + | 0.322115 | |
g3842 | DLA_04260 | GAOABQK02G7M1S | CDS | 705335 | 2826 | - | 0.363411 | |
g3843 | DLA_04262 | GAOABQK02G7M1S | CDS | 708702 | 558 | - | 0.317204 | |
g3844 | DLA_04263 | GAOABQK02G7M1S | CDS | 710196 | 2940 | - | 0.337415 | |
g3845 | DLA_04264 | GAOABQK02G7M1S | CDS | 714124 | 2442 | - | 0.354218 | |
g3846 | DLA_04266 | GAOABQK02G7M1S | CDS | 719009 | 1554 | - | 0.301802 | |
g3847 | DLA_04267 | GAOABQK02G7M1S | CDS | 723178 | 1035 | - | 0.25314 | |
g3848 | DLA_04268 | GAOABQK02G7M1S | CDS | 724718 | 5766 | - | 0.333333 | |
g3849 | DLA_04269 | GAOABQK02G7M1S | CDS | 731039 | 4038 | + | 0.337048 | |
g385 | DLA_00428 | contig05409_1.exp | CDS | 882874 | 2409 | + | 0.317974 | |
g3850 | DLA_04270 | GAOABQK02G7M1S | CDS | 735441 | 1416 | - | 0.358757 | |
g3851 | DLA_04271 | GAOABQK02G7M1S | CDS | 737197 | 1590 | + | 0.267925 | |
g3852 | DLA_04272 | GAOABQK02G7M1S | CDS | 738797 | 660 | - | 0.30303 | |
g3853 | DLA_04273 | GAOABQK02G7M1S | CDS | 740524 | 1050 | + | 0.328571 | |
g3854 | DLA_04274 | GAOABQK02G7M1S | CDS | 742966 | 426 | + | 0.276995 | |
g3855 | DLA_04275 | GAOABQK02G7M1S | CDS | 743511 | 1698 | - | 0.319788 | |
g3856 | DLA_04276 | GAOABQK02G7M1S | CDS | 745619 | 1431 | - | 0.406709 | |
g3857 | DLA_11579 | GAOABQK02G7M1S | CDS | 747536 | 318 | + | 0.273585 | |
g3858 | DLA_04277 | GAOABQK02G7M1S | CDS | 748426 | 450 | + | 0.24 | |
g3859 | DLA_04278 | GAOABQK02G7M1S | CDS | 749133 | 5775 | + | 0.319481 | |
g386 | DLA_00429 | contig05409_1.exp | CDS | 885585 | 2793 | - | 0.367347 | |
g3860 | DLA_04279 | GAOABQK02G7M1S | CDS | 755158 | 1089 | + | 0.280992 | |
g3861 | DLA_04281 | GAOABQK02G7M1S | CDS | 756703 | 675 | + | 0.308148 | |
g3862 | DLA_04282 | GAOABQK02G7M1S | CDS | 757683 | 1323 | - | 0.280423 | |
g3863 | DLA_04283 | GAOABQK02G7M1S | CDS | 759906 | 411 | + | 0.391728 | |
g3864 | DLA_04284 | GAOABQK02G7M1S | CDS | 761256 | 1530 | + | 0.336601 | |
g3865 | DLA_04285 | GAOABQK02G7M1S | CDS | 764308 | 2379 | + | 0.306011 | |
g3866 | DLA_04286 | GAOABQK02G7M1S | CDS | 768466 | 2067 | + | 0.305273 | |
g3867 | DLA_04287 | GAOABQK02G7M1S | CDS | 771459 | 2004 | - | 0.314371 | |
g3868 | DLA_04289 | GAOABQK02GQAQJ | CDS | 1080 | 1212 | + | 0.290429 | |
g3869 | DLA_04291 | GAOABQK02GQAQJ | CDS | 2867 | 2811 | + | 0.282818 | |
g387 | DLA_00431 | contig05409_1.exp | CDS | 888684 | 1251 | - | 0.278977 | |
g3870 | DLA_04292 | GAOABQK02GQAQJ | CDS | 5759 | 1623 | - | 0.264325 | |
g3871 | DLA_04293 | GAOABQK02GQAQJ | CDS | 7589 | 1095 | + | 0.315068 | |
g3872 | DLA_04294 | catalyzes the reaction ATP L-threonine tRNAThr AMP diphosphate L-threonyl-tRNAThr | GAOABQK02GQAQJ | CDS | 9022 | 2100 | + | 0.34619 |
g3873 | DLA_04295 | GAOABQK02GQAQJ | CDS | 11321 | 3717 | + | 0.304278 | |
g3874 | DLA_04296 | GAOABQK02GQAQJ | CDS | 15230 | 2094 | + | 0.2617 | |
g3875 | DLA_11580 | GAOABQK02GQAQJ | CDS | 17355 | 900 | + | 0.268889 | |
g3876 | DLA_04297 | GAOABQK02GQAQJ | CDS | 18461 | 510 | - | 0.35098 | |
g3877 | DLA_04298 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family expressed in pstO cells | GAOABQK02GQAQJ | CDS | 20246 | 1581 | + | 0.31246 |
g3878 | DLA_04299 | GAOABQK02GQAQJ | CDS | 22235 | 1458 | - | 0.312071 | |
g3879 | DLA_04301 | GAOABQK02GQAQJ | CDS | 24809 | 1356 | + | 0.276549 | |
g388 | DLA_00432 | contig05409_1.exp | CDS | 890059 | 348 | + | 0.275862 | |
g3880 | DLA_04302 | very similar to human GPSN2 contains a 3-oxo-5-alpha-steroid 4-dehydrogenase C-terminal domain and 4 putative transmembrane domains | GAOABQK02GQAQJ | CDS | 26461 | 885 | - | 0.325424 |
g3881 | DLA_04303 | GAOABQK02GQAQJ | CDS | 27927 | 3081 | + | 0.346641 | |
g3882 | DLA_04304 | GAOABQK02GQAQJ | CDS | 31412 | 1377 | + | 0.294118 | |
g3883 | DLA_04305 | GAOABQK02GQAQJ | CDS | 32831 | 864 | - | 0.278935 | |
g3884 | DLA_04306 | GAOABQK02GQAQJ | CDS | 33809 | 1815 | + | 0.272727 | |
g3885 | DLA_04308 | GAOABQK02GQAQJ | CDS | 35639 | 669 | - | 0.298954 | |
g3886 | DLA_04309 | GAOABQK02GQAQJ | CDS | 36507 | 630 | - | 0.277778 | |
g3887 | DLA_04310 | GAOABQK02GQAQJ | CDS | 37261 | 3075 | - | 0.275122 | |
g3888 | DLA_04311 | GAOABQK02GQAQJ | CDS | 40778 | 1596 | + | 0.281328 | |
g3889 | DLA_04312 | GAOABQK02GQAQJ | CDS | 42561 | 1743 | - | 0.423408 | |
g389 | DLA_00433 | contig05409_1.exp | CDS | 890516 | 936 | - | 0.313034 | |
g3890 | DLA_04313 | GAOABQK02GQAQJ | CDS | 44882 | 2739 | + | 0.318364 | |
g3891 | DLA_04314 | GAOABQK02GQAQJ | CDS | 47913 | 1554 | - | 0.258687 | |
g3892 | DLA_04315 | GAOABQK02GQAQJ | CDS | 49981 | 3153 | + | 0.313987 | |
g3893 | DLA_04316 | GAOABQK02GQAQJ | CDS | 53421 | 756 | + | 0.320106 | |
g3894 | DLA_04317 | homolog of the mammalian flavocytochrome B small subunit p22phox essential for spore formation | GAOABQK02GQAQJ | CDS | 54447 | 321 | - | 0.336449 |
g3895 | DLA_04318 | GAOABQK02GQAQJ | CDS | 55405 | 1104 | + | 0.291667 | |
g3896 | DLA_04320 | GAOABQK02GQAQJ | CDS | 57187 | 750 | - | 0.316 | |
g3897 | DLA_11581 | GAOABQK02GQAQJ | CDS | 58308 | 699 | + | 0.317597 | |
g3898 | DLA_04321 | GAOABQK02GQAQJ | CDS | 60841 | 1494 | + | 0.317938 | |
g3899 | DLA_11582 | GAOABQK02GQAQJ | CDS | 62736 | 381 | + | 0.244094 | |
g39 | DLA_00043 | contig05409_1.exp | CDS | 98061 | 3027 | - | 0.317146 | |
g390 | DLA_00434 | contig05409_1.exp | CDS | 892125 | 681 | + | 0.330396 | |
g3900 | DLA_04322 | GAOABQK02GQAQJ | CDS | 63307 | 1146 | - | 0.28534 | |
g3901 | DLA_04323 | GAOABQK02GQAQJ | CDS | 65005 | 573 | - | 0.326353 | |
g3902 | DLA_04324 | rab family small GTPase involved in vesicle fusion during endocytosis there is another rab7 homolog rab7B | GAOABQK02GQAQJ | CDS | 66343 | 606 | + | 0.344884 |
g3903 | DLA_04325 | GAOABQK02GQAQJ | CDS | 67354 | 5130 | + | 0.300585 | |
g3904 | DLA_04326 | GAOABQK02GQAQJ | CDS | 72926 | 816 | + | 0.341912 | |
g3905 | DLA_04327 | GAOABQK02GQAQJ | CDS | 74148 | 1413 | - | 0.277424 | |
g3906 | DLA_04328 | GAOABQK02GQAQJ | CDS | 75843 | 465 | + | 0.266667 | |
g3907 | DLA_04329 | GAOABQK02GQAQJ | CDS | 76501 | 2016 | - | 0.313988 | |
g3908 | DLA_04331 | conserved NMD3 protein which in S. cerevisiae is involved in the nuclear export of the large ribosomal subunit | GAOABQK02GQAQJ | CDS | 79531 | 1566 | + | 0.349298 |
g3909 | DLA_04333 | GAOABQK02GQAQJ | CDS | 81507 | 7707 | + | 0.359284 | |
g391 | DLA_00435 | contig05409_1.exp | CDS | 893058 | 660 | - | 0.290909 | |
g3910 | DLA_04334 | GAOABQK02GQAQJ | CDS | 89674 | 1590 | + | 0.271069 | |
g3911 | DLA_04335 | GAOABQK02GQAQJ | CDS | 91426 | 1416 | + | 0.292373 | |
g3912 | DLA_04336 | GAOABQK02GQAQJ | CDS | 93709 | 2934 | + | 0.304363 | |
g3913 | DLA_04337 | GAOABQK02GQAQJ | CDS | 96909 | 1896 | + | 0.310127 | |
g3914 | DLA_04338 | GAOABQK02GQAQJ | CDS | 99910 | 4308 | + | 0.275534 | |
g3915 | DLA_04339 | GAOABQK02GQAQJ | CDS | 104573 | 1161 | - | 0.3118 | |
g3916 | DLA_04340 | GAOABQK02GQAQJ | CDS | 106596 | 486 | + | 0.248971 | |
g3917 | DLA_04341 | GAOABQK02GQAQJ | CDS | 107209 | 2583 | - | 0.329462 | |
g3918 | DLA_04343 | GAOABQK02GQAQJ | CDS | 111354 | 2523 | - | 0.317876 | |
g3919 | DLA_04345 | GAOABQK02GQAQJ | CDS | 114626 | 1341 | - | 0.328859 | |
g392 | DLA_00436 | contig05409_1.exp | CDS | 893873 | 2271 | - | 0.317922 | |
g3920 | DLA_04346 | GAOABQK02GQAQJ | CDS | 117303 | 2034 | - | 0.362832 | |
g3921 | DLA_04348 | GAOABQK02GQAQJ | CDS | 124814 | 1776 | - | 0.346284 | |
g3922 | DLA_04349 | GAOABQK02GQAQJ | CDS | 127874 | 927 | + | 0.299892 | |
g3923 | DLA_04350 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis | GAOABQK02GQAQJ | CDS | 129732 | 1560 | + | 0.350641 |
g3924 | DLA_04351 | GAOABQK02GQAQJ | CDS | 131471 | 1107 | - | 0.285456 | |
g3925 | DLA_04352 | GAOABQK02GQAQJ | CDS | 133089 | 2337 | + | 0.348738 | |
g3926 | DLA_04353 | GAOABQK02GQAQJ | CDS | 136067 | 750 | + | 0.342667 | |
g3927 | DLA_04354 | GAOABQK02GQAQJ | CDS | 137417 | 1680 | + | 0.26131 | |
g3928 | DLA_04355 | GAOABQK02GQAQJ | CDS | 139507 | 1407 | - | 0.276475 | |
g3929 | DLA_04356 | GAOABQK02GQAQJ | CDS | 141452 | 1704 | + | 0.266432 | |
g393 | DLA_00437 | contig05409_1.exp | CDS | 897322 | 1281 | - | 0.360656 | |
g3930 | DLA_04357 | GAOABQK02GQAQJ | CDS | 143502 | 1746 | + | 0.271478 | |
g3931 | DLA_04360 | GAOABQK02GQAQJ | CDS | 146595 | 768 | + | 0.345052 | |
g3932 | DLA_04361 | GAOABQK02GQAQJ | CDS | 147541 | 963 | - | 0.292835 | |
g3933 | DLA_04362 | GAOABQK02GQAQJ | CDS | 149257 | 885 | + | 0.352542 | |
g3934 | DLA_04363 | GAOABQK02GQAQJ | CDS | 151071 | 2484 | + | 0.355878 | |
g3935 | DLA_04364 | GAOABQK02GQAQJ | CDS | 153849 | 1608 | - | 0.284204 | |
g3936 | DLA_04365 | GAOABQK02GQAQJ | CDS | 155844 | 531 | + | 0.365348 | |
g3937 | DLA_04366 | GAOABQK02GQAQJ | CDS | 156890 | 882 | + | 0.369615 | |
g3938 | DLA_04367 | GAOABQK02GQAQJ | CDS | 158155 | 1395 | + | 0.28172 | |
g3939 | DLA_04368 | similar to diaminopimelate decarboxylase which catalyzes the reaction meso-26-diaminoheptanedioate L-lysine COsub2sub | GAOABQK02GQAQJ | CDS | 159687 | 1287 | + | 0.351204 |
g394 | DLA_00438 | contig05409_1.exp | CDS | 899240 | 3717 | + | 0.347592 | |
g3940 | DLA_04369 | GAOABQK02GQAQJ | CDS | 161266 | 714 | - | 0.260504 | |
g3941 | DLA_04370 | GAOABQK02GQAQJ | CDS | 162548 | 1692 | + | 0.277187 | |
g3942 | DLA_04371 | GAOABQK02GQAQJ | CDS | 164289 | 921 | - | 0.283388 | |
g3943 | DLA_11583 | GAOABQK02GQAQJ | CDS | 165374 | 756 | + | 0.257937 | |
g3944 | DLA_11584 | GAOABQK02GQAQJ | CDS | 166360 | 564 | + | 0.27305 | |
g3945 | DLA_04372 | GAOABQK02GQAQJ | CDS | 166969 | 1644 | + | 0.294404 | |
g3946 | DLA_04374 | GAOABQK02GQAQJ | CDS | 169675 | 2571 | + | 0.33839 | |
g3947 | DLA_04375 | GAOABQK02GQAQJ | CDS | 172393 | 984 | + | 0.305894 | |
g3948 | DLA_04376 | GAOABQK02GQAQJ | CDS | 173549 | 1701 | + | 0.299824 | |
g3949 | DLA_04378 | GAOABQK02GQAQJ | CDS | 176910 | 1341 | + | 0.296793 | |
g395 | DLA_00439 | contig05409_1.exp | CDS | 903655 | 2490 | - | 0.322088 | |
g3950 | DLA_04379 | GAOABQK02GQAQJ | CDS | 178291 | 708 | - | 0.282486 | |
g3951 | DLA_04381 | GAOABQK02GQAQJ | CDS | 179670 | 243 | - | 0.292181 | |
g3952 | DLA_04382 | GAOABQK02GQAQJ | CDS | 181144 | 1773 | - | 0.275804 | |
g3953 | DLA_04383 | GAOABQK02GQAQJ | CDS | 182974 | 1767 | - | 0.2824 | |
g3954 | DLA_04384 | GAOABQK02GQAQJ | CDS | 184916 | 1560 | - | 0.280128 | |
g3955 | DLA_04385 | GAOABQK02GQAQJ | CDS | 188087 | 1497 | - | 0.275217 | |
g3956 | DLA_11585 | GAOABQK02GQAQJ | CDS | 190055 | 1566 | - | 0.283525 | |
g3957 | DLA_11586 | GAOABQK02GQAQJ | CDS | 191921 | 3147 | - | 0.271052 | |
g3958 | DLA_04387 | GAOABQK02GQAQJ | CDS | 195567 | 1605 | - | 0.299065 | |
g3959 | DLA_04388 | GAOABQK02GQAQJ | CDS | 198231 | 4212 | + | 0.315052 | |
g396 | DLA_00440 | contig05409_1.exp | CDS | 906513 | 717 | + | 0.351464 | |
g3960 | DLA_04389 | GAOABQK02GQAQJ | CDS | 202770 | 3390 | - | 0.314454 | |
g3961 | DLA_04390 | GAOABQK02GQAQJ | CDS | 206694 | 2529 | + | 0.326216 | |
g3962 | DLA_04391 | GAOABQK02GQAQJ | CDS | 209901 | 624 | - | 0.355769 | |
g3963 | DLA_04392 | GAOABQK02GQAQJ | CDS | 211270 | 897 | + | 0.345596 | |
g3964 | DLA_04393 | GAOABQK02GQAQJ | CDS | 212198 | 1650 | - | 0.294545 | |
g3965 | DLA_04394 | GAOABQK02GQAQJ | CDS | 214128 | 2352 | + | 0.299745 | |
g3966 | DLA_04395 | GAOABQK02GQAQJ | CDS | 216873 | 1713 | - | 0.280794 | |
g3967 | DLA_04396 | GAOABQK02GQAQJ | CDS | 218800 | 1065 | - | 0.34554 | |
g3968 | DLA_04397 | GAOABQK02GQAQJ | CDS | 220021 | 1092 | + | 0.311355 | |
g3969 | DLA_04399 | GAOABQK02GQAQJ | CDS | 221578 | 1881 | - | 0.299841 | |
g397 | DLA_00441 | contig05409_1.exp | CDS | 907288 | 2592 | - | 0.346065 | |
g3970 | DLA_04400 | GAOABQK02GQAQJ | CDS | 223975 | 786 | - | 0.28626 | |
g3971 | DLA_04401 | GAOABQK02GQAQJ | CDS | 225336 | 1803 | + | 0.283971 | |
g3972 | DLA_04402 | GAOABQK02GQAQJ | CDS | 227512 | 1854 | - | 0.357605 | |
g3973 | DLA_04403 | GAOABQK02GQAQJ | CDS | 229670 | 378 | - | 0.259259 | |
g3974 | DLA_04404 | GAOABQK02GQAQJ | CDS | 230653 | 6513 | + | 0.340243 | |
g3975 | DLA_04405 | GAOABQK02GQAQJ | CDS | 237427 | 8472 | - | 0.336402 | |
g3976 | DLA_04406 | GAOABQK02GQAQJ | CDS | 246596 | 2556 | + | 0.344679 | |
g3977 | DLA_04407 | contains a selenocysteine residue (U) at position 100 conserved protein which may be involved in protein folding in the endoplasmic reticulum | GAOABQK02GQAQJ | CDS | 249694 | 423 | - | 0.326241 |
g3978 | DLA_04408 | GAOABQK02GQAQJ | CDS | 250730 | 489 | - | 0.321063 | |
g3979 | DLA_04409 | GAOABQK02GQAQJ | CDS | 251452 | 1740 | + | 0.305747 | |
g398 | DLA_00442 | contig05409_1.exp | CDS | 911085 | 2340 | + | 0.334188 | |
g3980 | DLA_04411 | GAOABQK02GQAQJ | CDS | 255747 | 1710 | + | 0.278363 | |
g3981 | DLA_04412 | GAOABQK02GQAQJ | CDS | 257590 | 3237 | + | 0.272783 | |
g3982 | DLA_04414 | GAOABQK02GQAQJ | CDS | 261176 | 1530 | + | 0.290196 | |
g3983 | DLA_04415 | GAOABQK02GQAQJ | CDS | 262829 | 2295 | - | 0.285839 | |
g3984 | DLA_04419 | GAOABQK02GQAQJ | CDS | 268249 | 1218 | + | 0.287356 | |
g3985 | DLA_04420 | GAOABQK02GQAQJ | CDS | 269572 | 1137 | + | 0.313105 | |
g3986 | DLA_04421 | GAOABQK02GQAQJ | CDS | 271206 | 2544 | + | 0.291274 | |
g3987 | DLA_04423 | GAOABQK02GQAQJ | CDS | 274018 | 1083 | + | 0.296399 | |
g3988 | DLA_11587 | GAOABQK02GQAQJ | CDS | 275173 | 1140 | + | 0.347368 | |
g3989 | DLA_04424 | GAOABQK02GQAQJ | CDS | 276434 | 1509 | - | 0.300862 | |
g399 | DLA_00443 | contig05409_1.exp | CDS | 913600 | 978 | - | 0.299591 | |
g3990 | DLA_04425 | GAOABQK02GQAQJ | CDS | 278253 | 1068 | - | 0.367041 | |
g3991 | DLA_04426 | GAOABQK02GQAQJ | CDS | 279816 | 1689 | + | 0.352872 | |
g3992 | DLA_04427 | GAOABQK02GQAQJ | CDS | 281802 | 405 | - | 0.301235 | |
g3993 | DLA_04428 | highly similar to PRS involved in nucleotide histidine and tryptophan biosynthesis | GAOABQK02GQAQJ | CDS | 282706 | 957 | - | 0.3814 |
g3994 | DLA_04429 | GAOABQK02GQAQJ | CDS | 284410 | 6306 | + | 0.333492 | |
g3995 | DLA_04430 | GAOABQK02GQAQJ | CDS | 291152 | 696 | + | 0.258621 | |
g3996 | DLA_04431 | GAOABQK02GQAQJ | CDS | 292091 | 2061 | - | 0.360019 | |
g3997 | DLA_04432 | GAOABQK02GQAQJ | CDS | 296216 | 894 | + | 0.387025 | |
g3998 | DLA_04433 | GAOABQK02GQAQJ | CDS | 297376 | 1206 | + | 0.328358 | |
g3999 | DLA_04434 | GAOABQK02GQAQJ | CDS | 298928 | 4461 | + | 0.355974 | |
g4 | DLA_00005 | contig05409_1.exp | CDS | 9344 | 912 | - | 0.283991 | |
g40 | DLA_00045 | contig05409_1.exp | CDS | 102426 | 2979 | + | 0.327962 | |
g400 | DLA_00444 | contig05409_1.exp | CDS | 914889 | 855 | - | 0.336842 | |
g4000 | DLA_04435 | GAOABQK02GQAQJ | CDS | 303744 | 660 | - | 0.287879 | |
g4001 | DLA_04436 | GAOABQK02GQAQJ | CDS | 304733 | 1698 | + | 0.288575 | |
g4002 | DLA_04437 | GAOABQK02GQAQJ | CDS | 306561 | 1497 | - | 0.309953 | |
g4003 | DLA_04441 | GAOABQK02GQAQJ | CDS | 309821 | 1740 | + | 0.283908 | |
g4004 | DLA_04442 | GAOABQK02GQAQJ | CDS | 312196 | 1584 | + | 0.280303 | |
g4005 | DLA_04443 | GAOABQK02GQAQJ | CDS | 314158 | 1773 | + | 0.29216 | |
g4006 | DLA_04444 | GAOABQK02GQAQJ | CDS | 316239 | 531 | - | 0.33145 | |
g4007 | DLA_04445 | GAOABQK02GQAQJ | CDS | 317094 | 1740 | - | 0.352299 | |
g4008 | DLA_11588 | GAOABQK02GQAQJ | CDS | 319078 | 1617 | + | 0.298701 | |
g4009 | DLA_04446 | GAOABQK02GQAQJ | CDS | 320741 | 1608 | + | 0.284204 | |
g401 | DLA_00445 | contig05409_1.exp | CDS | 916031 | 372 | + | 0.314516 | |
g4010 | DLA_04447 | GAOABQK02GQAQJ | CDS | 322574 | 4710 | + | 0.337367 | |
g4011 | DLA_04450 | GAOABQK02GQAQJ | CDS | 329479 | 546 | + | 0.358974 | |
g4012 | DLA_04451 | GAOABQK02GQAQJ | CDS | 330396 | 939 | - | 0.342918 | |
g4013 | DLA_04452 | GAOABQK02GQAQJ | CDS | 332632 | 2295 | + | 0.332026 | |
g4014 | DLA_04453 | GAOABQK02GQAQJ | CDS | 335411 | 1302 | + | 0.367128 | |
g4015 | DLA_04454 | GAOABQK02GQAQJ | CDS | 338621 | 1038 | - | 0.313102 | |
g4016 | DLA_04455 | GAOABQK02GQAQJ | CDS | 340168 | 1005 | + | 0.351244 | |
g4017 | DLA_04456 | GAOABQK02GQAQJ | CDS | 341531 | 3360 | + | 0.324405 | |
g4018 | DLA_04457 | GAOABQK02GQAQJ | CDS | 345075 | 978 | - | 0.367076 | |
g4019 | DLA_04458 | GAOABQK02GQAQJ | CDS | 346864 | 1266 | + | 0.329384 | |
g402 | DLA_00446 | contig05409_1.exp | CDS | 917255 | 2877 | + | 0.346542 | |
g4020 | DLA_04459 | GAOABQK02GQAQJ | CDS | 348343 | 837 | - | 0.315412 | |
g4021 | DLA_04460 | GAOABQK02GQAQJ | CDS | 350621 | 2406 | + | 0.338321 | |
g4022 | DLA_04461 | GAOABQK02GQAQJ | CDS | 353418 | 750 | - | 0.358667 | |
g4023 | DLA_04463 | GAOABQK02GQAQJ | CDS | 354945 | 1227 | + | 0.376528 | |
g4024 | DLA_04464 | GAOABQK02GQAQJ | CDS | 356294 | 3474 | - | 0.342832 | |
g4025 | DLA_04465 | GAOABQK02GQAQJ | CDS | 361040 | 2100 | + | 0.377619 | |
g4026 | DLA_04466 | belongs to the drugmetabolite transporter (DMT) superfamily similar to D. melanogaster sll human SLC35B2 contains 8 predicted transmembrane domains | GAOABQK02GQAQJ | CDS | 363647 | 1137 | - | 0.373791 |
g4027 | DLA_04467 | GAOABQK02GQAQJ | CDS | 365050 | 1431 | - | 0.348008 | |
g4028 | DLA_04468 | catalyzes the reaction: N-acyl-L-amino acid H2O carboxylate L-amino acid (EC 3.5.1.14) | GAOABQK02GQAQJ | CDS | 366755 | 1248 | + | 0.371795 |
g4029 | DLA_04469 | GAOABQK02GQAQJ | CDS | 368218 | 2319 | - | 0.29323 | |
g403 | DLA_00447 | contig05409_1.exp | CDS | 920565 | 2895 | - | 0.331606 | |
g4030 | DLA_04470 | GAOABQK02GQAQJ | CDS | 371035 | 2208 | - | 0.288496 | |
g4031 | DLA_04471 | GAOABQK02GQAQJ | CDS | 374288 | 1326 | + | 0.294872 | |
g4032 | DLA_04472 | catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine | GAOABQK02GQAQJ | CDS | 375881 | 852 | - | 0.347418 |
g4033 | DLA_04473 | GAOABQK02GQAQJ | CDS | 378068 | 4164 | + | 0.321085 | |
g4034 | DLA_04474 | weakly similar to hssA2C7E family proteins has a similar gene structure with a N terminal 13 nt exon | GAOABQK02GQAQJ | CDS | 382657 | 222 | - | 0.324324 |
g4035 | DLA_04475 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | GAOABQK02GQAQJ | CDS | 383387 | 1971 | - | 0.33587 |
g4036 | DLA_04477 | GAOABQK02GQAQJ | CDS | 386246 | 1767 | - | 0.301075 | |
g4037 | DLA_04478 | GAOABQK02GQAQJ | CDS | 388513 | 2502 | + | 0.328137 | |
g4038 | DLA_04479 | GAOABQK02GQAQJ | CDS | 391506 | 795 | + | 0.283019 | |
g4039 | DLA_04480 | GAOABQK02GQAQJ | CDS | 392617 | 1245 | - | 0.360643 | |
g404 | DLA_00448 | contig05409_1.exp | CDS | 923911 | 1050 | + | 0.325714 | |
g4040 | DLA_04481 | GAOABQK02GQAQJ | CDS | 394557 | 1035 | - | 0.342995 | |
g4041 | DLA_04482 | GAOABQK02GQAQJ | CDS | 395900 | 225 | + | 0.302222 | |
g4042 | DLA_04483 | GAOABQK02GQAQJ | CDS | 396375 | 1032 | - | 0.309109 | |
g4043 | DLA_04485 | catalyzes the reaction RX glutathione HX R-S-glutathione | GAOABQK02GQAQJ | CDS | 398604 | 591 | + | 0.357022 |
g4044 | DLA_04486 | GAOABQK02GQAQJ | CDS | 399622 | 591 | + | 0.319797 | |
g4045 | DLA_04487 | GAOABQK02GQAQJ | CDS | 400910 | 1077 | + | 0.336119 | |
g4046 | DLA_04488 | GAOABQK02GQAQJ | CDS | 402195 | 2856 | - | 0.32458 | |
g4047 | DLA_04489 | GAOABQK02GQAQJ | CDS | 405489 | 2466 | - | 0.301298 | |
g4048 | DLA_04490 | GAOABQK02GQAQJ | CDS | 409309 | 1011 | + | 0.326409 | |
g4049 | DLA_04491 | GAOABQK02GQAQJ | CDS | 410702 | 240 | + | 0.329167 | |
g405 | DLA_00449 | contig05409_1.exp | CDS | 925376 | 498 | + | 0.381526 | |
g4050 | DLA_04492 | GAOABQK02GQAQJ | CDS | 411092 | 1170 | - | 0.351282 | |
g4051 | DLA_04494 | GAOABQK02GQAQJ | CDS | 413880 | 2538 | - | 0.300236 | |
g4052 | DLA_04495 | GAOABQK02GQAQJ | CDS | 417011 | 207 | + | 0.338164 | |
g4053 | DLA_04496 | GAOABQK02GQAQJ | CDS | 417761 | 258 | + | 0.317829 | |
g4054 | DLA_04497 | GAOABQK02GQAQJ | CDS | 418335 | 1023 | - | 0.312805 | |
g4055 | DLA_04498 | GAOABQK02GQAQJ | CDS | 420132 | 2526 | - | 0.337688 | |
g4056 | DLA_04499 | GAOABQK02GQAQJ | CDS | 423136 | 4071 | + | 0.338983 | |
g4057 | DLA_04500 | GAOABQK02GQAQJ | CDS | 427888 | 618 | - | 0.276699 | |
g4058 | DLA_04501 | GAOABQK02GQAQJ | CDS | 428695 | 3135 | - | 0.280702 | |
g4059 | DLA_04502 | GAOABQK02GQAQJ | CDS | 432284 | 3225 | + | 0.373643 | |
g406 | DLA_00450 | contig05409_1.exp | CDS | 926380 | 942 | - | 0.304671 | |
g4060 | DLA_04503 | GAOABQK02GQAQJ | CDS | 435813 | 933 | + | 0.332262 | |
g4061 | DLA_04504 | GAOABQK02GQAQJ | CDS | 437315 | 603 | + | 0.331675 | |
g4062 | DLA_04505 | GAOABQK02GQAQJ | CDS | 438051 | 5988 | - | 0.305945 | |
g4063 | DLA_04506 | GAOABQK02GQAQJ | CDS | 444325 | 1506 | - | 0.284861 | |
g4064 | DLA_04507 | GAOABQK02GQAQJ | CDS | 446181 | 3531 | + | 0.287737 | |
g4065 | DLA_04509 | GAOABQK02GQAQJ | CDS | 450958 | 357 | + | 0.333333 | |
g4066 | DLA_04510 | GAOABQK02GQAQJ | CDS | 451712 | 237 | + | 0.362869 | |
g4067 | DLA_04511 | GAOABQK02GQAQJ | CDS | 452517 | 513 | + | 0.335283 | |
g4068 | DLA_04512 | GAOABQK02GQAQJ | CDS | 453140 | 1473 | - | 0.283096 | |
g4069 | DLA_04513 | GAOABQK02GQAQJ | CDS | 454899 | 1164 | + | 0.305842 | |
g407 | DLA_00451 | component of the conserved Paf1 complex a multifunctional complex involved in histone methylation and plays a role in RNA elongation and processing defects in human CDC73 cause hyperparathyroidism-jaw tumor syndrome (HPT-JT) parathyroid carcinoma and hyperparathyroidism (FIHP) | contig05409_1.exp | CDS | 927626 | 1449 | - | 0.342995 |
g4070 | DLA_04514 | GAOABQK02GQAQJ | CDS | 456587 | 789 | + | 0.320659 | |
g4071 | DLA_04515 | GAOABQK02GQAQJ | CDS | 458487 | 3120 | + | 0.324038 | |
g4072 | DLA_04516 | GAOABQK02GQAQJ | CDS | 461947 | 666 | - | 0.364865 | |
g4073 | DLA_04517 | GAOABQK02GQAQJ | CDS | 463307 | 387 | + | 0.312661 | |
g4074 | DLA_04518 | similar to human TBC1D22B S. pombe gyp1 | GAOABQK02GQAQJ | CDS | 464498 | 1419 | + | 0.331924 |
g4075 | DLA_04519 | GAOABQK02GQAQJ | CDS | 466040 | 2841 | - | 0.339317 | |
g4076 | DLA_11589 | GAOABQK02GQAQJ | CDS | 469911 | 1095 | - | 0.32968 | |
g4077 | DLA_04520 | GAOABQK02GQAQJ | CDS | 471334 | 3888 | + | 0.33642 | |
g4078 | DLA_04521 | GAOABQK02GQAQJ | CDS | 475541 | 408 | - | 0.414216 | |
g4079 | DLA_04522 | GAOABQK02GQAQJ | CDS | 476325 | 1695 | - | 0.276106 | |
g408 | DLA_00453 | catalyzes the reaction L-glutaminyl-peptide 5-oxoprolyl-peptide NHsub3sub during the biosynthesis of pyroglutamyl peptides | contig05409_1.exp | CDS | 929912 | 1032 | - | 0.312984 |
g4080 | DLA_04523 | member of the alpha-actininspectrin superfamily dimerizes with cortexillin I involved in cytokinesis and development and associates with the actin cytoskeleton | GAOABQK02GQAQJ | CDS | 478736 | 1263 | + | 0.34521 |
g4081 | DLA_04524 | GAOABQK02GQAQJ | CDS | 480168 | 1824 | - | 0.332785 | |
g4082 | DLA_04525 | GAOABQK02GQAQJ | CDS | 482239 | 897 | - | 0.322185 | |
g4083 | DLA_04526 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | GAOABQK02GQAQJ | CDS | 483386 | 2190 | - | 0.336073 |
g4084 | DLA_04527 | GAOABQK02GQAQJ | CDS | 485696 | 1239 | + | 0.277643 | |
g4085 | DLA_04528 | contains a PPI_Ypi1 domain which is predicted to be involved in protein phosphatase regulation | GAOABQK02GQAQJ | CDS | 487132 | 318 | + | 0.308176 |
g4086 | DLA_04529 | GAOABQK02GQAQJ | CDS | 488304 | 657 | + | 0.340944 | |
g4087 | DLA_04530 | GAOABQK02GQAQJ | CDS | 489756 | 450 | - | 0.317778 | |
g4088 | DLA_04531 | GAOABQK02GQAQJ | CDS | 490671 | 2940 | + | 0.337415 | |
g4089 | DLA_04532 | GAOABQK02GQAQJ | CDS | 494608 | 471 | + | 0.265393 | |
g409 | DLA_00454 | contig05409_1.exp | CDS | 931801 | 3261 | - | 0.336093 | |
g4090 | DLA_04533 | GAOABQK02GQAQJ | CDS | 495469 | 1452 | + | 0.362948 | |
g4091 | DLA_04534 | GAOABQK02GQAQJ | CDS | 497049 | 930 | - | 0.319355 | |
g4092 | DLA_04535 | GAOABQK02GQAQJ | CDS | 498189 | 870 | + | 0.345977 | |
g4093 | DLA_04536 | GAOABQK02GQAQJ | CDS | 499569 | 666 | + | 0.339339 | |
g4094 | DLA_04537 | GAOABQK02GQAQJ | CDS | 500624 | 5160 | + | 0.332752 | |
g4095 | DLA_04539 | GAOABQK02GQAQJ | CDS | 508145 | 1467 | + | 0.362645 | |
g4096 | DLA_04540 | similar to importin-7 and importin-8 from numerous eukaryotes involved in nuclear protein import | GAOABQK02GQAQJ | CDS | 510001 | 3264 | - | 0.345588 |
g4097 | DLA_04541 | GAOABQK02GQAQJ | CDS | 513665 | 966 | + | 0.271222 | |
g4098 | DLA_04542 | GAOABQK02GQAQJ | CDS | 514858 | 1209 | - | 0.321754 | |
g4099 | DLA_04543 | GAOABQK02GQAQJ | CDS | 516529 | 2184 | - | 0.35989 | |
g41 | DLA_00046 | contig05409_1.exp | CDS | 106338 | 582 | + | 0.343643 | |
g410 | DLA_00455 | contig05409_1.exp | CDS | 935846 | 741 | + | 0.337382 | |
g4100 | DLA_04544 | GAOABQK02GQAQJ | CDS | 518878 | 1035 | + | 0.353623 | |
g4101 | DLA_04546 | GAOABQK02GQAQJ | CDS | 520839 | 1074 | - | 0.342644 | |
g4102 | DLA_04547 | GAOABQK02GQAQJ | CDS | 522307 | 2175 | + | 0.316322 | |
g4103 | DLA_04549 | GAOABQK02GQAQJ | CDS | 524927 | 930 | + | 0.335484 | |
g4104 | DLA_04550 | catalyzes the reaction (S)-malate NADPsupsup pyruvate COsub2sub NADPH Hsupsup transcriptionally regulated by SrfA | GAOABQK02GQAQJ | CDS | 526539 | 1635 | + | 0.382263 |
g4105 | DLA_04551 | GAOABQK02GQAQJ | CDS | 528894 | 3207 | + | 0.337387 | |
g4106 | DLA_04552 | GAOABQK02GQAQJ | CDS | 532254 | 225 | - | 0.275556 | |
g4107 | DLA_04553 | GAOABQK02GQAQJ | CDS | 532794 | 1113 | + | 0.327942 | |
g4108 | DLA_04554 | GAOABQK02GQAQJ | CDS | 534500 | 795 | + | 0.289308 | |
g4109 | DLA_04555 | GAOABQK02GQAQJ | CDS | 536126 | 693 | + | 0.324675 | |
g411 | DLA_00456 | component of the condensin I complex required for conversion of interphase chromatin into mitotic condensed chromosomes | contig05409_1.exp | CDS | 936869 | 4455 | + | 0.318294 |
g4110 | DLA_04556 | GAOABQK02GQAQJ | CDS | 537023 | 1875 | - | 0.293333 | |
g4111 | DLA_04558 | GAOABQK02GQAQJ | CDS | 540066 | 2472 | + | 0.343447 | |
g4112 | DLA_04559 | GAOABQK02GQAQJ | CDS | 542937 | 870 | - | 0.312644 | |
g4113 | DLA_04562 | GAOABQK02GQAQJ | CDS | 544754 | 258 | - | 0.344961 | |
g4114 | DLA_04563 | GAOABQK02GQAQJ | CDS | 545330 | 783 | + | 0.266922 | |
g4115 | DLA_04564 | conserved chaperone protein which promotes assembly of the 20S proteasome may form a dimer with psmG1 and act in concert with psmG3psmG4 | GAOABQK02GQAQJ | CDS | 546301 | 780 | - | 0.289744 |
g4116 | DLA_04565 | GAOABQK02GQAQJ | CDS | 547738 | 1404 | - | 0.36396 | |
g4117 | DLA_04566 | GAOABQK02GQAQJ | CDS | 549642 | 1053 | + | 0.311491 | |
g4118 | DLA_04567 | GAOABQK02GQAQJ | CDS | 550821 | 729 | + | 0.334705 | |
g4119 | DLA_04568 | GAOABQK02GQAQJ | CDS | 551695 | 2496 | - | 0.290064 | |
g412 | DLA_00457 | contig05409_1.exp | CDS | 941451 | 873 | - | 0.272623 | |
g4120 | DLA_11590 | GAOABQK02GQAQJ | CDS | 555164 | 423 | - | 0.316785 | |
g4121 | DLA_04569 | GAOABQK02GQAQJ | CDS | 555779 | 498 | - | 0.299197 | |
g4122 | DLA_04570 | GAOABQK02GQAQJ | CDS | 556631 | 2400 | + | 0.305 | |
g4123 | DLA_04571 | GAOABQK02GQAQJ | CDS | 559281 | 618 | - | 0.323625 | |
g4124 | DLA_04572 | GAOABQK02GQAQJ | CDS | 560413 | 2169 | - | 0.294606 | |
g4125 | DLA_04573 | GAOABQK02GQAQJ | CDS | 562647 | 1758 | + | 0.294653 | |
g4126 | DLA_04574 | GAOABQK02GQAQJ | CDS | 564596 | 351 | - | 0.450142 | |
g4127 | DLA_04575 | homolog of H. sapiens TNPO12 and S. cervisiae KAP104 (karyopherin 104) involved in nuclear protein import | GAOABQK02GQAQJ | CDS | 565957 | 2766 | - | 0.353941 |
g4128 | DLA_04576 | GAOABQK02GQAQJ | CDS | 569096 | 276 | + | 0.268116 | |
g4129 | DLA_04577 | contains at least three transmembrane domains ortholog of mannose-P-dolichol utilization defect 1 protein MPDU1 | GAOABQK02GQAQJ | CDS | 569562 | 705 | - | 0.347518 |
g413 | DLA_00458 | contig05409_1.exp | CDS | 942679 | 849 | + | 0.322733 | |
g4130 | DLA_04578 | belongs to the synaptobrevin family ortholog of human SEC22B contains a longin domain and a v-snare coiled-coil domain contains 1 predicted transmembrane domain | GAOABQK02GQAQJ | CDS | 570431 | 627 | - | 0.283892 |
g4131 | DLA_04579 | ortholog of the human CPSF4 and yeast YTH1 the 30 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs human CPSF4 binds RNA polymers with a preference for poly(U) | GAOABQK02GQAQJ | CDS | 571926 | 1626 | + | 0.376999 |
g4132 | DLA_04581 | GAOABQK02GQAQJ | CDS | 575009 | 1584 | - | 0.28346 | |
g4133 | DLA_04582 | GAOABQK02GQAQJ | CDS | 576666 | 600 | + | 0.283333 | |
g4134 | DLA_04583 | GAOABQK02GQAQJ | CDS | 577478 | 2601 | + | 0.315263 | |
g4135 | DLA_04584 | GAOABQK02GQAQJ | CDS | 580189 | 2076 | - | 0.310694 | |
g4136 | DLA_04585 | GAOABQK02GQAQJ | CDS | 582882 | 1491 | - | 0.369551 | |
g4137 | DLA_04586 | GAOABQK02GQAQJ | CDS | 585362 | 3645 | + | 0.340192 | |
g4138 | DLA_04587 | GAOABQK02GQAQJ | CDS | 589685 | 1446 | + | 0.301521 | |
g4139 | DLA_04588 | GAOABQK02GQAQJ | CDS | 591758 | 906 | + | 0.400662 | |
g414 | DLA_00459 | ortholog of human and S. pombe nucleolar protein 58 members of this family are involved in a variety of functions during pre-mRNA splicing | contig05409_1.exp | CDS | 943705 | 1881 | - | 0.353535 |
g4140 | DLA_04589 | GAOABQK02GQAQJ | CDS | 593088 | 900 | - | 0.343333 | |
g4141 | DLA_04590 | GAOABQK02GQAQJ | CDS | 594576 | 1932 | - | 0.365942 | |
g4142 | DLA_04591 | GAOABQK02GQAQJ | CDS | 598636 | 1410 | + | 0.364539 | |
g4143 | DLA_04592 | GAOABQK02GQAQJ | CDS | 600344 | 528 | + | 0.320076 | |
g4144 | DLA_04593 | GAOABQK02GQAQJ | CDS | 601402 | 2871 | + | 0.333682 | |
g4145 | DLA_04594 | ortholog of the human PPP2R4 (PTPA) that stimulates the phosphotyrosyl phosphatase activity of PP2A in the presence of ATP and Mg(2) in vitro | GAOABQK02GQAQJ | CDS | 604651 | 963 | - | 0.345794 |
g4146 | DLA_11591 | GAOABQK02GQAQJ | CDS | 605799 | 1113 | + | 0.319856 | |
g4147 | DLA_04595 | GAOABQK02GQAQJ | CDS | 607095 | 1614 | + | 0.348203 | |
g4148 | DLA_04596 | GAOABQK02GQAQJ | CDS | 608908 | 2157 | + | 0.265647 | |
g4149 | DLA_04597 | GAOABQK02GQAQJ | CDS | 611526 | 2625 | - | 0.32419 | |
g415 | DLA_00460 | contig05409_1.exp | CDS | 945875 | 1254 | + | 0.339713 | |
g4150 | DLA_04598 | GAOABQK02GQAQJ | CDS | 614909 | 678 | - | 0.312684 | |
g4151 | DLA_04599 | GAOABQK02GQAQJ | CDS | 616307 | 1068 | - | 0.34176 | |
g4152 | DLA_04600 | GAOABQK02GQAQJ | CDS | 618386 | 861 | + | 0.300813 | |
g4153 | DLA_04601 | GAOABQK02GQAQJ | CDS | 620307 | 2193 | + | 0.367533 | |
g4154 | DLA_04602 | similar to human PRSS16 (thymus-specific serine protease) contains a putative signal peptide | GAOABQK02GQAQJ | CDS | 622759 | 1473 | - | 0.382892 |
g4155 | DLA_11592 | GAOABQK02GQAQJ | CDS | 624444 | 1029 | - | 0.300292 | |
g4156 | DLA_04603 | GAOABQK02GQAQJ | CDS | 625870 | 1821 | - | 0.291049 | |
g4157 | DLA_04604 | GAOABQK02GQAQJ | CDS | 627845 | 1929 | + | 0.365993 | |
g4158 | DLA_04605 | GAOABQK02GQAQJ | CDS | 630116 | 7644 | + | 0.354003 | |
g4159 | DLA_04606 | GAOABQK02GQAQJ | CDS | 638077 | 1005 | - | 0.287562 | |
g416 | DLA_00461 | contig05409_1.exp | CDS | 947446 | 1215 | + | 0.412346 | |
g4160 | DLA_04607 | GAOABQK02GQAQJ | CDS | 639487 | 1248 | + | 0.345353 | |
g4161 | DLA_04609 | GAOABQK02GQAQJ | CDS | 641096 | 873 | + | 0.352806 | |
g4162 | DLA_11593 | GAOABQK02GQAQJ | CDS | 642114 | 288 | - | 0.239583 | |
g4163 | DLA_04610 | GAOABQK02GQAQJ | CDS | 643235 | 2076 | - | 0.307803 | |
g4164 | DLA_04611 | GAOABQK02GQAQJ | CDS | 645470 | 1110 | - | 0.313514 | |
g4165 | DLA_04612 | GAOABQK02GQAQJ | CDS | 647101 | 3552 | + | 0.341216 | |
g4166 | DLA_04613 | GAOABQK02GQAQJ | CDS | 650908 | 1155 | + | 0.4 | |
g4167 | DLA_04614 | GAOABQK02GQAQJ | CDS | 652471 | 2319 | - | 0.362656 | |
g4168 | DLA_04616 | GAOABQK02GQAQJ | CDS | 655797 | 1179 | + | 0.318914 | |
g4169 | DLA_04617 | GAOABQK02GQAQJ | CDS | 657047 | 3006 | - | 0.314039 | |
g417 | DLA_00462 | contig05409_1.exp | CDS | 949108 | 918 | + | 0.392157 | |
g4170 | DLA_04618 | GAOABQK02GQAQJ | CDS | 660765 | 2952 | - | 0.330285 | |
g4171 | DLA_04619 | GAOABQK02GQAQJ | CDS | 663991 | 369 | + | 0.314363 | |
g4172 | DLA_04620 | GAOABQK02GQAQJ | CDS | 664719 | 2034 | + | 0.360865 | |
g4173 | DLA_04621 | GAOABQK02GQAQJ | CDS | 667576 | 1077 | + | 0.413185 | |
g4174 | DLA_04622 | GAOABQK02GQAQJ | CDS | 668821 | 843 | - | 0.302491 | |
g4175 | DLA_04623 | GAOABQK02GQAQJ | CDS | 670078 | 690 | + | 0.402899 | |
g4176 | DLA_04624 | GAOABQK02GQAQJ | CDS | 671094 | 1299 | - | 0.342571 | |
g4177 | DLA_04625 | catalyzes the reaction ATP L-Tyrosine tRNATyr AMP diphosphate L-tyrosyl-tRNATyr | GAOABQK02GQAQJ | CDS | 672814 | 1173 | - | 0.333333 |
g4178 | DLA_11594 | GAOABQK02GQAQJ | CDS | 674161 | 1458 | - | 0.33882 | |
g4179 | DLA_11595 | GAOABQK02GQAQJ | CDS | 675950 | 945 | + | 0.330159 | |
g418 | DLA_00463 | contig05409_1.exp | CDS | 950309 | 531 | - | 0.374765 | |
g4180 | DLA_04626 | GAOABQK02GQAQJ | CDS | 677461 | 2697 | + | 0.31294 | |
g4181 | DLA_04627 | GAOABQK02GQAQJ | CDS | 680594 | 1872 | + | 0.341346 | |
g4182 | DLA_04628 | GAOABQK02GQAQJ | CDS | 682532 | 507 | - | 0.254438 | |
g4183 | DLA_11596 | GAOABQK02GQAQJ | CDS | 684628 | 2286 | + | 0.317148 | |
g4184 | DLA_04629 | GAOABQK02GQAQJ | CDS | 687366 | 594 | + | 0.358586 | |
g4185 | DLA_04630 | GAOABQK02GQAQJ | CDS | 688201 | 1161 | - | 0.296296 | |
g4186 | DLA_04631 | homolog of human EXOSC3 (exosome component 3) and S. cerevisiae RRP40 (Ribosomal RNA-processing protein 40) S. cerevisiae RRP40 is a component of the exosome 3'-5' exoribonuclease complex but lacks exonuclease activity | GAOABQK02GQAQJ | CDS | 690043 | 687 | + | 0.295488 |
g4187 | DLA_04632 | GAOABQK02GQAQJ | CDS | 690956 | 1743 | - | 0.343087 | |
g4188 | DLA_04633 | GAOABQK02GQAQJ | CDS | 693337 | 654 | - | 0.318043 | |
g4189 | DLA_04634 | GAOABQK02GQAQJ | CDS | 695751 | 2340 | - | 0.311111 | |
g419 | DLA_00464 | contig05409_1.exp | CDS | 951487 | 711 | + | 0.326301 | |
g4190 | DLA_04635 | GAOABQK02GQAQJ | CDS | 698291 | 2691 | - | 0.302861 | |
g4191 | DLA_04636 | GAOABQK02GQAQJ | CDS | 701272 | 678 | + | 0.330383 | |
g4192 | DLA_04637 | GAOABQK02GQAQJ | CDS | 702147 | 366 | - | 0.393443 | |
g4193 | DLA_04638 | GAOABQK02GQAQJ | CDS | 702683 | 1161 | - | 0.30491 | |
g4194 | DLA_04639 | GAOABQK02GQAQJ | CDS | 704404 | 2295 | + | 0.345098 | |
g4195 | DLA_04640 | GAOABQK02GQAQJ | CDS | 707986 | 828 | - | 0.283816 | |
g4196 | DLA_04641 | GAOABQK02GQAQJ | CDS | 709115 | 624 | - | 0.399038 | |
g4197 | DLA_04642 | GAOABQK02GQAQJ | CDS | 710350 | 417 | - | 0.378897 | |
g4198 | DLA_04643 | GAOABQK02GQAQJ | CDS | 711092 | 1665 | + | 0.287688 | |
g4199 | DLA_04644 | GAOABQK02GQAQJ | CDS | 713078 | 1503 | + | 0.322023 | |
g42 | DLA_00049 | contig05409_1.exp | CDS | 108002 | 546 | - | 0.340659 | |
g420 | DLA_00466 | contig05409_1.exp | CDS | 952728 | 1725 | + | 0.350145 | |
g4200 | DLA_04645 | GAOABQK02GQAQJ | CDS | 714652 | 1026 | + | 0.287524 | |
g4201 | DLA_04646 | GAOABQK02GQAQJ | CDS | 715895 | 1050 | + | 0.307619 | |
g4202 | DLA_04647 | GAOABQK02GQAQJ | CDS | 717302 | 945 | - | 0.293122 | |
g4203 | DLA_04648 | GAOABQK02GQAQJ | CDS | 718818 | 1494 | + | 0.309906 | |
g4204 | DLA_04649 | GAOABQK02GQAQJ | CDS | 721613 | 1611 | + | 0.343886 | |
g4205 | DLA_04650 | contains a sac phosphatase domain similar to D. discoideum sac1 similar to D. purpureum protein | GAOABQK02GQAQJ | CDS | 723389 | 3156 | - | 0.295627 |
g4206 | DLA_04652 | GAOABQK02GQAQJ | CDS | 728400 | 453 | - | 0.322296 | |
g4207 | DLA_04653 | GAOABQK02GQAQJ | CDS | 730463 | 612 | + | 0.30719 | |
g4208 | DLA_04654 | similar to animal and plant cystatin A3 member of the stefin cystatin family of cysteine protease inhibitors | GAOABQK02GQAQJ | CDS | 731378 | 297 | - | 0.367003 |
g4209 | DLA_04655 | GAOABQK02GQAQJ | CDS | 732097 | 1335 | + | 0.322846 | |
g421 | DLA_00467 | contig05409_1.exp | CDS | 954526 | 1515 | - | 0.308911 | |
g4210 | DLA_04656 | GAOABQK02GQAQJ | CDS | 733574 | 1152 | - | 0.352431 | |
g4211 | DLA_04658 | GAOABQK02GQAQJ | CDS | 735323 | 2208 | + | 0.317482 | |
g4212 | DLA_04659 | GAOABQK02GQAQJ | CDS | 738036 | 237 | - | 0.291139 | |
g4213 | DLA_04660 | GAOABQK02GQAQJ | CDS | 738437 | 2316 | + | 0.310017 | |
g4214 | DLA_04661 | GAOABQK02GQAQJ | CDS | 741297 | 837 | - | 0.383513 | |
g4215 | DLA_04662 | GAOABQK02GQAQJ | CDS | 742409 | 1620 | + | 0.280247 | |
g4216 | DLA_04663 | GAOABQK02GQAQJ | CDS | 744357 | 2100 | + | 0.32 | |
g4217 | DLA_04664 | putative ortholog of H. sapiens WDR7 also known as TGF-beta resistance-associated protein (TRAG) and rabconnectin-3 beta | GAOABQK02GQAQJ | CDS | 746948 | 3879 | + | 0.333849 |
g4218 | DLA_04665 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | GAOABQK02GQAQJ | CDS | 751139 | 1023 | - | 0.362659 |
g4219 | DLA_04666 | GAOABQK02GQAQJ | CDS | 752872 | 2856 | + | 0.358193 | |
g422 | DLA_00468 | contig05409_1.exp | CDS | 956594 | 576 | + | 0.300347 | |
g4220 | DLA_04667 | GAOABQK02GQAQJ | CDS | 756282 | 2670 | + | 0.341573 | |
g4221 | DLA_04668 | GAOABQK02GQAQJ | CDS | 759166 | 3513 | - | 0.318247 | |
g4222 | DLA_04669 | GAOABQK02GQAQJ | CDS | 763149 | 1296 | + | 0.328704 | |
g4223 | DLA_04670 | GAOABQK02GQAQJ | CDS | 764759 | 1152 | - | 0.293403 | |
g4224 | DLA_04671 | GAOABQK02GQAQJ | CDS | 767132 | 2847 | + | 0.32947 | |
g4225 | DLA_04672 | GAOABQK02GQAQJ | CDS | 770362 | 2007 | - | 0.337319 | |
g4226 | DLA_04673 | GAOABQK02GQAQJ | CDS | 772699 | 858 | + | 0.335664 | |
g4227 | DLA_04674 | GAOABQK02GQAQJ | CDS | 774305 | 2109 | + | 0.329066 | |
g4228 | DLA_04675 | GAOABQK02GQAQJ | CDS | 776472 | 840 | - | 0.32381 | |
g4229 | DLA_04676 | GAOABQK02GQAQJ | CDS | 777709 | 1710 | + | 0.339181 | |
g423 | DLA_00469 | contig05409_1.exp | CDS | 957371 | 1476 | + | 0.382114 | |
g4230 | DLA_04677 | GAOABQK02GQAQJ | CDS | 780151 | 1617 | - | 0.252938 | |
g4231 | DLA_04678 | ortholog of Werner helicase-interacting protein 1 a modulator for initiation or reinitiation events during DNA polymerase delta-mediated DNA synthesis | GAOABQK02GQAQJ | CDS | 782385 | 2436 | + | 0.309113 |
g4232 | DLA_04680 | GAOABQK02GQAQJ | CDS | 785792 | 2157 | + | 0.313398 | |
g4233 | DLA_04681 | GAOABQK02GQAQJ | CDS | 788021 | 867 | - | 0.247982 | |
g4234 | DLA_04682 | GAOABQK02GQAQJ | CDS | 789545 | 1029 | - | 0.316812 | |
g4235 | DLA_04683 | GAOABQK02GQAQJ | CDS | 791783 | 1278 | + | 0.364632 | |
g4236 | DLA_04684 | GAOABQK02GQAQJ | CDS | 793404 | 1899 | + | 0.339126 | |
g4237 | DLA_04685 | GAOABQK02GQAQJ | CDS | 795419 | 2172 | - | 0.337017 | |
g4238 | DLA_11597 | GAOABQK02GQAQJ | CDS | 798949 | 726 | + | 0.378788 | |
g4239 | DLA_11598 | GAOABQK02GQAQJ | CDS | 800106 | 1131 | + | 0.295314 | |
g424 | DLA_00470 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | contig05409_1.exp | CDS | 959789 | 4086 | + | 0.367107 |
g4240 | DLA_04687 | GAOABQK02GQAQJ | CDS | 801644 | 3270 | + | 0.336391 | |
g4241 | DLA_04688 | half transporter consisting of one ABC domain and one transmembrane domain | GAOABQK02GQAQJ | CDS | 805174 | 2526 | - | 0.335709 |
g4242 | DLA_04689 | half transporter consisting of one ABC domain and one transmembrane domain | GAOABQK02GQAQJ | CDS | 808176 | 2577 | + | 0.332557 |
g4243 | DLA_04690 | GAOABQK02GQAQJ | CDS | 810909 | 1698 | + | 0.277974 | |
g4244 | DLA_04691 | GAOABQK02GQAQJ | CDS | 812782 | 1419 | - | 0.338266 | |
g4245 | DLA_04692 | GAOABQK02GQAQJ | CDS | 814534 | 2502 | + | 0.323741 | |
g4246 | DLA_04693 | GAOABQK02GQAQJ | CDS | 817267 | 894 | - | 0.326622 | |
g4247 | DLA_04694 | GAOABQK02GQAQJ | CDS | 818685 | 1863 | - | 0.303274 | |
g4248 | DLA_04695 | GAOABQK02GQAQJ | CDS | 823264 | 1362 | - | 0.351689 | |
g4249 | DLA_04696 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | GAOABQK02GQAQJ | CDS | 825005 | 615 | - | 0.310569 |
g425 | DLA_00471 | contig05409_1.exp | CDS | 964177 | 498 | - | 0.325301 | |
g4250 | DLA_04697 | ortholog of TOP3 a nuclear topoisomerase responsible for relaxing single-stranded negatively-supercoiled DNA | GAOABQK02GQAQJ | CDS | 825795 | 2313 | - | 0.342412 |
g4251 | DLA_11599 | GAOABQK02GQAQJ | CDS | 828638 | 738 | - | 0.327913 | |
g4252 | DLA_04698 | GAOABQK02GQAQJ | CDS | 830244 | 1563 | - | 0.285988 | |
g4253 | DLA_04699 | identified as a suppressor of smlA null mutant cnr4 contains a Cue domain which may be involved in binding ubiquitin-conjugating enzymes | GAOABQK02GQAQJ | CDS | 832465 | 999 | + | 0.382382 |
g4254 | DLA_04700 | GAOABQK02GQAQJ | CDS | 834297 | 2067 | - | 0.355104 | |
g4255 | DLA_04701 | GAOABQK02GQAQJ | CDS | 836544 | 219 | - | 0.296804 | |
g4256 | DLA_04702 | GAOABQK02GQAQJ | CDS | 837570 | 1257 | + | 0.268894 | |
g4257 | DLA_04703 | GAOABQK02GQAQJ | CDS | 838889 | 2607 | - | 0.322593 | |
g4258 | DLA_04705 | GAOABQK02GQAQJ | CDS | 842046 | 2043 | - | 0.380813 | |
g4259 | DLA_04706 | GAOABQK02GQAQJ | CDS | 844698 | 2919 | + | 0.35149 | |
g426 | DLA_00473 | contig05409_1.exp | CDS | 965909 | 2373 | - | 0.326591 | |
g4260 | DLA_04707 | GAOABQK02GQAQJ | CDS | 849064 | 4197 | + | 0.394806 | |
g4261 | DLA_04708 | GAOABQK02GQAQJ | CDS | 853851 | 486 | - | 0.360082 | |
g4262 | DLA_04709 | GAOABQK02GQAQJ | CDS | 854739 | 1293 | + | 0.323279 | |
g4263 | DLA_04710 | GAOABQK02GQAQJ | CDS | 856888 | 486 | + | 0.36214 | |
g4264 | DLA_04711 | GAOABQK02GQAQJ | CDS | 857504 | 849 | - | 0.354535 | |
g4265 | DLA_04712 | GAOABQK02GQAQJ | CDS | 858765 | 528 | + | 0.293561 | |
g4266 | DLA_11600 | GAOABQK02GQAQJ | CDS | 859597 | 255 | - | 0.415686 | |
g4267 | DLA_04713 | GAOABQK02GQAQJ | CDS | 860607 | 1854 | - | 0.340345 | |
g4268 | DLA_04714 | GAOABQK02GQAQJ | CDS | 863577 | 1788 | + | 0.294183 | |
g4269 | DLA_11601 | GAOABQK02GQAQJ | CDS | 865784 | 516 | + | 0.374031 | |
g427 | DLA_00474 | contig05409_1.exp | CDS | 968607 | 879 | - | 0.32537 | |
g4270 | DLA_04715 | GAOABQK02GQAQJ | CDS | 866562 | 2244 | - | 0.299465 | |
g4271 | DLA_04716 | GAOABQK02GQAQJ | CDS | 869762 | 8682 | - | 0.349804 | |
g4272 | DLA_04717 | putative Ca2 channel similar to metazoan polycystin-2 (PKD2) defects in the human PKD2 causes polycystic kidney disease autosomal dominant type 2 (ADPKD2) characterized by progressive formation and enlargement of cysts in both kidneys contains 6 putative transmembrane domains | GAOABQK02GQAQJ | CDS | 878885 | 2247 | - | 0.307076 |
g4273 | DLA_04718 | GAOABQK02GQAQJ | CDS | 881726 | 2331 | - | 0.305877 | |
g4274 | DLA_04719 | GAOABQK02GQAQJ | CDS | 884353 | 2763 | + | 0.295331 | |
g4275 | DLA_04720 | GAOABQK02GQAQJ | CDS | 887264 | 1806 | + | 0.330011 | |
g4276 | DLA_04721 | GAOABQK02GQAQJ | CDS | 889531 | 945 | + | 0.329101 | |
g4277 | DLA_04722 | GAOABQK02GQAQJ | CDS | 890666 | 975 | + | 0.32 | |
g4278 | DLA_04723 | GAOABQK02GQAQJ | CDS | 891932 | 1137 | + | 0.373791 | |
g4279 | DLA_04725 | GAOABQK02GQAQJ | CDS | 894234 | 1044 | + | 0.355364 | |
g428 | DLA_00475 | contig05409_1.exp | CDS | 969756 | 1773 | - | 0.305133 | |
g4280 | DLA_04726 | GAOABQK02GQAQJ | CDS | 895678 | 2187 | + | 0.328304 | |
g4281 | DLA_04728 | GAOABQK02GQAQJ | CDS | 898225 | 873 | - | 0.337915 | |
g4282 | DLA_04729 | GAOABQK02GQAQJ | CDS | 899265 | 1680 | + | 0.29881 | |
g4283 | DLA_04730 | GAOABQK02GQAQJ | CDS | 901241 | 1908 | + | 0.302411 | |
g4284 | DLA_04731 | GAOABQK02GQAQJ | CDS | 903214 | 1701 | - | 0.285126 | |
g4285 | DLA_04732 | GAOABQK02GQAQJ | CDS | 905072 | 3132 | + | 0.304278 | |
g4286 | DLA_04733 | GAOABQK02GQAQJ | CDS | 908920 | 1350 | + | 0.268889 | |
g4287 | DLA_04734 | GAOABQK02GQAQJ | CDS | 910354 | 5298 | - | 0.360136 | |
g4288 | DLA_11602 | GAOABQK02GQAQJ | CDS | 916226 | 2115 | + | 0.289835 | |
g4289 | DLA_04735 | GAOABQK02GQAQJ | CDS | 918626 | 1182 | + | 0.291032 | |
g429 | DLA_00476 | contig05409_1.exp | CDS | 972503 | 1317 | - | 0.349279 | |
g4290 | DLA_04736 | GAOABQK02GQAQJ | CDS | 920116 | 1251 | - | 0.293365 | |
g4291 | DLA_04737 | GAOABQK02GQAQJ | CDS | 922001 | 1170 | + | 0.374359 | |
g4292 | DLA_04738 | GAOABQK02GQAQJ | CDS | 923857 | 828 | - | 0.316425 | |
g4293 | DLA_04739 | GAOABQK02GQAQJ | CDS | 925019 | 1179 | - | 0.318066 | |
g4294 | DLA_04740 | GAOABQK02GQAQJ | CDS | 927407 | 5724 | + | 0.408805 | |
g4295 | DLA_04741 | GAOABQK02GQAQJ | CDS | 933573 | 552 | - | 0.307971 | |
g4296 | DLA_04742 | GAOABQK02GQAQJ | CDS | 934578 | 4212 | - | 0.340456 | |
g4297 | DLA_04743 | catalyzes the reaction L-proline NAD(P)supsup 1-pyrroline-5-carboxylate NAD(P)H Hsupsup | GAOABQK02GQAQJ | CDS | 939860 | 1536 | + | 0.343099 |
g4298 | DLA_04744 | GAOABQK02GQAQJ | CDS | 941546 | 1119 | - | 0.321716 | |
g4299 | DLA_04745 | GAOABQK02GQAQJ | CDS | 942868 | 447 | + | 0.284116 | |
g43 | DLA_00052 | contig05409_1.exp | CDS | 110599 | 2445 | + | 0.271575 | |
g430 | DLA_00477 | contig05409_1.exp | CDS | 974153 | 4065 | + | 0.327429 | |
g4300 | DLA_04746 | GAOABQK02GQAQJ | CDS | 943988 | 1629 | - | 0.36771 | |
g4301 | DLA_04747 | GAOABQK02GQAQJ | CDS | 948296 | 1629 | + | 0.34868 | |
g4302 | DLA_04748 | GAOABQK02GQAQJ | CDS | 949983 | 1905 | - | 0.327559 | |
g4303 | DLA_04749 | GAOABQK02GQAQJ | CDS | 952334 | 1602 | + | 0.338951 | |
g4304 | DLA_04751 | GAOABQK02GQAQJ | CDS | 954602 | 2229 | - | 0.344101 | |
g4305 | DLA_04752 | GAOABQK02GQAQJ | CDS | 960673 | 1929 | - | 0.371695 | |
g4306 | DLA_04753 | GAOABQK02GQAQJ | CDS | 963209 | 3252 | - | 0.339176 | |
g4307 | DLA_04754 | GAOABQK02GQAQJ | CDS | 966859 | 786 | - | 0.344784 | |
g4308 | DLA_04755 | GAOABQK02GQAQJ | CDS | 968202 | 663 | + | 0.315234 | |
g4309 | DLA_04756 | GAOABQK02GQAQJ | CDS | 969059 | 657 | - | 0.420091 | |
g431 | DLA_00478 | contig05409_1.exp | CDS | 979245 | 849 | + | 0.366313 | |
g4310 | DLA_04757 | GAOABQK02GQAQJ | CDS | 969936 | 924 | - | 0.287879 | |
g4311 | DLA_04758 | GAOABQK02GQAQJ | CDS | 971256 | 2889 | - | 0.340602 | |
g4312 | DLA_04759 | GAOABQK02GQAQJ | CDS | 974718 | 3069 | + | 0.380254 | |
g4313 | DLA_04761 | GAOABQK02GQAQJ | CDS | 979729 | 486 | + | 0.26749 | |
g4314 | DLA_04762 | GAOABQK02GQAQJ | CDS | 980607 | 687 | - | 0.307132 | |
g4315 | DLA_04763 | GAOABQK02GQAQJ | CDS | 981628 | 726 | + | 0.285124 | |
g4316 | DLA_04764 | GAOABQK02GQAQJ | CDS | 982601 | 852 | + | 0.319249 | |
g4317 | DLA_04765 | GAOABQK02GQAQJ | CDS | 983660 | 2244 | - | 0.276292 | |
g4318 | DLA_04766 | GAOABQK02GQAQJ | CDS | 986492 | 1524 | - | 0.281496 | |
g4319 | DLA_04767 | GAOABQK02GQAQJ | CDS | 988886 | 1359 | + | 0.354673 | |
g432 | DLA_00480 | contig05409_1.exp | CDS | 981185 | 462 | + | 0.344156 | |
g4320 | DLA_04768 | GAOABQK02GQAQJ | CDS | 991147 | 3333 | - | 0.308731 | |
g4321 | DLA_04769 | GAOABQK02GQAQJ | CDS | 994903 | 1029 | + | 0.291545 | |
g4322 | DLA_04770 | GAOABQK02GQAQJ | CDS | 996101 | 6825 | - | 0.332015 | |
g4323 | DLA_04771 | GAOABQK02GQAQJ | CDS | 1003599 | 252 | + | 0.246032 | |
g4324 | DLA_04772 | GAOABQK02GQAQJ | CDS | 1004164 | 999 | - | 0.332332 | |
g4325 | DLA_04773 | GAOABQK02GQAQJ | CDS | 1005379 | 2721 | - | 0.329658 | |
g4326 | DLA_04774 | GAOABQK02GQAQJ | CDS | 1009911 | 858 | - | 0.395105 | |
g4327 | DLA_04775 | GAOABQK02GQAQJ | CDS | 1011298 | 1773 | + | 0.350818 | |
g4328 | DLA_04777 | GAOABQK02GQAQJ | CDS | 1015387 | 867 | + | 0.268743 | |
g4329 | DLA_04779 | GAOABQK02GQAQJ | CDS | 1017274 | 2826 | - | 0.295824 | |
g433 | DLA_00481 | contig05409_1.exp | CDS | 983170 | 1590 | + | 0.335849 | |
g4330 | DLA_04781 | GAOABQK02GQAQJ | CDS | 1021324 | 2493 | + | 0.271159 | |
g4331 | DLA_04782 | GAOABQK02GQAQJ | CDS | 1024516 | 549 | + | 0.298725 | |
g4332 | DLA_04783 | GAOABQK02GQAQJ | CDS | 1025738 | 11418 | - | 0.318795 | |
g4333 | DLA_04786 | GAOABQK02GQAQJ | CDS | 1041106 | 1323 | + | 0.32124 | |
g4334 | DLA_04787 | GAOABQK02GQAQJ | CDS | 1042465 | 675 | - | 0.305185 | |
g4335 | DLA_04788 | GAOABQK02GQAQJ | CDS | 1043860 | 2172 | - | 0.355893 | |
g4336 | DLA_04789 | GAOABQK02GQAQJ | CDS | 1046815 | 4053 | + | 0.339255 | |
g4337 | DLA_04791 | GAOABQK02GQAQJ | CDS | 1051527 | 450 | - | 0.402222 | |
g4338 | DLA_04792 | GAOABQK02GQAQJ | CDS | 1052595 | 2424 | + | 0.312706 | |
g4339 | DLA_04794 | GAOABQK02GQAQJ | CDS | 1056108 | 1185 | + | 0.276793 | |
g434 | DLA_00483 | contig05409_1.exp | CDS | 985729 | 450 | + | 0.32 | |
g4340 | DLA_04795 | GAOABQK02GQAQJ | CDS | 1057715 | 1140 | - | 0.355263 | |
g4341 | DLA_11603 | GAOABQK02GQAQJ | CDS | 1059345 | 357 | - | 0.294118 | |
g4342 | DLA_04796 | similar to human PLD a GPI (glycosylphosphatidylinositol)-specific phospholipase D | GAOABQK02GQAQJ | CDS | 1059948 | 2628 | - | 0.329148 |
g4343 | DLA_04797 | GAOABQK02GQAQJ | CDS | 1063492 | 1713 | - | 0.279043 | |
g4344 | DLA_04798 | GAOABQK02GQAQJ | CDS | 1065585 | 870 | + | 0.364368 | |
g4345 | DLA_04799 | GAOABQK02GQAQJ | CDS | 1066989 | 768 | + | 0.365885 | |
g4346 | DLA_04800 | GAOABQK02GQAQJ | CDS | 1068211 | 3357 | + | 0.327078 | |
g4347 | DLA_04802 | GAOABQK02GQAQJ | CDS | 1072189 | 1203 | + | 0.27182 | |
g4348 | DLA_04803 | GAOABQK02GQAQJ | CDS | 1074237 | 1086 | + | 0.341621 | |
g4349 | DLA_04805 | GAOABQK02GQAQJ | CDS | 1078207 | 1833 | + | 0.26132 | |
g435 | DLA_00484 | contig05409_1.exp | CDS | 986633 | 1572 | - | 0.321883 | |
g4350 | DLA_04806 | GAOABQK02GQAQJ | CDS | 1080315 | 369 | - | 0.292683 | |
g4351 | DLA_04808 | GAOABQK02GQAQJ | CDS | 1082463 | 7581 | + | 0.303258 | |
g4352 | DLA_04809 | GAOABQK02GQAQJ | CDS | 1090298 | 1194 | - | 0.322446 | |
g4353 | DLA_04811 | GAOABQK02GQAQJ | CDS | 1093282 | 369 | - | 0.273713 | |
g4354 | DLA_04812 | GAOABQK02GQAQJ | CDS | 1095272 | 1263 | + | 0.361837 | |
g4355 | DLA_04814 | GAOABQK02GQAQJ | CDS | 1097737 | 651 | - | 0.357911 | |
g4356 | DLA_04815 | ortholog of S. cerevisiae TAM41 a mitochondrial protein involved in protein import into the mitochondrial matrix | GAOABQK02GRIAE | CDS | 2140 | 2220 | + | 0.281081 |
g4357 | DLA_04816 | GAOABQK02GRIAE | CDS | 4785 | 3231 | - | 0.316311 | |
g4358 | DLA_04817 | GAOABQK02GRIAE | CDS | 8618 | 555 | + | 0.336937 | |
g4359 | DLA_04818 | GAOABQK02GRIAE | CDS | 9656 | 1917 | - | 0.324465 | |
g436 | DLA_00485 | contig05409_1.exp | CDS | 988907 | 453 | - | 0.353201 | |
g4360 | DLA_04819 | GAOABQK02GRIAE | CDS | 11780 | 3618 | - | 0.300719 | |
g4361 | DLA_04820 | GAOABQK02GRIAE | CDS | 17839 | 2421 | - | 0.336225 | |
g4362 | DLA_04821 | GAOABQK02GRIAE | CDS | 20539 | 2247 | - | 0.315532 | |
g4363 | DLA_04822 | GAOABQK02GRIAE | CDS | 23497 | 3804 | + | 0.339642 | |
g4364 | DLA_04823 | GAOABQK02GRIAE | CDS | 27917 | 2184 | + | 0.31685 | |
g4365 | DLA_04824 | GAOABQK02GRIAE | CDS | 30234 | 594 | - | 0.323232 | |
g4366 | DLA_04825 | GAOABQK02GRIAE | CDS | 31375 | 1116 | + | 0.305556 | |
g4367 | DLA_04826 | GAOABQK02GRIAE | CDS | 32950 | 375 | - | 0.394667 | |
g4368 | DLA_04827 | GAOABQK02GRIAE | CDS | 34463 | 1149 | - | 0.307224 | |
g4369 | DLA_04828 | GAOABQK02GRIAE | CDS | 36687 | 5133 | + | 0.263589 | |
g437 | DLA_00486 | Dictyostelium ortholog of the conserved midasin a large protein containing an AAA ATPase domain and a C-terminal VWFA domain S. cerevisiae MDN1 is a rRNA processing ATPase. | contig05409_1.exp | CDS | 990202 | 16743 | + | 0.335663 |
g4370 | DLA_04830 | GAOABQK02GRIAE | CDS | 44001 | 3402 | - | 0.368313 | |
g4371 | DLA_04831 | GAOABQK02GRIAE | CDS | 48218 | 3375 | + | 0.357333 | |
g4372 | DLA_04832 | ortholog of the conserved CIA1 (S. cerevisiae) or CIAO1 (Mammals) which in yeast is essential for assembly of cytosolic and nuclear iron-sulfur proteins contains 7 WD40 repeats | GAOABQK02GRIAE | CDS | 51833 | 987 | + | 0.348531 |
g4373 | DLA_04833 | GAOABQK02GRIAE | CDS | 52860 | 831 | - | 0.327316 | |
g4374 | DLA_04834 | GAOABQK02GRIAE | CDS | 53831 | 6273 | + | 0.326957 | |
g4375 | DLA_04835 | GAOABQK02GRIAE | CDS | 60378 | 1338 | - | 0.294469 | |
g4376 | DLA_04836 | GAOABQK02GRIAE | CDS | 62023 | 888 | - | 0.279279 | |
g4377 | DLA_04838 | GAOABQK02GRIAE | CDS | 65266 | 9915 | + | 0.320625 | |
g4378 | DLA_04839 | GAOABQK02GRIAE | CDS | 75425 | 1020 | + | 0.253922 | |
g4379 | DLA_04840 | GAOABQK02GRIAE | CDS | 76672 | 567 | + | 0.266314 | |
g438 | DLA_00487 | contig05409_1.exp | CDS | 1007255 | 2724 | - | 0.30837 | |
g4380 | DLA_04841 | GAOABQK02GRIAE | CDS | 77679 | 2385 | - | 0.374004 | |
g4381 | DLA_04842 | GAOABQK02GRIAE | CDS | 82259 | 1353 | + | 0.297857 | |
g4382 | DLA_04843 | GAOABQK02GRIAE | CDS | 83934 | 1602 | + | 0.325218 | |
g4383 | DLA_04845 | GAOABQK02GRIAE | CDS | 86199 | 786 | + | 0.30916 | |
g4384 | DLA_04846 | GAOABQK02GRIAE | CDS | 87383 | 1194 | + | 0.345059 | |
g4385 | DLA_04848 | GAOABQK02GRIAE | CDS | 89099 | 246 | - | 0.337398 | |
g4386 | DLA_04849 | GAOABQK02GRIAE | CDS | 89763 | 588 | + | 0.336735 | |
g4387 | DLA_04850 | NAP proteins act as histone chaperones shuttling both core and linker histones from their site of synthesis in the cytoplasm to the nucleus | GAOABQK02GRIAE | CDS | 90607 | 942 | + | 0.361996 |
g4388 | DLA_04851 | belongs to a family of zinc transporters that are integral membrane proteins which are found to increase tolerance to divalent metal ions contains 6 putative transmembrane domains | GAOABQK02GRIAE | CDS | 91802 | 1668 | - | 0.317746 |
g4389 | DLA_04852 | GAOABQK02GRIAE | CDS | 93825 | 909 | + | 0.325633 | |
g439 | DLA_00488 | contig05409_1.exp | CDS | 1010422 | 2394 | - | 0.327485 | |
g4390 | DLA_04853 | GAOABQK02GRIAE | CDS | 95100 | 1842 | + | 0.327362 | |
g4391 | DLA_04854 | GAOABQK02GRIAE | CDS | 97101 | 2892 | - | 0.33852 | |
g4392 | DLA_04855 | GAOABQK02GRIAE | CDS | 101265 | 1704 | - | 0.348005 | |
g4393 | DLA_04856 | GAOABQK02GRIAE | CDS | 107439 | 675 | - | 0.383704 | |
g4394 | DLA_04857 | GAOABQK02GRIAE | CDS | 109131 | 1053 | - | 0.329535 | |
g4395 | DLA_04858 | GAOABQK02GRIAE | CDS | 110904 | 657 | + | 0.378995 | |
g4396 | DLA_04859 | GAOABQK02GRIAE | CDS | 112322 | 543 | - | 0.290976 | |
g4397 | DLA_04860 | GAOABQK02GRIAE | CDS | 113254 | 1716 | + | 0.277972 | |
g4398 | DLA_04861 | GAOABQK02GRIAE | CDS | 118926 | 1323 | - | 0.352986 | |
g4399 | DLA_11604 | GAOABQK02GRIAE | CDS | 123217 | 1224 | + | 0.319444 | |
g44 | DLA_00053 | contig05409_1.exp | CDS | 113335 | 4518 | - | 0.340859 | |
g440 | DLA_00489 | contig05409_1.exp | CDS | 1013074 | 2718 | - | 0.306107 | |
g4400 | DLA_04862 | GAOABQK02GRIAE | CDS | 124812 | 489 | + | 0.300613 | |
g4401 | DLA_04863 | GAOABQK02GRIAE | CDS | 128848 | 537 | + | 0.292365 | |
g4402 | DLA_04864 | GAOABQK02GRIAE | CDS | 130046 | 594 | - | 0.319865 | |
g4403 | DLA_04867 | GAOABQK02GRIAE | CDS | 131300 | 2673 | - | 0.320239 | |
g4404 | DLA_04868 | GAOABQK02GRIAE | CDS | 136633 | 1623 | + | 0.371534 | |
g4405 | DLA_04869 | GAOABQK02GRIAE | CDS | 138667 | 3420 | - | 0.334503 | |
g4406 | DLA_04871 | GAOABQK02GRIAE | CDS | 143302 | 1827 | + | 0.321839 | |
g4407 | DLA_04872 | ortholog of the human CPSF3 and yeast YSH1 the 73 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs | GAOABQK02GRIAE | CDS | 145279 | 2223 | - | 0.338731 |
g4408 | DLA_04873 | catalyzes the reaction Hsub2subO dCTP - NH3 dUTP in de novo biosynthesis of pyrimidine deoxyribonucleotides | GAOABQK02GRIAE | CDS | 147649 | 738 | - | 0.304878 |
g4409 | DLA_04874 | GAOABQK02GRIAE | CDS | 149654 | 1803 | + | 0.380477 | |
g441 | DLA_11442 | contig05409_1.exp | CDS | 1016219 | 1113 | - | 0.263252 | |
g4410 | DLA_04875 | GAOABQK02GRIAE | CDS | 151919 | 864 | + | 0.298611 | |
g4411 | DLA_04876 | GAOABQK02GRIAE | CDS | 153333 | 765 | + | 0.295425 | |
g4412 | DLA_04878 | GAOABQK02GRIAE | CDS | 155358 | 4623 | + | 0.307376 | |
g4413 | DLA_04879 | GAOABQK02GRIAE | CDS | 160195 | 1650 | - | 0.310303 | |
g4414 | DLA_04880 | GAOABQK02GRIAE | CDS | 162629 | 2166 | - | 0.301939 | |
g4415 | DLA_04881 | GAOABQK02GRIAE | CDS | 165148 | 990 | + | 0.347475 | |
g4416 | DLA_04882 | GAOABQK02GRIAE | CDS | 166338 | 2568 | + | 0.308801 | |
g4417 | DLA_04883 | GAOABQK02GRIAE | CDS | 169464 | 897 | + | 0.352285 | |
g4418 | DLA_04884 | GAOABQK02GRIAE | CDS | 170647 | 846 | + | 0.353428 | |
g4419 | DLA_04886 | GAOABQK02GRIAE | CDS | 172157 | 2103 | + | 0.292915 | |
g442 | DLA_00490 | contig05409_1.exp | CDS | 1017632 | 1248 | + | 0.327724 | |
g4420 | DLA_04887 | GAOABQK02GRIAE | CDS | 174565 | 1338 | - | 0.289238 | |
g4421 | DLA_04888 | GAOABQK02GRIAE | CDS | 176092 | 225 | + | 0.293333 | |
g4422 | DLA_04889 | GAOABQK02GRIAE | CDS | 176484 | 1617 | - | 0.303649 | |
g4423 | DLA_04890 | GAOABQK02GRIAE | CDS | 178156 | 447 | + | 0.270694 | |
g4424 | DLA_04891 | GAOABQK02GRIAE | CDS | 178690 | 960 | - | 0.308333 | |
g4425 | DLA_04892 | GAOABQK02GRIAE | CDS | 179861 | 516 | + | 0.294574 | |
g4426 | DLA_04893 | GAOABQK02GRIAE | CDS | 180489 | 921 | - | 0.416938 | |
g4427 | DLA_04894 | GAOABQK02GRIAE | CDS | 181916 | 1023 | + | 0.356794 | |
g4428 | DLA_04895 | GAOABQK02GRIAE | CDS | 183019 | 2127 | - | 0.348848 | |
g4429 | DLA_04896 | GAOABQK02GRIAE | CDS | 186938 | 3063 | + | 0.335619 | |
g443 | DLA_00491 | contig05409_1.exp | CDS | 1018959 | 993 | - | 0.303122 | |
g4430 | DLA_04899 | catalyzes the reaction cystathionine Hsub2subO 2-oxobutanoate L-cysteine NHsub3sub | GAOABQK02GRIAE | CDS | 194004 | 1152 | + | 0.377604 |
g4431 | DLA_04900 | GAOABQK02GRIAE | CDS | 195274 | 2445 | + | 0.283436 | |
g4432 | DLA_04901 | GAOABQK02GRIAE | CDS | 197855 | 660 | - | 0.298485 | |
g4433 | DLA_04902 | GAOABQK02GRIAE | CDS | 198902 | 1545 | + | 0.242071 | |
g4434 | DLA_04903 | GAOABQK02GRIAE | CDS | 200678 | 1572 | + | 0.315522 | |
g4435 | DLA_04906 | GAOABQK02GRIAE | CDS | 205193 | 1446 | - | 0.291148 | |
g4436 | DLA_04907 | GAOABQK02GRIAE | CDS | 207516 | 3198 | + | 0.331457 | |
g4437 | DLA_04909 | GAOABQK02GRIAE | CDS | 211845 | 804 | + | 0.262438 | |
g4438 | DLA_04911 | GAOABQK02GRIAE | CDS | 213590 | 1617 | - | 0.369821 | |
g4439 | DLA_04912 | GAOABQK02GRIAE | CDS | 215650 | 372 | + | 0.346774 | |
g444 | DLA_11443 | contig05409_1.exp | CDS | 1020252 | 723 | - | 0.29184 | |
g4440 | DLA_04913 | ortholog of peroxin 4 a peroxisomal ubiquitin conjugating enzyme required for peroxisomal matrix protein import and peroxisome biogenesis | GAOABQK02GRIAE | CDS | 216161 | 447 | + | 0.288591 |
g4441 | DLA_04914 | GAOABQK02GRIAE | CDS | 216906 | 537 | + | 0.3054 | |
g4442 | DLA_04916 | GAOABQK02GRIAE | CDS | 218825 | 1521 | + | 0.365549 | |
g4443 | DLA_04917 | GAOABQK02GRIAE | CDS | 220710 | 2406 | + | 0.266833 | |
g4444 | DLA_04919 | GAOABQK02GRIAE | CDS | 225089 | 405 | - | 0.28642 | |
g4445 | DLA_04922 | GAOABQK02GSVD1 | CDS | 113 | 1479 | - | 0.282623 | |
g4446 | DLA_04923 | GAOABQK02GSVD1 | CDS | 1845 | 444 | - | 0.337838 | |
g4447 | DLA_04924 | GAOABQK02GSVD1 | CDS | 2815 | 579 | + | 0.288428 | |
g4448 | DLA_04926 | GAOABQK02H81I9 | CDS | 1090 | 4572 | - | 0.27909 | |
g4449 | DLA_04927 | GAOABQK02H81I9 | CDS | 5974 | 660 | + | 0.298485 | |
g445 | DLA_00492 | contig05409_1.exp | CDS | 1021410 | 618 | - | 0.322006 | |
g4450 | DLA_04928 | GAOABQK02H81I9 | CDS | 6871 | 4566 | - | 0.286027 | |
g4451 | DLA_04929 | GAOABQK02H81I9 | CDS | 11985 | 3048 | + | 0.283136 | |
g4452 | DLA_04930 | GAOABQK02H81I9 | CDS | 16971 | 1119 | + | 0.303843 | |
g4453 | DLA_04932 | GAOABQK02H81I9 | CDS | 20597 | 1620 | + | 0.299383 | |
g4454 | DLA_04933 | GAOABQK02H81I9 | CDS | 22642 | 444 | + | 0.288288 | |
g4455 | DLA_04934 | component of the RNA polymerase II complex ortholog of S. cerevisiae RPB9 | GAOABQK02H81I9 | CDS | 23321 | 327 | - | 0.348624 |
g4456 | DLA_04935 | GAOABQK02H81I9 | CDS | 23754 | 2466 | - | 0.345904 | |
g4457 | DLA_04936 | GAOABQK02H81I9 | CDS | 26587 | 2580 | - | 0.312403 | |
g4458 | DLA_04937 | GAOABQK02H81I9 | CDS | 29274 | 1683 | + | 0.322044 | |
g4459 | DLA_04938 | GAOABQK02H81I9 | CDS | 31029 | 1170 | - | 0.309402 | |
g446 | DLA_00493 | contig05409_1.exp | CDS | 1022388 | 2244 | - | 0.3418 | |
g4460 | DLA_04939 | GAOABQK02H81I9 | CDS | 32465 | 933 | + | 0.289389 | |
g4461 | DLA_04940 | GAOABQK02H81I9 | CDS | 33421 | 1080 | - | 0.281481 | |
g4462 | DLA_04941 | ortholog of mammalian NARG1 and yeast NAT1 part of a complex that displays alpha (N-terminal) acetyltransferase activity | GAOABQK02H81I9 | CDS | 34817 | 2520 | + | 0.325 |
g4463 | DLA_04942 | GAOABQK02H81I9 | CDS | 37895 | 318 | + | 0.305031 | |
g4464 | DLA_04944 | GAOABQK02H81I9 | CDS | 40895 | 2850 | - | 0.291579 | |
g4465 | DLA_11605 | GAOABQK02H81I9 | CDS | 43898 | 3429 | - | 0.265967 | |
g4466 | DLA_04945 | involved in the degradation of misfolded glycosylated proteins required for normal multicellular development belongs to the transglutaminase-like superfamily | GAOABQK02H81I9 | CDS | 47687 | 2256 | + | 0.317376 |
g4467 | DLA_04946 | GAOABQK02H81I9 | CDS | 50045 | 2025 | - | 0.230123 | |
g4468 | DLA_04947 | GAOABQK02H81I9 | CDS | 52421 | 1572 | - | 0.291985 | |
g4469 | DLA_04948 | GAOABQK02H81I9 | CDS | 54369 | 1437 | + | 0.334029 | |
g447 | DLA_00495 | contig05409_1.exp | CDS | 1025554 | 1761 | + | 0.33674 | |
g4470 | DLA_04949 | GAOABQK02H81I9 | CDS | 55881 | 414 | - | 0.277778 | |
g4471 | DLA_04954 | GAOABQK02H81I9 | CDS | 60096 | 393 | - | 0.368957 | |
g4472 | DLA_11606 | GAOABQK02H81I9 | CDS | 60638 | 285 | - | 0.291228 | |
g4473 | DLA_04955 | GAOABQK02H81I9 | CDS | 61020 | 1341 | + | 0.280388 | |
g4474 | DLA_11607 | GAOABQK02H81I9 | CDS | 62868 | 870 | + | 0.285057 | |
g4475 | DLA_04956 | GAOABQK02H81I9 | CDS | 63836 | 1956 | - | 0.292945 | |
g4476 | DLA_04957 | GAOABQK02H81I9 | CDS | 66089 | 3852 | + | 0.317497 | |
g4477 | DLA_04958 | GAOABQK02H81I9 | CDS | 70591 | 3831 | + | 0.308536 | |
g4478 | DLA_04959 | GAOABQK02H81I9 | CDS | 75090 | 3807 | + | 0.312319 | |
g4479 | DLA_04960 | GAOABQK02H81I9 | CDS | 79895 | 1290 | + | 0.343411 | |
g448 | DLA_00496 | ortholog of S. cerevisiae SGT1 and mammalian SUGT1 associated with the SCF (Skp1pCdc53pF box protein) ubiquitin ligase complex | contig05409_1.exp | CDS | 1027524 | 1056 | - | 0.339015 |
g4480 | DLA_04961 | GAOABQK02H81I9 | CDS | 81878 | 1056 | + | 0.272727 | |
g4481 | DLA_04962 | GAOABQK02H81I9 | CDS | 83048 | 483 | + | 0.310559 | |
g4482 | DLA_04963 | GAOABQK02H81I9 | CDS | 83618 | 495 | - | 0.357576 | |
g4483 | DLA_04964 | GAOABQK02H81I9 | CDS | 84430 | 3258 | - | 0.296194 | |
g4484 | DLA_04965 | GAOABQK02H81I9 | CDS | 88024 | 1497 | + | 0.299265 | |
g4485 | DLA_04966 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | GAOABQK02H81I9 | CDS | 89714 | 1668 | + | 0.351319 |
g4486 | DLA_04967 | GAOABQK02H81I9 | CDS | 91781 | 2508 | + | 0.329346 | |
g4487 | DLA_04968 | GAOABQK02H81I9 | CDS | 94787 | 1464 | - | 0.304645 | |
g4488 | DLA_04969 | GAOABQK02H81I9 | CDS | 96865 | 666 | + | 0.267267 | |
g4489 | DLA_04970 | GAOABQK02H81I9 | CDS | 97703 | 8262 | + | 0.26398 | |
g449 | DLA_00497 | contig05409_1.exp | CDS | 1029008 | 1596 | - | 0.370301 | |
g4490 | DLA_04973 | N-terminal kinase-like (NTKL) protein does not contain the consensus sequences required for kinase function however the SCY1 family encodes highly conserved non-canonical kinases that are believed to function | GAOABQK02H81I9 | CDS | 107685 | 2367 | + | 0.286439 |
g4491 | DLA_04974 | GAOABQK02H81I9 | CDS | 110403 | 924 | + | 0.350649 | |
g4492 | DLA_04975 | GAOABQK02H81I9 | CDS | 111821 | 798 | + | 0.367168 | |
g4493 | DLA_04976 | GAOABQK02H81I9 | CDS | 112900 | 2298 | + | 0.289817 | |
g4494 | DLA_11608 | GAOABQK02H81I9 | CDS | 115732 | 228 | + | 0.307018 | |
g4495 | DLA_04977 | catalyzes the reaction ATP a long-chain carboxylic acid CoA AMP diphosphate an acyl-CoA | GAOABQK02H81I9 | CDS | 116081 | 1728 | + | 0.337384 |
g4496 | DLA_04978 | GAOABQK02H81I9 | CDS | 118060 | 2229 | - | 0.302378 | |
g4497 | DLA_04979 | GAOABQK02H81I9 | CDS | 121111 | 603 | - | 0.363184 | |
g4498 | DLA_04980 | GAOABQK02H81I9 | CDS | 122357 | 609 | - | 0.367816 | |
g4499 | DLA_04981 | GAOABQK02H81I9 | CDS | 123591 | 516 | + | 0.339147 | |
g45 | DLA_00054 | contig05409_1.exp | CDS | 118405 | 5565 | + | 0.296676 | |
g450 | DLA_00498 | contig05409_1.exp | CDS | 1032003 | 3207 | + | 0.346118 | |
g4500 | DLA_04984 | GAOABQK02H81I9 | CDS | 125925 | 2370 | - | 0.283966 | |
g4501 | DLA_04987 | GAOABQK02H81I9 | CDS | 128805 | 1245 | - | 0.281928 | |
g4502 | DLA_04988 | GAOABQK02H81I9 | CDS | 130212 | 816 | + | 0.253676 | |
g4503 | DLA_04989 | GAOABQK02H81I9 | CDS | 131193 | 1047 | - | 0.379179 | |
g4504 | DLA_04990 | GAOABQK02H81I9 | CDS | 133637 | 717 | + | 0.309623 | |
g4505 | DLA_04992 | GAOABQK02H81I9 | CDS | 135825 | 810 | - | 0.303704 | |
g4506 | DLA_04993 | GAOABQK02H81I9 | CDS | 137938 | 792 | - | 0.309343 | |
g4507 | DLA_04994 | GAOABQK02H81I9 | CDS | 139185 | 3006 | + | 0.312708 | |
g4508 | DLA_04995 | GAOABQK02H81I9 | CDS | 142902 | 3027 | + | 0.315494 | |
g4509 | DLA_04997 | GAOABQK02H81I9 | CDS | 147020 | 2955 | + | 0.317428 | |
g451 | DLA_00499 | contig05409_1.exp | CDS | 1035324 | 1050 | - | 0.27619 | |
g4510 | DLA_04999 | GAOABQK02H81I9 | CDS | 150479 | 1059 | - | 0.341832 | |
g4511 | DLA_05000 | GAOABQK02H81I9 | CDS | 152471 | 3168 | + | 0.324811 | |
g4512 | DLA_05002 | GAOABQK02H81I9 | CDS | 156045 | 3822 | + | 0.321821 | |
g4513 | DLA_05003 | GAOABQK02H81I9 | CDS | 160775 | 4557 | + | 0.31885 | |
g4514 | DLA_05004 | GAOABQK02H81I9 | CDS | 165813 | 1008 | + | 0.375 | |
g4515 | DLA_05005 | contains one thioredoxin domain similar to human PDIA6 (protein disulfide isomerase A6) | GAOABQK02H81I9 | CDS | 167084 | 1254 | + | 0.333333 |
g4516 | DLA_05006 | catalyzes the reaction L-methylmalonyl-CoA D-methylmalonyl-CoA | GAOABQK02H81I9 | CDS | 168523 | 498 | - | 0.299197 |
g4517 | DLA_05007 | GAOABQK02H81I9 | CDS | 169460 | 1371 | + | 0.378556 | |
g4518 | DLA_05008 | GAOABQK02H81I9 | CDS | 171288 | 666 | - | 0.351351 | |
g4519 | DLA_05009 | GAOABQK02H81I9 | CDS | 172448 | 780 | + | 0.344872 | |
g452 | DLA_00500 | contig05409_1.exp | CDS | 1036689 | 1746 | - | 0.321306 | |
g4520 | DLA_05010 | GAOABQK02H81I9 | CDS | 173524 | 972 | + | 0.341564 | |
g4521 | DLA_05011 | GAOABQK02H81I9 | CDS | 174890 | 1251 | + | 0.303757 | |
g4522 | DLA_05012 | GAOABQK02H81I9 | CDS | 176240 | 1347 | - | 0.279881 | |
g4523 | DLA_05013 | GAOABQK02H81I9 | CDS | 177698 | 2418 | + | 0.301902 | |
g4524 | DLA_05014 | GAOABQK02H81I9 | CDS | 181124 | 5421 | + | 0.33278 | |
g4525 | DLA_05015 | GAOABQK02H81I9 | CDS | 186706 | 642 | - | 0.342679 | |
g4526 | DLA_05016 | GAOABQK02H81I9 | CDS | 188618 | 3891 | + | 0.311488 | |
g4527 | DLA_05017 | GAOABQK02H81I9 | CDS | 192626 | 2370 | - | 0.253165 | |
g4528 | DLA_05018 | GAOABQK02H81I9 | CDS | 195376 | 1617 | - | 0.235622 | |
g4529 | DLA_05020 | GAOABQK02H81I9 | CDS | 198017 | 1677 | + | 0.325581 | |
g453 | DLA_00502 | contig05409_1.exp | CDS | 1039273 | 1131 | + | 0.342175 | |
g4530 | DLA_05021 | GAOABQK02H81I9 | CDS | 199991 | 1722 | + | 0.325203 | |
g4531 | DLA_05022 | GAOABQK02H81I9 | CDS | 202178 | 2760 | + | 0.334783 | |
g4532 | DLA_05023 | putative ortholog of mammalian sorting nexin and S. cerevisiae VPS5 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | GAOABQK02H81I9 | CDS | 205815 | 1629 | + | 0.364027 |
g4533 | DLA_05024 | GAOABQK02H81I9 | CDS | 208039 | 1245 | + | 0.361446 | |
g4534 | DLA_05025 | GAOABQK02H81I9 | CDS | 209603 | 3888 | + | 0.316872 | |
g4535 | DLA_05026 | GAOABQK02H81I9 | CDS | 214301 | 3846 | + | 0.310192 | |
g4536 | DLA_05027 | GAOABQK02H81I9 | CDS | 219062 | 3903 | + | 0.305662 | |
g4537 | DLA_05028 | GAOABQK02H81I9 | CDS | 223619 | 3909 | + | 0.308775 | |
g4538 | DLA_05029 | GAOABQK02H81I9 | CDS | 228244 | 4599 | - | 0.346815 | |
g4539 | DLA_05030 | GAOABQK02H81I9 | CDS | 233403 | 1422 | + | 0.315752 | |
g454 | DLA_00503 | contig05409_1.exp | CDS | 1040478 | 1761 | - | 0.354344 | |
g4540 | DLA_05031 | GAOABQK02H81I9 | CDS | 235605 | 1560 | + | 0.337179 | |
g4541 | DLA_05032 | GAOABQK02H81I9 | CDS | 237598 | 576 | - | 0.314236 | |
g4542 | DLA_05033 | GAOABQK02H81I9 | CDS | 239017 | 447 | - | 0.33557 | |
g4543 | DLA_05034 | GAOABQK02H81I9 | CDS | 239809 | 360 | + | 0.263889 | |
g4544 | DLA_05035 | GAOABQK02H81I9 | CDS | 240327 | 1449 | - | 0.311939 | |
g4545 | DLA_05036 | GAOABQK02H81I9 | CDS | 242788 | 537 | + | 0.337058 | |
g4546 | DLA_05037 | GAOABQK02H81I9 | CDS | 243794 | 2862 | + | 0.326345 | |
g4547 | DLA_05039 | GAOABQK02H81I9 | CDS | 248282 | 2757 | - | 0.322815 | |
g4548 | DLA_05040 | CK2 family protein kinase a ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | GAOABQK02H81I9 | CDS | 251379 | 1047 | + | 0.325692 |
g4549 | DLA_05041 | GAOABQK02H81I9 | CDS | 252821 | 480 | - | 0.302083 | |
g455 | DLA_00504 | contig05409_1.exp | CDS | 1042485 | 999 | - | 0.311311 | |
g4550 | DLA_05043 | GAOABQK02H81I9 | CDS | 253731 | 1731 | + | 0.33911 | |
g4551 | DLA_05044 | GAOABQK02H81I9 | CDS | 255889 | 2142 | + | 0.323996 | |
g4552 | DLA_05045 | GAOABQK02H81I9 | CDS | 258290 | 432 | + | 0.298611 | |
g4553 | DLA_05046 | GAOABQK02H81I9 | CDS | 259124 | 924 | + | 0.322511 | |
g4554 | DLA_05047 | GAOABQK02H81I9 | CDS | 260609 | 963 | - | 0.364486 | |
g4555 | DLA_05048 | GAOABQK02H81I9 | CDS | 262440 | 1518 | - | 0.373518 | |
g4556 | DLA_05049 | GAOABQK02H81I9 | CDS | 264313 | 708 | + | 0.289548 | |
g4557 | DLA_05050 | GAOABQK02H81I9 | CDS | 265305 | 1029 | + | 0.417881 | |
g4558 | DLA_05051 | GAOABQK02H81I9 | CDS | 266847 | 3897 | - | 0.322812 | |
g4559 | DLA_05052 | GAOABQK02H81I9 | CDS | 271994 | 525 | + | 0.285714 | |
g456 | DLA_00505 | contig05409_1.exp | CDS | 1044865 | 417 | + | 0.318945 | |
g4560 | DLA_05053 | GAOABQK02H81I9 | CDS | 272669 | 2781 | - | 0.291262 | |
g4561 | DLA_05055 | GAOABQK02H81I9 | CDS | 276079 | 3147 | + | 0.346044 | |
g4562 | DLA_05056 | GAOABQK02H81I9 | CDS | 279835 | 2310 | + | 0.323377 | |
g4563 | DLA_11609 | GAOABQK02H81I9 | CDS | 282392 | 966 | - | 0.310559 | |
g4564 | DLA_05057 | GAOABQK02H81I9 | CDS | 283533 | 2481 | - | 0.326078 | |
g4565 | DLA_05058 | GAOABQK02H81I9 | CDS | 286396 | 477 | - | 0.408805 | |
g4566 | DLA_05060 | GAOABQK02H81I9 | CDS | 288226 | 1305 | + | 0.318008 | |
g4567 | DLA_05061 | GAOABQK02H81I9 | CDS | 289818 | 330 | + | 0.3 | |
g4568 | DLA_05062 | GAOABQK02H81I9 | CDS | 290627 | 477 | - | 0.289308 | |
g4569 | DLA_05065 | composed of approx. 35 copies of a 24-amino-acid cysteine-rich repeat expression is decreased in | GAOABQK02H81I9 | CDS | 292738 | 3582 | + | 0.37493 |
g457 | DLA_00506 | contig05409_1.exp | CDS | 1047084 | 2517 | - | 0.326182 | |
g4570 | DLA_05066 | GAOABQK02H81I9 | CDS | 296557 | 741 | - | 0.303644 | |
g4571 | DLA_11610 | GAOABQK02H81I9 | CDS | 297445 | 606 | + | 0.29703 | |
g4572 | DLA_11611 | GAOABQK02H81I9 | CDS | 298550 | 3153 | + | 0.330796 | |
g4573 | DLA_05067 | GAOABQK02H81I9 | CDS | 302078 | 5169 | + | 0.336235 | |
g4574 | DLA_05069 | GAOABQK02H81I9 | CDS | 309518 | 1008 | + | 0.368056 | |
g4575 | DLA_05070 | GAOABQK02H81I9 | CDS | 311055 | 231 | + | 0.311688 | |
g4576 | DLA_05071 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | GAOABQK02H81I9 | CDS | 311445 | 2517 | + | 0.319825 |
g4577 | DLA_05072 | GAOABQK02H81I9 | CDS | 314015 | 1854 | - | 0.326321 | |
g4578 | DLA_05073 | GAOABQK02H81I9 | CDS | 315953 | 3183 | - | 0.278982 | |
g4579 | DLA_05074 | GAOABQK02H81I9 | CDS | 319505 | 474 | + | 0.280591 | |
g458 | DLA_00507 | contig05409_1.exp | CDS | 1049859 | 4731 | - | 0.345804 | |
g4580 | DLA_05075 | GAOABQK02H81I9 | CDS | 320402 | 1383 | - | 0.467824 | |
g4581 | DLA_05076 | GAOABQK02H81I9 | CDS | 322281 | 960 | + | 0.342708 | |
g4582 | DLA_05077 | GAOABQK02H81I9 | CDS | 323941 | 198 | + | 0.277778 | |
g4583 | DLA_05079 | GAOABQK02H81I9 | CDS | 325351 | 4026 | + | 0.360656 | |
g4584 | DLA_05080 | GAOABQK02H81I9 | CDS | 329562 | 288 | - | 0.309028 | |
g4585 | DLA_05081 | GAOABQK02H81I9 | CDS | 330597 | 5763 | + | 0.33906 | |
g4586 | DLA_05082 | GAOABQK02H81I9 | CDS | 336610 | 981 | - | 0.345566 | |
g4587 | DLA_05083 | GAOABQK02H81I9 | CDS | 337976 | 633 | - | 0.330174 | |
g4588 | DLA_05084 | GAOABQK02H81I9 | CDS | 338906 | 384 | + | 0.291667 | |
g4589 | DLA_05085 | GAOABQK02H81I9 | CDS | 339742 | 1095 | + | 0.336073 | |
g459 | DLA_00508 | contig05409_1.exp | CDS | 1055256 | 324 | - | 0.283951 | |
g4590 | DLA_05086 | GAOABQK02H81I9 | CDS | 340992 | 2823 | - | 0.314559 | |
g4591 | DLA_11612 | GAOABQK02H81I9 | CDS | 344694 | 882 | + | 0.291383 | |
g4592 | DLA_05087 | GAOABQK02H81I9 | CDS | 346046 | 441 | + | 0.324263 | |
g4593 | DLA_05088 | GAOABQK02H81I9 | CDS | 346910 | 1011 | + | 0.238378 | |
g4594 | DLA_11613 | GAOABQK02H81I9 | CDS | 348059 | 861 | + | 0.259001 | |
g4595 | DLA_05089 | GAOABQK02H81I9 | CDS | 349544 | 1509 | - | 0.355865 | |
g4596 | DLA_05090 | GAOABQK02H81I9 | CDS | 352560 | 1077 | - | 0.312906 | |
g4597 | DLA_05091 | GAOABQK02H81I9 | CDS | 353901 | 2172 | - | 0.345304 | |
g4598 | DLA_05093 | GAOABQK02H81I9 | CDS | 358939 | 3615 | + | 0.307054 | |
g4599 | DLA_05094 | GAOABQK02H81I9 | CDS | 363645 | 1575 | - | 0.290794 | |
g46 | DLA_00055 | very similar to the H. sapiens PISD a mitochondrial proenzyme that is cleaved into a phosphatidylserine decarboxylase alpha and beta chain contains one putative transmembrane domain | contig05409_1.exp | CDS | 124344 | 1062 | + | 0.3371 |
g460 | DLA_00509 | contig05409_1.exp | CDS | 1056108 | 363 | - | 0.294766 | |
g4600 | DLA_05095 | GAOABQK02H81I9 | CDS | 365480 | 840 | + | 0.294048 | |
g4601 | DLA_05096 | GAOABQK02H81I9 | CDS | 366473 | 1737 | - | 0.332758 | |
g4602 | DLA_05097 | GAOABQK02H81I9 | CDS | 368555 | 3192 | - | 0.331454 | |
g4603 | DLA_05098 | GAOABQK02H81I9 | CDS | 373722 | 939 | + | 0.324814 | |
g4604 | DLA_05099 | GAOABQK02H81I9 | CDS | 375330 | 2349 | + | 0.325671 | |
g4605 | DLA_05100 | GAOABQK02H81I9 | CDS | 378002 | 5517 | - | 0.355084 | |
g4606 | DLA_05101 | GAOABQK02H81I9 | CDS | 384086 | 2265 | - | 0.291391 | |
g4607 | DLA_05102 | GAOABQK02H81I9 | CDS | 387363 | 1539 | + | 0.357375 | |
g4608 | DLA_05103 | GAOABQK02H81I9 | CDS | 388977 | 1629 | - | 0.365255 | |
g4609 | DLA_05104 | GAOABQK02H81I9 | CDS | 390945 | 768 | - | 0.292969 | |
g461 | DLA_00511 | contig05409_1.exp | CDS | 1057177 | 375 | + | 0.288 | |
g4610 | DLA_05105 | GAOABQK02H81I9 | CDS | 391940 | 558 | - | 0.417563 | |
g4611 | DLA_05107 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | GAOABQK02H81I9 | CDS | 394523 | 3450 | + | 0.346087 |
g4612 | DLA_05108 | GAOABQK02H81I9 | CDS | 399265 | 1425 | + | 0.286316 | |
g4613 | DLA_05110 | GAOABQK02H81I9 | CDS | 401463 | 315 | + | 0.336508 | |
g4614 | DLA_05111 | GAOABQK02H81I9 | CDS | 402148 | 1809 | - | 0.3267 | |
g4615 | DLA_05112 | GAOABQK02H81I9 | CDS | 404366 | 2184 | - | 0.322344 | |
g4616 | DLA_05113 | GAOABQK02H81I9 | CDS | 406848 | 849 | - | 0.260306 | |
g4617 | DLA_05114 | GAOABQK02H81I9 | CDS | 407807 | 1650 | - | 0.316364 | |
g4618 | DLA_05115 | GAOABQK02H81I9 | CDS | 409558 | 4971 | - | 0.345001 | |
g4619 | DLA_05116 | GAOABQK02H81I9 | CDS | 415520 | 3084 | + | 0.32393 | |
g462 | DLA_00512 | contig05409_1.exp | CDS | 1058034 | 933 | - | 0.326902 | |
g4620 | DLA_05117 | GAOABQK02H81I9 | CDS | 418960 | 702 | - | 0.293447 | |
g4621 | DLA_05118 | GAOABQK02H81I9 | CDS | 419880 | 618 | + | 0.355987 | |
g4622 | DLA_05119 | GAOABQK02H81I9 | CDS | 420860 | 1371 | + | 0.36178 | |
g4623 | DLA_05120 | GAOABQK02H81I9 | CDS | 422821 | 948 | - | 0.296414 | |
g4624 | DLA_05122 | GAOABQK02H81I9 | CDS | 425875 | 945 | + | 0.307937 | |
g4625 | DLA_05123 | GAOABQK02H81I9 | CDS | 427647 | 1128 | + | 0.309397 | |
g4626 | DLA_05124 | GAOABQK02H81I9 | CDS | 429375 | 2094 | - | 0.344317 | |
g4627 | DLA_11614 | GAOABQK02H81I9 | CDS | 431673 | 1224 | + | 0.311274 | |
g4628 | DLA_05125 | GAOABQK02H81I9 | CDS | 434500 | 4944 | + | 0.344053 | |
g4629 | DLA_05126 | GAOABQK02H81I9 | CDS | 440362 | 2097 | - | 0.379113 | |
g463 | DLA_00513 | contig05409_1.exp | CDS | 1059390 | 642 | - | 0.311526 | |
g4630 | DLA_05127 | GAOABQK02H81I9 | CDS | 442861 | 378 | + | 0.261905 | |
g4631 | DLA_05128 | GAOABQK02H81I9 | CDS | 443410 | 1434 | - | 0.341702 | |
g4632 | DLA_05129 | GAOABQK02H81I9 | CDS | 445151 | 1266 | + | 0.325434 | |
g4633 | DLA_05130 | 32 kDa subunit of heterodimeric actin capping protein cap3234 34 kDa subunit is encoded by acpB contributes to the dynactin complex | GAOABQK02H81I9 | CDS | 446735 | 813 | - | 0.351784 |
g4634 | DLA_05131 | GAOABQK02H81I9 | CDS | 448234 | 198 | - | 0.30303 | |
g4635 | DLA_05132 | GAOABQK02H81I9 | CDS | 448847 | 1134 | - | 0.306878 | |
g4636 | DLA_05133 | GAOABQK02H81I9 | CDS | 450095 | 2898 | - | 0.329538 | |
g4637 | DLA_05134 | introduces a double bond at the delta position of fatty acids during the biosynthesis of monounsaturated fatty acids there is a second copy of this gene | GAOABQK02H81I9 | CDS | 453330 | 2007 | + | 0.290982 |
g4638 | DLA_05135 | GAOABQK02H81I9 | CDS | 455596 | 2094 | - | 0.39255 | |
g4639 | DLA_05137 | GAOABQK02H81I9 | CDS | 458245 | 3429 | - | 0.305628 | |
g464 | DLA_00514 | contig05409_1.exp | CDS | 1060493 | 582 | - | 0.293814 | |
g4640 | DLA_05138 | GAOABQK02H81I9 | CDS | 461863 | 1905 | - | 0.283989 | |
g4641 | DLA_05139 | GAOABQK02H81I9 | CDS | 464371 | 993 | + | 0.289023 | |
g4642 | DLA_05140 | GAOABQK02H81I9 | CDS | 466100 | 1581 | + | 0.392789 | |
g4643 | DLA_05141 | GAOABQK02H81I9 | CDS | 468799 | 1236 | + | 0.311489 | |
g4644 | DLA_05142 | GAOABQK02H81I9 | CDS | 471938 | 888 | + | 0.346847 | |
g4645 | DLA_05143 | GAOABQK02H81I9 | CDS | 472960 | 663 | - | 0.319759 | |
g4646 | DLA_05144 | GAOABQK02H81I9 | CDS | 474368 | 1326 | + | 0.310709 | |
g4647 | DLA_05145 | GAOABQK02H81I9 | CDS | 477470 | 990 | - | 0.284848 | |
g4648 | DLA_05146 | GAOABQK02H81I9 | CDS | 479260 | 3003 | + | 0.345987 | |
g4649 | DLA_05147 | GAOABQK02H81I9 | CDS | 482828 | 483 | + | 0.26501 | |
g465 | DLA_00515 | contig05409_1.exp | CDS | 1061562 | 1713 | - | 0.290718 | |
g4650 | DLA_05148 | GAOABQK02H81I9 | CDS | 483370 | 1431 | - | 0.317261 | |
g4651 | DLA_05149 | GAOABQK02H81I9 | CDS | 485411 | 1143 | - | 0.287839 | |
g4652 | DLA_05150 | GAOABQK02H81I9 | CDS | 486952 | 1659 | + | 0.317661 | |
g4653 | DLA_05151 | GAOABQK02H81I9 | CDS | 488758 | 999 | + | 0.313313 | |
g4654 | DLA_05152 | GAOABQK02H81I9 | CDS | 489833 | 1032 | - | 0.29845 | |
g4655 | DLA_05153 | GAOABQK02H81I9 | CDS | 491302 | 1122 | - | 0.302139 | |
g4656 | DLA_05154 | GAOABQK02H81I9 | CDS | 493101 | 1419 | + | 0.302326 | |
g4657 | DLA_05155 | GAOABQK02H81I9 | CDS | 494831 | 3852 | + | 0.300623 | |
g4658 | DLA_05156 | GAOABQK02H81I9 | CDS | 499080 | 258 | - | 0.313953 | |
g4659 | DLA_05157 | GAOABQK02H81I9 | CDS | 499913 | 5685 | + | 0.319085 | |
g466 | DLA_00516 | contig05409_1.exp | CDS | 1064300 | 3774 | + | 0.330419 | |
g4660 | DLA_05158 | GAOABQK02H81I9 | CDS | 505775 | 1137 | - | 0.347405 | |
g4661 | DLA_05159 | GAOABQK02H81I9 | CDS | 508706 | 1284 | - | 0.250779 | |
g4662 | DLA_05160 | GAOABQK02H81I9 | CDS | 510260 | 2514 | - | 0.397375 | |
g4663 | DLA_05161 | GAOABQK02H81I9 | CDS | 513663 | 1545 | + | 0.239482 | |
g4664 | DLA_05162 | GAOABQK02H81I9 | CDS | 516119 | 2649 | + | 0.333333 | |
g4665 | DLA_05163 | GAOABQK02H81I9 | CDS | 518915 | 4089 | + | 0.344828 | |
g4666 | DLA_05164 | GAOABQK02H81I9 | CDS | 523548 | 1218 | + | 0.286535 | |
g4667 | DLA_05165 | GAOABQK02H81I9 | CDS | 525606 | 2379 | + | 0.356032 | |
g4668 | DLA_05167 | GAOABQK02H81I9 | CDS | 528501 | 1167 | - | 0.308483 | |
g4669 | DLA_05168 | GAOABQK02H81I9 | CDS | 529948 | 1911 | - | 0.315542 | |
g467 | DLA_00519 | contig05409_1.exp | CDS | 1069362 | 1425 | + | 0.261754 | |
g4670 | DLA_05169 | GAOABQK02H81I9 | CDS | 532004 | 837 | + | 0.252091 | |
g4671 | DLA_05171 | GAOABQK02H81I9 | CDS | 533272 | 2589 | - | 0.298185 | |
g4672 | DLA_05172 | GAOABQK02H81I9 | CDS | 536309 | 1569 | + | 0.354366 | |
g4673 | DLA_05173 | GAOABQK02H81I9 | CDS | 538297 | 957 | - | 0.336468 | |
g4674 | DLA_05175 | GAOABQK02H81I9 | CDS | 539720 | 828 | + | 0.339372 | |
g4675 | DLA_05176 | GAOABQK02H81I9 | CDS | 540739 | 1557 | + | 0.321773 | |
g4676 | DLA_05177 | GAOABQK02H81I9 | CDS | 542687 | 4617 | + | 0.357375 | |
g4677 | DLA_05178 | GAOABQK02H81I9 | CDS | 547620 | 1284 | + | 0.281931 | |
g4678 | DLA_05179 | GAOABQK02H81I9 | CDS | 549332 | 1062 | - | 0.297552 | |
g4679 | DLA_05180 | similar to plant and fungi NADH dehydrogenases such as S. cerevisiae NDE1 and NDE2 the external mitochondrial NADH dehydrogenases that catalyze the oxidation of cytosolic NADH | GAOABQK02H81I9 | CDS | 550928 | 1839 | + | 0.340946 |
g468 | DLA_00520 | contig05409_1.exp | CDS | 1070907 | 1311 | - | 0.343249 | |
g4680 | DLA_05181 | GAOABQK02H81I9 | CDS | 553088 | 1659 | + | 0.335744 | |
g4681 | DLA_05182 | GAOABQK02H81I9 | CDS | 554984 | 3123 | + | 0.32789 | |
g4682 | DLA_05183 | GAOABQK02H81I9 | CDS | 558390 | 900 | - | 0.294444 | |
g4683 | DLA_05184 | GAOABQK02H81I9 | CDS | 559866 | 1626 | - | 0.346248 | |
g4684 | DLA_05185 | GAOABQK02H81I9 | CDS | 561941 | 3432 | + | 0.323135 | |
g4685 | DLA_05186 | GAOABQK02H81I9 | CDS | 565576 | 2376 | + | 0.301347 | |
g4686 | DLA_11615 | GAOABQK02H81I9 | CDS | 569021 | 285 | + | 0.259649 | |
g4687 | DLA_05187 | GAOABQK02H81I9 | CDS | 570034 | 5094 | + | 0.3936 | |
g4688 | DLA_05189 | GAOABQK02H81I9 | CDS | 576721 | 726 | - | 0.278237 | |
g4689 | DLA_05192 | GAOABQK02H81I9 | CDS | 578951 | 4812 | + | 0.341854 | |
g469 | DLA_00521 | contig05409_1.exp | CDS | 1073050 | 1794 | - | 0.283724 | |
g4690 | DLA_05193 | GAOABQK02H81I9 | CDS | 583930 | 228 | + | 0.350877 | |
g4691 | DLA_05194 | GAOABQK02H81I9 | CDS | 584597 | 849 | - | 0.351001 | |
g4692 | DLA_05195 | GAOABQK02H81I9 | CDS | 586104 | 2238 | + | 0.32529 | |
g4693 | DLA_05196 | GAOABQK02H81I9 | CDS | 588581 | 867 | - | 0.327566 | |
g4694 | DLA_05197 | GAOABQK02H81I9 | CDS | 589804 | 1263 | - | 0.360253 | |
g4695 | DLA_05198 | GAOABQK02H81I9 | CDS | 591173 | 1695 | + | 0.292035 | |
g4696 | DLA_05199 | GAOABQK02H81I9 | CDS | 593090 | 1014 | + | 0.259369 | |
g4697 | DLA_05200 | GAOABQK02H81I9 | CDS | 594278 | 1791 | - | 0.367393 | |
g4698 | DLA_05201 | GAOABQK02H81I9 | CDS | 596562 | 471 | - | 0.246284 | |
g4699 | DLA_05203 | GAOABQK02H81I9 | CDS | 597680 | 2328 | - | 0.341065 | |
g47 | DLA_00056 | contig05409_1.exp | CDS | 125462 | 1800 | - | 0.28 | |
g470 | DLA_11444 | contig05409_1.exp | CDS | 1075769 | 1794 | - | 0.29097 | |
g4700 | DLA_05204 | GAOABQK02H81I9 | CDS | 600487 | 378 | + | 0.301587 | |
g4701 | DLA_05205 | GAOABQK02H81I9 | CDS | 600927 | 1524 | - | 0.312992 | |
g4702 | DLA_05206 | GAOABQK02H81I9 | CDS | 602736 | 1104 | + | 0.413043 | |
g4703 | DLA_05208 | GAOABQK02H81I9 | CDS | 604510 | 1080 | + | 0.35463 | |
g4704 | DLA_05210 | GAOABQK02H81I9 | CDS | 606799 | 1722 | + | 0.372242 | |
g4705 | DLA_05211 | GAOABQK02H81I9 | CDS | 609105 | 603 | + | 0.320066 | |
g4706 | DLA_11616 | GAOABQK02H81I9 | CDS | 609851 | 549 | + | 0.300546 | |
g4707 | DLA_05212 | GAOABQK02H81I9 | CDS | 610450 | 1050 | - | 0.361905 | |
g4708 | DLA_05214 | GAOABQK02H81I9 | CDS | 611690 | 465 | + | 0.393548 | |
g4709 | DLA_05215 | GAOABQK02H81I9 | CDS | 612728 | 2121 | + | 0.345592 | |
g471 | DLA_00522 | contig05409_1.exp | CDS | 1077970 | 993 | + | 0.299094 | |
g4710 | DLA_05216 | GAOABQK02H81I9 | CDS | 615246 | 3444 | + | 0.31417 | |
g4711 | DLA_05217 | GAOABQK02H81I9 | CDS | 618941 | 2283 | - | 0.406483 | |
g4712 | DLA_05219 | GAOABQK02H81I9 | CDS | 623137 | 1818 | - | 0.326733 | |
g4713 | DLA_05220 | GAOABQK02H81I9 | CDS | 625114 | 3246 | + | 0.385089 | |
g4714 | DLA_05221 | GAOABQK02H81I9 | CDS | 628551 | 1014 | - | 0.281065 | |
g4715 | DLA_05222 | GAOABQK02H81I9 | CDS | 629973 | 1425 | + | 0.322807 | |
g4716 | DLA_11617 | GAOABQK02H81I9 | CDS | 631455 | 603 | + | 0.33665 | |
g4717 | DLA_05223 | GAOABQK02H81I9 | CDS | 632704 | 2310 | + | 0.321645 | |
g4718 | DLA_05224 | GAOABQK02H81I9 | CDS | 635593 | 2496 | + | 0.338141 | |
g4719 | DLA_05225 | GAOABQK02H81I9 | CDS | 638237 | 2286 | - | 0.316273 | |
g472 | DLA_00523 | contig05409_1.exp | CDS | 1079189 | 1794 | - | 0.291527 | |
g4720 | DLA_05226 | GAOABQK02H81I9 | CDS | 640685 | 2472 | + | 0.305825 | |
g4721 | DLA_05227 | GAOABQK02H81I9 | CDS | 643943 | 1890 | - | 0.285185 | |
g4722 | DLA_05228 | GAOABQK02H81I9 | CDS | 647116 | 1509 | + | 0.293572 | |
g4723 | DLA_05229 | GAOABQK02H81I9 | CDS | 649346 | 2100 | + | 0.284286 | |
g4724 | DLA_05230 | GAOABQK02H81I9 | CDS | 652842 | 1569 | + | 0.298279 | |
g4725 | DLA_05231 | GAOABQK02H81I9 | CDS | 655814 | 1572 | + | 0.295165 | |
g4726 | DLA_05232 | GAOABQK02H81I9 | CDS | 658227 | 2241 | + | 0.297189 | |
g4727 | DLA_05233 | ortholog of QDPR which catalyzes the NADH-mediated reduction of quinonoid dihydrobiopterin (a 5678-tetrahydropteridine NAD(P) a 67-dihydropteridine NAD(P)H H) the last step of tetrahydrobiopterin (BH4) recycling in higher eukaryotes an essential cofactor | GAOABQK02H81I9 | CDS | 660832 | 693 | - | 0.382395 |
g4728 | DLA_05234 | GAOABQK02H81I9 | CDS | 661847 | 1650 | + | 0.358788 | |
g4729 | DLA_05235 | GAOABQK02H81I9 | CDS | 663654 | 1107 | + | 0.439024 | |
g473 | DLA_00524 | contig05409_1.exp | CDS | 1082442 | 4092 | + | 0.384409 | |
g4730 | DLA_05237 | GAOABQK02H81I9 | CDS | 665742 | 13893 | + | 0.388181 | |
g4731 | DLA_05238 | GAOABQK02H81I9 | CDS | 679874 | 2391 | - | 0.327896 | |
g4732 | DLA_05239 | GAOABQK02H81I9 | CDS | 682753 | 1710 | - | 0.34152 | |
g4733 | DLA_05240 | GAOABQK02H81I9 | CDS | 684946 | 783 | - | 0.330779 | |
g4734 | DLA_05241 | GAOABQK02H81I9 | CDS | 686309 | 1311 | - | 0.321129 | |
g4735 | DLA_05242 | GAOABQK02H81I9 | CDS | 688150 | 3072 | + | 0.349284 | |
g4736 | DLA_05243 | GAOABQK02H81I9 | CDS | 691670 | 678 | - | 0.256637 | |
g4737 | DLA_05244 | GAOABQK02H81I9 | CDS | 692587 | 3522 | - | 0.35406 | |
g4738 | DLA_05245 | GAOABQK02H81I9 | CDS | 696574 | 504 | - | 0.388889 | |
g4739 | DLA_05246 | GAOABQK02H81I9 | CDS | 697251 | 1788 | - | 0.323826 | |
g474 | DLA_00525 | contig05409_1.exp | CDS | 1087035 | 3075 | + | 0.292358 | |
g4740 | DLA_05249 | GAOABQK02H81I9 | CDS | 703002 | 1683 | + | 0.332145 | |
g4741 | DLA_05250 | GAOABQK02H81I9 | CDS | 705051 | 555 | - | 0.371171 | |
g4742 | DLA_11618 | GAOABQK02H81I9 | CDS | 706058 | 1098 | + | 0.331512 | |
g4743 | DLA_05251 | GAOABQK02H81I9 | CDS | 707370 | 3147 | + | 0.328249 | |
g4744 | DLA_05252 | GAOABQK02H81I9 | CDS | 710775 | 3687 | + | 0.335503 | |
g4745 | DLA_05253 | GAOABQK02H81I9 | CDS | 714553 | 507 | - | 0.343195 | |
g4746 | DLA_05254 | GAOABQK02H81I9 | CDS | 715647 | 582 | + | 0.33677 | |
g4747 | DLA_05255 | GAOABQK02H81I9 | CDS | 716446 | 417 | - | 0.335731 | |
g4748 | DLA_05256 | GAOABQK02H81I9 | CDS | 717459 | 1539 | - | 0.354776 | |
g4749 | DLA_05257 | conserved protein that is part of a post-splicing multiprotein complex involved in mRNA nuclear export the human ortholog interacts with | GAOABQK02H81I9 | CDS | 719662 | 558 | - | 0.302867 |
g475 | DLA_00526 | contig05409_1.exp | CDS | 1090252 | 270 | - | 0.414815 | |
g4750 | DLA_05258 | GAOABQK02H81I9 | CDS | 720529 | 2163 | + | 0.336107 | |
g4751 | DLA_05259 | GAOABQK02H81I9 | CDS | 722858 | 555 | - | 0.318919 | |
g4752 | DLA_05260 | GAOABQK02H81I9 | CDS | 724058 | 1770 | - | 0.30226 | |
g4753 | DLA_05261 | GAOABQK02H81I9 | CDS | 726932 | 558 | + | 0.318996 | |
g4754 | DLA_05262 | GAOABQK02H81I9 | CDS | 727833 | 3069 | - | 0.285761 | |
g4755 | DLA_05263 | GAOABQK02H81I9 | CDS | 731419 | 3042 | - | 0.286982 | |
g4756 | DLA_05264 | GAOABQK02H81I9 | CDS | 735023 | 3078 | - | 0.288499 | |
g4757 | DLA_05265 | GAOABQK02H81I9 | CDS | 738634 | 2073 | + | 0.302943 | |
g4758 | DLA_05266 | GAOABQK02H81I9 | CDS | 740766 | 4119 | - | 0.334547 | |
g4759 | DLA_05267 | GAOABQK02H81I9 | CDS | 745289 | 3912 | + | 0.304703 | |
g476 | DLA_00527 | contig05409_1.exp | CDS | 1090993 | 2856 | + | 0.306022 | |
g4760 | DLA_05268 | GAOABQK02H81I9 | CDS | 749552 | 3879 | + | 0.310131 | |
g4761 | DLA_11619 | GAOABQK02H81I9 | CDS | 753710 | 1008 | + | 0.295635 | |
g4762 | DLA_05269 | GAOABQK02H81I9 | CDS | 754854 | 2766 | + | 0.310557 | |
g4763 | DLA_05270 | GAOABQK02H81I9 | CDS | 757797 | 3900 | + | 0.304615 | |
g4764 | DLA_05271 | GAOABQK02H81I9 | CDS | 761824 | 1086 | - | 0.338858 | |
g4765 | DLA_05272 | GAOABQK02H81I9 | CDS | 763188 | 3198 | + | 0.300188 | |
g4766 | DLA_05275 | GAOABQK02H81I9 | CDS | 767724 | 4059 | + | 0.292929 | |
g4767 | DLA_05276 | GAOABQK02H81I9 | CDS | 771912 | 1455 | - | 0.341581 | |
g4768 | DLA_05277 | GAOABQK02H81I9 | CDS | 773592 | 669 | + | 0.272048 | |
g4769 | DLA_05278 | GAOABQK02H81I9 | CDS | 774378 | 2373 | - | 0.334598 | |
g477 | DLA_00529 | contig05409_1.exp | CDS | 1093998 | 2502 | - | 0.338129 | |
g4770 | DLA_05279 | GAOABQK02H81I9 | CDS | 777621 | 537 | + | 0.337058 | |
g4771 | DLA_05280 | GAOABQK02H81I9 | CDS | 778487 | 750 | - | 0.312 | |
g4772 | DLA_05281 | GAOABQK02H81I9 | CDS | 779593 | 4461 | + | 0.335351 | |
g4773 | DLA_05282 | GAOABQK02H81I9 | CDS | 784686 | 2667 | + | 0.32021 | |
g4774 | DLA_05283 | GAOABQK02H81I9 | CDS | 787377 | 876 | - | 0.317352 | |
g4775 | DLA_05287 | GAOABQK02H81I9 | CDS | 790281 | 2946 | - | 0.350645 | |
g4776 | DLA_05288 | GAOABQK02H81I9 | CDS | 793736 | 747 | + | 0.30656 | |
g4777 | DLA_05289 | GAOABQK02H81I9 | CDS | 795672 | 387 | + | 0.361757 | |
g4778 | DLA_05290 | GAOABQK02H81I9 | CDS | 796339 | 921 | - | 0.314875 | |
g4779 | DLA_05291 | GAOABQK02H81I9 | CDS | 797559 | 387 | - | 0.346253 | |
g478 | DLA_00530 | contig05409_1.exp | CDS | 1096723 | 1077 | - | 0.359331 | |
g4780 | DLA_05292 | GAOABQK02H81I9 | CDS | 798763 | 1227 | - | 0.315403 | |
g4781 | DLA_11620 | GAOABQK02H81I9 | CDS | 800461 | 381 | + | 0.296588 | |
g4782 | DLA_05294 | GAOABQK02H81I9 | CDS | 801108 | 2241 | + | 0.327532 | |
g4783 | DLA_11621 | GAOABQK02H81I9 | CDS | 803570 | 3294 | + | 0.329387 | |
g4784 | DLA_05295 | GAOABQK02H81I9 | CDS | 806986 | 5853 | - | 0.320178 | |
g4785 | DLA_05296 | GAOABQK02H81I9 | CDS | 813575 | 954 | + | 0.309224 | |
g4786 | DLA_05297 | GAOABQK02H81I9 | CDS | 814656 | 228 | + | 0.29386 | |
g4787 | DLA_05298 | GAOABQK02H81I9 | CDS | 815038 | 3195 | - | 0.305164 | |
g4788 | DLA_05299 | GAOABQK02H81I9 | CDS | 818911 | 1635 | - | 0.334557 | |
g4789 | DLA_11622 | GAOABQK02H81I9 | CDS | 821379 | 321 | - | 0.34891 | |
g479 | DLA_00531 | contig05409_1.exp | CDS | 1098948 | 4128 | + | 0.349806 | |
g4790 | DLA_05300 | GAOABQK02H81I9 | CDS | 822421 | 219 | + | 0.315068 | |
g4791 | DLA_05301 | GAOABQK02H81I9 | CDS | 823230 | 1413 | - | 0.303609 | |
g4792 | DLA_05303 | GAOABQK02H81I9 | CDS | 825304 | 1197 | - | 0.315789 | |
g4793 | DLA_05305 | controls the topological state of DNA by transient double-strand breakage and subsequent rejoining of DNA strands this is predicted to be a nuclear topoisomerase II | GAOABQK02H81I9 | CDS | 826964 | 3756 | - | 0.305644 |
g4794 | DLA_05306 | GAOABQK02H81I9 | CDS | 830981 | 906 | + | 0.336645 | |
g4795 | DLA_05307 | GAOABQK02H81I9 | CDS | 831961 | 1068 | - | 0.273408 | |
g4796 | DLA_05308 | GAOABQK02H81I9 | CDS | 833131 | 2166 | - | 0.256694 | |
g4797 | DLA_05309 | GAOABQK02H81I9 | CDS | 835682 | 222 | + | 0.346847 | |
g4798 | DLA_05310 | GAOABQK02H81I9 | CDS | 836495 | 252 | - | 0.420635 | |
g4799 | DLA_05311 | GAOABQK02H81I9 | CDS | 837212 | 1719 | - | 0.250727 | |
g48 | DLA_00057 | contig05409_1.exp | CDS | 127351 | 864 | + | 0.287037 | |
g480 | DLA_00532 | contig05409_1.exp | CDS | 1103482 | 2301 | + | 0.300304 | |
g4800 | DLA_05313 | GAOABQK02H81I9 | CDS | 839363 | 3039 | - | 0.336624 | |
g4801 | DLA_05314 | GAOABQK02H81I9 | CDS | 842823 | 516 | + | 0.25969 | |
g4802 | DLA_05315 | GAOABQK02H81I9 | CDS | 843458 | 306 | - | 0.267974 | |
g4803 | DLA_05320 | GAOABQK02H81I9 | CDS | 848662 | 291 | + | 0.319588 | |
g4804 | DLA_05321 | GAOABQK02H81I9 | CDS | 849549 | 1623 | - | 0.376463 | |
g4805 | DLA_05322 | GAOABQK02H81I9 | CDS | 851639 | 384 | + | 0.393229 | |
g4806 | DLA_05323 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | GAOABQK02H81I9 | CDS | 853023 | 3603 | - | 0.352206 |
g4807 | DLA_05324 | GAOABQK02H81I9 | CDS | 856796 | 849 | - | 0.365135 | |
g4808 | DLA_05325 | GAOABQK02H81I9 | CDS | 858970 | 1842 | - | 0.315961 | |
g4809 | DLA_05326 | GAOABQK02H81I9 | CDS | 861777 | 900 | + | 0.285556 | |
g481 | DLA_00533 | contig05409_1.exp | CDS | 1105888 | 2304 | + | 0.323785 | |
g4810 | DLA_05327 | GAOABQK02H81I9 | CDS | 862921 | 1608 | - | 0.341418 | |
g4811 | DLA_05328 | GAOABQK02H81I9 | CDS | 864922 | 1761 | + | 0.284497 | |
g4812 | DLA_05329 | GAOABQK02H81I9 | CDS | 867194 | 1119 | - | 0.310992 | |
g4813 | DLA_11623 | GAOABQK02H81I9 | CDS | 868566 | 228 | + | 0.267544 | |
g4814 | DLA_05330 | GAOABQK02H81I9 | CDS | 870660 | 1269 | + | 0.322301 | |
g4815 | DLA_05331 | GAOABQK02H81I9 | CDS | 872232 | 585 | + | 0.251282 | |
g4816 | DLA_05332 | GAOABQK02H81I9 | CDS | 873335 | 2250 | - | 0.326667 | |
g4817 | DLA_05334 | GAOABQK02HF6HV | CDS | 2 | 3076 | - | 0.414824 | |
g4818 | DLA_05335 | CAZy family GT57 catalyzes N-linked glucosylation | GAOABQK02HOVEJ | CDS | 808 | 1344 | + | 0.276786 |
g4819 | DLA_05336 | GAOABQK02HOVEJ | CDS | 2719 | 3027 | - | 0.268913 | |
g482 | DLA_00534 | protein component of the small (40S) ribosomal subunit there is a second copy of this gene | contig05409_1.exp | CDS | 1108352 | 198 | - | 0.388889 |
g4820 | DLA_05337 | GAOABQK02HOVEJ | CDS | 6001 | 1035 | + | 0.323671 | |
g4821 | DLA_05338 | GAOABQK02HOVEJ | CDS | 7375 | 309 | - | 0.381877 | |
g4822 | DLA_05339 | GAOABQK02HOVEJ | CDS | 7922 | 681 | + | 0.295154 | |
g4823 | DLA_05340 | GAOABQK02HOVEJ | CDS | 9343 | 843 | - | 0.309609 | |
g4824 | DLA_11624 | GAOABQK02HUB3S | CDS | 3 | 207 | + | 0.188406 | |
g4825 | DLA_05341 | GAOABQK02HUB3S | CDS | 281 | 3021 | - | 0.289639 | |
g4826 | DLA_05342 | GAOABQK02HUB3S | CDS | 3437 | 327 | - | 0.266055 | |
g4827 | DLA_05343 | GAOABQK02HUB3S | CDS | 4998 | 1944 | - | 0.309156 | |
g4828 | DLA_05344 | GAOABQK02HUB3S | CDS | 7038 | 978 | - | 0.290389 | |
g4829 | DLA_05347 | GAOABQK02HUB3S | CDS | 10460 | 573 | + | 0.303665 | |
g483 | DLA_00535 | similar to H. sapiens REXO2 and S. cerevisiae REX2 a mitochondrial 3'-5' RNA exonuclease there is a second copy of this gene | contig05409_1.exp | CDS | 1109180 | 636 | + | 0.311321 |
g4830 | DLA_05348 | GAOABQK02HUB3S | CDS | 11346 | 1809 | - | 0.319514 | |
g4831 | DLA_05349 | GAOABQK02HUB3S | CDS | 13534 | 3093 | - | 0.2871 | |
g4832 | DLA_05350 | GAOABQK02HUB3S | CDS | 16828 | 1536 | - | 0.266927 | |
g4833 | DLA_05351 | GAOABQK02HUB3S | CDS | 18635 | 1593 | + | 0.338983 | |
g4834 | DLA_05352 | GAOABQK02HUB3S | CDS | 20660 | 402 | - | 0.328358 | |
g4835 | DLA_05353 | GAOABQK02HUB3S | CDS | 21104 | 204 | - | 0.313726 | |
g4836 | DLA_05354 | GAOABQK02HUB3S | CDS | 21622 | 4881 | - | 0.331694 | |
g4837 | DLA_05355 | GAOABQK02HUB3S | CDS | 26955 | 1776 | + | 0.282658 | |
g4838 | DLA_05356 | GAOABQK02HUB3S | CDS | 28813 | 714 | - | 0.259104 | |
g4839 | DLA_05357 | GAOABQK02HUB3S | CDS | 29952 | 1026 | - | 0.28655 | |
g484 | DLA_00536 | shares a short region of similarity with the human gene TEX2 (expressed in testis) there is a second copy of this gene | contig05409_1.exp | CDS | 1109911 | 2463 | - | 0.332115 |
g4840 | DLA_05358 | GAOABQK02HUB3S | CDS | 32577 | 4410 | - | 0.314512 | |
g4841 | DLA_05359 | GAOABQK02HUB3S | CDS | 38007 | 1365 | - | 0.317216 | |
g4842 | DLA_05360 | GAOABQK02HUB3S | CDS | 39619 | 1707 | - | 0.298184 | |
g4843 | DLA_05361 | GAOABQK02HUB3S | CDS | 41559 | 612 | + | 0.25817 | |
g4844 | DLA_05363 | GAOABQK02HUB3S | CDS | 42808 | 564 | - | 0.283688 | |
g4845 | DLA_05364 | GAOABQK02HUB3S | CDS | 43490 | 1908 | + | 0.34434 | |
g4846 | DLA_05365 | GAOABQK02HUB3S | CDS | 45595 | 804 | - | 0.324627 | |
g4847 | DLA_05366 | GAOABQK02HUB3S | CDS | 47127 | 969 | - | 0.338493 | |
g4848 | DLA_05367 | catalyzes the reaction succinyl-CoA enzyme N6-(dihydrolipoyl)lysine CoA enzyme N6-(S-succinyldihydrolipoyl) lysine E2 component of the multienzyme 2-oxoglutarate dehydrogenase complex | GAOABQK02HUB3S | CDS | 48947 | 1356 | + | 0.338496 |
g4849 | DLA_05368 | GAOABQK02HUB3S | CDS | 50661 | 528 | + | 0.361742 | |
g485 | DLA_00537 | contig05409_1.exp | CDS | 1113170 | 1707 | + | 0.343292 | |
g4850 | DLA_05369 | protein with a beigeBEACH domain a weak protein kinase domain and N-terminal WD40 repeats does not contain the consensus sequences required for kinase function | GAOABQK02HUB3S | CDS | 51787 | 5412 | + | 0.301737 |
g4851 | DLA_05372 | GAOABQK02HUB3S | CDS | 57856 | 1383 | + | 0.274042 | |
g4852 | DLA_05373 | GAOABQK02HUB3S | CDS | 59716 | 3984 | - | 0.296436 | |
g4853 | DLA_05374 | GAOABQK02HUB3S | CDS | 64717 | 993 | - | 0.314199 | |
g4854 | DLA_05375 | GAOABQK02HUB3S | CDS | 66509 | 1611 | + | 0.325264 | |
g4855 | DLA_05376 | GAOABQK02HUB3S | CDS | 69940 | 2490 | + | 0.326908 | |
g4856 | DLA_05377 | GAOABQK02HUB3S | CDS | 72989 | 1815 | - | 0.296419 | |
g4857 | DLA_05378 | GAOABQK02HUB3S | CDS | 74972 | 636 | - | 0.272013 | |
g4858 | DLA_05379 | GAOABQK02HUB3S | CDS | 75924 | 1365 | - | 0.275458 | |
g4859 | DLA_05380 | GAOABQK02HUB3S | CDS | 77483 | 1095 | + | 0.353425 | |
g486 | DLA_00538 | contig05409_1.exp | CDS | 1115144 | 207 | - | 0.338164 | |
g4860 | DLA_05381 | GAOABQK02HUB3S | CDS | 78868 | 924 | + | 0.316017 | |
g4861 | DLA_05382 | GAOABQK02HUB3S | CDS | 80067 | 1020 | - | 0.352941 | |
g4862 | DLA_05383 | involved in regulation of aggregate size member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | GAOABQK02HUB3S | CDS | 81730 | 894 | - | 0.326622 |
g4863 | DLA_05385 | GAOABQK02HUB3S | CDS | 82935 | 5202 | + | 0.328143 | |
g4864 | DLA_05386 | GAOABQK02HUB3S | CDS | 88899 | 4290 | + | 0.293706 | |
g4865 | DLA_05387 | GAOABQK02HUB3S | CDS | 93561 | 675 | + | 0.322963 | |
g4866 | DLA_05388 | GAOABQK02HUB3S | CDS | 94289 | 987 | - | 0.291793 | |
g4867 | DLA_05389 | GAOABQK02HUB3S | CDS | 95609 | 603 | + | 0.313433 | |
g4868 | DLA_05390 | GAOABQK02HUB3S | CDS | 96467 | 561 | - | 0.301248 | |
g4869 | DLA_05392 | GAOABQK02HUB3S | CDS | 98602 | 2964 | - | 0.337045 | |
g487 | DLA_00539 | contig05409_1.exp | CDS | 1115813 | 951 | + | 0.343849 | |
g4870 | DLA_05393 | class 1 myosin lacking the traditional tail domains common to short-tailed myosins binds actin and is in complex with several other proteins involved in phagocytosis maintenance of cortical tension and motility | GAOABQK02HUB3S | CDS | 104164 | 2583 | - | 0.388695 |
g4871 | DLA_05394 | GAOABQK02HUB3S | CDS | 107721 | 1341 | + | 0.343028 | |
g4872 | DLA_05395 | GAOABQK02HUB3S | CDS | 109604 | 1632 | - | 0.340074 | |
g4873 | DLA_05396 | GAOABQK02HUB3S | CDS | 111775 | 909 | + | 0.278328 | |
g4874 | DLA_05397 | GAOABQK02HUB3S | CDS | 112856 | 4044 | - | 0.315529 | |
g4875 | DLA_05399 | GAOABQK02HUB3S | CDS | 118065 | 1359 | + | 0.308315 | |
g4876 | DLA_05400 | promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form required for adenylate cyclase activation and chemotaxis | GAOABQK02HUB3S | CDS | 119654 | 2454 | - | 0.321108 |
g4877 | DLA_05401 | GAOABQK02HUB3S | CDS | 123004 | 7272 | + | 0.331958 | |
g4878 | DLA_05402 | GAOABQK02HUB3S | CDS | 131170 | 1236 | + | 0.324434 | |
g4879 | DLA_05403 | GAOABQK02HUB3S | CDS | 132771 | 2211 | + | 0.303935 | |
g488 | DLA_00540 | contig05409_1.exp | CDS | 1116892 | 1542 | + | 0.28275 | |
g4880 | DLA_05404 | GAOABQK02HUB3S | CDS | 135164 | 1641 | - | 0.316271 | |
g4881 | DLA_05405 | GAOABQK02HUB3S | CDS | 137029 | 330 | - | 0.263636 | |
g4882 | DLA_05406 | GAOABQK02HUB3S | CDS | 137743 | 1446 | + | 0.330567 | |
g4883 | DLA_05407 | GAOABQK02HUB3S | CDS | 139579 | 654 | + | 0.279817 | |
g4884 | DLA_05408 | putative Ca2 channel similar to metazoan polycystin-2 (PKD2) defects in the human PKD2 causes polycystic kidney disease autosomal dominant type 2 (ADPKD2) characterized by progressive formation and enlargement of cysts in both kidneys contains 6 putative transmembrane domains | GAOABQK02HUB3S | CDS | 140430 | 2349 | - | 0.290762 |
g4885 | DLA_05409 | GAOABQK02HUB3S | CDS | 143288 | 537 | - | 0.320298 | |
g4886 | DLA_05410 | GAOABQK02HUB3S | CDS | 144754 | 3432 | + | 0.33042 | |
g4887 | DLA_05411 | GAOABQK02HUB3S | CDS | 148443 | 1041 | - | 0.329491 | |
g4888 | DLA_05412 | GAOABQK02HUB3S | CDS | 149655 | 492 | - | 0.302846 | |
g4889 | DLA_05413 | GAOABQK02HUB3S | CDS | 152112 | 2007 | + | 0.310414 | |
g489 | DLA_00541 | contig05409_1.exp | CDS | 1118581 | 1500 | + | 0.278667 | |
g4890 | DLA_05414 | GAOABQK02HUB3S | CDS | 154454 | 3750 | + | 0.316267 | |
g4891 | DLA_05415 | GAOABQK02HUB3S | CDS | 158319 | 3612 | - | 0.299557 | |
g4892 | DLA_05417 | GAOABQK02HUB3S | CDS | 164700 | 1116 | + | 0.344982 | |
g4893 | DLA_11625 | GAOABQK02HUB3S | CDS | 166149 | 855 | + | 0.28655 | |
g4894 | DLA_11626 | GAOABQK02HUB3S | CDS | 167145 | 1851 | + | 0.288493 | |
g4895 | DLA_05418 | ortholog of human CD2 binding proteinproline-serine-threonine phosphatase-interacting protein 1 | GAOABQK02HUB3S | CDS | 169483 | 1155 | + | 0.315152 |
g4896 | DLA_05419 | GAOABQK02HUB3S | CDS | 171383 | 699 | + | 0.329041 | |
g4897 | DLA_05420 | GAOABQK02HUB3S | CDS | 172197 | 870 | + | 0.27931 | |
g4898 | DLA_05421 | GAOABQK02HUB3S | CDS | 173274 | 1485 | + | 0.36229 | |
g4899 | DLA_05423 | GAOABQK02HUB3S | CDS | 176252 | 405 | + | 0.325926 | |
g49 | DLA_00058 | contig05409_1.exp | CDS | 128252 | 1062 | - | 0.322034 | |
g490 | DLA_00542 | contig05409_1.exp | CDS | 1120143 | 3522 | - | 0.329926 | |
g4900 | DLA_05424 | GAOABQK02HUB3S | CDS | 176828 | 1302 | + | 0.395545 | |
g4901 | DLA_11627 | GAOABQK02HUB3S | CDS | 178675 | 828 | - | 0.301932 | |
g4902 | DLA_05425 | GAOABQK02HUB3S | CDS | 179887 | 4707 | - | 0.369875 | |
g4903 | DLA_05426 | GAOABQK02HUB3S | CDS | 185193 | 921 | + | 0.313789 | |
g4904 | DLA_05427 | GAOABQK02HUB3S | CDS | 187169 | 1647 | + | 0.352155 | |
g4905 | DLA_05428 | GAOABQK02HUB3S | CDS | 189774 | 1716 | - | 0.317599 | |
g4906 | DLA_05429 | GAOABQK02HUB3S | CDS | 191873 | 1194 | + | 0.268844 | |
g4907 | DLA_05430 | GAOABQK02HUB3S | CDS | 193524 | 1392 | - | 0.329741 | |
g4908 | DLA_05431 | GAOABQK02HUB3S | CDS | 197237 | 942 | + | 0.299363 | |
g4909 | DLA_05432 | GAOABQK02HUB3S | CDS | 198696 | 1263 | - | 0.285036 | |
g491 | DLA_00543 | contig05409_1.exp | CDS | 1125165 | 1923 | + | 0.453978 | |
g4910 | DLA_05434 | GAOABQK02HUB3S | CDS | 201883 | 1608 | - | 0.297886 | |
g4911 | DLA_05435 | GAOABQK02HUB3S | CDS | 204157 | 2544 | - | 0.315645 | |
g4912 | DLA_05436 | GAOABQK02HUB3S | CDS | 209415 | 1434 | + | 0.297071 | |
g4913 | DLA_05437 | GAOABQK02HUB3S | CDS | 211177 | 999 | + | 0.282282 | |
g4914 | DLA_05438 | GAOABQK02HUB3S | CDS | 212394 | 2262 | - | 0.318744 | |
g4915 | DLA_05441 | GAOABQK02HUB3S | CDS | 215230 | 534 | - | 0.327715 | |
g4916 | DLA_05442 | GAOABQK02HUB3S | CDS | 215959 | 2430 | + | 0.292593 | |
g4917 | DLA_05443 | GAOABQK02HUB3S | CDS | 218537 | 4035 | + | 0.294176 | |
g4918 | DLA_05445 | GAOABQK02HUB3S | CDS | 224290 | 1515 | - | 0.255446 | |
g4919 | DLA_05446 | GAOABQK02HUB3S | CDS | 226348 | 1632 | + | 0.252451 | |
g492 | DLA_00544 | contig05409_1.exp | CDS | 1127337 | 1959 | - | 0.331291 | |
g4920 | DLA_05447 | GAOABQK02HUB3S | CDS | 228159 | 1572 | - | 0.322519 | |
g4921 | DLA_05448 | GAOABQK02HUB3S | CDS | 229933 | 765 | + | 0.364706 | |
g4922 | DLA_05449 | GAOABQK02HUB3S | CDS | 230833 | 921 | - | 0.295331 | |
g4923 | DLA_05450 | GAOABQK02HUB3S | CDS | 232799 | 849 | + | 0.285041 | |
g4924 | DLA_05452 | GAOABQK02HUB3S | CDS | 234122 | 2382 | + | 0.308984 | |
g4925 | DLA_05453 | GAOABQK02HUB3S | CDS | 236552 | 2322 | - | 0.306632 | |
g4926 | DLA_05454 | GAOABQK02HUB3S | CDS | 239569 | 1560 | + | 0.317949 | |
g4927 | DLA_05455 | GAOABQK02HUB3S | CDS | 241170 | 297 | + | 0.30303 | |
g4928 | DLA_05456 | similar to metazoan TRAP1 member of the HSP90 family translocates to mitochondria during the prestarvation response | GAOABQK02HUB3S | CDS | 242188 | 2121 | - | 0.330976 |
g4929 | DLA_05457 | GAOABQK02HUB3S | CDS | 244548 | 1584 | - | 0.313131 | |
g493 | DLA_00545 | contig05409_1.exp | CDS | 1129831 | 630 | + | 0.28254 | |
g4930 | DLA_11628 | GAOABQK02HUB3S | CDS | 246344 | 969 | + | 0.268318 | |
g4931 | DLA_05458 | GAOABQK02HUB3S | CDS | 247590 | 3984 | + | 0.320783 | |
g4932 | DLA_05459 | GAOABQK02HUB3S | CDS | 251911 | 2541 | - | 0.340024 | |
g4933 | DLA_05460 | GAOABQK02HUB3S | CDS | 255026 | 1092 | - | 0.326923 | |
g4934 | DLA_05461 | membrane ion channel activated by ATP may be involved in intracellular calcium signaling | GAOABQK02HUB3S | CDS | 256447 | 1152 | - | 0.337674 |
g4935 | DLA_05462 | GAOABQK02HUB3S | CDS | 257896 | 2493 | - | 0.318492 | |
g4936 | DLA_05464 | GAOABQK02HUB3S | CDS | 261635 | 1611 | - | 0.290503 | |
g4937 | DLA_05465 | GAOABQK02HUB3S | CDS | 263483 | 723 | - | 0.294606 | |
g4938 | DLA_05466 | GAOABQK02HUB3S | CDS | 264509 | 1287 | - | 0.355089 | |
g4939 | DLA_05467 | GAOABQK02HUB3S | CDS | 266219 | 870 | - | 0.317241 | |
g494 | DLA_00546 | contig05409_1.exp | CDS | 1131494 | 1059 | - | 0.325779 | |
g4940 | DLA_05469 | GAOABQK02HUB3S | CDS | 267817 | 300 | - | 0.293333 | |
g4941 | DLA_05470 | GAOABQK02HUB3S | CDS | 268370 | 972 | - | 0.307613 | |
g4942 | DLA_05471 | GAOABQK02HUB3S | CDS | 269785 | 885 | - | 0.326554 | |
g4943 | DLA_05472 | GAOABQK02HUB3S | CDS | 271101 | 936 | - | 0.311966 | |
g4944 | DLA_05473 | GAOABQK02HUB3S | CDS | 272308 | 903 | + | 0.315615 | |
g4945 | DLA_05474 | GAOABQK02HUB3S | CDS | 273646 | 654 | + | 0.385321 | |
g4946 | DLA_05475 | GAOABQK02HUB3S | CDS | 274521 | 1611 | + | 0.268156 | |
g4947 | DLA_05476 | GAOABQK02HUB3S | CDS | 276961 | 2271 | - | 0.323206 | |
g4948 | DLA_05477 | GAOABQK02HUB3S | CDS | 279782 | 852 | - | 0.342723 | |
g4949 | DLA_05479 | GAOABQK02HUB3S | CDS | 281350 | 1311 | + | 0.249428 | |
g495 | DLA_00547 | contig05409_1.exp | CDS | 1132796 | 3402 | - | 0.320988 | |
g4950 | DLA_05480 | GAOABQK02HUB3S | CDS | 282694 | 5865 | - | 0.299233 | |
g4951 | DLA_05481 | GAOABQK02HUB3S | CDS | 289405 | 1629 | - | 0.284223 | |
g4952 | DLA_05482 | GAOABQK02HUB3S | CDS | 291570 | 654 | + | 0.302752 | |
g4953 | DLA_05483 | GAOABQK02HUB3S | CDS | 292317 | 1140 | - | 0.322807 | |
g4954 | DLA_05484 | GAOABQK02HUB3S | CDS | 293988 | 2682 | - | 0.306861 | |
g4955 | DLA_05485 | expressed in prespore cells ortholog of peroxiredoxin 4 catalyzes the reaction reduced thioredoxin Hsub2subOsub2sub oxidized thioredoxin Hsub2subO | GAOABQK02HUB3S | CDS | 297755 | 633 | + | 0.383886 |
g4956 | DLA_05486 | GAOABQK02HUB3S | CDS | 298661 | 501 | - | 0.333333 | |
g4957 | DLA_05487 | GAOABQK02HUB3S | CDS | 299983 | 666 | + | 0.301802 | |
g4958 | DLA_05488 | GAOABQK02HUB3S | CDS | 300833 | 1170 | - | 0.321368 | |
g4959 | DLA_05489 | GAOABQK02HUB3S | CDS | 302421 | 1539 | - | 0.31319 | |
g496 | DLA_00548 | contig05409_1.exp | CDS | 1136551 | 987 | - | 0.342452 | |
g4960 | DLA_05490 | GAOABQK02HUB3S | CDS | 304164 | 663 | + | 0.3273 | |
g4961 | DLA_05491 | GAOABQK02HUB3S | CDS | 305018 | 4104 | - | 0.371589 | |
g4962 | DLA_05492 | GAOABQK02HUB3S | CDS | 309976 | 9201 | + | 0.34018 | |
g4963 | DLA_05493 | GAOABQK02HUB3S | CDS | 319345 | 1308 | + | 0.282875 | |
g4964 | DLA_11629 | GAOABQK02HUB3S | CDS | 320667 | 1365 | - | 0.289377 | |
g4965 | DLA_05494 | GAOABQK02HUB3S | CDS | 322199 | 1278 | - | 0.277778 | |
g4966 | DLA_05496 | GAOABQK02HUB3S | CDS | 323934 | 786 | + | 0.278626 | |
g4967 | DLA_05497 | GAOABQK02HUB3S | CDS | 324958 | 1785 | + | 0.32549 | |
g4968 | DLA_05498 | GAOABQK02HUB3S | CDS | 326938 | 1095 | - | 0.331507 | |
g4969 | DLA_05500 | GAOABQK02HUB3S | CDS | 328178 | 1584 | - | 0.266414 | |
g497 | DLA_00550 | contig05409_1.exp | CDS | 1139170 | 624 | + | 0.339744 | |
g4970 | DLA_05501 | GAOABQK02HUB3S | CDS | 330121 | 4398 | + | 0.351069 | |
g4971 | DLA_05503 | GAOABQK02HUB3S | CDS | 336459 | 1224 | + | 0.345588 | |
g4972 | DLA_05504 | contains 1 C2H2-type zinc finger homolog of human ZNF593 and S. cerevisiae BUD20 (bud site selection protein 20) | GAOABQK02HUB3S | CDS | 338127 | 408 | + | 0.311274 |
g4973 | DLA_05505 | similar to human NOC4L belongs to the CBFMAK21 family contains a CCAAT-binding_factor domain | GAOABQK02HUB3S | CDS | 338698 | 2022 | - | 0.320969 |
g4974 | DLA_05506 | GAOABQK02HUB3S | CDS | 341784 | 1617 | - | 0.29932 | |
g4975 | DLA_05507 | ortholog of the mammalian ATG16l1 which is involved in autophagy defects in human cause inflammatory bowel disease type 10 in D. discoideum involved in early development and tip formation | GAOABQK02HUB3S | CDS | 344440 | 1773 | + | 0.380711 |
g4976 | DLA_05508 | GAOABQK02HUB3S | CDS | 347052 | 1443 | + | 0.327096 | |
g4977 | DLA_05509 | GAOABQK02HUB3S | CDS | 349089 | 693 | + | 0.292929 | |
g4978 | DLA_05511 | GAOABQK02HUB3S | CDS | 350528 | 3336 | - | 0.344125 | |
g4979 | DLA_05512 | GAOABQK02HUB3S | CDS | 354598 | 909 | + | 0.339934 | |
g498 | DLA_00551 | contig05409_1.exp | CDS | 1140187 | 4632 | + | 0.330743 | |
g4980 | DLA_05513 | GAOABQK02HUB3S | CDS | 355576 | 471 | - | 0.307856 | |
g4981 | DLA_05514 | GAOABQK02HUB3S | CDS | 356402 | 927 | - | 0.283711 | |
g4982 | DLA_05515 | GAOABQK02HUB3S | CDS | 357944 | 366 | + | 0.295082 | |
g4983 | DLA_05516 | GAOABQK02HUB3S | CDS | 358351 | 8616 | - | 0.355966 | |
g4984 | DLA_05517 | GAOABQK02HUB3S | CDS | 367257 | 1614 | - | 0.286865 | |
g4985 | DLA_11630 | GAOABQK02HUB3S | CDS | 369000 | 1656 | + | 0.299517 | |
g4986 | DLA_05518 | GAOABQK02HUB3S | CDS | 370724 | 1563 | - | 0.315419 | |
g4987 | DLA_05519 | GAOABQK02HUB3S | CDS | 372387 | 1641 | + | 0.296161 | |
g4988 | DLA_05520 | GAOABQK02HUB3S | CDS | 374079 | 3261 | + | 0.289788 | |
g4989 | DLA_05521 | GAOABQK02HUB3S | CDS | 377592 | 1602 | + | 0.282147 | |
g499 | DLA_00552 | contig05409_1.exp | CDS | 1145161 | 921 | + | 0.35722 | |
g4990 | DLA_05522 | GAOABQK02HUB3S | CDS | 379447 | 990 | + | 0.338384 | |
g4991 | DLA_05525 | GAOABQK02HUB3S | CDS | 383190 | 1203 | - | 0.320033 | |
g4992 | DLA_05526 | GAOABQK02HUB3S | CDS | 384463 | 243 | - | 0.329218 | |
g4993 | DLA_05527 | GAOABQK02HUB3S | CDS | 385563 | 792 | + | 0.305556 | |
g4994 | DLA_05529 | GAOABQK02HUB3S | CDS | 386617 | 2148 | - | 0.325419 | |
g4995 | DLA_05530 | GAOABQK02HUB3S | CDS | 389156 | 813 | + | 0.297663 | |
g4996 | DLA_05531 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | GAOABQK02HUB3S | CDS | 390510 | 2007 | + | 0.39711 |
g4997 | DLA_05532 | GAOABQK02HUB3S | CDS | 392757 | 2364 | + | 0.278342 | |
g4998 | DLA_05533 | GAOABQK02HUB3S | CDS | 395597 | 1230 | + | 0.287805 | |
g4999 | DLA_05535 | GAOABQK02HUB3S | CDS | 398255 | 543 | - | 0.296501 | |
g5 | DLA_00006 | contig05409_1.exp | CDS | 10703 | 1887 | + | 0.259671 | |
g50 | DLA_00059 | contig05409_1.exp | CDS | 130429 | 660 | + | 0.327273 | |
g500 | DLA_00553 | contig05409_1.exp | CDS | 1146688 | 912 | + | 0.345395 | |
g5000 | DLA_05537 | catalyzes the reaction ATP L-phenylalanine tRNAPhe AMP diphosphate L-phenylalanyl-tRNAPhe | GAOABQK02HUB3S | CDS | 399206 | 1263 | + | 0.335709 |
g5001 | DLA_05538 | GAOABQK02HUB3S | CDS | 401139 | 1557 | + | 0.326268 | |
g5002 | DLA_05539 | GAOABQK02HUB3S | CDS | 402987 | 747 | - | 0.267738 | |
g5003 | DLA_05541 | GAOABQK02HUB3S | CDS | 404306 | 810 | - | 0.334568 | |
g5004 | DLA_05542 | GAOABQK02HUB3S | CDS | 405276 | 1542 | - | 0.302853 | |
g5005 | DLA_05543 | GAOABQK02HUB3S | CDS | 407066 | 858 | + | 0.322844 | |
g5006 | DLA_05544 | GAOABQK02HUB3S | CDS | 407970 | 1065 | - | 0.337089 | |
g5007 | DLA_05545 | GAOABQK02HUB3S | CDS | 409718 | 1875 | + | 0.352533 | |
g5008 | DLA_05546 | GAOABQK02HUB3S | CDS | 411859 | 1245 | + | 0.307631 | |
g5009 | DLA_11631 | GAOABQK02HUB3S | CDS | 413134 | 315 | - | 0.298413 | |
g501 | DLA_00554 | contig05409_1.exp | CDS | 1147813 | 1587 | + | 0.328923 | |
g5010 | DLA_05547 | GAOABQK02HUB3S | CDS | 414389 | 1524 | + | 0.410105 | |
g5011 | DLA_05550 | GAOABQK02HUB3S | CDS | 417367 | 1092 | - | 0.299451 | |
g5012 | DLA_05551 | GAOABQK02HUB3S | CDS | 419927 | 1536 | - | 0.281901 | |
g5013 | DLA_05552 | GAOABQK02HUB3S | CDS | 422006 | 1698 | + | 0.375147 | |
g5014 | DLA_05553 | GAOABQK02HUB3S | CDS | 423848 | 651 | + | 0.308756 | |
g5015 | DLA_05554 | GAOABQK02HUB3S | CDS | 424743 | 2100 | - | 0.321429 | |
g5016 | DLA_05555 | GAOABQK02HUB3S | CDS | 427700 | 1356 | + | 0.311947 | |
g5017 | DLA_05556 | GAOABQK02HUB3S | CDS | 429206 | 945 | - | 0.355556 | |
g5018 | DLA_05557 | GAOABQK02HUB3S | CDS | 430650 | 948 | + | 0.322785 | |
g5019 | DLA_05558 | GAOABQK02HUB3S | CDS | 431829 | 1227 | - | 0.267319 | |
g502 | DLA_00555 | contig05409_1.exp | CDS | 1149478 | 2172 | + | 0.336096 | |
g5020 | DLA_05559 | GAOABQK02HUB3S | CDS | 433306 | 1278 | + | 0.320814 | |
g5021 | DLA_05560 | GAOABQK02HUB3S | CDS | 434802 | 7788 | - | 0.351181 | |
g5022 | DLA_05562 | GAOABQK02HUB3S | CDS | 443405 | 1116 | - | 0.278674 | |
g5023 | DLA_05563 | GAOABQK02HUB3S | CDS | 445177 | 570 | + | 0.324561 | |
g5024 | DLA_05564 | GAOABQK02HUB3S | CDS | 447129 | 1587 | - | 0.269691 | |
g5025 | DLA_05565 | GAOABQK02HUB3S | CDS | 448957 | 3624 | + | 0.327263 | |
g5026 | DLA_05566 | GAOABQK02HUB3S | CDS | 452673 | 240 | - | 0.391667 | |
g5027 | DLA_05567 | GAOABQK02HUB3S | CDS | 453169 | 1458 | - | 0.301097 | |
g5028 | DLA_05568 | GAOABQK02HUB3S | CDS | 455025 | 642 | + | 0.352025 | |
g5029 | DLA_05569 | GAOABQK02HUB3S | CDS | 458627 | 759 | + | 0.293808 | |
g503 | DLA_00556 | contig05409_1.exp | CDS | 1151893 | 1089 | + | 0.362718 | |
g5030 | DLA_05570 | GAOABQK02HUB3S | CDS | 460304 | 1029 | + | 0.367347 | |
g5031 | DLA_05571 | GAOABQK02HUB3S | CDS | 461404 | 2952 | - | 0.32893 | |
g5032 | DLA_05572 | GAOABQK02HUB3S | CDS | 464705 | 1032 | + | 0.319767 | |
g5033 | DLA_05574 | GAOABQK02HUB3S | CDS | 466269 | 474 | + | 0.293249 | |
g5034 | DLA_05575 | GAOABQK02HUB3S | CDS | 468534 | 1458 | + | 0.353909 | |
g5035 | DLA_05576 | GAOABQK02HUB3S | CDS | 470323 | 1911 | + | 0.276818 | |
g5036 | DLA_05577 | GAOABQK02HUB3S | CDS | 473141 | 1350 | + | 0.346667 | |
g5037 | DLA_05578 | GAOABQK02HUB3S | CDS | 474758 | 3843 | - | 0.342961 | |
g5038 | DLA_05580 | GAOABQK02HUB3S | CDS | 480282 | 2535 | + | 0.358185 | |
g5039 | DLA_05581 | GAOABQK02HUB3S | CDS | 483219 | 450 | + | 0.36 | |
g504 | DLA_00557 | contig05409_1.exp | CDS | 1153319 | 1896 | + | 0.312764 | |
g5040 | DLA_05582 | GAOABQK02HUB3S | CDS | 483913 | 768 | - | 0.300781 | |
g5041 | DLA_05583 | GAOABQK02HUB3S | CDS | 485316 | 306 | + | 0.401961 | |
g5042 | DLA_05584 | GAOABQK02HUB3S | CDS | 486421 | 852 | + | 0.33216 | |
g5043 | DLA_05585 | GAOABQK02HUB3S | CDS | 487469 | 603 | - | 0.3466 | |
g5044 | DLA_05586 | GAOABQK02HUB3S | CDS | 488387 | 1941 | - | 0.309119 | |
g5045 | DLA_05587 | GAOABQK02HUB3S | CDS | 490528 | 552 | + | 0.240942 | |
g5046 | DLA_05588 | GAOABQK02HUB3S | CDS | 491194 | 1341 | + | 0.353468 | |
g5047 | DLA_05590 | GAOABQK02HUB3S | CDS | 493463 | 1287 | + | 0.272727 | |
g5048 | DLA_05591 | GAOABQK02HUB3S | CDS | 495003 | 1041 | - | 0.329491 | |
g5049 | DLA_05592 | GAOABQK02HUB3S | CDS | 496212 | 4731 | - | 0.355739 | |
g505 | DLA_00558 | contig05409_1.exp | CDS | 1155622 | 1032 | + | 0.325581 | |
g5050 | DLA_05593 | GAOABQK02HUB3S | CDS | 501681 | 3468 | - | 0.341695 | |
g5051 | DLA_05594 | GAOABQK02HUB3S | CDS | 505898 | 3144 | + | 0.338422 | |
g5052 | DLA_05595 | contains a predicted signal peptide there is a second copy of this gene | GAOABQK02HUB3S | CDS | 509163 | 4179 | - | 0.354152 |
g5053 | DLA_11632 | catalyzes the reaction ATP HCOsub3subsup-sup propionyl-CoA ADP phosphate D-methylmalonyl-CoA | GAOABQK02HUB3S | CDS | 513803 | 2064 | - | 0.380814 |
g5054 | DLA_11633 | GAOABQK02HUB3S | CDS | 516199 | 2838 | + | 0.340028 | |
g5055 | DLA_05596 | GAOABQK02HUB3S | CDS | 520123 | 3354 | + | 0.330352 | |
g5056 | DLA_05597 | GAOABQK02HUB3S | CDS | 523639 | 1836 | - | 0.318627 | |
g5057 | DLA_05598 | GAOABQK02HUB3S | CDS | 525762 | 507 | + | 0.266272 | |
g5058 | DLA_11634 | GAOABQK02HUB3S | CDS | 526388 | 327 | + | 0.266055 | |
g5059 | DLA_05599 | GAOABQK02HUB3S | CDS | 526810 | 1863 | - | 0.3489 | |
g506 | DLA_00559 | has similarity to the S. cerevisisae ATP10 a mitochondrial inner membrane protein required for assembly of the mitochondrial F1F0 ATP synthase there is a second copy of this gene | contig05409_1.exp | CDS | 1157091 | 792 | + | 0.296717 |
g5060 | DLA_05600 | GAOABQK02HUB3S | CDS | 528768 | 2805 | + | 0.318004 | |
g5061 | DLA_05603 | GAOABQK02HUB3S | CDS | 533018 | 972 | + | 0.343621 | |
g5062 | DLA_05604 | GAOABQK02HUB3S | CDS | 534928 | 1914 | - | 0.324974 | |
g5063 | DLA_05606 | GAOABQK02HUB3S | CDS | 538701 | 1482 | - | 0.251687 | |
g5064 | DLA_05607 | GAOABQK02HUB3S | CDS | 540250 | 1596 | + | 0.246867 | |
g5065 | DLA_05608 | GAOABQK02HUB3S | CDS | 542699 | 1077 | + | 0.290622 | |
g5066 | DLA_05609 | GAOABQK02HUB3S | CDS | 543862 | 1773 | - | 0.337281 | |
g5067 | DLA_05611 | ortholog of the conserved RMD5 which in yeast has has an E3-like ubiquitin ligase activity | GAOABQK02HUB3S | CDS | 546474 | 1215 | + | 0.331687 |
g5068 | DLA_05612 | catalyzes the reaction ATP ethanolamine ADP O-phosphoethanolamine | GAOABQK02HUB3S | CDS | 548355 | 1491 | + | 0.319249 |
g5069 | DLA_05614 | very similar in the C-terminal RING Zn finger domain belongs to the BRE1 family | GAOABQK02HUB3S | CDS | 550800 | 2736 | + | 0.327485 |
g507 | DLA_00560 | contig05409_1.exp | CDS | 1158108 | 5679 | + | 0.296883 | |
g5070 | DLA_05615 | GAOABQK02HUB3S | CDS | 553749 | 6030 | - | 0.315091 | |
g5071 | DLA_05616 | catalyzes the reaction ATP uridine ADP UMP | GAOABQK02HUB3S | CDS | 560099 | 1386 | - | 0.336219 |
g5072 | DLA_05617 | GAOABQK02HUB3S | CDS | 562088 | 336 | + | 0.327381 | |
g5073 | DLA_05618 | GAOABQK02HUB3S | CDS | 562805 | 2460 | - | 0.314634 | |
g5074 | DLA_05619 | GAOABQK02HUB3S | CDS | 566617 | 2586 | - | 0.317479 | |
g5075 | DLA_11635 | GAOABQK02HUB3S | CDS | 569779 | 258 | - | 0.372093 | |
g5076 | DLA_05620 | GAOABQK02HUB3S | CDS | 571491 | 5514 | + | 0.353283 | |
g5077 | DLA_05621 | GAOABQK02HUB3S | CDS | 577248 | 813 | - | 0.268143 | |
g5078 | DLA_05622 | GAOABQK02HUB3S | CDS | 578407 | 1176 | - | 0.284014 | |
g5079 | DLA_05624 | GAOABQK02HUB3S | CDS | 579638 | 3105 | + | 0.295652 | |
g508 | DLA_00561 | contig05409_1.exp | CDS | 1164257 | 1440 | - | 0.359028 | |
g5080 | DLA_05625 | GAOABQK02HUB3S | CDS | 583295 | 444 | + | 0.236486 | |
g5081 | DLA_05626 | GAOABQK02HUB3S | CDS | 583974 | 780 | - | 0.302564 | |
g5082 | DLA_05627 | GAOABQK02HUB3S | CDS | 584948 | 777 | - | 0.34749 | |
g5083 | DLA_05628 | GAOABQK02HUB3S | CDS | 586125 | 855 | - | 0.353216 | |
g5084 | DLA_05629 | phosphorylates pyridoxal to pyridoxal 5'-phosphate member of the TKL (tyrosine kinase-like) group of protein kinases belongs to the MLK protein kinase family | GAOABQK02HUB3S | CDS | 587208 | 903 | + | 0.295681 |
g5085 | DLA_05630 | GAOABQK02HUB3S | CDS | 588330 | 2022 | - | 0.333828 | |
g5086 | DLA_05634 | GAOABQK02HUB3S | CDS | 592531 | 969 | - | 0.324045 | |
g5087 | DLA_05635 | GAOABQK02HUB3S | CDS | 593660 | 1707 | - | 0.313415 | |
g5088 | DLA_05636 | GAOABQK02HUB3S | CDS | 596247 | 2346 | + | 0.36445 | |
g5089 | DLA_05637 | GAOABQK02HUB3S | CDS | 598752 | 8223 | + | 0.332117 | |
g509 | DLA_00562 | contig05409_1.exp | CDS | 1165985 | 294 | + | 0.285714 | |
g5090 | DLA_05638 | GAOABQK02HUB3S | CDS | 607415 | 1278 | + | 0.335681 | |
g5091 | DLA_05639 | GAOABQK02HUB3S | CDS | 608950 | 4611 | + | 0.317719 | |
g5092 | DLA_05640 | GAOABQK02HUB3S | CDS | 613814 | 1563 | - | 0.358285 | |
g5093 | DLA_05641 | very similar to H. sapiens di-N-acetylchitobiase (CBTS) a hydrolase involved in the degradation of asparagine-linked glycoproteins contains a putative N-terminal signal sequence | GAOABQK02HUB3S | CDS | 615803 | 1116 | - | 0.350358 |
g5094 | DLA_05642 | GAOABQK02HUB3S | CDS | 617107 | 492 | - | 0.276423 | |
g5095 | DLA_05643 | GAOABQK02HUB3S | CDS | 617928 | 531 | - | 0.404896 | |
g5096 | DLA_05644 | GAOABQK02HUB3S | CDS | 619305 | 1980 | - | 0.375253 | |
g5097 | DLA_05645 | GAOABQK02HUB3S | CDS | 622219 | 6897 | + | 0.345658 | |
g5098 | DLA_05646 | putative ortholog of S. cerevisiae BUB2 a mitotic checkpoint protein | GAOABQK02HUB3S | CDS | 629459 | 993 | + | 0.306143 |
g5099 | DLA_05647 | GAOABQK02HUB3S | CDS | 630627 | 687 | - | 0.295488 | |
g51 | DLA_00060 | contig05409_1.exp | CDS | 131668 | 1317 | - | 0.351557 | |
g510 | DLA_00563 | contig05409_1.exp | CDS | 1166350 | 270 | - | 0.403704 | |
g5100 | DLA_05648 | GAOABQK02HUB3S | CDS | 631506 | 987 | + | 0.288754 | |
g5101 | DLA_05649 | GAOABQK02HUB3S | CDS | 632679 | 1317 | + | 0.355353 | |
g5102 | DLA_05650 | GAOABQK02HUB3S | CDS | 634110 | 1521 | + | 0.335306 | |
g5103 | DLA_05652 | highly conserved protein ortholog of human NAT10 and yeast KRE33 predicted to localize to the nucleolus | GAOABQK02HUB3S | CDS | 636366 | 3360 | + | 0.32619 |
g5104 | DLA_05653 | GAOABQK02HUB3S | CDS | 640198 | 1047 | + | 0.295129 | |
g5105 | DLA_05654 | GAOABQK02HUB3S | CDS | 641462 | 1251 | - | 0.341327 | |
g5106 | DLA_05655 | GAOABQK02HUB3S | CDS | 642993 | 2706 | + | 0.335181 | |
g5107 | DLA_05656 | GAOABQK02HUB3S | CDS | 645929 | 2625 | - | 0.374857 | |
g5108 | DLA_05657 | GAOABQK02HUB3S | CDS | 648858 | 2475 | - | 0.298586 | |
g5109 | DLA_05658 | GAOABQK02HUB3S | CDS | 651949 | 360 | - | 0.319444 | |
g511 | DLA_00564 | contig05409_1.exp | CDS | 1167449 | 291 | + | 0.33677 | |
g5110 | DLA_05659 | GAOABQK02HUB3S | CDS | 653033 | 2154 | - | 0.361653 | |
g5111 | DLA_05660 | GAOABQK02HUB3S | CDS | 657512 | 1434 | - | 0.357043 | |
g5112 | DLA_05661 | GAOABQK02HUB3S | CDS | 659019 | 1668 | - | 0.293765 | |
g5113 | DLA_05662 | GAOABQK02HUB3S | CDS | 662072 | 1938 | + | 0.344169 | |
g5114 | DLA_05663 | GAOABQK02HUB3S | CDS | 664256 | 1881 | - | 0.307815 | |
g5115 | DLA_05664 | very similar to A. thaliana AHL and SAL1 phosphatases and S. pombe tol1 (halotolerance protein) all related to the S. cerevisiae HAL2 these proteins are 3'-phosphoadenosine-5'-phosphate (PAP) phosphatases that also act as inositol polyphosphate 1-phosphatases. | GAOABQK02HUB3S | CDS | 667626 | 1011 | - | 0.339268 |
g5116 | DLA_05665 | GAOABQK02HUB3S | CDS | 669026 | 2424 | - | 0.331683 | |
g5117 | DLA_05666 | GAOABQK02HUB3S | CDS | 671872 | 993 | - | 0.330312 | |
g5118 | DLA_05668 | GAOABQK02HUB3S | CDS | 673172 | 1290 | + | 0.272093 | |
g5119 | DLA_05669 | GAOABQK02HUB3S | CDS | 674700 | 711 | + | 0.293952 | |
g512 | DLA_00565 | contig05409_1.exp | CDS | 1167857 | 270 | - | 0.4 | |
g5120 | DLA_05670 | GAOABQK02HUB3S | CDS | 675645 | 2913 | - | 0.325781 | |
g5121 | DLA_05671 | GAOABQK02HUB3S | CDS | 678704 | 1239 | + | 0.326877 | |
g5122 | DLA_05672 | GAOABQK02HUB3S | CDS | 680009 | 1767 | - | 0.307301 | |
g5123 | DLA_05673 | GAOABQK02HUB3S | CDS | 682192 | 1398 | + | 0.319027 | |
g5124 | DLA_05674 | GAOABQK02HUB3S | CDS | 683688 | 2823 | - | 0.335104 | |
g5125 | DLA_05675 | GAOABQK02HUB3S | CDS | 687081 | 1143 | + | 0.353456 | |
g5126 | DLA_05676 | GAOABQK02HUB3S | CDS | 688665 | 2088 | + | 0.299329 | |
g5127 | DLA_05677 | GAOABQK02HUB3S | CDS | 690962 | 510 | + | 0.298039 | |
g5128 | DLA_05678 | GAOABQK02HUB3S | CDS | 691579 | 984 | - | 0.24187 | |
g5129 | DLA_05679 | GAOABQK02HUB3S | CDS | 692830 | 1473 | + | 0.325866 | |
g513 | DLA_00566 | contig05409_1.exp | CDS | 1168704 | 2820 | + | 0.292199 | |
g5130 | DLA_05680 | GAOABQK02HUB3S | CDS | 694851 | 2775 | + | 0.323964 | |
g5131 | DLA_05681 | GAOABQK02HUB3S | CDS | 698121 | 765 | + | 0.330719 | |
g5132 | DLA_05682 | GAOABQK02HUB3S | CDS | 699437 | 3183 | + | 0.322652 | |
g5133 | DLA_05685 | GAOABQK02HUB3S | CDS | 703693 | 3501 | - | 0.350757 | |
g5134 | DLA_05686 | GAOABQK02HUB3S | CDS | 708017 | 1431 | - | 0.361286 | |
g5135 | DLA_05687 | GAOABQK02HUB3S | CDS | 709936 | 2475 | + | 0.30101 | |
g5136 | DLA_05688 | GAOABQK02HUB3S | CDS | 712544 | 1281 | - | 0.261514 | |
g5137 | DLA_05689 | GAOABQK02HUB3S | CDS | 715626 | 1443 | + | 0.250866 | |
g5138 | DLA_05693 | GAOABQK02HUB3S | CDS | 718237 | 474 | + | 0.295359 | |
g5139 | DLA_05698 | GAOABQK02HUB3S | CDS | 722409 | 1365 | - | 0.352381 | |
g514 | DLA_00568 | contig05409_1.exp | CDS | 1171930 | 2079 | - | 0.378547 | |
g5140 | DLA_05700 | GAOABQK02HUB3S | CDS | 724158 | 3018 | - | 0.270378 | |
g5141 | DLA_05701 | GAOABQK02HUB3S | CDS | 728826 | 4296 | + | 0.30703 | |
g5142 | DLA_05702 | GAOABQK02HUB3S | CDS | 733229 | 2988 | - | 0.282798 | |
g5143 | DLA_05703 | GAOABQK02HUB3S | CDS | 736719 | 1491 | - | 0.336016 | |
g5144 | DLA_05704 | GAOABQK02HUB3S | CDS | 739651 | 3900 | + | 0.332564 | |
g5145 | DLA_05705 | GAOABQK02HUB3S | CDS | 743695 | 1308 | - | 0.355505 | |
g5146 | DLA_05706 | GAOABQK02HUB3S | CDS | 745347 | 4065 | + | 0.342927 | |
g5147 | DLA_05708 | GAOABQK02HUB3S | CDS | 749810 | 1146 | - | 0.34555 | |
g5148 | DLA_05709 | GAOABQK02HUB3S | CDS | 751578 | 657 | + | 0.30137 | |
g5149 | DLA_05710 | GAOABQK02HUB3S | CDS | 752623 | 576 | - | 0.375 | |
g515 | DLA_00569 | contig05409_1.exp | CDS | 1174401 | 1557 | - | 0.370584 | |
g5150 | DLA_05712 | GAOABQK02HUB3S | CDS | 754117 | 1869 | - | 0.323167 | |
g5151 | DLA_05713 | GAOABQK02HUB3S | CDS | 756235 | 6708 | - | 0.317382 | |
g5152 | DLA_05714 | GAOABQK02HUB3S | CDS | 764149 | 1134 | + | 0.353616 | |
g5153 | DLA_05715 | GAOABQK02HUB3S | CDS | 765958 | 1125 | + | 0.354667 | |
g5154 | DLA_05716 | GAOABQK02HUB3S | CDS | 767263 | 1008 | + | 0.280754 | |
g5155 | DLA_05717 | GAOABQK02HUB3S | CDS | 768415 | 1602 | - | 0.353308 | |
g5156 | DLA_05718 | GAOABQK02HUB3S | CDS | 770571 | 702 | - | 0.361823 | |
g5157 | DLA_05720 | GAOABQK02HUB3S | CDS | 772075 | 1080 | + | 0.343519 | |
g5158 | DLA_05722 | GAOABQK02HUB3S | CDS | 774281 | 405 | + | 0.34321 | |
g5159 | DLA_05723 | GAOABQK02HUB3S | CDS | 774808 | 1152 | - | 0.346354 | |
g516 | DLA_00570 | highly similar to other short proteins expressed in the prestalk region expressed in pstAO cells | contig05409_1.exp | CDS | 1176096 | 270 | - | 0.403704 |
g5160 | DLA_05724 | catalyzes the removal of the carboxylate group of S-adenosylmethionine to form S-adenosyl-5'-3-methylpropylamine which then acts as the n-propylamine group donor in the synthesis of the polyamines spermidine and sperminebr bNomenclature conflict: b Do not confuse this gene with amdA encoding AMP deaminase | GAOABQK02HUB3S | CDS | 776975 | 1149 | + | 0.376849 |
g5161 | DLA_05726 | GAOABQK02HUB3S | CDS | 779799 | 351 | + | 0.2849 | |
g5162 | DLA_05727 | GAOABQK02HUB3S | CDS | 780230 | 2280 | + | 0.339035 | |
g5163 | DLA_05728 | GAOABQK02HUB3S | CDS | 782651 | 2133 | - | 0.342241 | |
g5164 | DLA_05729 | GAOABQK02HUB3S | CDS | 785504 | 2463 | + | 0.326837 | |
g5165 | DLA_05730 | GAOABQK02HUB3S | CDS | 788372 | 435 | - | 0.351724 | |
g5166 | DLA_05731 | GAOABQK02HUB3S | CDS | 789142 | 501 | - | 0.337325 | |
g5167 | DLA_05733 | GAOABQK02HUB3S | CDS | 790678 | 1080 | + | 0.373148 | |
g5168 | DLA_05734 | GAOABQK02HUB3S | CDS | 791982 | 351 | - | 0.356125 | |
g5169 | DLA_05735 | GAOABQK02HUB3S | CDS | 793033 | 3303 | + | 0.367847 | |
g517 | DLA_00571 | contig05409_1.exp | CDS | 1177610 | 243 | + | 0.415638 | |
g5170 | DLA_05736 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | GAOABQK02HUB3S | CDS | 796937 | 1710 | + | 0.322222 |
g5171 | DLA_05737 | GAOABQK02HUB3S | CDS | 799193 | 17223 | + | 0.328863 | |
g5172 | DLA_05738 | GAOABQK02HUB3S | CDS | 816900 | 1398 | - | 0.364807 | |
g5173 | DLA_05739 | GAOABQK02HUB3S | CDS | 818651 | 996 | + | 0.315261 | |
g5174 | DLA_05740 | GAOABQK02HUB3S | CDS | 820029 | 771 | + | 0.311284 | |
g5175 | DLA_05741 | GAOABQK02HUB3S | CDS | 821262 | 2721 | + | 0.331128 | |
g5176 | DLA_05742 | GAOABQK02HUB3S | CDS | 824904 | 7947 | - | 0.307663 | |
g5177 | DLA_05743 | GAOABQK02HUB3S | CDS | 833073 | 2523 | + | 0.320254 | |
g5178 | DLA_11636 | GAOABQK02HUB3S | CDS | 836737 | 16356 | - | 0.314013 | |
g5179 | DLA_11637 | GAOABQK02HUB3S | CDS | 855266 | 690 | - | 0.317391 | |
g518 | DLA_11445 | contig05409_1.exp | CDS | 1178028 | 363 | - | 0.250689 | |
g5180 | DLA_05744 | GAOABQK02HUB3S | CDS | 856339 | 13416 | - | 0.316413 | |
g5181 | DLA_05745 | GAOABQK02HUB3S | CDS | 870072 | 846 | + | 0.309693 | |
g5182 | DLA_05746 | GAOABQK02HUB3S | CDS | 871130 | 1071 | - | 0.376284 | |
g5183 | DLA_05747 | GAOABQK02HUB3S | CDS | 873649 | 1515 | + | 0.345875 | |
g5184 | DLA_05748 | GAOABQK02HUB3S | CDS | 875626 | 2385 | + | 0.398323 | |
g5185 | DLA_05749 | GAOABQK02HUB3S | CDS | 878548 | 378 | + | 0.256614 | |
g5186 | DLA_05750 | GAOABQK02HUB3S | CDS | 879086 | 2442 | - | 0.362817 | |
g5187 | DLA_05752 | member of the SNARE family (Soluble NSF Attachment Protein REceptor) localizes to endosome and interacts with syn7A | GAOABQK02HUB3S | CDS | 882792 | 438 | + | 0.321918 |
g5188 | DLA_05755 | GAOABQK02HUB3S | CDS | 884884 | 678 | + | 0.333333 | |
g5189 | DLA_05756 | GAOABQK02HUB3S | CDS | 885905 | 897 | + | 0.322185 | |
g519 | DLA_00572 | catalyzes the reaction Hsub2subO allantoin allantoate expressed in upper cup cells during culmination | contig05409_1.exp | CDS | 1178580 | 1956 | - | 0.373722 |
g5190 | DLA_05758 | GAOABQK02HUB3S | CDS | 887016 | 2760 | - | 0.278261 | |
g5191 | DLA_05759 | GAOABQK02HUB3S | CDS | 890932 | 1029 | + | 0.285714 | |
g5192 | DLA_05760 | GAOABQK02HUB3S | CDS | 892126 | 2388 | + | 0.327889 | |
g5193 | DLA_05761 | GAOABQK02HUB3S | CDS | 894993 | 1248 | + | 0.297276 | |
g5194 | DLA_05764 | GAOABQK02HUB3S | CDS | 898624 | 1107 | + | 0.277326 | |
g5195 | DLA_05765 | GAOABQK02HUB3S | CDS | 899811 | 2913 | - | 0.28081 | |
g5196 | DLA_05766 | GAOABQK02HUB3S | CDS | 903028 | 4074 | - | 0.303142 | |
g5197 | DLA_05769 | GAOABQK02HUB3S | CDS | 908585 | 4353 | - | 0.33655 | |
g5198 | DLA_05770 | GAOABQK02HUB3S | CDS | 913522 | 312 | + | 0.326923 | |
g5199 | DLA_05771 | GAOABQK02HUB3S | CDS | 914036 | 834 | - | 0.306954 | |
g52 | DLA_00061 | contig05409_1.exp | CDS | 136141 | 264 | - | 0.412879 | |
g520 | DLA_00573 | contig05409_1.exp | CDS | 1181037 | 522 | - | 0.287356 | |
g5200 | DLA_05772 | GAOABQK02HUB3S | CDS | 915455 | 2523 | + | 0.349187 | |
g5201 | DLA_05773 | GAOABQK02HUB3S | CDS | 918191 | 1362 | + | 0.314978 | |
g5202 | DLA_05774 | putative ortholog of S. cerevisiae VPS52 component of the GARP (Golgi-associated retrograde protein) complex | GAOABQK02HUB3S | CDS | 919673 | 2370 | + | 0.336287 |
g5203 | DLA_05775 | GAOABQK02HUB3S | CDS | 922590 | 1137 | + | 0.310466 | |
g5204 | DLA_05776 | GAOABQK02HUB3S | CDS | 925127 | 3027 | + | 0.355467 | |
g5205 | DLA_05777 | GAOABQK02HUB3S | CDS | 928233 | 3237 | + | 0.314798 | |
g5206 | DLA_05778 | GAOABQK02HUB3S | CDS | 932143 | 1695 | - | 0.379941 | |
g5207 | DLA_05779 | GAOABQK02HUB3S | CDS | 934318 | 2625 | - | 0.314667 | |
g5208 | DLA_05781 | GAOABQK02HUB3S | CDS | 939271 | 2745 | + | 0.317668 | |
g5209 | DLA_05782 | GAOABQK02HUB3S | CDS | 942240 | 822 | - | 0.323601 | |
g521 | DLA_00574 | contig05409_1.exp | CDS | 1181707 | 837 | - | 0.377539 | |
g5210 | DLA_05783 | GAOABQK02HUB3S | CDS | 943443 | 423 | + | 0.326241 | |
g5211 | DLA_11638 | GAOABQK02HUB3S | CDS | 944103 | 666 | - | 0.345345 | |
g5212 | DLA_05784 | GAOABQK02HUB3S | CDS | 944935 | 1326 | - | 0.317496 | |
g5213 | DLA_05785 | GAOABQK02HUB3S | CDS | 946843 | 1488 | + | 0.284946 | |
g5214 | DLA_05786 | GAOABQK02HUB3S | CDS | 948883 | 480 | + | 0.347917 | |
g5215 | DLA_11639 | GAOABQK02HUB3S | CDS | 950473 | 459 | - | 0.261438 | |
g5216 | DLA_05787 | GAOABQK02HUB3S | CDS | 951458 | 3252 | + | 0.301661 | |
g5217 | DLA_05788 | GAOABQK02HUB3S | CDS | 954846 | 420 | - | 0.395238 | |
g5218 | DLA_05789 | GAOABQK02HUB3S | CDS | 955277 | 2424 | - | 0.347772 | |
g5219 | DLA_05790 | GAOABQK02HUB3S | CDS | 959356 | 1185 | + | 0.374684 | |
g522 | DLA_00575 | contig05409_1.exp | CDS | 1183526 | 840 | - | 0.336905 | |
g5220 | DLA_05791 | GAOABQK02HUB3S | CDS | 960681 | 1719 | - | 0.329843 | |
g5221 | DLA_05792 | GAOABQK02HUB3S | CDS | 963705 | 1140 | + | 0.349123 | |
g5222 | DLA_05793 | GAOABQK02HUB3S | CDS | 965157 | 1992 | + | 0.329819 | |
g5223 | DLA_05795 | GAOABQK02HUB3S | CDS | 968334 | 849 | + | 0.299176 | |
g5224 | DLA_05796 | GAOABQK02HUB3S | CDS | 969501 | 255 | + | 0.262745 | |
g5225 | DLA_05797 | GAOABQK02HUB3S | CDS | 970101 | 789 | + | 0.362484 | |
g5226 | DLA_05799 | GAOABQK02HUB3S | CDS | 971524 | 2406 | + | 0.316708 | |
g5227 | DLA_05800 | GAOABQK02HUB3S | CDS | 974737 | 864 | + | 0.28588 | |
g5228 | DLA_05801 | GAOABQK02HUB3S | CDS | 975770 | 705 | - | 0.310638 | |
g5229 | DLA_05802 | GAOABQK02HUB3S | CDS | 976806 | 666 | + | 0.328829 | |
g523 | DLA_00576 | contig05409_1.exp | CDS | 1185030 | 5907 | - | 0.346707 | |
g5230 | DLA_05803 | GAOABQK02HUB3S | CDS | 977585 | 807 | - | 0.325898 | |
g5231 | DLA_05804 | GAOABQK02HUB3S | CDS | 978467 | 1056 | + | 0.272727 | |
g5232 | DLA_05805 | GAOABQK02HUB3S | CDS | 979636 | 2847 | - | 0.336495 | |
g5233 | DLA_05806 | GAOABQK02HUB3S | CDS | 983055 | 5760 | - | 0.358681 | |
g5234 | DLA_05807 | GAOABQK02HUB3S | CDS | 989588 | 1956 | + | 0.324642 | |
g5235 | DLA_05808 | GAOABQK02HUB3S | CDS | 991609 | 2892 | - | 0.317773 | |
g5236 | DLA_05809 | GAOABQK02HUB3S | CDS | 994845 | 2769 | - | 0.326111 | |
g5237 | DLA_05811 | GAOABQK02HUB3S | CDS | 1000291 | 4923 | + | 0.29088 | |
g5238 | DLA_05812 | GAOABQK02HUB3S | CDS | 1005470 | 1524 | - | 0.322178 | |
g5239 | DLA_05813 | GAOABQK02HUB3S | CDS | 1007273 | 1401 | - | 0.309779 | |
g524 | DLA_00577 | contig05409_1.exp | CDS | 1192156 | 6693 | + | 0.356492 | |
g5240 | DLA_05815 | GAOABQK02HUB3S | CDS | 1009232 | 1158 | + | 0.343696 | |
g5241 | DLA_05816 | GAOABQK02HUB3S | CDS | 1010565 | 399 | + | 0.223058 | |
g5242 | DLA_05817 | GAOABQK02HUB3S | CDS | 1011321 | 1725 | - | 0.293333 | |
g5243 | DLA_05818 | GAOABQK02HUB3S | CDS | 1013829 | 939 | - | 0.27902 | |
g5244 | DLA_05819 | GAOABQK02HUB3S | CDS | 1014974 | 1746 | + | 0.230813 | |
g5245 | DLA_05820 | GAOABQK02HUB3S | CDS | 1016882 | 3063 | - | 0.24094 | |
g5246 | DLA_05821 | GAOABQK02HUB3S | CDS | 1020589 | 1410 | + | 0.343972 | |
g5247 | DLA_05822 | GAOABQK02HUB3S | CDS | 1022135 | 1938 | - | 0.28999 | |
g5248 | DLA_05824 | GAOABQK02HUB3S | CDS | 1024401 | 324 | - | 0.314815 | |
g5249 | DLA_05825 | GAOABQK02HUB3S | CDS | 1028711 | 1488 | - | 0.305108 | |
g525 | DLA_00578 | contig05409_1.exp | CDS | 1199877 | 1041 | + | 0.270893 | |
g5250 | DLA_05826 | GAOABQK02HUB3S | CDS | 1030493 | 2619 | + | 0.237495 | |
g5251 | DLA_05828 | GAOABQK02HUB3S | CDS | 1033963 | 744 | + | 0.302419 | |
g5252 | DLA_05829 | GAOABQK02HUB3S | CDS | 1034819 | 933 | - | 0.316184 | |
g5253 | DLA_05830 | GAOABQK02HUB3S | CDS | 1036962 | 960 | + | 0.344792 | |
g5254 | DLA_05831 | contains 7 WD repeats belongs to the WD repeat WDSOF1 family homolog of human WDSOF1 S. cerevisiae SOF1 S. cerevisiae SOF1 is required for ribosomal RNA processing | GAOABQK02HUB3S | CDS | 1038002 | 1371 | - | 0.342815 |
g5255 | DLA_05832 | similar to antiquitin aldehyde dehydrogenase family 7 catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | GAOABQK02HUB3S | CDS | 1039684 | 1533 | + | 0.3803 |
g5256 | DLA_05833 | GAOABQK02HUB3S | CDS | 1041496 | 1680 | + | 0.284524 | |
g5257 | DLA_05834 | GAOABQK02HUB3S | CDS | 1043503 | 1593 | + | 0.277464 | |
g5258 | DLA_05835 | GAOABQK02HUB3S | CDS | 1045122 | 2844 | - | 0.353024 | |
g5259 | DLA_05836 | GAOABQK02HUB3S | CDS | 1048215 | 756 | + | 0.318783 | |
g526 | DLA_00579 | contig05409_1.exp | CDS | 1201208 | 3444 | + | 0.305168 | |
g5260 | DLA_05837 | GAOABQK02HUB3S | CDS | 1049622 | 420 | + | 0.309524 | |
g5261 | DLA_05838 | GAOABQK02HUB3S | CDS | 1050392 | 1218 | - | 0.293103 | |
g5262 | DLA_05840 | GAOABQK02HUB3S | CDS | 1052924 | 3171 | - | 0.252286 | |
g5263 | DLA_05841 | GAOABQK02HUB3S | CDS | 1056268 | 1080 | + | 0.318519 | |
g5264 | DLA_05842 | GAOABQK02HUB3S | CDS | 1057689 | 1941 | - | 0.36373 | |
g5265 | DLA_05843 | GAOABQK02HUB3S | CDS | 1060924 | 945 | + | 0.319577 | |
g5266 | DLA_05844 | GAOABQK02HUB3S | CDS | 1062024 | 2304 | + | 0.310764 | |
g5267 | DLA_05845 | GAOABQK02HUB3S | CDS | 1064384 | 897 | - | 0.352285 | |
g5268 | DLA_05846 | ortholog of the conserved COQ9 a protein which in S. cerevisiae is required for ubiquinone (coenzyme Q) biosynthesis | GAOABQK02HUB3S | CDS | 1065509 | 876 | + | 0.27968 |
g5269 | DLA_05847 | GAOABQK02HUB3S | CDS | 1066629 | 1572 | - | 0.255725 | |
g527 | DLA_00580 | contig05409_1.exp | CDS | 1205702 | 633 | + | 0.28594 | |
g5270 | DLA_05848 | contains 2 GRAM domains one RabGAPTBC domain and one EF hand domain | GAOABQK02HUB3S | CDS | 1069188 | 3243 | - | 0.307431 |
g5271 | DLA_11640 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane brbr bCommunity annotation:b Overview of the | GAOABQK02HUB3S | CDS | 1074058 | 942 | - | 0.33758 |
g5272 | DLA_05849 | GAOABQK02HUB3S | CDS | 1077639 | 756 | - | 0.309524 | |
g5273 | DLA_05850 | GAOABQK02HUB3S | CDS | 1080440 | 1767 | - | 0.320317 | |
g5274 | DLA_05851 | GAOABQK02HUB3S | CDS | 1082614 | 1737 | + | 0.332758 | |
g5275 | DLA_05852 | GAOABQK02HUB3S | CDS | 1084467 | 1605 | + | 0.305919 | |
g5276 | DLA_05853 | GAOABQK02HUB3S | CDS | 1086420 | 3279 | + | 0.345837 | |
g5277 | DLA_05854 | GAOABQK02HUB3S | CDS | 1089837 | 912 | - | 0.314693 | |
g5278 | DLA_05855 | GAOABQK02HUB3S | CDS | 1091054 | 1833 | + | 0.314239 | |
g5279 | DLA_05856 | GAOABQK02HUB3S | CDS | 1093676 | 948 | + | 0.35865 | |
g528 | DLA_00581 | contig05409_1.exp | CDS | 1206739 | 267 | - | 0.284644 | |
g5280 | DLA_05861 | GAOABQK02HUB3S | CDS | 1098276 | 4662 | - | 0.302445 | |
g5281 | DLA_05862 | member of the alpha-actininspectrin superfamily dimerizes with cortexillin I involved in cytokinesis and development and associates with the actin cytoskeleton | GAOABQK02HUB3S | CDS | 1103799 | 1329 | - | 0.343868 |
g5282 | DLA_11641 | GAOABQK02HUB3S | CDS | 1105821 | 2667 | + | 0.285714 | |
g5283 | DLA_05864 | GAOABQK02HUB3S | CDS | 1108726 | 5511 | + | 0.293232 | |
g5284 | DLA_05865 | GAOABQK02HUB3S | CDS | 1114611 | 3675 | + | 0.319456 | |
g5285 | DLA_05866 | GAOABQK02HUB3S | CDS | 1120661 | 2448 | - | 0.330474 | |
g5286 | DLA_05867 | GAOABQK02HUB3S | CDS | 1123346 | 3384 | - | 0.30792 | |
g5287 | DLA_05868 | GAOABQK02HUB3S | CDS | 1127229 | 1563 | - | 0.329495 | |
g5288 | DLA_05869 | GAOABQK02HUB3S | CDS | 1129286 | 1221 | + | 0.352989 | |
g5289 | DLA_05871 | GAOABQK02HUB3S | CDS | 1133331 | 1881 | + | 0.259968 | |
g529 | DLA_00582 | contig05409_1.exp | CDS | 1207838 | 4317 | + | 0.351633 | |
g5290 | DLA_05872 | GAOABQK02HUB3S | CDS | 1135244 | 1200 | - | 0.2875 | |
g5291 | DLA_05874 | GAOABQK02HUB3S | CDS | 1137048 | 1767 | + | 0.273345 | |
g5292 | DLA_05875 | GAOABQK02HUB3S | CDS | 1139252 | 585 | + | 0.292308 | |
g5293 | DLA_05878 | GAOABQK02HUB3S | CDS | 1140427 | 2184 | - | 0.282967 | |
g5294 | DLA_05879 | GAOABQK02HUB3S | CDS | 1142841 | 2157 | + | 0.278628 | |
g5295 | DLA_05881 | GAOABQK02HUB3S | CDS | 1146303 | 369 | + | 0.384824 | |
g5296 | DLA_05883 | GAOABQK02HUB3S | CDS | 1147298 | 1584 | + | 0.303662 | |
g5297 | DLA_05884 | GAOABQK02HUB3S | CDS | 1149106 | 837 | - | 0.317802 | |
g5298 | DLA_05885 | GAOABQK02HUB3S | CDS | 1151440 | 1539 | + | 0.367122 | |
g5299 | DLA_05886 | GAOABQK02HUB3S | CDS | 1153628 | 1752 | + | 0.333333 | |
g53 | DLA_00062 | contig05409_1.exp | CDS | 136958 | 2331 | - | 0.357357 | |
g530 | DLA_00583 | contig05409_1.exp | CDS | 1212352 | 2052 | - | 0.332846 | |
g5300 | DLA_05887 | GAOABQK02HUB3S | CDS | 1155634 | 1212 | + | 0.267327 | |
g5301 | DLA_05889 | GAOABQK02HUB3S | CDS | 1157724 | 2223 | - | 0.329735 | |
g5302 | DLA_05891 | GAOABQK02HUB3S | CDS | 1161498 | 576 | + | 0.302083 | |
g5303 | DLA_05892 | GAOABQK02HUB3S | CDS | 1162273 | 1578 | - | 0.287706 | |
g5304 | DLA_05893 | GAOABQK02HUB3S | CDS | 1164984 | 519 | + | 0.271676 | |
g5305 | DLA_05894 | GAOABQK02HUB3S | CDS | 1165794 | 3834 | - | 0.325248 | |
g5306 | DLA_05895 | GAOABQK02HUB3S | CDS | 1171951 | 843 | - | 0.31554 | |
g5307 | DLA_05898 | GAOABQK02HUB3S | CDS | 1174131 | 867 | + | 0.347174 | |
g5308 | DLA_05899 | GAOABQK02HUB3S | CDS | 1175289 | 2052 | - | 0.305556 | |
g5309 | DLA_11642 | GAOABQK02HUB3S | CDS | 1177712 | 1602 | - | 0.322097 | |
g531 | DLA_00584 | contig05409_1.exp | CDS | 1214742 | 1788 | + | 0.313758 | |
g5310 | DLA_05900 | GAOABQK02HUB3S | CDS | 1179641 | 2886 | + | 0.288635 | |
g5311 | DLA_05902 | GAOABQK02HUB3S | CDS | 1182935 | 594 | + | 0.328283 | |
g5312 | DLA_05904 | GAOABQK02HUB3S | CDS | 1183851 | 1608 | - | 0.346393 | |
g5313 | DLA_05905 | GAOABQK02HUB3S | CDS | 1185974 | 1605 | + | 0.340187 | |
g5314 | DLA_05907 | GAOABQK02HUB3S | CDS | 1192296 | 4218 | - | 0.317923 | |
g5315 | DLA_05908 | GAOABQK02HUB3S | CDS | 1196895 | 750 | + | 0.301333 | |
g5316 | DLA_05909 | GAOABQK02HUB3S | CDS | 1198196 | 1797 | + | 0.319978 | |
g5317 | DLA_05910 | GAOABQK02HUB3S | CDS | 1200351 | 4206 | + | 0.298859 | |
g5318 | DLA_05912 | GAOABQK02HUB3S | CDS | 1204790 | 366 | - | 0.281421 | |
g5319 | DLA_05913 | GAOABQK02HUB3S | CDS | 1205322 | 1737 | + | 0.28152 | |
g532 | DLA_00585 | contig05409_1.exp | CDS | 1216825 | 3339 | - | 0.292603 | |
g5320 | DLA_05914 | GAOABQK02HUB3S | CDS | 1207145 | 1515 | - | 0.328713 | |
g5321 | DLA_05916 | GAOABQK02HUB3S | CDS | 1209550 | 417 | + | 0.371703 | |
g5322 | DLA_05917 | GAOABQK02HUB3S | CDS | 1210067 | 984 | - | 0.314024 | |
g5323 | DLA_05918 | GAOABQK02HUB3S | CDS | 1211262 | 1065 | + | 0.288263 | |
g5324 | DLA_05919 | GAOABQK02HUB3S | CDS | 1212357 | 1665 | - | 0.306306 | |
g5325 | DLA_05920 | GAOABQK02HUB3S | CDS | 1214313 | 2619 | - | 0.306606 | |
g5326 | DLA_05921 | GAOABQK02HUB3S | CDS | 1217120 | 930 | - | 0.25914 | |
g5327 | DLA_05922 | GAOABQK02HUB3S | CDS | 1218451 | 828 | + | 0.306763 | |
g5328 | DLA_05923 | GAOABQK02HUB3S | CDS | 1219407 | 1734 | - | 0.336794 | |
g5329 | DLA_05924 | GAOABQK02HUB3S | CDS | 1221514 | 1767 | + | 0.327108 | |
g533 | DLA_00586 | contig05409_1.exp | CDS | 1220530 | 1668 | - | 0.361511 | |
g5330 | DLA_05928 | GAOABQK02HUB3S | CDS | 1228722 | 942 | - | 0.300425 | |
g5331 | DLA_05929 | GAOABQK02HUB3S | CDS | 1230362 | 1122 | - | 0.290553 | |
g5332 | DLA_05930 | GAOABQK02HUB3S | CDS | 1232455 | 360 | - | 0.327778 | |
g5333 | DLA_05931 | GAOABQK02HUB3S | CDS | 1233276 | 3234 | - | 0.372294 | |
g5334 | DLA_05932 | GAOABQK02HUB3S | CDS | 1236802 | 2988 | - | 0.323628 | |
g5335 | DLA_05933 | GAOABQK02HUB3S | CDS | 1239974 | 240 | + | 0.370833 | |
g5336 | DLA_05934 | GAOABQK02HUB3S | CDS | 1241031 | 3873 | + | 0.32662 | |
g5337 | DLA_05935 | GAOABQK02HUB3S | CDS | 1245381 | 936 | - | 0.323718 | |
g5338 | DLA_05936 | GAOABQK02HUB3S | CDS | 1248106 | 453 | + | 0.267108 | |
g5339 | DLA_05937 | GAOABQK02HUB3S | CDS | 1248666 | 957 | - | 0.310345 | |
g534 | DLA_00587 | contig05409_1.exp | CDS | 1222361 | 714 | - | 0.331933 | |
g5340 | DLA_05938 | GAOABQK02HUB3S | CDS | 1249860 | 1029 | - | 0.294461 | |
g5341 | DLA_05939 | GAOABQK02HUB3S | CDS | 1251738 | 2730 | + | 0.312821 | |
g5342 | DLA_05942 | GAOABQK02HUB3S | CDS | 1256890 | 1440 | + | 0.285417 | |
g5343 | DLA_05944 | GAOABQK02HUB3S | CDS | 1259691 | 1401 | + | 0.294076 | |
g5344 | DLA_05945 | GAOABQK02HUB3S | CDS | 1261425 | 951 | + | 0.299685 | |
g5345 | DLA_05946 | GAOABQK02HUB3S | CDS | 1262494 | 951 | + | 0.294427 | |
g5346 | DLA_05947 | GAOABQK02HUB3S | CDS | 1263549 | 453 | - | 0.278146 | |
g5347 | DLA_05948 | GAOABQK02HUB3S | CDS | 1264118 | 354 | + | 0.29661 | |
g5348 | DLA_05949 | GAOABQK02HUB3S | CDS | 1264815 | 1056 | + | 0.336174 | |
g5349 | DLA_05952 | GAOABQK02HUB3S | CDS | 1269523 | 1641 | - | 0.305302 | |
g535 | DLA_00588 | contig05409_1.exp | CDS | 1223548 | 528 | - | 0.32197 | |
g5350 | DLA_05953 | GAOABQK02HUB3S | CDS | 1271811 | 1602 | + | 0.285268 | |
g5351 | DLA_11643 | GAOABQK02HUB3S | CDS | 1274338 | 633 | + | 0.322275 | |
g5352 | DLA_05954 | similar to Ixodes scapularis U2 small nuclear ribonucleoprotein A human c10orf11 has 3 leucine-rich repeats which are involved in protein-protein interactions | GAOABQK02HUB3S | CDS | 1275407 | 663 | - | 0.28356 |
g5353 | DLA_05955 | GAOABQK02HUB3S | CDS | 1276586 | 1011 | - | 0.293769 | |
g5354 | DLA_05956 | contains a cyclase domain 7 transmembrane helices a histidine kinase domain and two receiver domains | GAOABQK02HUB3S | CDS | 1277865 | 4821 | - | 0.340178 |
g5355 | DLA_05957 | CAZy family GT58 catalyzes N-linked mannosylation | GAOABQK02HUB3S | CDS | 1283209 | 4092 | + | 0.319892 |
g5356 | DLA_05959 | GAOABQK02HUB3S | CDS | 1288437 | 1143 | + | 0.31846 | |
g5357 | DLA_05961 | GAOABQK02HUB3S | CDS | 1291226 | 10626 | - | 0.378788 | |
g5358 | DLA_05962 | GAOABQK02HUB3S | CDS | 1302941 | 3519 | + | 0.305485 | |
g5359 | DLA_11644 | GAOABQK02HUB3S | CDS | 1306937 | 801 | + | 0.297129 | |
g536 | DLA_00589 | contig05409_1.exp | CDS | 1224362 | 1917 | + | 0.304643 | |
g5360 | DLA_05963 | GAOABQK02HUB3S | CDS | 1308831 | 2589 | + | 0.337968 | |
g5361 | DLA_05964 | GAOABQK02HUB3S | CDS | 1311522 | 3345 | + | 0.277429 | |
g5362 | DLA_05966 | GAOABQK02HUB3S | CDS | 1315617 | 900 | - | 0.322222 | |
g5363 | DLA_05967 | GAOABQK02HUB3S | CDS | 1317327 | 1182 | - | 0.309645 | |
g5364 | DLA_05968 | GAOABQK02HUB3S | CDS | 1319257 | 1641 | + | 0.340646 | |
g5365 | DLA_05969 | GAOABQK02HUB3S | CDS | 1321176 | 2610 | - | 0.355172 | |
g5366 | DLA_05970 | GAOABQK02HUB3S | CDS | 1324154 | 1119 | + | 0.330652 | |
g5367 | DLA_05971 | GAOABQK02HUB3S | CDS | 1325424 | 1011 | + | 0.281899 | |
g5368 | DLA_05973 | GAOABQK02HUB3S | CDS | 1327475 | 1053 | - | 0.319088 | |
g5369 | DLA_05974 | GAOABQK02HUB3S | CDS | 1329499 | 957 | - | 0.335423 | |
g537 | DLA_00590 | contig05409_1.exp | CDS | 1226454 | 2037 | - | 0.375061 | |
g5370 | DLA_05976 | GAOABQK02HUB3S | CDS | 1331748 | 423 | + | 0.248227 | |
g5371 | DLA_05977 | GAOABQK02HUB3S | CDS | 1332472 | 1851 | - | 0.353323 | |
g5372 | DLA_05978 | GAOABQK02HUB3S | CDS | 1334607 | 3846 | - | 0.358814 | |
g5373 | DLA_05979 | GAOABQK02HUB3S | CDS | 1338937 | 1242 | + | 0.309179 | |
g5374 | DLA_05981 | ortholog of H. sapiens xeroderma pigmentosum group D (XPD) M. musculus ERCC2 and S. cerevisiae RAD3 | GAOABQK02HUB3S | CDS | 1341303 | 2334 | + | 0.344045 |
g5375 | DLA_05982 | GAOABQK02HUB3S | CDS | 1343966 | 486 | + | 0.323045 | |
g5376 | DLA_05983 | GAOABQK02HUB3S | CDS | 1344825 | 576 | + | 0.276042 | |
g5377 | DLA_05984 | GAOABQK02HUB3S | CDS | 1345555 | 561 | - | 0.340463 | |
g5378 | DLA_05985 | GAOABQK02HUB3S | CDS | 1346218 | 1341 | + | 0.319911 | |
g5379 | DLA_05986 | GAOABQK02HUB3S | CDS | 1347789 | 966 | - | 0.28882 | |
g538 | DLA_00591 | contig05409_1.exp | CDS | 1228927 | 3024 | - | 0.295635 | |
g5380 | DLA_05987 | GAOABQK02HUB3S | CDS | 1349332 | 750 | + | 0.32 | |
g5381 | DLA_05988 | GAOABQK02HUB3S | CDS | 1350141 | 381 | - | 0.270341 | |
g5382 | DLA_05989 | GAOABQK02HUB3S | CDS | 1351053 | 354 | + | 0.251412 | |
g5383 | DLA_05990 | GAOABQK02HUB3S | CDS | 1351598 | 339 | - | 0.324484 | |
g5384 | DLA_05991 | GAOABQK02HUB3S | CDS | 1352145 | 1392 | - | 0.280891 | |
g5385 | DLA_05992 | GAOABQK02HUB3S | CDS | 1353919 | 822 | + | 0.344282 | |
g5386 | DLA_05993 | GAOABQK02HUB3S | CDS | 1354918 | 711 | - | 0.315049 | |
g5387 | DLA_05994 | GAOABQK02HUB3S | CDS | 1356000 | 3702 | + | 0.290924 | |
g5388 | DLA_05995 | GAOABQK02HUB3S | CDS | 1359885 | 3264 | - | 0.31924 | |
g5389 | DLA_05996 | GAOABQK02HUB3S | CDS | 1363391 | 3576 | - | 0.349553 | |
g539 | DLA_00592 | contig05409_1.exp | CDS | 1232519 | 1503 | + | 0.328011 | |
g5390 | DLA_05999 | GAOABQK02HUB3S | CDS | 1372852 | 1533 | + | 0.308545 | |
g5391 | DLA_06000 | GAOABQK02HUB3S | CDS | 1374570 | 753 | - | 0.273572 | |
g5392 | DLA_06001 | GAOABQK02HUB3S | CDS | 1375627 | 558 | + | 0.295699 | |
g5393 | DLA_06002 | GAOABQK02HUB3S | CDS | 1376464 | 2598 | + | 0.324865 | |
g5394 | DLA_06003 | GAOABQK02HUB3S | CDS | 1379122 | 1671 | + | 0.281867 | |
g5395 | DLA_06004 | GAOABQK02HUB3S | CDS | 1380899 | 2292 | + | 0.294066 | |
g5396 | DLA_06005 | GAOABQK02HUB3S | CDS | 1383618 | 2184 | - | 0.340201 | |
g5397 | DLA_06006 | GAOABQK02HUB3S | CDS | 1386244 | 438 | + | 0.280822 | |
g5398 | DLA_06007 | GAOABQK02HUB3S | CDS | 1386925 | 1515 | - | 0.266007 | |
g5399 | DLA_06008 | GAOABQK02HUB3S | CDS | 1388822 | 2781 | + | 0.317152 | |
g54 | DLA_00063 | contig05409_1.exp | CDS | 139541 | 1737 | - | 0.302821 | |
g540 | DLA_00593 | contig05409_1.exp | CDS | 1234054 | 3429 | - | 0.300087 | |
g5400 | DLA_06009 | GAOABQK02HUB3S | CDS | 1391779 | 450 | + | 0.311111 | |
g5401 | DLA_06010 | GAOABQK02HUB3S | CDS | 1392391 | 1083 | - | 0.347184 | |
g5402 | DLA_06011 | GAOABQK02HUB3S | CDS | 1393578 | 1938 | - | 0.328689 | |
g5403 | DLA_06012 | GAOABQK02HUB3S | CDS | 1396194 | 1935 | + | 0.352455 | |
g5404 | DLA_06013 | GAOABQK02HUB3S | CDS | 1398433 | 1575 | + | 0.299683 | |
g5405 | DLA_06015 | GAOABQK02HUB3S | CDS | 1400538 | 1989 | + | 0.352438 | |
g5406 | DLA_06016 | GAOABQK02HUB3S | CDS | 1402680 | 3453 | + | 0.306111 | |
g5407 | DLA_06017 | GAOABQK02HUB3S | CDS | 1406216 | 705 | - | 0.320567 | |
g5408 | DLA_06018 | GAOABQK02HUB3S | CDS | 1407794 | 828 | + | 0.311594 | |
g5409 | DLA_06019 | GAOABQK02HUB3S | CDS | 1409031 | 549 | - | 0.249545 | |
g541 | DLA_00595 | contig05409_1.exp | CDS | 1237784 | 1563 | - | 0.321177 | |
g5410 | DLA_06020 | GAOABQK02HUB3S | CDS | 1410213 | 882 | + | 0.311791 | |
g5411 | DLA_06021 | GAOABQK02HUB3S | CDS | 1411414 | 537 | - | 0.333333 | |
g5412 | DLA_06022 | highly similar to mammalian SAHH (catalyzes the hydrolysis of S-adenosyl-L-homocysteine into adenosine and homocysteine) localizes to actin rods found in spores | GAOABQK02HUB3S | CDS | 1412763 | 1296 | + | 0.421296 |
g5413 | DLA_06023 | GAOABQK02HUB3S | CDS | 1414370 | 5595 | + | 0.31546 | |
g5414 | DLA_06024 | GAOABQK02HUB3S | CDS | 1421234 | 219 | + | 0.374429 | |
g5415 | DLA_06026 | GAOABQK02HUB3S | CDS | 1422238 | 3381 | - | 0.335699 | |
g5416 | DLA_06028 | GAOABQK02HUB3S | CDS | 1426759 | 1896 | + | 0.306435 | |
g5417 | DLA_06029 | GAOABQK02HUB3S | CDS | 1428820 | 2505 | - | 0.30978 | |
g5418 | DLA_06031 | GAOABQK02HUB3S | CDS | 1431770 | 2691 | - | 0.353772 | |
g5419 | DLA_06032 | GAOABQK02HUB3S | CDS | 1434819 | 1683 | + | 0.335116 | |
g542 | DLA_00597 | contig05409_1.exp | CDS | 1239561 | 270 | - | 0.27037 | |
g5420 | DLA_06033 | GAOABQK02HUB3S | CDS | 1436722 | 1842 | + | 0.323018 | |
g5421 | DLA_06034 | GAOABQK02HUB3S | CDS | 1438764 | 3732 | - | 0.322615 | |
g5422 | DLA_06035 | GAOABQK02HUB3S | CDS | 1442808 | 711 | + | 0.296765 | |
g5423 | DLA_06036 | GAOABQK02HUB3S | CDS | 1444879 | 1842 | + | 0.389251 | |
g5424 | DLA_06037 | GAOABQK02HUB3S | CDS | 1447064 | 1482 | - | 0.326586 | |
g5425 | DLA_06038 | GAOABQK02HUB3S | CDS | 1448988 | 582 | - | 0.314433 | |
g5426 | DLA_06039 | GAOABQK02HUB3S | CDS | 1450251 | 1089 | + | 0.323232 | |
g5427 | DLA_06041 | GAOABQK02HUB3S | CDS | 1452294 | 1320 | + | 0.324242 | |
g5428 | DLA_06042 | GAOABQK02HUB3S | CDS | 1453817 | 2178 | + | 0.305785 | |
g5429 | DLA_06044 | GAOABQK02HUB3S | CDS | 1456878 | 606 | + | 0.338284 | |
g543 | DLA_00598 | contig05409_1.exp | CDS | 1240640 | 540 | + | 0.281481 | |
g5430 | DLA_06045 | GAOABQK02HUB3S | CDS | 1457941 | 1248 | + | 0.338141 | |
g5431 | DLA_06046 | GAOABQK02HUB3S | CDS | 1459581 | 462 | - | 0.378788 | |
g5432 | DLA_06047 | GAOABQK02HUB3S | CDS | 1461035 | 201 | + | 0.273632 | |
g5433 | DLA_06049 | GAOABQK02HUB3S | CDS | 1461570 | 2115 | - | 0.340898 | |
g5434 | DLA_06050 | GAOABQK02HUB3S | CDS | 1464215 | 1347 | + | 0.245731 | |
g5435 | DLA_06051 | GAOABQK02HUB3S | CDS | 1465705 | 1890 | - | 0.289947 | |
g5436 | DLA_06052 | GAOABQK02HUB3S | CDS | 1468561 | 1839 | + | 0.358347 | |
g5437 | DLA_06056 | GAOABQK02HUB3S | CDS | 1471922 | 2574 | - | 0.320901 | |
g5438 | DLA_06058 | GAOABQK02HUB3S | CDS | 1475227 | 2574 | - | 0.328283 | |
g5439 | DLA_06059 | GAOABQK02HUB3S | CDS | 1478354 | 375 | - | 0.274667 | |
g544 | DLA_11446 | contig05409_1.exp | CDS | 1241313 | 564 | + | 0.287234 | |
g5440 | DLA_06060 | GAOABQK02HUB3S | CDS | 1479046 | 1611 | - | 0.387337 | |
g5441 | DLA_06061 | GAOABQK02HUB3S | CDS | 1481957 | 1038 | + | 0.370906 | |
g5442 | DLA_06062 | GAOABQK02HUB3S | CDS | 1483101 | 4170 | - | 0.328297 | |
g5443 | DLA_06063 | GAOABQK02HUB3S | CDS | 1487946 | 1059 | - | 0.288008 | |
g5444 | DLA_06064 | GAOABQK02HUB3S | CDS | 1491776 | 2694 | + | 0.306236 | |
g5445 | DLA_06065 | GAOABQK02HUB3S | CDS | 1494646 | 993 | + | 0.316213 | |
g5446 | DLA_06066 | catalyzes the reaction 2-phospho-D-glycerate phosphoenolpyruvate Hsub2subO | GAOABQK02HUB3S | CDS | 1496409 | 1293 | - | 0.369683 |
g5447 | DLA_06067 | GAOABQK02HUB3S | CDS | 1499697 | 2229 | + | 0.336025 | |
g5448 | DLA_06068 | GAOABQK02HUB3S | CDS | 1502068 | 3438 | - | 0.331006 | |
g5449 | DLA_06069 | GAOABQK02HUB3S | CDS | 1507220 | 2934 | + | 0.407975 | |
g545 | DLA_00599 | contig05409_1.exp | CDS | 1242291 | 2505 | + | 0.306986 | |
g5450 | DLA_06070 | GAOABQK02HUB3S | CDS | 1510494 | 1935 | + | 0.31938 | |
g5451 | DLA_06071 | GAOABQK02HUB3S | CDS | 1512664 | 501 | - | 0.313373 | |
g5452 | DLA_06072 | GAOABQK02HUB3S | CDS | 1513745 | 540 | - | 0.314815 | |
g5453 | DLA_06073 | GAOABQK02HUB3S | CDS | 1515061 | 2583 | + | 0.351529 | |
g5454 | DLA_06074 | component of the RNA polymerase III complex has similarity to H. sapiens RPC6RPC39 and S. cerevisiae RPC34 | GAOABQK02HUB3S | CDS | 1517942 | 885 | - | 0.325424 |
g5455 | DLA_06075 | GAOABQK02HUB3S | CDS | 1519174 | 513 | + | 0.282651 | |
g5456 | DLA_06077 | GAOABQK02HUB3S | CDS | 1520165 | 4575 | + | 0.302951 | |
g5457 | DLA_06079 | GAOABQK02HUB3S | CDS | 1525823 | 876 | + | 0.27968 | |
g5458 | DLA_06080 | GAOABQK02HUB3S | CDS | 1527496 | 1254 | + | 0.336523 | |
g5459 | DLA_06081 | GAOABQK02HUB3S | CDS | 1529006 | 477 | + | 0.287212 | |
g546 | DLA_00601 | contig05409_1.exp | CDS | 1246084 | 3921 | + | 0.294313 | |
g5460 | DLA_06082 | GAOABQK02HUB3S | CDS | 1529954 | 2778 | + | 0.339813 | |
g5461 | DLA_06083 | GAOABQK02HUB3S | CDS | 1533098 | 1314 | + | 0.306697 | |
g5462 | DLA_06084 | GAOABQK02HUB3S | CDS | 1534693 | 993 | - | 0.328298 | |
g5463 | DLA_06087 | GAOABQK02HUB3S | CDS | 1536442 | 1011 | + | 0.294758 | |
g5464 | DLA_06088 | GAOABQK02HUB3S | CDS | 1537886 | 579 | + | 0.331606 | |
g5465 | DLA_06090 | GAOABQK02HUB3S | CDS | 1539993 | 1443 | - | 0.342342 | |
g5466 | DLA_06091 | GAOABQK02HUB3S | CDS | 1542528 | 1707 | + | 0.291154 | |
g5467 | DLA_06092 | catalyzes the reaction isocitrate NADP 2-oxoglutarate CO2 NADPH | GAOABQK02HUB3S | CDS | 1544425 | 1257 | - | 0.38027 |
g5468 | DLA_06093 | GAOABQK02HUB3S | CDS | 1546733 | 414 | - | 0.330918 | |
g5469 | DLA_06094 | GAOABQK02HUB3S | CDS | 1547524 | 3300 | + | 0.321818 | |
g547 | DLA_00603 | contig05409_1.exp | CDS | 1250336 | 3906 | + | 0.32002 | |
g5470 | DLA_06095 | GAOABQK02HUB3S | CDS | 1550989 | 795 | - | 0.357233 | |
g5471 | DLA_06097 | GAOABQK02HUB3S | CDS | 1552913 | 936 | - | 0.320513 | |
g5472 | DLA_06098 | GAOABQK02HUB3S | CDS | 1554432 | 1749 | - | 0.331046 | |
g5473 | DLA_06100 | GAOABQK02HUB3S | CDS | 1557324 | 2205 | + | 0.320635 | |
g5474 | DLA_06101 | GAOABQK02HUB3S | CDS | 1559587 | 582 | - | 0.281787 | |
g5475 | DLA_06102 | GAOABQK02HUB3S | CDS | 1560306 | 798 | - | 0.283208 | |
g5476 | DLA_06103 | GAOABQK02HUB3S | CDS | 1561289 | 1536 | - | 0.321615 | |
g5477 | DLA_06104 | GAOABQK02HUB3S | CDS | 1563011 | 288 | + | 0.302083 | |
g5478 | DLA_06105 | GAOABQK02HUB3S | CDS | 1563808 | 234 | - | 0.405983 | |
g5479 | DLA_06106 | GAOABQK02HUB3S | CDS | 1564607 | 1050 | - | 0.340952 | |
g548 | DLA_00604 | contig05409_1.exp | CDS | 1254325 | 1593 | - | 0.300691 | |
g5480 | DLA_06107 | GAOABQK02HUB3S | CDS | 1565814 | 2001 | + | 0.34083 | |
g5481 | DLA_06108 | GAOABQK02HUB3S | CDS | 1567935 | 1623 | - | 0.309304 | |
g5482 | DLA_06110 | GAOABQK02HUB3S | CDS | 1570812 | 3024 | + | 0.341601 | |
g5483 | DLA_06111 | GAOABQK02HUB3S | CDS | 1574140 | 2898 | + | 0.335059 | |
g5484 | DLA_06112 | similar to discoidin I almost identical to its downstream gene DD7-1 | GAOABQK02HUB3S | CDS | 1578181 | 771 | + | 0.339818 |
g5485 | DLA_06113 | GAOABQK02HUB3S | CDS | 1579214 | 312 | + | 0.320513 | |
g5486 | DLA_06115 | GAOABQK02HUB3S | CDS | 1580083 | 3816 | + | 0.35718 | |
g5487 | DLA_06116 | GAOABQK02HUB3S | CDS | 1584053 | 507 | + | 0.307692 | |
g5488 | DLA_06118 | GAOABQK02HUB3S | CDS | 1584634 | 402 | - | 0.325871 | |
g5489 | DLA_06119 | catalyzes the reaction CDP-choline 12-diacylglycerol CMP a phosphatidylcholine | GAOABQK02HUB3S | CDS | 1586206 | 1185 | - | 0.342616 |
g549 | DLA_00605 | contig05409_1.exp | CDS | 1256123 | 3600 | - | 0.341389 | |
g5490 | DLA_06120 | GAOABQK02HUB3S | CDS | 1587723 | 3159 | + | 0.304527 | |
g5491 | DLA_11645 | GAOABQK02HUB3S | CDS | 1590990 | 237 | - | 0.308017 | |
g5492 | DLA_06121 | GAOABQK02HUB3S | CDS | 1591514 | 1812 | - | 0.381347 | |
g5493 | DLA_06122 | GAOABQK02HUB3S | CDS | 1593918 | 3222 | + | 0.346058 | |
g5494 | DLA_06124 | GAOABQK02HUB3S | CDS | 1597707 | 2163 | - | 0.297272 | |
g5495 | DLA_06125 | GAOABQK02HUB3S | CDS | 1600848 | 2223 | - | 0.304094 | |
g5496 | DLA_06126 | GAOABQK02HUB3S | CDS | 1604298 | 3276 | + | 0.356838 | |
g5497 | DLA_06127 | GAOABQK02HUB3S | CDS | 1607720 | 1308 | + | 0.309633 | |
g5498 | DLA_06128 | GAOABQK02HUB3S | CDS | 1609153 | 990 | - | 0.334343 | |
g5499 | DLA_06129 | GAOABQK02HUB3S | CDS | 1611066 | 354 | + | 0.310734 | |
g55 | DLA_00065 | contig05409_1.exp | CDS | 142683 | 519 | + | 0.325626 | |
g550 | DLA_00606 | contig05409_1.exp | CDS | 1260908 | 3054 | + | 0.332351 | |
g5500 | DLA_06130 | GAOABQK02HUB3S | CDS | 1611743 | 1152 | - | 0.335069 | |
g5501 | DLA_06131 | GAOABQK02HUB3S | CDS | 1613133 | 864 | - | 0.403935 | |
g5502 | DLA_06133 | GAOABQK02HUB3S | CDS | 1616160 | 888 | + | 0.353604 | |
g5503 | DLA_06134 | GAOABQK02HUB3S | CDS | 1617278 | 915 | + | 0.35082 | |
g5504 | DLA_06135 | GAOABQK02HUB3S | CDS | 1618445 | 1308 | - | 0.307339 | |
g5505 | DLA_06136 | GAOABQK02HUB3S | CDS | 1620569 | 1578 | + | 0.37199 | |
g5506 | DLA_06137 | GAOABQK02HUB3S | CDS | 1622539 | 1359 | + | 0.343635 | |
g5507 | DLA_06138 | GAOABQK02HUB3S | CDS | 1624230 | 3615 | + | 0.355463 | |
g5508 | DLA_06139 | GAOABQK02HUB3S | CDS | 1628003 | 3441 | - | 0.334786 | |
g5509 | DLA_06140 | conserved peptidase M20 family zinc metallopeptidases which are glutamate carboxypeptidases contains peptidase dimerization domain | GAOABQK02HUB3S | CDS | 1631814 | 1527 | - | 0.35167 |
g551 | DLA_00607 | contig05409_1.exp | CDS | 1264265 | 558 | + | 0.315412 | |
g5510 | DLA_06141 | GAOABQK02HUB3S | CDS | 1633658 | 942 | + | 0.313163 | |
g5511 | DLA_06142 | GAOABQK02HUB3S | CDS | 1635011 | 2298 | + | 0.355962 | |
g5512 | DLA_06143 | GAOABQK02HUB3S | CDS | 1637494 | 1845 | - | 0.337669 | |
g5513 | DLA_06144 | GAOABQK02HUB3S | CDS | 1639598 | 7839 | - | 0.391632 | |
g5514 | DLA_06145 | GAOABQK02HUB3S | CDS | 1649195 | 345 | - | 0.249275 | |
g5515 | DLA_06146 | GAOABQK02HUB3S | CDS | 1649646 | 2163 | - | 0.344429 | |
g5516 | DLA_06147 | GAOABQK02HUB3S | CDS | 1652776 | 1491 | + | 0.323273 | |
g5517 | DLA_06148 | GAOABQK02HUB3S | CDS | 1654680 | 2013 | - | 0.330353 | |
g5518 | DLA_06149 | GAOABQK02HUB3S | CDS | 1657395 | 3720 | - | 0.302151 | |
g5519 | DLA_06150 | GAOABQK02HUB3S | CDS | 1661476 | 3723 | - | 0.295998 | |
g552 | DLA_00608 | contig05409_1.exp | CDS | 1265949 | 1362 | + | 0.339207 | |
g5520 | DLA_06151 | GAOABQK02HUB3S | CDS | 1665833 | 3756 | - | 0.297657 | |
g5521 | DLA_06152 | GAOABQK02HUB3S | CDS | 1669851 | 1974 | - | 0.338906 | |
g5522 | DLA_06153 | GAOABQK02HUB3S | CDS | 1673333 | 2061 | + | 0.3246 | |
g5523 | DLA_06154 | GAOABQK02HUB3S | CDS | 1675987 | 375 | + | 0.312 | |
g5524 | DLA_06155 | cytochrome b5 is a membrane bound hemoprotein that functions as an electron carrier for several membrane bound oxygenases contains a single C-terminal transmembrane domain | GAOABQK02HUB3S | CDS | 1677051 | 330 | + | 0.321212 |
g5525 | DLA_06156 | GAOABQK02HUB3S | CDS | 1677557 | 954 | - | 0.287212 | |
g5526 | DLA_06158 | GAOABQK02HUB3S | CDS | 1679356 | 2919 | - | 0.332648 | |
g5527 | DLA_06159 | GAOABQK02HUB3S | CDS | 1682658 | 2637 | - | 0.323474 | |
g5528 | DLA_06160 | GAOABQK02HUB3S | CDS | 1685610 | 1227 | - | 0.410758 | |
g5529 | DLA_06161 | GAOABQK02HUB3S | CDS | 1687311 | 5418 | + | 0.307309 | |
g553 | DLA_00609 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | contig05409_1.exp | CDS | 1267677 | 456 | - | 0.309211 |
g5530 | DLA_06162 | GAOABQK02HUB3S | CDS | 1693115 | 1713 | + | 0.346176 | |
g5531 | DLA_06163 | GAOABQK02HUB3S | CDS | 1695704 | 459 | - | 0.346405 | |
g5532 | DLA_06164 | GAOABQK02HUB3S | CDS | 1697229 | 1470 | + | 0.34966 | |
g5533 | DLA_06165 | GAOABQK02HUB3S | CDS | 1698996 | 810 | - | 0.340741 | |
g5534 | DLA_06166 | GAOABQK02HUB3S | CDS | 1700973 | 3390 | + | 0.307965 | |
g5535 | DLA_06167 | GAOABQK02HUB3S | CDS | 1704535 | 444 | - | 0.353604 | |
g5536 | DLA_06168 | GAOABQK02HUB3S | CDS | 1705673 | 1164 | + | 0.311856 | |
g5537 | DLA_06169 | GAOABQK02HUB3S | CDS | 1707055 | 207 | - | 0.294686 | |
g5538 | DLA_06170 | GAOABQK02HUB3S | CDS | 1707826 | 2439 | + | 0.345223 | |
g5539 | DLA_06171 | GAOABQK02HUB3S | CDS | 1711237 | 777 | + | 0.337194 | |
g554 | DLA_00610 | contig05409_1.exp | CDS | 1268467 | 996 | + | 0.25502 | |
g5540 | DLA_06172 | similar to the conserved survival of motor neuron-related splicing factor 30 (SMNDC1 SPF30) the tudor domain is found in many proteins that colocalize with ribonucleoprotein or single-strand DNA-associated complexes | GAOABQK02HUB3S | CDS | 1712138 | 897 | + | 0.268673 |
g5541 | DLA_06173 | GAOABQK02HUB3S | CDS | 1713441 | 600 | - | 0.323333 | |
g5542 | DLA_06174 | GAOABQK02HUB3S | CDS | 1714166 | 3621 | + | 0.286385 | |
g5543 | DLA_06175 | GAOABQK02HUB3S | CDS | 1718240 | 543 | + | 0.302026 | |
g5544 | DLA_06176 | GAOABQK02HUB3S | CDS | 1719698 | 585 | + | 0.326496 | |
g5545 | DLA_06177 | GAOABQK02HUB3S | CDS | 1721108 | 477 | - | 0.33543 | |
g5546 | DLA_06178 | GAOABQK02HUB3S | CDS | 1721971 | 2142 | + | 0.29085 | |
g5547 | DLA_06179 | GAOABQK02HUB3S | CDS | 1724199 | 3735 | + | 0.243373 | |
g5548 | DLA_06181 | GAOABQK02HUB3S | CDS | 1728235 | 15423 | - | 0.319458 | |
g5549 | DLA_06183 | GAOABQK02HUB3S | CDS | 1745187 | 255 | + | 0.384314 | |
g555 | DLA_00611 | contig05409_1.exp | CDS | 1269641 | 534 | - | 0.29588 | |
g5550 | DLA_06184 | GAOABQK02HUB3S | CDS | 1745943 | 603 | + | 0.386401 | |
g5551 | DLA_06186 | GAOABQK02HUB3S | CDS | 1748039 | 1797 | - | 0.316639 | |
g5552 | DLA_06187 | GAOABQK02HUB3S | CDS | 1750162 | 537 | + | 0.340782 | |
g5553 | DLA_06188 | GAOABQK02HUB3S | CDS | 1750730 | 585 | - | 0.353846 | |
g5554 | DLA_11646 | GAOABQK02HUB3S | CDS | 1751505 | 231 | - | 0.363636 | |
g5555 | DLA_06189 | GAOABQK02HUB3S | CDS | 1752495 | 4401 | + | 0.304703 | |
g5556 | DLA_11647 | GAOABQK02HUB3S | CDS | 1757752 | 2301 | + | 0.262495 | |
g5557 | DLA_06190 | GAOABQK02HUB3S | CDS | 1760320 | 894 | + | 0.253915 | |
g5558 | DLA_06193 | GAOABQK02HUB3S | CDS | 1762996 | 2718 | - | 0.346946 | |
g5559 | DLA_06194 | GAOABQK02HUB3S | CDS | 1765900 | 3456 | - | 0.325231 | |
g556 | DLA_00612 | contig05409_1.exp | CDS | 1270367 | 2211 | + | 0.352782 | |
g5560 | DLA_06195 | GAOABQK02HUB3S | CDS | 1770035 | 816 | + | 0.29902 | |
g5561 | DLA_06196 | GAOABQK02HUB3S | CDS | 1771189 | 1764 | + | 0.296485 | |
g5562 | DLA_06197 | GAOABQK02HUB3S | CDS | 1773724 | 1989 | + | 0.291101 | |
g5563 | DLA_06199 | GAOABQK02HUB3S | CDS | 1778119 | 507 | + | 0.303748 | |
g5564 | DLA_06200 | GAOABQK02HUB3S | CDS | 1779865 | 669 | - | 0.355755 | |
g5565 | DLA_06201 | similar to human SYS1 which is involved in protein trafficking contains 4 putative transmembrane domains | GAOABQK02HUB3S | CDS | 1780650 | 804 | + | 0.273632 |
g5566 | DLA_06202 | similar to Rad1 a component of a heterotrimeric clamp (the 9-1-1 complex) that recognizes damaged DNA and initiates signal transduction for repair | GAOABQK02HUB3S | CDS | 1781586 | 981 | - | 0.309888 |
g5567 | DLA_06203 | GAOABQK02HUB3S | CDS | 1782785 | 849 | + | 0.287397 | |
g5568 | DLA_06204 | GAOABQK02HUB3S | CDS | 1783728 | 861 | + | 0.296167 | |
g5569 | DLA_06205 | GAOABQK02HUB3S | CDS | 1784848 | 3456 | - | 0.320891 | |
g557 | DLA_00613 | contig05409_1.exp | CDS | 1272889 | 660 | - | 0.395455 | |
g5570 | DLA_06206 | GAOABQK02HUB3S | CDS | 1788767 | 360 | - | 0.236111 | |
g5571 | DLA_06208 | GAOABQK02HUB3S | CDS | 1790422 | 891 | + | 0.309764 | |
g5572 | DLA_06209 | GAOABQK02HUB3S | CDS | 1791664 | 324 | + | 0.29321 | |
g5573 | DLA_06210 | GAOABQK02HUB3S | CDS | 1792010 | 990 | - | 0.318182 | |
g5574 | DLA_06211 | GAOABQK02HUB3S | CDS | 1793370 | 1065 | + | 0.373709 | |
g5575 | DLA_06212 | GAOABQK02HUB3S | CDS | 1794723 | 999 | + | 0.324324 | |
g5576 | DLA_06214 | GAOABQK02HUB3S | CDS | 1796393 | 1752 | + | 0.29395 | |
g5577 | DLA_06217 | GAOABQK02HUB3S | CDS | 1802982 | 849 | + | 0.302709 | |
g5578 | DLA_06218 | GAOABQK02HUB3S | CDS | 1803980 | 888 | - | 0.289414 | |
g5579 | DLA_06219 | GAOABQK02HUB3S | CDS | 1805526 | 303 | + | 0.280528 | |
g558 | DLA_00614 | contig05409_1.exp | CDS | 1274105 | 2472 | + | 0.337783 | |
g5580 | DLA_06220 | GAOABQK02HUB3S | CDS | 1806194 | 1173 | + | 0.330776 | |
g5581 | DLA_06221 | GAOABQK02HUB3S | CDS | 1807559 | 1044 | + | 0.327586 | |
g5582 | DLA_06222 | GAOABQK02HUB3S | CDS | 1808930 | 2490 | - | 0.300803 | |
g5583 | DLA_06223 | GAOABQK02HUB3S | CDS | 1812442 | 573 | + | 0.321117 | |
g5584 | DLA_06224 | GAOABQK02HUB3S | CDS | 1813096 | 2007 | - | 0.286497 | |
g5585 | DLA_06225 | GAOABQK02HUB3S | CDS | 1815884 | 945 | - | 0.303704 | |
g5586 | DLA_06229 | GAOABQK02HUB3S | CDS | 1822025 | 444 | + | 0.292793 | |
g5587 | DLA_06231 | GAOABQK02HUB3S | CDS | 1823015 | 1125 | - | 0.362667 | |
g5588 | DLA_06232 | GAOABQK02HUB3S | CDS | 1824721 | 3891 | + | 0.316114 | |
g5589 | DLA_06234 | very similar to the human 25 kDa cleavage and polyadenylation specificity factor component of the cleavage factor Im (CFIm) complex that plays a key role in pre-mRNA 3' processing | GAOABQK02HUB3S | CDS | 1829010 | 615 | - | 0.299187 |
g559 | DLA_00615 | contig05409_1.exp | CDS | 1276767 | 1959 | - | 0.346605 | |
g5590 | DLA_06235 | GAOABQK02HUB3S | CDS | 1829907 | 1581 | + | 0.359899 | |
g5591 | DLA_06236 | GAOABQK02HUB3S | CDS | 1831573 | 1944 | - | 0.319444 | |
g5592 | DLA_06237 | GAOABQK02HUB3S | CDS | 1833710 | 3480 | - | 0.314943 | |
g5593 | DLA_06238 | GAOABQK02HUB3S | CDS | 1837693 | 915 | - | 0.325683 | |
g5594 | DLA_06239 | GAOABQK02HUB3S | CDS | 1838972 | 303 | + | 0.356436 | |
g5595 | DLA_06240 | GAOABQK02HUB3S | CDS | 1839632 | 1023 | - | 0.313783 | |
g5596 | DLA_06241 | GAOABQK02HUB3S | CDS | 1840953 | 684 | - | 0.280702 | |
g5597 | DLA_06242 | GAOABQK02HUB3S | CDS | 1841711 | 666 | + | 0.268769 | |
g5598 | DLA_06243 | GAOABQK02HUB3S | CDS | 1842440 | 417 | - | 0.270983 | |
g5599 | DLA_06244 | GAOABQK02HUB3S | CDS | 1843423 | 1248 | + | 0.329327 | |
g56 | DLA_00066 | contig05409_1.exp | CDS | 143247 | 2988 | - | 0.319946 | |
g560 | DLA_00616 | contig05409_1.exp | CDS | 1278889 | 1833 | + | 0.357338 | |
g5600 | DLA_06245 | GAOABQK02HUB3S | CDS | 1844890 | 1230 | - | 0.301626 | |
g5601 | DLA_06246 | GAOABQK02HUB3S | CDS | 1846655 | 711 | - | 0.338959 | |
g5602 | DLA_06247 | GAOABQK02HUB3S | CDS | 1847928 | 1800 | + | 0.329444 | |
g5603 | DLA_06248 | the DCUN1 domain is found in the eukaryotic 'defective in cullin neddylation' (DCN) protein family | GAOABQK02HUB3S | CDS | 1849906 | 780 | + | 0.302564 |
g5604 | DLA_06249 | GAOABQK02HUB3S | CDS | 1851186 | 1101 | - | 0.294278 | |
g5605 | DLA_06250 | GAOABQK02HUB3S | CDS | 1852556 | 753 | + | 0.257636 | |
g5606 | DLA_06251 | GAOABQK02HUB3S | CDS | 1853533 | 1482 | - | 0.294872 | |
g5607 | DLA_06252 | GAOABQK02HUB3S | CDS | 1855354 | 1551 | - | 0.324307 | |
g5608 | DLA_06253 | GAOABQK02HUB3S | CDS | 1857833 | 4560 | + | 0.311184 | |
g5609 | DLA_06254 | GAOABQK02HUB3S | CDS | 1863011 | 609 | + | 0.311987 | |
g561 | DLA_00617 | contig05409_1.exp | CDS | 1280986 | 912 | - | 0.358553 | |
g5610 | DLA_06255 | GAOABQK02IBA3P | CDS | 206 | 2055 | + | 0.32944 | |
g5611 | DLA_06256 | GAOABQK02IBA3P | CDS | 2432 | 945 | - | 0.299471 | |
g5612 | DLA_06257 | GAOABQK02IBA3P | CDS | 4134 | 1986 | + | 0.330312 | |
g5613 | DLA_06258 | GAOABQK02IBA3P | CDS | 6230 | 819 | - | 0.291819 | |
g5614 | DLA_06259 | GAOABQK02IBA3P | CDS | 7687 | 2964 | + | 0.291161 | |
g5615 | DLA_06260 | similar to the IRSp53 and MIM families of I-BAR domains co-localizes with clathrin spots and seems to be involved in clathrin-mediated endocytosis does not localize to filopodia and is not involved in filopodium formation | GAOABQK02IBA3P | CDS | 11414 | 1050 | - | 0.30381 |
g5616 | DLA_06261 | GAOABQK02IBA3P | CDS | 13386 | 1188 | + | 0.319024 | |
g5617 | DLA_06262 | GAOABQK02IBA3P | CDS | 15305 | 1743 | + | 0.388411 | |
g5618 | DLA_06263 | GAOABQK02IBA3P | CDS | 17254 | 1911 | - | 0.324961 | |
g5619 | DLA_06264 | GAOABQK02IBA3P | CDS | 19449 | 765 | + | 0.288889 | |
g562 | DLA_00619 | contig05409_1.exp | CDS | 1283918 | 1182 | + | 0.406937 | |
g5620 | DLA_06265 | GAOABQK02IBA3P | CDS | 20757 | 1743 | + | 0.277682 | |
g5621 | DLA_06266 | GAOABQK02IBA3P | CDS | 23758 | 1545 | + | 0.299676 | |
g5622 | DLA_06267 | GAOABQK02IBA3P | CDS | 25572 | 693 | + | 0.291486 | |
g5623 | DLA_06269 | GAOABQK02IBA3P | CDS | 27290 | 1902 | - | 0.302313 | |
g5624 | DLA_06270 | GAOABQK02IBA3P | CDS | 29597 | 3363 | + | 0.296461 | |
g5625 | DLA_06271 | GAOABQK02IBA3P | CDS | 33164 | 2073 | + | 0.312108 | |
g5626 | DLA_06272 | GAOABQK02IBA3P | CDS | 35682 | 744 | + | 0.288978 | |
g5627 | DLA_06273 | GAOABQK02IBA3P | CDS | 36551 | 3156 | - | 0.324144 | |
g5628 | DLA_06274 | GAOABQK02IBA3P | CDS | 41340 | 3612 | + | 0.314784 | |
g5629 | DLA_06275 | GAOABQK02IBA3P | CDS | 45567 | 570 | + | 0.285965 | |
g563 | DLA_00620 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide has similarity to D. discoideum counting factor components cf50 and cf45-1. | contig05409_1.exp | CDS | 1286182 | 915 | + | 0.4 |
g5630 | DLA_06276 | GAOABQK02IBA3P | CDS | 46576 | 999 | - | 0.317317 | |
g5631 | DLA_06278 | GAOABQK02IBA3P | CDS | 48582 | 693 | + | 0.347763 | |
g5632 | DLA_06279 | EIF3A ortholog the eukaryotic initiation factor theta subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | GAOABQK02IBA3P | CDS | 49444 | 3186 | - | 0.348399 |
g5633 | DLA_06280 | EIF3L ortholog has been shown in human to bind EIF3E | GAOABQK02IBA3P | CDS | 53067 | 1842 | + | 0.32139 |
g5634 | DLA_06281 | GAOABQK02IBA3P | CDS | 55645 | 1767 | + | 0.353141 | |
g5635 | DLA_11648 | GAOABQK02IBA3P | CDS | 57940 | 519 | - | 0.310212 | |
g5636 | DLA_06282 | GAOABQK02IBA3P | CDS | 58631 | 1086 | - | 0.309392 | |
g5637 | DLA_06283 | GAOABQK02IBA3P | CDS | 59877 | 1746 | + | 0.269759 | |
g5638 | DLA_06284 | GAOABQK02IBA3P | CDS | 61690 | 1737 | - | 0.307427 | |
g5639 | DLA_06285 | GAOABQK02IBA3P | CDS | 64210 | 894 | + | 0.284116 | |
g564 | DLA_00621 | contig05409_1.exp | CDS | 1287428 | 3990 | - | 0.31604 | |
g5640 | DLA_06286 | GAOABQK02IBA3P | CDS | 65298 | 3513 | - | 0.321662 | |
g5641 | DLA_06287 | GAOABQK02IBA3P | CDS | 69480 | 3513 | + | 0.325648 | |
g5642 | DLA_06288 | GAOABQK02IBA3P | CDS | 73559 | 2757 | + | 0.300689 | |
g5643 | DLA_06289 | GAOABQK02IBA3P | CDS | 77074 | 1599 | + | 0.333959 | |
g5644 | DLA_06290 | GAOABQK02IBA3P | CDS | 78894 | 1023 | + | 0.29521 | |
g5645 | DLA_06291 | ortholog of S. cerevisiae OAC1 involved in transport of oxaloacetate sulfate and thiosulfate across the mitochondrial membrane contains two transmembrane domains | GAOABQK02IBA3P | CDS | 80113 | 972 | - | 0.335391 |
g5646 | DLA_06293 | GAOABQK02IBA3P | CDS | 82956 | 2109 | + | 0.322902 | |
g5647 | DLA_06294 | GAOABQK02IBA3P | CDS | 85170 | 930 | - | 0.291398 | |
g5648 | DLA_06295 | GAOABQK02IBA3P | CDS | 87434 | 1659 | + | 0.290536 | |
g5649 | DLA_06296 | GAOABQK02IBA3P | CDS | 89360 | 969 | - | 0.292054 | |
g565 | DLA_00622 | contig05409_1.exp | CDS | 1291713 | 2670 | - | 0.320225 | |
g5650 | DLA_06297 | GAOABQK02IBA3P | CDS | 91201 | 1005 | + | 0.303483 | |
g5651 | DLA_06298 | GAOABQK02IBA3P | CDS | 93638 | 3111 | - | 0.287367 | |
g5652 | DLA_11649 | GAOABQK02IBA3P | CDS | 97262 | 1521 | + | 0.26693 | |
g5653 | DLA_06299 | GAOABQK02IBA3P | CDS | 98937 | 741 | + | 0.318489 | |
g5654 | DLA_06300 | GAOABQK02IBA3P | CDS | 100124 | 4236 | - | 0.344901 | |
g5655 | DLA_06301 | GAOABQK02IBA3P | CDS | 105239 | 3180 | + | 0.367925 | |
g5656 | DLA_06302 | GAOABQK02IBA3P | CDS | 108795 | 564 | + | 0.296099 | |
g5657 | DLA_06303 | GAOABQK02IBA3P | CDS | 109736 | 4614 | - | 0.310576 | |
g5658 | DLA_06304 | GAOABQK02IBA3P | CDS | 114650 | 3585 | - | 0.318828 | |
g5659 | DLA_06305 | GAOABQK02IBA3P | CDS | 119528 | 4551 | + | 0.307185 | |
g566 | DLA_00623 | contig05409_1.exp | CDS | 1294672 | 1509 | - | 0.37442 | |
g5660 | DLA_06306 | contains 5 putative transmembrane domains similar to D. purpureum protein | GAOABQK02IBA3P | CDS | 124665 | 1809 | + | 0.331675 |
g5661 | DLA_06307 | GAOABQK02IBA3P | CDS | 126787 | 225 | - | 0.28 | |
g5662 | DLA_06308 | GAOABQK02IBA3P | CDS | 127226 | 600 | + | 0.343333 | |
g5663 | DLA_06309 | GAOABQK02IBA3P | CDS | 127922 | 1002 | - | 0.347305 | |
g5664 | DLA_06310 | GAOABQK02IBA3P | CDS | 129244 | 969 | - | 0.336429 | |
g5665 | DLA_06311 | GAOABQK02IBA3P | CDS | 130956 | 2592 | + | 0.345293 | |
g5666 | DLA_06312 | catalytic subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase | GAOABQK02IBA3P | CDS | 133718 | 1569 | + | 0.333971 |
g5667 | DLA_06313 | GAOABQK02IBA3P | CDS | 135440 | 4092 | - | 0.305718 | |
g5668 | DLA_06314 | GAOABQK02IBA3P | CDS | 139957 | 1665 | + | 0.361562 | |
g5669 | DLA_06315 | GAOABQK02IBA3P | CDS | 142689 | 1431 | + | 0.317261 | |
g567 | DLA_00625 | contig05409_1.exp | CDS | 1297697 | 1677 | - | 0.252832 | |
g5670 | DLA_06316 | GAOABQK02IBA3P | CDS | 144291 | 600 | + | 0.243333 | |
g5671 | DLA_06317 | GAOABQK02IBA3P | CDS | 145093 | 420 | - | 0.242857 | |
g5672 | DLA_06318 | GAOABQK02IBA3P | CDS | 145851 | 1854 | - | 0.318231 | |
g5673 | DLA_06319 | GAOABQK02IBA3P | CDS | 150404 | 1575 | - | 0.293968 | |
g5674 | DLA_06321 | GAOABQK02IBA3P | CDS | 153167 | 237 | - | 0.299578 | |
g5675 | DLA_06322 | GAOABQK02IBA3P | CDS | 154496 | 3345 | + | 0.339611 | |
g5676 | DLA_06323 | GAOABQK02IBA3P | CDS | 157975 | 990 | - | 0.288889 | |
g5677 | DLA_06324 | GAOABQK02IBA3P | CDS | 159784 | 813 | + | 0.311193 | |
g5678 | DLA_06325 | GAOABQK02IBA3P | CDS | 160924 | 723 | + | 0.327801 | |
g5679 | DLA_06327 | GAOABQK02IBA3P | CDS | 163438 | 1125 | - | 0.335111 | |
g568 | DLA_00626 | contig05409_1.exp | CDS | 1299767 | 1692 | - | 0.299054 | |
g5680 | DLA_06328 | GAOABQK02IBA3P | CDS | 165720 | 1671 | + | 0.299222 | |
g5681 | DLA_06329 | GAOABQK02IBA3P | CDS | 167791 | 1395 | + | 0.375627 | |
g5682 | DLA_06330 | GAOABQK02IBA3P | CDS | 170238 | 1788 | + | 0.294743 | |
g5683 | DLA_06331 | GAOABQK02IBA3P | CDS | 172824 | 1467 | + | 0.386503 | |
g5684 | DLA_06333 | GAOABQK02IBA3P | CDS | 176984 | 1476 | + | 0.275068 | |
g5685 | DLA_06334 | GAOABQK02IBA3P | CDS | 178605 | 2376 | + | 0.31271 | |
g5686 | DLA_06335 | GAOABQK02IBA3P | CDS | 181171 | 282 | - | 0.27305 | |
g5687 | DLA_06336 | GAOABQK02IBA3P | CDS | 181871 | 1077 | + | 0.334262 | |
g5688 | DLA_06337 | contains an N-terminal oxidoreductase domain and a partial C-terminal oxidoreductase domain the GfoIdhMocA family proteins utilize NADP or NAD | GAOABQK02IBA3P | CDS | 182992 | 1338 | - | 0.323617 |
g5689 | DLA_06339 | GAOABQK02IBA3P | CDS | 185206 | 2403 | - | 0.293799 | |
g569 | DLA_00627 | contig05409_1.exp | CDS | 1302253 | 3717 | + | 0.334409 | |
g5690 | DLA_06340 | GAOABQK02IBA3P | CDS | 188605 | 1425 | - | 0.322807 | |
g5691 | DLA_06341 | GAOABQK02IBA3P | CDS | 190338 | 1497 | + | 0.336673 | |
g5692 | DLA_06342 | GAOABQK02IBA3P | CDS | 191924 | 846 | - | 0.320331 | |
g5693 | DLA_06343 | GAOABQK02IBA3P | CDS | 193156 | 2175 | - | 0.331954 | |
g5694 | DLA_06345 | GAOABQK02IBA3P | CDS | 195723 | 6309 | - | 0.319702 | |
g5695 | DLA_06346 | GAOABQK02IBA3P | CDS | 202584 | 2334 | - | 0.37018 | |
g5696 | DLA_06347 | GAOABQK02IBA3P | CDS | 205257 | 1188 | + | 0.299663 | |
g5697 | DLA_06349 | GAOABQK02IBA3P | CDS | 206637 | 243 | - | 0.271605 | |
g5698 | DLA_06350 | GAOABQK02IBA3P | CDS | 207988 | 3138 | - | 0.314532 | |
g5699 | DLA_06352 | GAOABQK02IBA3P | CDS | 212325 | 753 | + | 0.320053 | |
g57 | DLA_00067 | contig05409_1.exp | CDS | 146543 | 270 | + | 0.340741 | |
g570 | DLA_00629 | contig05409_1.exp | CDS | 1306356 | 3144 | + | 0.309796 | |
g5700 | DLA_06353 | GAOABQK02IBA3P | CDS | 213493 | 846 | + | 0.323877 | |
g5701 | DLA_06354 | GAOABQK02IBA3P | CDS | 214575 | 654 | - | 0.270642 | |
g5702 | DLA_06355 | GAOABQK02IBA3P | CDS | 215900 | 1233 | - | 0.297648 | |
g5703 | DLA_06356 | GAOABQK02IBA3P | CDS | 217747 | 4431 | - | 0.349131 | |
g5704 | DLA_11650 | GAOABQK02IBA3P | CDS | 222520 | 213 | + | 0.253521 | |
g5705 | DLA_06357 | GAOABQK02IBA3P | CDS | 223679 | 2946 | + | 0.334691 | |
g5706 | DLA_06359 | GAOABQK02IBA3P | CDS | 227474 | 1104 | - | 0.289855 | |
g5707 | DLA_06360 | GAOABQK02IBA3P | CDS | 229013 | 1719 | + | 0.307155 | |
g5708 | DLA_06361 | GAOABQK02IBA3P | CDS | 230973 | 1905 | + | 0.289239 | |
g5709 | DLA_06363 | GAOABQK02IBA3P | CDS | 234110 | 1617 | + | 0.289425 | |
g571 | DLA_00631 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane expressed in pstAO cells and in upper and lower cups during culminationbrbr bCommunity annotation:b Overview of the | contig05409_1.exp | CDS | 1310001 | 894 | + | 0.381432 |
g5710 | DLA_06364 | GAOABQK02IBA3P | CDS | 235762 | 495 | - | 0.375758 | |
g5711 | DLA_06365 | GAOABQK02IBA3P | CDS | 236744 | 1392 | + | 0.389368 | |
g5712 | DLA_06367 | GAOABQK02IBA3P | CDS | 238671 | 2769 | + | 0.313109 | |
g5713 | DLA_06368 | GAOABQK02IBA3P | CDS | 241491 | 1197 | - | 0.320802 | |
g5714 | DLA_06369 | GAOABQK02IBA3P | CDS | 242993 | 864 | - | 0.357639 | |
g5715 | DLA_06370 | GAOABQK02IBA3P | CDS | 244597 | 2223 | - | 0.340531 | |
g5716 | DLA_06371 | GAOABQK02IBA3P | CDS | 247103 | 639 | + | 0.320814 | |
g5717 | DLA_06372 | GAOABQK02IBA3P | CDS | 247933 | 1053 | - | 0.242165 | |
g5718 | DLA_06373 | GAOABQK02IBA3P | CDS | 249382 | 666 | + | 0.421922 | |
g5719 | DLA_06377 | GAOABQK02IBA3P | CDS | 252839 | 810 | + | 0.291358 | |
g572 | DLA_00632 | contig05409_1.exp | CDS | 1311038 | 1035 | - | 0.296618 | |
g5720 | DLA_06378 | GAOABQK02IBA3P | CDS | 253864 | 28059 | - | 0.323105 | |
g5721 | DLA_06379 | GAOABQK02IBA3P | CDS | 282793 | 3195 | - | 0.358372 | |
g5722 | DLA_06380 | GAOABQK02IBA3P | CDS | 286661 | 1371 | + | 0.312181 | |
g5723 | DLA_06381 | GAOABQK02IBA3P | CDS | 288304 | 660 | - | 0.365152 | |
g5724 | DLA_06382 | GAOABQK02IBA3P | CDS | 289709 | 5442 | - | 0.332598 | |
g5725 | DLA_06384 | GAOABQK02IBA3P | CDS | 295842 | 594 | - | 0.328283 | |
g5726 | DLA_06385 | GAOABQK02IBA3P | CDS | 296684 | 1692 | - | 0.353428 | |
g5727 | DLA_06386 | GAOABQK02IBA3P | CDS | 298528 | 1398 | - | 0.329041 | |
g5728 | DLA_06390 | GAOABQK02IBA3P | CDS | 303541 | 1962 | - | 0.275229 | |
g5729 | DLA_06391 | GAOABQK02IBA3P | CDS | 305679 | 2820 | - | 0.324823 | |
g573 | DLA_00633 | catalyzes the reaction isocitrate NAD 2-oxoglutarate CO2 NADH | contig05409_1.exp | CDS | 1312355 | 1092 | + | 0.387363 |
g5730 | DLA_06392 | GAOABQK02IBA3P | CDS | 308551 | 1104 | - | 0.298913 | |
g5731 | DLA_06393 | involved in regulation of aggregate size member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | GAOABQK02IBA3P | CDS | 310003 | 912 | + | 0.346491 |
g5732 | DLA_06394 | GAOABQK02IBA3P | CDS | 311185 | 1728 | - | 0.328125 | |
g5733 | DLA_06395 | GAOABQK02IBA3P | CDS | 313602 | 5910 | - | 0.318105 | |
g5734 | DLA_06396 | GAOABQK02IBA3P | CDS | 320520 | 288 | + | 0.322917 | |
g5735 | DLA_06397 | GAOABQK02IBA3P | CDS | 321075 | 894 | - | 0.309843 | |
g5736 | DLA_06398 | GAOABQK02IBA3P | CDS | 322686 | 810 | - | 0.376543 | |
g5737 | DLA_06399 | GAOABQK02IBA3P | CDS | 323853 | 1539 | - | 0.326836 | |
g5738 | DLA_06400 | GAOABQK02IBA3P | CDS | 325958 | 906 | + | 0.321192 | |
g5739 | DLA_06401 | GAOABQK02IBA3P | CDS | 327191 | 3069 | - | 0.358749 | |
g574 | DLA_00634 | contig05409_1.exp | CDS | 1313757 | 879 | + | 0.242321 | |
g5740 | DLA_06403 | GAOABQK02IBA3P | CDS | 330956 | 2391 | - | 0.368047 | |
g5741 | DLA_06404 | GAOABQK02IBA3P | CDS | 333524 | 210 | + | 0.290476 | |
g5742 | DLA_06405 | GAOABQK02IBA3P | CDS | 333890 | 336 | - | 0.241071 | |
g5743 | DLA_06406 | GAOABQK02IBA3P | CDS | 334439 | 2538 | + | 0.326241 | |
g5744 | DLA_11651 | GAOABQK02IBA3P | CDS | 337103 | 4110 | + | 0.326277 | |
g5745 | DLA_06407 | GAOABQK02IBA3P | CDS | 341553 | 3891 | + | 0.332562 | |
g5746 | DLA_06408 | GAOABQK02IBA3P | CDS | 345827 | 4107 | + | 0.327977 | |
g5747 | DLA_06409 | GAOABQK02IBA3P | CDS | 350455 | 3795 | + | 0.334914 | |
g5748 | DLA_06410 | GAOABQK02IBA3P | CDS | 354331 | 1455 | - | 0.303093 | |
g5749 | DLA_06412 | GAOABQK02IBA3P | CDS | 356799 | 1758 | - | 0.293515 | |
g575 | DLA_00636 | contig05409_1.exp | CDS | 1314714 | 432 | - | 0.259259 | |
g5750 | DLA_06413 | GAOABQK02IBA3P | CDS | 358729 | 2043 | - | 0.314244 | |
g5751 | DLA_06414 | GAOABQK02IBA3P | CDS | 360993 | 1308 | + | 0.29052 | |
g5752 | DLA_06415 | GAOABQK02IBA3P | CDS | 362764 | 1143 | - | 0.339458 | |
g5753 | DLA_06416 | GAOABQK02IBA3P | CDS | 365076 | 2937 | + | 0.336398 | |
g5754 | DLA_06417 | GAOABQK02IBA3P | CDS | 368506 | 2937 | + | 0.335036 | |
g5755 | DLA_06418 | GAOABQK02IBA3P | CDS | 371791 | 1371 | - | 0.308534 | |
g5756 | DLA_06419 | GAOABQK02IBA3P | CDS | 373614 | 1512 | + | 0.28836 | |
g5757 | DLA_06420 | GAOABQK02IBA3P | CDS | 375342 | 822 | + | 0.254258 | |
g5758 | DLA_06422 | GAOABQK02IBA3P | CDS | 377139 | 4905 | - | 0.332518 | |
g5759 | DLA_06423 | GAOABQK02IBA3P | CDS | 382665 | 1047 | - | 0.35148 | |
g576 | DLA_00637 | contig05409_1.exp | CDS | 1315407 | 1557 | + | 0.324342 | |
g5760 | DLA_06424 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase defects in the human MOCOS cause xanthinuria type II (XU-II) | GAOABQK02IBA3P | CDS | 384204 | 2544 | + | 0.342767 |
g5761 | DLA_06425 | GAOABQK02IBA3P | CDS | 387451 | 2007 | + | 0.308421 | |
g5762 | DLA_06427 | similar to S. cerevisiae UDF1 together with npl4 and cdcD involved in recognition of polyubiquitinated proteins and their presentation to the 26S proteasome for degradation | GAOABQK02IBA3P | CDS | 390636 | 963 | + | 0.318795 |
g5763 | DLA_06428 | GAOABQK02IBA3P | CDS | 391763 | 975 | - | 0.242051 | |
g5764 | DLA_06429 | GAOABQK02IBA3P | CDS | 393481 | 1029 | + | 0.394558 | |
g5765 | DLA_06430 | GAOABQK02IBA3P | CDS | 395182 | 2124 | - | 0.330508 | |
g5766 | DLA_06431 | GAOABQK02IBA3P | CDS | 397662 | 222 | + | 0.310811 | |
g5767 | DLA_06432 | GAOABQK02IBA3P | CDS | 398059 | 801 | - | 0.338327 | |
g5768 | DLA_06433 | ortholog of human FHIT which is a possible tumor suppressor for specific tissues numerous tumor types are associated with aberrant forms of human FHIT protein | GAOABQK02IBA3P | CDS | 399414 | 435 | + | 0.333333 |
g5769 | DLA_06434 | GAOABQK02IBA3P | CDS | 399983 | 774 | - | 0.341085 | |
g577 | DLA_00638 | contig05409_1.exp | CDS | 1317346 | 600 | + | 0.348333 | |
g5770 | DLA_06436 | ortholog of the mammalian aquarius (AQR) protein an intron-binding spliceosomal protein required to link pre-mRNA splicing and snoRNP (small nucleolar ribonucleoprotein) biogenesis | GAOABQK02IBA3P | CDS | 401701 | 4101 | + | 0.320897 |
g5771 | DLA_06437 | GAOABQK02IBA3P | CDS | 405975 | 3036 | - | 0.323123 | |
g5772 | DLA_06438 | GAOABQK02IBA3P | CDS | 410080 | 357 | - | 0.338936 | |
g5773 | DLA_06439 | GAOABQK02IBA3P | CDS | 411080 | 2640 | - | 0.371591 | |
g5774 | DLA_06440 | GAOABQK02IBA3P | CDS | 414375 | 2274 | + | 0.346526 | |
g5775 | DLA_06441 | protein component of the small (40S) ribosomal subunit ribosomal protein S25 homolog | GAOABQK02IBA3P | CDS | 416834 | 336 | + | 0.395833 |
g5776 | DLA_06442 | GAOABQK02IBA3P | CDS | 417877 | 546 | + | 0.282051 | |
g5777 | DLA_06443 | GAOABQK02IBA3P | CDS | 418948 | 1335 | - | 0.323595 | |
g5778 | DLA_11652 | GAOABQK02IBA3P | CDS | 421230 | 984 | - | 0.36687 | |
g5779 | DLA_06444 | GAOABQK02IBA3P | CDS | 422765 | 1071 | + | 0.331466 | |
g578 | DLA_00639 | contig05409_1.exp | CDS | 1318219 | 612 | + | 0.277778 | |
g5780 | DLA_06445 | GAOABQK02IBA3P | CDS | 423939 | 978 | - | 0.370143 | |
g5781 | DLA_06447 | GAOABQK02IBA3P | CDS | 425395 | 3099 | + | 0.31494 | |
g5782 | DLA_06448 | GAOABQK02IBA3P | CDS | 428950 | 3291 | + | 0.294439 | |
g5783 | DLA_06450 | GAOABQK02IBA3P | CDS | 434811 | 1488 | + | 0.336694 | |
g5784 | DLA_06451 | GAOABQK02IBA3P | CDS | 437317 | 2775 | + | 0.343784 | |
g5785 | DLA_06452 | GAOABQK02IBA3P | CDS | 440360 | 4989 | + | 0.338144 | |
g5786 | DLA_06453 | GAOABQK02IBA3P | CDS | 445809 | 648 | + | 0.351852 | |
g5787 | DLA_06454 | GAOABQK02IBA3P | CDS | 446948 | 558 | + | 0.335125 | |
g5788 | DLA_06455 | GAOABQK02IBA3P | CDS | 447538 | 1749 | - | 0.294454 | |
g5789 | DLA_06456 | GAOABQK02IBA3P | CDS | 449355 | 615 | + | 0.305691 | |
g579 | DLA_00640 | contig05409_1.exp | CDS | 1318963 | 909 | - | 0.326733 | |
g5790 | DLA_06457 | GAOABQK02IBA3P | CDS | 450086 | 1008 | + | 0.311508 | |
g5791 | DLA_06458 | GAOABQK02IBA3P | CDS | 451397 | 885 | + | 0.372881 | |
g5792 | DLA_06459 | GAOABQK02IBA3P | CDS | 452548 | 642 | - | 0.436137 | |
g5793 | DLA_06460 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | GAOABQK02IBA3P | CDS | 453719 | 2019 | - | 0.327885 |
g5794 | DLA_06461 | catalyzes the reaction ATP D-fructose 6-phosphate ADP D-fructose 16-bisphosphate the Dictyostelium PFK has been found to be a non-allosteric enzyme that binds to tubulin and inhibits tubulin polymerization | GAOABQK02IBA3P | CDS | 456155 | 2367 | + | 0.377693 |
g5795 | DLA_06462 | GAOABQK02IBA3P | CDS | 460491 | 657 | + | 0.354642 | |
g5796 | DLA_06463 | belongs to the thiolase family similar to human ACAA1 | GAOABQK02IBA3P | CDS | 461596 | 1260 | - | 0.399206 |
g5797 | DLA_06464 | catalyzes the reaction dolichyl diphosphate Hsub2subO dolichyl phosphate phosphate contains 4 putative transmembrane domains | GAOABQK02IBA3P | CDS | 463369 | 714 | + | 0.29972 |
g5798 | DLA_11653 | GAOABQK02IBA3P | CDS | 464115 | 1845 | - | 0.289973 | |
g5799 | DLA_06465 | GAOABQK02IBA3P | CDS | 466208 | 3795 | - | 0.311199 | |
g58 | DLA_00068 | contig05409_1.exp | CDS | 147186 | 2382 | + | 0.342989 | |
g580 | DLA_00641 | contig05409_1.exp | CDS | 1320633 | 1473 | + | 0.303462 | |
g5800 | DLA_06466 | GAOABQK02IBA3P | CDS | 470727 | 1437 | + | 0.306193 | |
g5801 | DLA_06467 | GAOABQK02IBA3P | CDS | 472374 | 1722 | + | 0.283391 | |
g5802 | DLA_06468 | GAOABQK02IBA3P | CDS | 474321 | 867 | + | 0.317186 | |
g5803 | DLA_06469 | GAOABQK02IBA3P | CDS | 475424 | 993 | - | 0.296073 | |
g5804 | DLA_06470 | GAOABQK02IBA3P | CDS | 476918 | 1482 | - | 0.317139 | |
g5805 | DLA_06471 | GAOABQK02IBA3P | CDS | 478846 | 753 | - | 0.270916 | |
g5806 | DLA_06475 | A6 family protein kinase very similar to human and mouse twinfilin (A6 protein) which is a tyrosine kinase and an actin monomer binding protein contains two ADF domains (actin depolymerization factorcofilin-like domains) | GAOABQK02IBA3P | CDS | 481599 | 1011 | - | 0.352127 |
g5807 | DLA_06476 | protein component of the large (60S) ribosomal subunit ribosomal protein L8 homolog | GAOABQK02IBA3P | CDS | 483162 | 762 | + | 0.430446 |
g5808 | DLA_06477 | GAOABQK02IBA3P | CDS | 484395 | 1359 | - | 0.287712 | |
g5809 | DLA_06478 | GAOABQK02IBA3P | CDS | 486188 | 1662 | - | 0.380866 | |
g581 | DLA_00642 | contig05409_1.exp | CDS | 1322612 | 1473 | + | 0.298031 | |
g5810 | DLA_06479 | GAOABQK02IBA3P | CDS | 488224 | 504 | + | 0.271825 | |
g5811 | DLA_06480 | GAOABQK02IBA3P | CDS | 488940 | 1839 | - | 0.32137 | |
g5812 | DLA_06481 | GAOABQK02IBA3P | CDS | 491442 | 1083 | - | 0.339797 | |
g5813 | DLA_06482 | GAOABQK02IBA3P | CDS | 493049 | 2448 | + | 0.299428 | |
g5814 | DLA_06483 | GAOABQK02IBA3P | CDS | 496332 | 1233 | + | 0.310624 | |
g5815 | DLA_06485 | GAOABQK02IBA3P | CDS | 499171 | 1422 | + | 0.342475 | |
g5816 | DLA_06488 | GAOABQK02IBA3P | CDS | 502384 | 864 | + | 0.30787 | |
g5817 | DLA_06490 | GAOABQK02IBA3P | CDS | 503468 | 3159 | - | 0.348845 | |
g5818 | DLA_06491 | GAOABQK02IBA3P | CDS | 506763 | 222 | + | 0.247748 | |
g5819 | DLA_06492 | GAOABQK02IBA3P | CDS | 507262 | 1731 | - | 0.275563 | |
g582 | DLA_00643 | contig05409_1.exp | CDS | 1324993 | 3417 | - | 0.307872 | |
g5820 | DLA_06493 | GAOABQK02IBA3P | CDS | 509312 | 969 | + | 0.359133 | |
g5821 | DLA_06494 | GAOABQK02IBA3P | CDS | 510741 | 1128 | + | 0.340426 | |
g5822 | DLA_06495 | GAOABQK02IBA3P | CDS | 512692 | 3099 | + | 0.334947 | |
g5823 | DLA_06496 | GAOABQK02IBA3P | CDS | 515864 | 699 | - | 0.246066 | |
g5824 | DLA_06497 | GAOABQK02IBA3P | CDS | 516660 | 792 | - | 0.268939 | |
g5825 | DLA_06498 | GAOABQK02IBA3P | CDS | 518153 | 3813 | + | 0.303698 | |
g5826 | DLA_06499 | GAOABQK02IBA3P | CDS | 522277 | 897 | + | 0.294314 | |
g5827 | DLA_11654 | GAOABQK02IBA3P | CDS | 523356 | 699 | + | 0.314735 | |
g5828 | DLA_06500 | GAOABQK02IBA3P | CDS | 524202 | 1902 | - | 0.321767 | |
g5829 | DLA_06501 | GAOABQK02IBA3P | CDS | 526363 | 399 | - | 0.300752 | |
g583 | DLA_00644 | contig05409_1.exp | CDS | 1328886 | 522 | + | 0.369732 | |
g5830 | DLA_06502 | GAOABQK02IBA3P | CDS | 527165 | 2028 | + | 0.29783 | |
g5831 | DLA_06503 | GAOABQK02IBA3P | CDS | 529447 | 1281 | - | 0.320062 | |
g5832 | DLA_06504 | GAOABQK02IBA3P | CDS | 531170 | 2241 | - | 0.318162 | |
g5833 | DLA_06505 | GAOABQK02IBA3P | CDS | 533689 | 4170 | - | 0.356115 | |
g5834 | DLA_06506 | subunit VIb of cytochrome c oxidase the terminal member of the mitochondrial inner membrane electron transport chain | GAOABQK02IBA3P | CDS | 538246 | 303 | + | 0.277228 |
g5835 | DLA_06507 | GAOABQK02IBA3P | CDS | 538712 | 1815 | - | 0.305234 | |
g5836 | DLA_06508 | GAOABQK02IBA3P | CDS | 540736 | 2946 | + | 0.339104 | |
g5837 | DLA_06509 | GAOABQK02IBA3P | CDS | 543827 | 2214 | - | 0.287715 | |
g5838 | DLA_06510 | GAOABQK02IBA3P | CDS | 546420 | 783 | + | 0.316731 | |
g5839 | DLA_06513 | GAOABQK02IBA3P | CDS | 548866 | 705 | + | 0.337589 | |
g584 | DLA_00645 | contig05409_1.exp | CDS | 1329817 | 1587 | - | 0.289855 | |
g5840 | DLA_06514 | GAOABQK02IBA3P | CDS | 549833 | 1281 | - | 0.338798 | |
g5841 | DLA_06515 | GAOABQK02IBA3P | CDS | 552310 | 1395 | - | 0.324731 | |
g5842 | DLA_06516 | GAOABQK02IBA3P | CDS | 553910 | 3255 | - | 0.349309 | |
g5843 | DLA_06517 | GAOABQK02IBA3P | CDS | 557758 | 2001 | + | 0.323838 | |
g5844 | DLA_06518 | GAOABQK02IBA3P | CDS | 560097 | 546 | + | 0.35348 | |
g5845 | DLA_06519 | GAOABQK02IBA3P | CDS | 560845 | 387 | - | 0.312661 | |
g5846 | DLA_06520 | GAOABQK02IBA3P | CDS | 561659 | 825 | + | 0.30303 | |
g5847 | DLA_06522 | GAOABQK02IBA3P | CDS | 563547 | 966 | - | 0.278468 | |
g5848 | DLA_06523 | GAOABQK02IBA3P | CDS | 565103 | 2235 | - | 0.311409 | |
g5849 | DLA_06524 | GAOABQK02IBA3P | CDS | 568174 | 1335 | + | 0.326592 | |
g585 | DLA_00646 | contig05409_1.exp | CDS | 1331666 | 3348 | - | 0.344086 | |
g5850 | DLA_06525 | GAOABQK02IBA3P | CDS | 570201 | 1470 | + | 0.344898 | |
g5851 | DLA_06526 | GAOABQK02IBA3P | CDS | 571753 | 1461 | - | 0.347023 | |
g5852 | DLA_06527 | GAOABQK02IBA3P | CDS | 573481 | 759 | - | 0.328063 | |
g5853 | DLA_06528 | GAOABQK02IBA3P | CDS | 574396 | 1449 | - | 0.287785 | |
g5854 | DLA_06529 | ortholog of the human SOD2 the mitochondrial superoxide dismutase belongs to the ironmanganese superoxide dismutase family | GAOABQK02IBA3P | CDS | 575948 | 660 | - | 0.365152 |
g5855 | DLA_06530 | GAOABQK02IBA3P | CDS | 577025 | 1674 | - | 0.311828 | |
g5856 | DLA_06531 | GAOABQK02IBA3P | CDS | 579167 | 951 | - | 0.263933 | |
g5857 | DLA_06532 | GAOABQK02IBA3P | CDS | 580403 | 990 | - | 0.251515 | |
g5858 | DLA_11655 | GAOABQK02IBA3P | CDS | 582513 | 504 | - | 0.232143 | |
g5859 | DLA_06533 | GAOABQK02IBA3P | CDS | 583288 | 792 | - | 0.262626 | |
g586 | DLA_00647 | contig05409_1.exp | CDS | 1335627 | 1506 | + | 0.35591 | |
g5860 | DLA_06534 | GAOABQK02IBA3P | CDS | 585008 | 882 | - | 0.250567 | |
g5861 | DLA_06535 | GAOABQK02IBA3P | CDS | 586433 | 1005 | - | 0.255721 | |
g5862 | DLA_06536 | GAOABQK02IBA3P | CDS | 587566 | 1002 | - | 0.256487 | |
g5863 | DLA_06537 | GAOABQK02IBA3P | CDS | 589430 | 1599 | - | 0.37586 | |
g5864 | DLA_06538 | GAOABQK02IBA3P | CDS | 591603 | 657 | + | 0.30137 | |
g5865 | DLA_06539 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | GAOABQK02IBA3P | CDS | 592701 | 1761 | + | 0.376491 |
g5866 | DLA_06540 | GAOABQK02IBA3P | CDS | 594716 | 1509 | + | 0.306163 | |
g5867 | DLA_06541 | GAOABQK02IBA3P | CDS | 597009 | 2496 | + | 0.330929 | |
g5868 | DLA_06542 | GAOABQK02IBA3P | CDS | 599746 | 1014 | + | 0.260355 | |
g5869 | DLA_06543 | GAOABQK02IBA3P | CDS | 601243 | 2475 | - | 0.317576 | |
g587 | DLA_00648 | contig05409_1.exp | CDS | 1337264 | 2793 | + | 0.274973 | |
g5870 | DLA_06544 | GAOABQK02IBA3P | CDS | 604806 | 876 | - | 0.33105 | |
g5871 | DLA_06545 | GAOABQK02IBA3P | CDS | 606117 | 939 | - | 0.369542 | |
g5872 | DLA_06546 | GAOABQK02IBA3P | CDS | 607739 | 1356 | + | 0.312684 | |
g5873 | DLA_06547 | GAOABQK02IBA3P | CDS | 609366 | 1617 | - | 0.284477 | |
g5874 | DLA_06548 | GAOABQK02IBA3P | CDS | 611093 | 1299 | + | 0.403387 | |
g5875 | DLA_06549 | GAOABQK02IBA3P | CDS | 613097 | 9525 | + | 0.338583 | |
g5876 | DLA_06550 | GAOABQK02IBA3P | CDS | 623208 | 9186 | + | 0.33649 | |
g5877 | DLA_11656 | GAOABQK02IBA3P | CDS | 632489 | 237 | - | 0.329114 | |
g5878 | DLA_06551 | GAOABQK02IBA3P | CDS | 633221 | 489 | + | 0.276074 | |
g5879 | DLA_06552 | GAOABQK02IBA3P | CDS | 633887 | 2169 | - | 0.261411 | |
g588 | DLA_00649 | contig05409_1.exp | CDS | 1340372 | 762 | - | 0.33727 | |
g5880 | DLA_06553 | GAOABQK02IBA3P | CDS | 636291 | 2019 | - | 0.292224 | |
g5881 | DLA_11657 | GAOABQK02IBA3P | CDS | 638553 | 630 | - | 0.322222 | |
g5882 | DLA_06554 | distant relative of CAZy family GT4 contains a central glycosyltransferase domain and a C-terminal sulfotransferase domain | GAOABQK02IBA3P | CDS | 639356 | 3453 | - | 0.348972 |
g5883 | DLA_11658 | GAOABQK02IBA3P | CDS | 643068 | 894 | - | 0.334452 | |
g5884 | DLA_06555 | contains a predicted signal peptide there is a second copy of this gene | GAOABQK02IBA3P | CDS | 644500 | 3309 | + | 0.378362 |
g5885 | DLA_06556 | GAOABQK02IBA3P | CDS | 648018 | 1281 | - | 0.398907 | |
g5886 | DLA_06557 | GAOABQK02IBA3P | CDS | 649601 | 657 | + | 0.333333 | |
g5887 | DLA_06559 | GAOABQK02IBA3P | CDS | 652072 | 1149 | + | 0.311575 | |
g5888 | DLA_06560 | GAOABQK02IBA3P | CDS | 654139 | 1140 | + | 0.317544 | |
g5889 | DLA_06561 | GAOABQK02IBA3P | CDS | 655419 | 3693 | - | 0.355808 | |
g589 | DLA_00650 | contig05409_1.exp | CDS | 1341281 | 2694 | - | 0.298441 | |
g5890 | DLA_06562 | GAOABQK02IBA3P | CDS | 659686 | 1731 | + | 0.271519 | |
g5891 | DLA_06563 | GAOABQK02IBA3P | CDS | 661867 | 963 | + | 0.352025 | |
g5892 | DLA_06564 | GAOABQK02IBA3P | CDS | 663042 | 1170 | - | 0.322222 | |
g5893 | DLA_06566 | GAOABQK02IBA3P | CDS | 666483 | 813 | + | 0.293973 | |
g5894 | DLA_11659 | widely conserved protein very similar to M. musculus Myg1 (melanocyte proliferating gene 1) | GAOABQK02IBA3P | CDS | 667406 | 1059 | - | 0.327668 |
g5895 | DLA_06567 | GAOABQK02IBA3P | CDS | 668694 | 4401 | - | 0.335378 | |
g5896 | DLA_06569 | GAOABQK02IBA3P | CDS | 673422 | 1083 | - | 0.354571 | |
g5897 | DLA_06570 | GAOABQK02IBA3P | CDS | 677079 | 1071 | + | 0.343604 | |
g5898 | DLA_06571 | GAOABQK02IBA3P | CDS | 678603 | 771 | + | 0.32166 | |
g5899 | DLA_06572 | GAOABQK02IBA3P | CDS | 679548 | 540 | + | 0.32963 | |
g59 | DLA_00069 | contig05409_1.exp | CDS | 150114 | 1017 | + | 0.304818 | |
g590 | DLA_00651 | contig05409_1.exp | CDS | 1344093 | 768 | + | 0.285156 | |
g5900 | DLA_06573 | GAOABQK02IBA3P | CDS | 680470 | 3729 | + | 0.324484 | |
g5901 | DLA_06574 | GAOABQK02IBA3P | CDS | 684789 | 9243 | - | 0.321432 | |
g5902 | DLA_06575 | GAOABQK02IBA3P | CDS | 694587 | 9294 | - | 0.316979 | |
g5903 | DLA_06576 | GAOABQK02IBA3P | CDS | 704612 | 11448 | - | 0.325122 | |
g5904 | DLA_06579 | GAOABQK02IBA3P | CDS | 716669 | 561 | - | 0.313726 | |
g5905 | DLA_06580 | GAOABQK02IBA3P | CDS | 717982 | 423 | + | 0.326241 | |
g5906 | DLA_06581 | GAOABQK02IBA3P | CDS | 719108 | 822 | + | 0.317518 | |
g5907 | DLA_06582 | GAOABQK02IBA3P | CDS | 720147 | 1032 | + | 0.33624 | |
g5908 | DLA_06583 | GAOABQK02IBA3P | CDS | 721382 | 1710 | - | 0.347368 | |
g5909 | DLA_06584 | GAOABQK02IBA3P | CDS | 724502 | 333 | + | 0.3003 | |
g591 | DLA_00652 | contig05409_1.exp | CDS | 1344998 | 1935 | + | 0.286305 | |
g5910 | DLA_06585 | GAOABQK02IBA3P | CDS | 725063 | 1677 | - | 0.378056 | |
g5911 | DLA_06586 | GAOABQK02IBA3P | CDS | 727332 | 1125 | + | 0.321778 | |
g5912 | DLA_06587 | GAOABQK02IBA3P | CDS | 728608 | 267 | - | 0.284644 | |
g5913 | DLA_06588 | GAOABQK02IBA3P | CDS | 729210 | 1722 | + | 0.321719 | |
g5914 | DLA_06590 | GAOABQK02IBA3P | CDS | 731425 | 1725 | + | 0.327536 | |
g5915 | DLA_06591 | GAOABQK02IBA3P | CDS | 733421 | 1188 | - | 0.309764 | |
g5916 | DLA_06592 | GAOABQK02IBA3P | CDS | 734928 | 1422 | + | 0.331224 | |
g5917 | DLA_06593 | GAOABQK02IBA3P | CDS | 738791 | 3045 | + | 0.309688 | |
g5918 | DLA_06595 | ortholog of PAN2 a member of the Pan2p-Pan3p poly(A)-ribonuclease complex which acts to control poly(A) tail length and regulate the stoichiometry and activity of postreplication repair complexes | GAOABQK02IBA3P | CDS | 743565 | 3777 | - | 0.350543 |
g5919 | DLA_06596 | GAOABQK02IBA3P | CDS | 747600 | 909 | + | 0.354235 | |
g592 | DLA_00653 | contig05409_1.exp | CDS | 1347369 | 4791 | + | 0.342517 | |
g5920 | DLA_06597 | GAOABQK02IBA3P | CDS | 748876 | 2547 | - | 0.352964 | |
g5921 | DLA_06598 | GAOABQK02IBA3P | CDS | 752988 | 513 | + | 0.387914 | |
g5922 | DLA_06599 | GAOABQK02IBA3P | CDS | 753807 | 4353 | + | 0.316334 | |
g5923 | DLA_06600 | GAOABQK02IBA3P | CDS | 759395 | 2211 | + | 0.289914 | |
g5924 | DLA_06601 | GAOABQK02IBA3P | CDS | 762982 | 1317 | - | 0.279423 | |
g5925 | DLA_06602 | GAOABQK02IBA3P | CDS | 764511 | 3048 | - | 0.370407 | |
g5926 | DLA_06603 | GAOABQK02IBA3P | CDS | 768107 | 504 | - | 0.333333 | |
g5927 | DLA_06604 | GAOABQK02IBA3P | CDS | 769846 | 4020 | + | 0.340547 | |
g5928 | DLA_06605 | GAOABQK02IBA3P | CDS | 774129 | 1236 | + | 0.334951 | |
g5929 | DLA_06606 | contains an actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domain near its N-terminus and a C-terminal SH3 (src Homology-3) domain predicted to have an N-terminal signal peptide | GAOABQK02IBA3P | CDS | 776451 | 885 | + | 0.462147 |
g593 | DLA_00654 | contig05409_1.exp | CDS | 1352469 | 2931 | - | 0.354145 | |
g5930 | DLA_06608 | GAOABQK02IBA3P | CDS | 778046 | 759 | + | 0.274045 | |
g5931 | DLA_11660 | GAOABQK02IBA3P | CDS | 782088 | 273 | - | 0.29304 | |
g5932 | DLA_06609 | GAOABQK02IBA3P | CDS | 784027 | 2964 | + | 0.324899 | |
g5933 | DLA_06610 | GAOABQK02IBA3P | CDS | 787183 | 1245 | - | 0.284337 | |
g5934 | DLA_06612 | GAOABQK02IBA3P | CDS | 790674 | 633 | + | 0.366509 | |
g5935 | DLA_06613 | catalyzes the reaction 4-fumarylacetoacetate Hsub2subO acetoacetate fumarate | GAOABQK02IBA3P | CDS | 791537 | 1266 | + | 0.363349 |
g5936 | DLA_06615 | GAOABQK02IBA3P | CDS | 793458 | 720 | - | 0.294444 | |
g5937 | DLA_06616 | GAOABQK02IBA3P | CDS | 794404 | 747 | - | 0.269076 | |
g5938 | DLA_06617 | GAOABQK02IBA3P | CDS | 795638 | 1086 | + | 0.326888 | |
g5939 | DLA_06618 | GAOABQK02IBA3P | CDS | 796917 | 1128 | - | 0.291667 | |
g594 | DLA_00655 | contig05409_1.exp | CDS | 1355654 | 477 | - | 0.289308 | |
g5940 | DLA_06619 | GAOABQK02IBA3P | CDS | 798822 | 2127 | + | 0.308886 | |
g5941 | DLA_06620 | GAOABQK02IBA3P | CDS | 801603 | 2190 | + | 0.346119 | |
g5942 | DLA_06621 | GAOABQK02IBA3P | CDS | 804389 | 1857 | + | 0.31664 | |
g5943 | DLA_06622 | GAOABQK02IBA3P | CDS | 806351 | 3066 | + | 0.283105 | |
g5944 | DLA_06623 | GAOABQK02IBA3P | CDS | 809683 | 3165 | + | 0.338389 | |
g5945 | DLA_06624 | GAOABQK02IBA3P | CDS | 813032 | 3834 | - | 0.304643 | |
g5946 | DLA_06625 | GAOABQK02IBA3P | CDS | 817438 | 612 | + | 0.248366 | |
g5947 | DLA_06626 | GAOABQK02IBA3P | CDS | 818187 | 663 | - | 0.309201 | |
g5948 | DLA_06627 | GAOABQK02IBA3P | CDS | 819430 | 1584 | + | 0.299242 | |
g5949 | DLA_06628 | GAOABQK02IBA3P | CDS | 821083 | 732 | - | 0.319672 | |
g595 | DLA_00656 | contig05409_1.exp | CDS | 1356589 | 2517 | - | 0.301152 | |
g5950 | DLA_06629 | GAOABQK02IBA3P | CDS | 821951 | 330 | + | 0.40303 | |
g5951 | DLA_06630 | GAOABQK02IBA3P | CDS | 823941 | 591 | + | 0.285956 | |
g5952 | DLA_06631 | GAOABQK02IBA3P | CDS | 824711 | 705 | - | 0.307801 | |
g5953 | DLA_06632 | GAOABQK02IBA3P | CDS | 825486 | 1197 | + | 0.282373 | |
g5954 | DLA_06633 | GAOABQK02IBA3P | CDS | 827107 | 591 | + | 0.328257 | |
g5955 | DLA_06634 | GAOABQK02IBA3P | CDS | 828379 | 1857 | - | 0.322563 | |
g5956 | DLA_06635 | GAOABQK02IBA3P | CDS | 830534 | 1674 | + | 0.323775 | |
g5957 | DLA_06636 | GAOABQK02IBA3P | CDS | 832449 | 1824 | + | 0.339912 | |
g5958 | DLA_06637 | GAOABQK02IBA3P | CDS | 834390 | 4008 | - | 0.307635 | |
g5959 | DLA_11661 | GAOABQK02IBA3P | CDS | 839364 | 762 | - | 0.368766 | |
g596 | DLA_00657 | contig05409_1.exp | CDS | 1359869 | 804 | + | 0.330846 | |
g5960 | DLA_06638 | GAOABQK02IBA3P | CDS | 840559 | 1410 | - | 0.308511 | |
g5961 | DLA_06639 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | GAOABQK02IBA3P | CDS | 842234 | 660 | + | 0.272727 |
g5962 | DLA_11662 | ortholog of the conserved COQ10 a Coenzyme Q (ubiquinone) binding protein in S. cerevisiae there is a second copy of this gene | GAOABQK02IBA3P | CDS | 843020 | 645 | - | 0.333333 |
g5963 | DLA_06640 | GAOABQK02IBA3P | CDS | 843853 | 462 | + | 0.266234 | |
g5964 | DLA_06641 | GAOABQK02IBA3P | CDS | 844661 | 405 | - | 0.308642 | |
g5965 | DLA_06643 | catalyzes the reaction ATP uridine ADP UMP | GAOABQK02IBA3P | CDS | 846253 | 759 | + | 0.333333 |
g5966 | DLA_06644 | GAOABQK02IBA3P | CDS | 847549 | 1014 | + | 0.342209 | |
g5967 | DLA_06645 | GAOABQK02IBA3P | CDS | 848714 | 2208 | - | 0.367754 | |
g5968 | DLA_06646 | GAOABQK02IBA3P | CDS | 851479 | 798 | - | 0.33584 | |
g5969 | DLA_06647 | catalyzes the reaction ATP N-acetyl-L-glutamate ADP N-acetyl-L-glutamate 5-phosphate | GAOABQK02IBA3P | CDS | 852768 | 2619 | - | 0.348988 |
g597 | DLA_00658 | contig05409_1.exp | CDS | 1361288 | 2010 | + | 0.31194 | |
g5970 | DLA_06648 | GAOABQK02IBA3P | CDS | 857550 | 2571 | + | 0.340335 | |
g5971 | DLA_06649 | GAOABQK02IBA3P | CDS | 860823 | 2349 | + | 0.306513 | |
g5972 | DLA_11663 | GAOABQK02IBA3P | CDS | 863650 | 1575 | - | 0.309206 | |
g5973 | DLA_06650 | GAOABQK02IBA3P | CDS | 866675 | 3330 | - | 0.296997 | |
g5974 | DLA_06651 | catalyzes the reaction L-glutamine PRPP Hsub2subO 5-phospho-beta-D-ribosyl-amine pyrophosphate L-glutamate the first step in de novo DNA synthesis | GAOABQK02IBA3P | CDS | 870949 | 1605 | - | 0.356386 |
g5975 | DLA_06652 | GAOABQK02IBA3P | CDS | 873201 | 1065 | + | 0.300469 | |
g5976 | DLA_06653 | GAOABQK02IBA3P | CDS | 874544 | 582 | - | 0.328179 | |
g5977 | DLA_06654 | GAOABQK02IBA3P | CDS | 875281 | 1146 | - | 0.304538 | |
g5978 | DLA_06655 | GAOABQK02IBA3P | CDS | 876625 | 1059 | - | 0.321058 | |
g5979 | DLA_06656 | partial similarity to cry34 the Bacillus thuringiensis proteinaceous crystal and insecticidal toxin formed during sporulation contains an endonucleaseexonucleasephosphatase domain which is found in proteins such as magnesium dependent endonucleases and phosphatases involved in intracellular signalling | GAOABQK02IBA3P | CDS | 877818 | 3279 | + | 0.322049 |
g598 | DLA_00660 | contig05409_1.exp | CDS | 1365424 | 1941 | + | 0.308604 | |
g5980 | DLA_06657 | GAOABQK02IBA3P | CDS | 881238 | 672 | - | 0.299107 | |
g5981 | DLA_06658 | GAOABQK02IBA3P | CDS | 882024 | 1491 | - | 0.316566 | |
g5982 | DLA_06660 | GAOABQK02IBA3P | CDS | 884074 | 2871 | + | 0.302682 | |
g5983 | DLA_06661 | GAOABQK02IBA3P | CDS | 887735 | 1989 | + | 0.317245 | |
g5984 | DLA_06662 | GAOABQK02IBA3P | CDS | 890254 | 924 | + | 0.353896 | |
g5985 | DLA_06663 | GAOABQK02IBA3P | CDS | 891598 | 1905 | + | 0.314436 | |
g5986 | DLA_06664 | GAOABQK02IBA3P | CDS | 894230 | 3849 | + | 0.302936 | |
g5987 | DLA_06667 | GAOABQK02IBA3P | CDS | 899294 | 2088 | - | 0.330939 | |
g5988 | DLA_06668 | GAOABQK02IBA3P | CDS | 902080 | 2700 | + | 0.346296 | |
g5989 | DLA_06670 | EIF4E ortholog the eukaryotic initiation factor 4E recognizes and binds the RNA cap during protein synthesis | GAOABQK02IBA3P | CDS | 905932 | 726 | + | 0.330579 |
g599 | DLA_00661 | contig05409_1.exp | CDS | 1367849 | 339 | - | 0.430678 | |
g5990 | DLA_06671 | GAOABQK02IBA3P | CDS | 907162 | 2505 | + | 0.290619 | |
g5991 | DLA_06672 | GAOABQK02IBA3P | CDS | 909843 | 3057 | + | 0.298659 | |
g5992 | DLA_06673 | ortholog of S. cerevisiae DIS3 and H. sapiens KIAA1008 component of the nucleolar exosome involved in RNA processing | GAOABQK02IBA3P | CDS | 913124 | 2943 | - | 0.326538 |
g5993 | DLA_06674 | GAOABQK02IBA3P | CDS | 916263 | 3255 | + | 0.288479 | |
g5994 | DLA_06675 | GAOABQK02IBA3P | CDS | 920189 | 7371 | + | 0.338624 | |
g5995 | DLA_06676 | GAOABQK02IBA3P | CDS | 928650 | 7143 | + | 0.343973 | |
g5996 | DLA_06678 | GAOABQK02IBA3P | CDS | 936358 | 7389 | + | 0.348085 | |
g5997 | DLA_06679 | homologous to bacterial genes that are involved in the transport of arsenate selenate and other anionic compounds outside the cell | GAOABQK02IBA3P | CDS | 944113 | 993 | - | 0.311178 |
g5998 | DLA_06680 | GAOABQK02IBA3P | CDS | 945382 | 1122 | - | 0.336007 | |
g5999 | DLA_06681 | GAOABQK02IBA3P | CDS | 947125 | 1239 | + | 0.355125 | |
g6 | DLA_00007 | contig05409_1.exp | CDS | 12758 | 660 | - | 0.366667 | |
g60 | DLA_00070 | contig05409_1.exp | CDS | 152183 | 387 | + | 0.284238 | |
g600 | DLA_00662 | contig05409_1.exp | CDS | 1369071 | 5961 | + | 0.311357 | |
g6000 | DLA_06682 | protein component of the small (40S) ribosomal subunit expressed in vegetative cells and in prestalk cells during culmination | GAOABQK02IBA3P | CDS | 948545 | 825 | - | 0.442424 |
g6001 | DLA_06683 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | GAOABQK02IBA3P | CDS | 949933 | 825 | + | 0.335758 |
g6002 | DLA_06684 | GAOABQK02IBA3P | CDS | 951201 | 2358 | - | 0.337574 | |
g6003 | DLA_06685 | GAOABQK02IBA3P | CDS | 954157 | 2217 | + | 0.298151 | |
g6004 | DLA_06686 | GAOABQK02IBA3P | CDS | 956813 | 804 | - | 0.364428 | |
g6005 | DLA_11664 | GAOABQK02IBA3P | CDS | 957917 | 2136 | - | 0.326779 | |
g6006 | DLA_06687 | GAOABQK02IBA3P | CDS | 962016 | 2868 | - | 0.331939 | |
g6007 | DLA_06688 | GAOABQK02IBA3P | CDS | 965323 | 3618 | + | 0.292427 | |
g6008 | DLA_06690 | GAOABQK02IBA3P | CDS | 969761 | 1743 | - | 0.253586 | |
g6009 | DLA_06691 | GAOABQK02IBA3P | CDS | 971567 | 3495 | + | 0.307296 | |
g601 | DLA_00663 | contig05409_1.exp | CDS | 1375394 | 2061 | + | 0.324115 | |
g6010 | DLA_06692 | GAOABQK02IBA3P | CDS | 975320 | 792 | - | 0.337121 | |
g6011 | DLA_06693 | similar to bacterial proteins of the YjgF superfamily homolog of Psedomonas sp. amnD (2-aminomuconate deaminase) also matches PFAM HMM for endoribonuclease L-PSP | GAOABQK02IBA3P | CDS | 976471 | 486 | - | 0.316872 |
g6012 | DLA_06694 | GAOABQK02IBA3P | CDS | 977217 | 1278 | + | 0.368545 | |
g6013 | DLA_06695 | GAOABQK02IBA3P | CDS | 979393 | 291 | + | 0.298969 | |
g6014 | DLA_06697 | GAOABQK02IBA3P | CDS | 979879 | 390 | - | 0.276923 | |
g6015 | DLA_06698 | GAOABQK02IBA3P | CDS | 980737 | 657 | - | 0.330289 | |
g6016 | DLA_06700 | GAOABQK02IBA3P | CDS | 982381 | 2901 | + | 0.307135 | |
g6017 | DLA_06701 | GAOABQK02IBA3P | CDS | 985960 | 2268 | + | 0.338624 | |
g6018 | DLA_06702 | GAOABQK02IBA3P | CDS | 988770 | 474 | + | 0.303797 | |
g6019 | DLA_06703 | GAOABQK02IBA3P | CDS | 990607 | 1182 | - | 0.335025 | |
g602 | DLA_00664 | wealky similar to acid ceramidase which catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine | contig05409_1.exp | CDS | 1377640 | 1317 | - | 0.365224 |
g6020 | DLA_06704 | GAOABQK02IBA3P | CDS | 992439 | 1743 | + | 0.251865 | |
g6021 | DLA_06705 | GAOABQK02IBA3P | CDS | 994380 | 1305 | - | 0.316475 | |
g6022 | DLA_06706 | GAOABQK02IBA3P | CDS | 996296 | 2979 | + | 0.265861 | |
g6023 | DLA_06707 | ortholog of human SLC25A4 which catalyzes the exchange of ADP and ATP across the mitochondrial inner membrane contains six predicted transmembrane domains brbrbCommunity annotation:b Overview of the | GAOABQK02IBA3P | CDS | 1000089 | 933 | + | 0.404073 |
g6024 | DLA_06711 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains | GAOABQK02IBA3P | CDS | 1003562 | 5019 | - | 0.328751 |
g6025 | DLA_06712 | GAOABQK02IBA3P | CDS | 1009441 | 1149 | - | 0.288947 | |
g6026 | DLA_06713 | GAOABQK02IBA3P | CDS | 1010831 | 1341 | - | 0.301268 | |
g6027 | DLA_06714 | GAOABQK02IBA3P | CDS | 1012536 | 2217 | - | 0.352278 | |
g6028 | DLA_06715 | GAOABQK02IBA3P | CDS | 1015161 | 1608 | - | 0.380597 | |
g6029 | DLA_06716 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | GAOABQK02IBA3P | CDS | 1017519 | 462 | + | 0.30303 |
g603 | DLA_00665 | contig05409_1.exp | CDS | 1379233 | 894 | - | 0.279642 | |
g6030 | DLA_06717 | GAOABQK02IBA3P | CDS | 1018353 | 1458 | + | 0.353909 | |
g6031 | DLA_06718 | GAOABQK02IBA3P | CDS | 1020126 | 852 | + | 0.267606 | |
g6032 | DLA_06719 | GAOABQK02IBA3P | CDS | 1021385 | 1077 | + | 0.348189 | |
g6033 | DLA_06720 | GAOABQK02IBA3P | CDS | 1022975 | 1392 | + | 0.3125 | |
g6034 | DLA_06721 | GAOABQK02IBA3P | CDS | 1024547 | 777 | - | 0.263835 | |
g6035 | DLA_06722 | GAOABQK02IBA3P | CDS | 1025523 | 588 | + | 0.311224 | |
g6036 | DLA_06723 | GAOABQK02IBA3P | CDS | 1026967 | 1110 | - | 0.332432 | |
g6037 | DLA_06724 | GAOABQK02IBA3P | CDS | 1028735 | 429 | + | 0.240093 | |
g6038 | DLA_11665 | GAOABQK02IBA3P | CDS | 1029448 | 276 | + | 0.278986 | |
g6039 | DLA_06725 | GAOABQK02IBA3P | CDS | 1030130 | 2187 | + | 0.346136 | |
g604 | DLA_00666 | contig05409_1.exp | CDS | 1380295 | 642 | + | 0.342679 | |
g6040 | DLA_06726 | one of many putative Dictyostelium potassium channels contains 3 pentapeptide repeats | GAOABQK02IBA3P | CDS | 1032468 | 1038 | - | 0.331407 |
g6041 | DLA_06727 | GAOABQK02IBA3P | CDS | 1034562 | 3390 | + | 0.3 | |
g6042 | DLA_06728 | GAOABQK02IBA3P | CDS | 1038272 | 3960 | - | 0.290404 | |
g6043 | DLA_06730 | GAOABQK02IBA3P | CDS | 1043040 | 615 | - | 0.331707 | |
g6044 | DLA_06732 | GAOABQK02IBA3P | CDS | 1044342 | 1818 | - | 0.343234 | |
g6045 | DLA_06733 | GAOABQK02IBA3P | CDS | 1046601 | 750 | + | 0.333333 | |
g6046 | DLA_06734 | GAOABQK02IBA3P | CDS | 1047580 | 1809 | + | 0.283029 | |
g6047 | DLA_06735 | GAOABQK02IBA3P | CDS | 1049743 | 2889 | - | 0.300104 | |
g6048 | DLA_06736 | GAOABQK02IBA3P | CDS | 1053550 | 1959 | + | 0.273609 | |
g6049 | DLA_06737 | GAOABQK02IBA3P | CDS | 1055595 | 603 | - | 0.290216 | |
g605 | DLA_00667 | contig05409_1.exp | CDS | 1381287 | 1077 | + | 0.371402 | |
g6050 | DLA_06738 | GAOABQK02IBA3P | CDS | 1056482 | 3309 | + | 0.289816 | |
g6051 | DLA_06739 | GAOABQK02IBA3P | CDS | 1060888 | 1035 | - | 0.342995 | |
g6052 | DLA_06740 | GAOABQK02IBA3P | CDS | 1062418 | 276 | + | 0.25 | |
g6053 | DLA_11666 | GAOABQK02IBA3P | CDS | 1062790 | 456 | - | 0.276316 | |
g6054 | DLA_06741 | GAOABQK02IBA3P | CDS | 1063337 | 1011 | - | 0.302671 | |
g6055 | DLA_06742 | similar to Dictyostelium pakA and other mitogen-activated protein kinases (Ste20PAK family) putative p21-activated kinase contains a calponin-like actin-binding domain a p21-Rho-binding domain and a PKC conserved region 1 (C1) regulates the actin cytoskeleton response during chemotaxis to cAMP | GAOABQK02IBA3P | CDS | 1064531 | 3954 | + | 0.309054 |
g6056 | DLA_06743 | GAOABQK02IBA3P | CDS | 1068804 | 753 | - | 0.313413 | |
g6057 | DLA_06744 | GAOABQK02IBA3P | CDS | 1070039 | 2121 | + | 0.33239 | |
g6058 | DLA_06745 | GAOABQK02IBA3P | CDS | 1072192 | 702 | - | 0.242165 | |
g6059 | DLA_06746 | GAOABQK02IBA3P | CDS | 1073232 | 1716 | + | 0.320513 | |
g606 | DLA_00668 | contig05409_1.exp | CDS | 1382769 | 765 | + | 0.287582 | |
g6060 | DLA_06747 | GAOABQK02IBA3P | CDS | 1075190 | 1629 | - | 0.300798 | |
g6061 | DLA_06748 | GAOABQK02IBA3P | CDS | 1077036 | 3759 | - | 0.320032 | |
g6062 | DLA_06749 | GAOABQK02IBA3P | CDS | 1081008 | 1905 | - | 0.329659 | |
g6063 | DLA_06750 | GAOABQK02IBA3P | CDS | 1083418 | 1008 | + | 0.350198 | |
g6064 | DLA_06751 | identified as a suppressor of smlA null mutant cnr3 has a predicted signal anchor sequence | GAOABQK02IBA3P | CDS | 1085177 | 1377 | - | 0.30719 |
g6065 | DLA_06752 | GAOABQK02IBA3P | CDS | 1086758 | 780 | - | 0.280769 | |
g6066 | DLA_06753 | inositol 5-phosphatase similar to the human protein OCRL which when defect causes Lowe syndrome involved in Dictyostelium growth development and phagocytosis | GAOABQK02IBA3P | CDS | 1087916 | 2187 | + | 0.328761 |
g6067 | DLA_11667 | GAOABQK02IBA3P | CDS | 1090245 | 1581 | + | 0.288425 | |
g6068 | DLA_06754 | GAOABQK02IBA3P | CDS | 1091884 | 1239 | - | 0.351897 | |
g6069 | DLA_06755 | GAOABQK02IBA3P | CDS | 1093337 | 777 | + | 0.301158 | |
g607 | DLA_00669 | contig05409_1.exp | CDS | 1383576 | 1308 | - | 0.313456 | |
g6070 | DLA_06756 | contains one 5'-3' exonuclease domain and one 3'-5' exonuclease domain | GAOABQK02IBA3P | CDS | 1094275 | 6369 | - | 0.302245 |
g6071 | DLA_06758 | GAOABQK02IBA3P | CDS | 1101299 | 408 | + | 0.303922 | |
g6072 | DLA_06759 | GAOABQK02IBA3P | CDS | 1102208 | 2892 | + | 0.307746 | |
g6073 | DLA_06760 | GAOABQK02IBA3P | CDS | 1107703 | 3453 | + | 0.312192 | |
g6074 | DLA_06761 | GAOABQK02IBA3P | CDS | 1111452 | 369 | - | 0.306233 | |
g6075 | DLA_06762 | GAOABQK02IBA3P | CDS | 1112301 | 1005 | + | 0.262687 | |
g6076 | DLA_06763 | GAOABQK02IBA3P | CDS | 1113711 | 1299 | + | 0.251732 | |
g6077 | DLA_06765 | GAOABQK02IBA3P | CDS | 1115772 | 3627 | - | 0.292528 | |
g6078 | DLA_06766 | GAOABQK02IBA3P | CDS | 1119614 | 2031 | + | 0.250615 | |
g6079 | DLA_06767 | GAOABQK02IBA3P | CDS | 1121898 | 2040 | - | 0.323039 | |
g608 | DLA_00670 | contig05409_1.exp | CDS | 1385384 | 579 | + | 0.290155 | |
g6080 | DLA_06768 | GAOABQK02INHKB | CDS | 589 | 3240 | + | 0.304321 | |
g6081 | DLA_06769 | GAOABQK02INHKB | CDS | 4515 | 1569 | + | 0.314213 | |
g6082 | DLA_06770 | GAOABQK02INHKB | CDS | 6408 | 1899 | - | 0.294365 | |
g6083 | DLA_06771 | GAOABQK02INHKB | CDS | 9919 | 3717 | - | 0.313963 | |
g6084 | DLA_06772 | GAOABQK02INHKB | CDS | 14180 | 1545 | - | 0.368285 | |
g6085 | DLA_06773 | GAOABQK02INHKB | CDS | 16363 | 2622 | + | 0.307018 | |
g6086 | DLA_06774 | GAOABQK02INHKB | CDS | 19513 | 852 | + | 0.338028 | |
g6087 | DLA_06775 | GAOABQK02INHKB | CDS | 20627 | 1986 | + | 0.345921 | |
g6088 | DLA_06776 | GAOABQK02INHKB | CDS | 22792 | 1212 | - | 0.35066 | |
g6089 | DLA_06778 | GAOABQK02IO52T | CDS | 2675 | 1566 | + | 0.265006 | |
g609 | DLA_00671 | contig05409_1.exp | CDS | 1386207 | 540 | - | 0.287037 | |
g6090 | DLA_06779 | GAOABQK02IO52T | CDS | 4517 | 837 | + | 0.261649 | |
g6091 | DLA_11668 | GAOABQK02IO52T | CDS | 5975 | 2301 | + | 0.262495 | |
g6092 | DLA_06780 | GAOABQK02IO52T | CDS | 8543 | 894 | + | 0.253915 | |
g6093 | DLA_06783 | GAOABQK02IO52T | CDS | 11210 | 693 | - | 0.233766 | |
g6094 | DLA_06786 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide | GAOABQK02IO52T | CDS | 13496 | 840 | + | 0.35 |
g6095 | DLA_06788 | GAOABQK02IO52T | CDS | 16304 | 3150 | - | 0.235873 | |
g6096 | DLA_06789 | GAOABQK02IO52T | CDS | 19727 | 582 | - | 0.441581 | |
g6097 | DLA_06790 | GAOABQK02IO52T | CDS | 20587 | 1419 | + | 0.251586 | |
g6098 | DLA_06791 | GAOABQK02IO52T | CDS | 22177 | 2427 | + | 0.233622 | |
g6099 | DLA_06792 | GAOABQK02IO52T | CDS | 24816 | 2145 | + | 0.307692 | |
g61 | DLA_00071 | contig05409_1.exp | CDS | 152795 | 501 | - | 0.335329 | |
g610 | DLA_00672 | contig05409_1.exp | CDS | 1386975 | 1047 | - | 0.359121 | |
g6100 | DLA_06793 | GAOABQK02IO52T | CDS | 27199 | 414 | + | 0.350242 | |
g6101 | DLA_06794 | GAOABQK02IO52T | CDS | 27816 | 1317 | - | 0.290053 | |
g6102 | DLA_06795 | GAOABQK02IO52T | CDS | 30437 | 1989 | + | 0.306184 | |
g6103 | DLA_06796 | GAOABQK02IO52T | CDS | 32661 | 1725 | + | 0.292174 | |
g6104 | DLA_06797 | GAOABQK02IO52T | CDS | 34493 | 996 | - | 0.365462 | |
g6105 | DLA_06798 | GAOABQK02IO52T | CDS | 35913 | 1800 | + | 0.297222 | |
g6106 | DLA_06799 | GAOABQK02IO52T | CDS | 37861 | 609 | + | 0.311987 | |
g6107 | DLA_06800 | conserved protein involved in contractile vacuole discharge upon osmotic stressbr bNomenclature conflict: b Do not confuse this gene with phg1a encoding the putative phagocytic receptor 1a or with the phgA locus ( | GAOABQK02IO52T | CDS | 38525 | 978 | - | 0.340491 |
g6108 | DLA_06801 | GAOABQK02IO52T | CDS | 39597 | 843 | - | 0.342823 | |
g6109 | DLA_06802 | GAOABQK02IO52T | CDS | 40992 | 801 | - | 0.337079 | |
g611 | DLA_00674 | contig05409_1.exp | CDS | 1388866 | 762 | + | 0.314961 | |
g6110 | DLA_06803 | GAOABQK02IO52T | CDS | 41983 | 1542 | + | 0.286641 | |
g6111 | DLA_06804 | GAOABQK02IO52T | CDS | 43669 | 4935 | - | 0.358865 | |
g6112 | DLA_06805 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) | GAOABQK02IO52T | CDS | 49054 | 1587 | + | 0.360428 |
g6113 | DLA_06806 | GAOABQK02IO52T | CDS | 51884 | 1800 | + | 0.324444 | |
g6114 | DLA_06808 | GAOABQK02IO52T | CDS | 54390 | 1089 | + | 0.331497 | |
g6115 | DLA_06810 | GAOABQK02IO52T | CDS | 55740 | 309 | - | 0.346278 | |
g6116 | DLA_06811 | GAOABQK02IO52T | CDS | 56795 | 1080 | + | 0.383333 | |
g6117 | DLA_06812 | GAOABQK02IO52T | CDS | 58106 | 1263 | + | 0.355503 | |
g6118 | DLA_06813 | GAOABQK02IO52T | CDS | 59682 | 489 | - | 0.364008 | |
g6119 | DLA_06814 | GAOABQK02IO52T | CDS | 60772 | 1845 | + | 0.299729 | |
g612 | DLA_00675 | contig05409_1.exp | CDS | 1390296 | 336 | + | 0.315476 | |
g6120 | DLA_06815 | GAOABQK02IO52T | CDS | 63029 | 1314 | + | 0.352359 | |
g6121 | DLA_06816 | GAOABQK02IO52T | CDS | 64421 | 1767 | - | 0.301075 | |
g6122 | DLA_06817 | GAOABQK02IO52T | CDS | 66465 | 2757 | - | 0.328255 | |
g6123 | DLA_06819 | GAOABQK02IO52T | CDS | 69545 | 2439 | + | 0.339073 | |
g6124 | DLA_06820 | GAOABQK02IO52T | CDS | 72537 | 1269 | + | 0.325453 | |
g6125 | DLA_06821 | GAOABQK02IO52T | CDS | 73832 | 1698 | - | 0.30212 | |
g6126 | DLA_06822 | GAOABQK02IO52T | CDS | 75745 | 2961 | - | 0.342452 | |
g6127 | DLA_06823 | GAOABQK02IO52T | CDS | 78960 | 3399 | - | 0.293027 | |
g6128 | DLA_06825 | GAOABQK02IO52T | CDS | 83539 | 417 | + | 0.333333 | |
g6129 | DLA_06826 | GAOABQK02IO52T | CDS | 84324 | 870 | - | 0.309195 | |
g613 | DLA_00677 | contig05409_1.exp | CDS | 1396015 | 1221 | + | 0.249795 | |
g6130 | DLA_06827 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity contains a predicted signal peptide | GAOABQK02IO52T | CDS | 85422 | 891 | - | 0.352413 |
g6131 | DLA_06828 | GAOABQK02IO52T | CDS | 86744 | 4974 | - | 0.334942 | |
g6132 | DLA_06830 | GAOABQK02IO52T | CDS | 92613 | 2925 | - | 0.285128 | |
g6133 | DLA_06832 | GAOABQK02IO52T | CDS | 95848 | 2091 | - | 0.313726 | |
g6134 | DLA_06833 | GAOABQK02IO52T | CDS | 97950 | 240 | - | 0.25 | |
g6135 | DLA_06834 | GAOABQK02IO52T | CDS | 98563 | 3009 | - | 0.306414 | |
g6136 | DLA_06835 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family kinase activity stimulated by hyperosmolarity and heat shock there is a second copy of this gene | GAOABQK02IO52T | CDS | 102489 | 4140 | - | 0.322947 |
g6137 | DLA_06836 | GAOABQK02IO52T | CDS | 107367 | 3732 | - | 0.353966 | |
g6138 | DLA_06837 | GAOABQK02IO52T | CDS | 111590 | 1314 | - | 0.354642 | |
g6139 | DLA_06838 | GAOABQK02IO52T | CDS | 113411 | 1434 | + | 0.281729 | |
g614 | DLA_00678 | contig05409_1.exp | CDS | 1397455 | 1068 | - | 0.328652 | |
g6140 | DLA_06839 | GAOABQK02IO52T | CDS | 114984 | 2319 | + | 0.336783 | |
g6141 | DLA_06840 | GAOABQK02IO52T | CDS | 117375 | 1032 | + | 0.295543 | |
g6142 | DLA_06841 | GAOABQK02IO52T | CDS | 118547 | 3090 | - | 0.303883 | |
g6143 | DLA_06842 | GAOABQK02IO52T | CDS | 122493 | 1692 | + | 0.287825 | |
g6144 | DLA_06843 | GAOABQK02IO52T | CDS | 124233 | 2037 | - | 0.309278 | |
g6145 | DLA_06844 | GAOABQK02IO52T | CDS | 126540 | 999 | + | 0.378378 | |
g6146 | DLA_06845 | GAOABQK02IO52T | CDS | 127874 | 1875 | + | 0.314133 | |
g6147 | DLA_06847 | GAOABQK02IO52T | CDS | 130231 | 789 | + | 0.269962 | |
g6148 | DLA_06848 | GAOABQK02IO52T | CDS | 131650 | 6594 | + | 0.327571 | |
g6149 | DLA_06849 | GAOABQK02IO52T | CDS | 138582 | 3204 | + | 0.334582 | |
g615 | DLA_00679 | contig05409_1.exp | CDS | 1398720 | 1905 | + | 0.308661 | |
g6150 | DLA_06852 | GAOABQK02IO52T | CDS | 142304 | 1197 | + | 0.333333 | |
g6151 | DLA_06853 | GAOABQK02IO52T | CDS | 143752 | 1821 | - | 0.343767 | |
g6152 | DLA_06854 | GAOABQK02IO52T | CDS | 146019 | 2202 | + | 0.310173 | |
g6153 | DLA_06855 | GAOABQK02IO52T | CDS | 148438 | 1251 | - | 0.309353 | |
g6154 | DLA_06856 | GAOABQK02IO52T | CDS | 149796 | 1230 | + | 0.303252 | |
g6155 | DLA_06857 | conserved hypothetical protein similar to esophageal cancer associated protein there is a second copy of this gene | GAOABQK02IO52T | CDS | 151129 | 2898 | - | 0.31677 |
g6156 | DLA_06858 | GAOABQK02IO52T | CDS | 154724 | 480 | - | 0.316667 | |
g6157 | DLA_06859 | GAOABQK02IO52T | CDS | 155969 | 2106 | - | 0.315764 | |
g6158 | DLA_06860 | GAOABQK02IO52T | CDS | 158498 | 702 | + | 0.306268 | |
g6159 | DLA_06861 | GAOABQK02IO52T | CDS | 159354 | 393 | - | 0.284987 | |
g616 | DLA_00681 | DDLF0006c05.r1 | CDS | 2 | 3991 | - | 0.401153 | |
g6160 | DLA_06863 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | GAOABQK02IO52T | CDS | 160544 | 2301 | - | 0.348979 |
g6161 | DLA_06864 | GAOABQK02IO52T | CDS | 163473 | 2073 | + | 0.327062 | |
g6162 | DLA_06865 | GAOABQK02IO52T | CDS | 165952 | 1149 | + | 0.318538 | |
g6163 | DLA_06866 | GAOABQK02IO52T | CDS | 167124 | 1911 | - | 0.323391 | |
g6164 | DLA_06867 | GAOABQK02IO52T | CDS | 169190 | 2802 | + | 0.275161 | |
g6165 | DLA_06869 | GAOABQK02IO52T | CDS | 172244 | 540 | - | 0.368519 | |
g6166 | DLA_06870 | GAOABQK02IO52T | CDS | 173040 | 726 | + | 0.30854 | |
g6167 | DLA_06871 | ortholog of the magnesium transporter MMGT1 contains a putative signal sequence and one transmembrane domain | GAOABQK02IO52T | CDS | 173974 | 291 | - | 0.237113 |
g6168 | DLA_06872 | GAOABQK02IO52T | CDS | 174537 | 270 | + | 0.296296 | |
g6169 | DLA_11669 | GAOABQK02IO52T | CDS | 175395 | 651 | - | 0.347158 | |
g617 | DLA_00682 | DDLF0038h09.f4 | CDS | 188 | 393 | + | 0.312977 | |
g6170 | DLA_06873 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | GAOABQK02IO52T | CDS | 176715 | 450 | - | 0.333333 |
g6171 | DLA_06874 | GAOABQK02IO52T | CDS | 177709 | 2208 | - | 0.319746 | |
g6172 | DLA_06875 | GAOABQK02IO52T | CDS | 180700 | 1071 | + | 0.325864 | |
g6173 | DLA_06878 | GAOABQK02IO52T | CDS | 182524 | 528 | + | 0.304924 | |
g6174 | DLA_06879 | GAOABQK02IO52T | CDS | 184321 | 615 | - | 0.338211 | |
g6175 | DLA_06883 | GAOABQK02IO52T | CDS | 187216 | 1746 | - | 0.313288 | |
g6176 | DLA_06884 | GAOABQK02IO52T | CDS | 189381 | 3627 | + | 0.27764 | |
g6177 | DLA_06885 | GAOABQK02IO52T | CDS | 193209 | 540 | - | 0.272222 | |
g6178 | DLA_06886 | GAOABQK02IO52T | CDS | 193948 | 900 | + | 0.286667 | |
g6179 | DLA_06887 | GAOABQK02IO52T | CDS | 195119 | 1185 | + | 0.278481 | |
g618 | DLA_00683 | DDLF0038h09.f4 | CDS | 1426 | 1761 | - | 0.293015 | |
g6180 | DLA_06888 | GAOABQK02IO52T | CDS | 196483 | 1353 | + | 0.280857 | |
g6181 | DLA_06891 | GAOABQK02IO52T | CDS | 198295 | 1560 | - | 0.373077 | |
g6182 | DLA_06892 | GAOABQK02IO52T | CDS | 200784 | 1593 | + | 0.313873 | |
g6183 | DLA_06893 | GAOABQK02IO52T | CDS | 203312 | 987 | + | 0.300912 | |
g6184 | DLA_06894 | GAOABQK02IO52T | CDS | 205344 | 4128 | + | 0.341328 | |
g6185 | DLA_06895 | ortholog of Huntington's disease protein Huntingtin (HTT not to be confused with the human serotonin transporter now named SLC6A4) in Dictyostelium regulates myosin II phosphorylation through phosphatase PP2A affecting chemotaxis and cytokinesis also involved in osmoregulation bivalent cation maintenance with effects on development including presporespore differentiation | GAOABQK02IO52T | CDS | 210495 | 8700 | + | 0.330115 |
g6186 | DLA_06896 | catalyzes the reaction D-ribose-5-phosphate D-xylulose-5-phosphate D-sedoheptulose-7-phosphate D-glyceraldehyde-3-phosphate there is a second copy of this gene | GAOABQK02IO52T | CDS | 219448 | 1983 | - | 0.395865 |
g6187 | DLA_11670 | GAOABQK02IO52T | CDS | 221715 | 2754 | - | 0.306826 | |
g6188 | DLA_06897 | GAOABQK02IO52T | CDS | 224860 | 951 | - | 0.320715 | |
g6189 | DLA_06898 | GAOABQK02IO52T | CDS | 226095 | 837 | - | 0.322581 | |
g619 | DLA_00684 | DDLF0038h09.f4 | CDS | 3360 | 228 | + | 0.29386 | |
g6190 | DLA_06899 | GAOABQK02IO52T | CDS | 227597 | 2031 | + | 0.321516 | |
g6191 | DLA_06900 | GAOABQK02IO52T | CDS | 230165 | 2697 | + | 0.311828 | |
g6192 | DLA_06901 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form similar to son of sevenless | GAOABQK02IO52T | CDS | 233724 | 3675 | + | 0.323265 |
g6193 | DLA_06904 | GAOABQK02IO52T | CDS | 238698 | 2793 | - | 0.324024 | |
g6194 | DLA_06905 | component of the gamma-secretase complex which executes the intramembrane proteolysis of type I integral membrane proteins | GAOABQK02IO52T | CDS | 241828 | 999 | - | 0.309309 |
g6195 | DLA_06906 | GAOABQK02IO52T | CDS | 243026 | 1500 | + | 0.308 | |
g6196 | DLA_06907 | GAOABQK02IO52T | CDS | 244624 | 1221 | - | 0.314496 | |
g6197 | DLA_06908 | GAOABQK02IO52T | CDS | 246045 | 954 | - | 0.272537 | |
g6198 | DLA_06909 | GAOABQK02IO52T | CDS | 247376 | 1623 | + | 0.32101 | |
g6199 | DLA_06910 | GAOABQK02IO52T | CDS | 249203 | 426 | - | 0.384977 | |
g62 | DLA_00072 | contig05409_1.exp | CDS | 153753 | 1725 | + | 0.32058 | |
g620 | DLA_00686 | DDLF0038h09.f4 | CDS | 4403 | 1788 | + | 0.291387 | |
g6200 | DLA_06911 | GAOABQK02IO52T | CDS | 250152 | 288 | + | 0.291667 | |
g6201 | DLA_06912 | GAOABQK02IO52T | CDS | 251039 | 330 | - | 0.348485 | |
g6202 | DLA_06913 | GAOABQK02IO52T | CDS | 251587 | 1764 | - | 0.325964 | |
g6203 | DLA_06914 | GAOABQK02IO52T | CDS | 258001 | 2196 | + | 0.362022 | |
g6204 | DLA_06915 | GAOABQK02IO52T | CDS | 260528 | 1869 | + | 0.326378 | |
g6205 | DLA_06916 | GAOABQK02IO52T | CDS | 262549 | 783 | - | 0.296296 | |
g6206 | DLA_11671 | GAOABQK02IO52T | CDS | 263677 | 567 | + | 0.310406 | |
g6207 | DLA_06917 | GAOABQK02IO52T | CDS | 265073 | 4674 | + | 0.345315 | |
g6208 | DLA_06918 | GAOABQK02IO52T | CDS | 270258 | 1809 | + | 0.347706 | |
g6209 | DLA_06919 | GAOABQK02IO52T | CDS | 272235 | 678 | + | 0.30531 | |
g621 | DLA_00687 | DDLF0038h09.f4 | CDS | 6383 | 1383 | + | 0.321041 | |
g6210 | DLA_06920 | belongs to the Sec7 superfamily involved in phagocytosis and cell motility | GAOABQK02IO52T | CDS | 273684 | 2421 | + | 0.344486 |
g6211 | DLA_06921 | GAOABQK02IO52T | CDS | 276308 | 543 | + | 0.335175 | |
g6212 | DLA_06922 | GAOABQK02IO52T | CDS | 277059 | 1482 | - | 0.357625 | |
g6213 | DLA_06923 | GAOABQK02IO52T | CDS | 279060 | 1587 | + | 0.31821 | |
g6214 | DLA_06924 | GAOABQK02IO52T | CDS | 280771 | 573 | + | 0.326353 | |
g6215 | DLA_06925 | GAOABQK02IO52T | CDS | 281483 | 1110 | - | 0.328829 | |
g6216 | DLA_06926 | GAOABQK02IO52T | CDS | 282728 | 1095 | - | 0.309589 | |
g6217 | DLA_06927 | GAOABQK02IO52T | CDS | 284074 | 1239 | - | 0.330105 | |
g6218 | DLA_06929 | GAOABQK02IO52T | CDS | 286642 | 1476 | + | 0.348916 | |
g6219 | DLA_06930 | GAOABQK02IO52T | CDS | 288711 | 1182 | + | 0.27665 | |
g622 | DLA_00688 | DDLF0038h09.f4 | CDS | 7986 | 1059 | - | 0.355996 | |
g6220 | DLA_06931 | GAOABQK02IO52T | CDS | 290009 | 1014 | - | 0.311637 | |
g6221 | DLA_06932 | GAOABQK02IO52T | CDS | 291490 | 1233 | + | 0.300892 | |
g6222 | DLA_06933 | GAOABQK02IO52T | CDS | 292942 | 504 | - | 0.28373 | |
g6223 | DLA_06934 | GAOABQK02IO52T | CDS | 293652 | 1794 | - | 0.330546 | |
g6224 | DLA_06936 | GAOABQK02IO52T | CDS | 296793 | 2274 | - | 0.346966 | |
g6225 | DLA_06937 | GAOABQK02IO52T | CDS | 300296 | 543 | + | 0.267035 | |
g6226 | DLA_06938 | GAOABQK02IO52T | CDS | 301000 | 1266 | - | 0.345182 | |
g6227 | DLA_06939 | GAOABQK02IO52T | CDS | 302551 | 2001 | + | 0.30085 | |
g6228 | DLA_06940 | GAOABQK02IO52T | CDS | 304716 | 1059 | + | 0.303116 | |
g6229 | DLA_06941 | GAOABQK02IO52T | CDS | 306315 | 834 | + | 0.322542 | |
g623 | DLA_00689 | DDLF0038h09.f4 | CDS | 9468 | 3960 | + | 0.301768 | |
g6230 | DLA_06942 | GAOABQK02IO52T | CDS | 307606 | 831 | + | 0.32852 | |
g6231 | DLA_06943 | contains one C2 domain one MHD1 (Munc13-homology) domain and one MHD2 domain | GAOABQK02IO52T | CDS | 308697 | 3792 | + | 0.314873 |
g6232 | DLA_06945 | GAOABQK02IO52T | CDS | 312965 | 1083 | - | 0.289935 | |
g6233 | DLA_06946 | GAOABQK02IO52T | CDS | 314692 | 1926 | + | 0.363448 | |
g6234 | DLA_06947 | GAOABQK02IO52T | CDS | 316825 | 2715 | - | 0.331492 | |
g6235 | DLA_06948 | GAOABQK02IO52T | CDS | 320800 | 555 | + | 0.403604 | |
g6236 | DLA_06949 | GAOABQK02IO52T | CDS | 322203 | 915 | - | 0.353005 | |
g6237 | DLA_06950 | GAOABQK02IO52T | CDS | 324527 | 1281 | + | 0.282592 | |
g6238 | DLA_06951 | GAOABQK02IO52T | CDS | 326148 | 726 | + | 0.319559 | |
g6239 | DLA_06952 | GAOABQK02IO52T | CDS | 326950 | 5052 | - | 0.321853 | |
g624 | DLA_00690 | DDLF0038h09.f4 | CDS | 13804 | 1047 | - | 0.255969 | |
g6240 | DLA_06953 | GAOABQK02IO52T | CDS | 332362 | 1953 | + | 0.315412 | |
g6241 | DLA_06954 | GAOABQK02IO52T | CDS | 334461 | 1596 | - | 0.295739 | |
g6242 | DLA_06956 | GAOABQK02IO52T | CDS | 337730 | 426 | - | 0.284038 | |
g6243 | DLA_11672 | GAOABQK02IO52T | CDS | 338424 | 426 | - | 0.319249 | |
g6244 | DLA_06957 | GAOABQK02IO52T | CDS | 338974 | 1620 | - | 0.29321 | |
g6245 | DLA_06958 | GAOABQK02IO52T | CDS | 340681 | 270 | + | 0.277778 | |
g6246 | DLA_06959 | GAOABQK02IO52T | CDS | 341219 | 1992 | - | 0.318775 | |
g6247 | DLA_06961 | GAOABQK02IO52T | CDS | 344194 | 1281 | + | 0.293521 | |
g6248 | DLA_06962 | GAOABQK02IO52T | CDS | 346923 | 2586 | + | 0.338747 | |
g6249 | DLA_06963 | GAOABQK02IO52T | CDS | 349959 | 5151 | + | 0.317608 | |
g625 | DLA_00691 | DDLF0038h09.f4 | CDS | 15443 | 759 | - | 0.249012 | |
g6250 | DLA_06964 | GAOABQK02IO52T | CDS | 356092 | 636 | + | 0.366352 | |
g6251 | DLA_06965 | GAOABQK02IO52T | CDS | 356924 | 708 | + | 0.289548 | |
g6252 | DLA_06966 | GAOABQK02IO52T | CDS | 357817 | 3051 | + | 0.303507 | |
g6253 | DLA_06967 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | GAOABQK02IO52T | CDS | 361252 | 696 | - | 0.341954 |
g6254 | DLA_06968 | GAOABQK02IO52T | CDS | 362243 | 2244 | + | 0.295009 | |
g6255 | DLA_06969 | GAOABQK02IO52T | CDS | 364514 | 789 | - | 0.258555 | |
g6256 | DLA_06970 | GAOABQK02IO52T | CDS | 365848 | 1383 | + | 0.340564 | |
g6257 | DLA_06971 | GAOABQK02IO52T | CDS | 367324 | 2175 | - | 0.329655 | |
g6258 | DLA_06972 | GAOABQK02IO52T | CDS | 370044 | 384 | + | 0.382812 | |
g6259 | DLA_06973 | GAOABQK02IO52T | CDS | 370784 | 1821 | + | 0.315761 | |
g626 | DLA_00693 | DDLF0038h09.f4 | CDS | 18281 | 1704 | + | 0.297535 | |
g6260 | DLA_06974 | GAOABQK02IO52T | CDS | 373105 | 1275 | + | 0.294902 | |
g6261 | DLA_06975 | GAOABQK02IO52T | CDS | 374940 | 633 | + | 0.301738 | |
g6262 | DLA_06976 | GAOABQK02IO52T | CDS | 376039 | 981 | + | 0.331295 | |
g6263 | DLA_06977 | GAOABQK02IO52T | CDS | 377430 | 3825 | - | 0.324444 | |
g6264 | DLA_06978 | GAOABQK02IO52T | CDS | 381832 | 300 | - | 0.303333 | |
g6265 | DLA_06979 | GAOABQK02IO52T | CDS | 382382 | 1770 | + | 0.311299 | |
g6266 | DLA_06980 | GAOABQK02IO52T | CDS | 384308 | 1248 | - | 0.339744 | |
g6267 | DLA_06981 | GAOABQK02IO52T | CDS | 386011 | 360 | + | 0.291667 | |
g6268 | DLA_06982 | GAOABQK02IO52T | CDS | 386719 | 1077 | - | 0.301764 | |
g6269 | DLA_06985 | GAOABQK02IO52T | CDS | 390510 | 1839 | - | 0.353997 | |
g627 | DLA_00694 | DDLF0038h09.f4 | CDS | 20330 | 1023 | + | 0.316716 | |
g6270 | DLA_06986 | GAOABQK02IO52T | CDS | 394984 | 4206 | + | 0.362102 | |
g6271 | DLA_06987 | GAOABQK02IO52T | CDS | 399341 | 414 | - | 0.333333 | |
g6272 | DLA_06988 | GAOABQK02IO52T | CDS | 400319 | 231 | + | 0.320346 | |
g6273 | DLA_11673 | GAOABQK02IO52T | CDS | 400817 | 816 | + | 0.430147 | |
g6274 | DLA_06989 | GAOABQK02IO52T | CDS | 401737 | 2016 | - | 0.323909 | |
g6275 | DLA_06990 | GAOABQK02IO52T | CDS | 404089 | 1203 | + | 0.334996 | |
g6276 | DLA_06991 | GAOABQK02IO52T | CDS | 405378 | 1617 | - | 0.31107 | |
g6277 | DLA_11674 | GAOABQK02IO52T | CDS | 407984 | 390 | + | 0.312821 | |
g6278 | DLA_06992 | GAOABQK02IO52T | CDS | 408495 | 3780 | + | 0.298413 | |
g6279 | DLA_06993 | GAOABQK02IO52T | CDS | 413957 | 3456 | - | 0.303241 | |
g628 | DLA_00695 | DDLF0038h09.f4 | CDS | 21559 | 2373 | - | 0.307627 | |
g6280 | DLA_06994 | GAOABQK02IO52T | CDS | 417905 | 2673 | - | 0.295922 | |
g6281 | DLA_06996 | GAOABQK02IO52T | CDS | 422502 | 1737 | + | 0.315486 | |
g6282 | DLA_11675 | GAOABQK02IO52T | CDS | 425969 | 1512 | + | 0.417328 | |
g6283 | DLA_06997 | GAOABQK02IO52T | CDS | 427854 | 981 | + | 0.377166 | |
g6284 | DLA_06998 | GAOABQK02IO52T | CDS | 429085 | 2832 | + | 0.322034 | |
g6285 | DLA_06999 | GAOABQK02IO52T | CDS | 432203 | 1323 | + | 0.298564 | |
g6286 | DLA_07000 | ATP-dependent DNA ligase required for the ligation of Okazaki fragments during lagging-strand DNA synthesis | GAOABQK02IO52T | CDS | 433888 | 2760 | + | 0.334058 |
g6287 | DLA_07001 | GAOABQK02IO52T | CDS | 436769 | 1008 | - | 0.286706 | |
g6288 | DLA_07002 | GAOABQK02IO52T | CDS | 437914 | 1413 | + | 0.319887 | |
g6289 | DLA_07004 | GAOABQK02IO52T | CDS | 440071 | 1605 | - | 0.302804 | |
g629 | DLA_00696 | DDLF0038h09.f4 | CDS | 24005 | 612 | + | 0.281046 | |
g6290 | DLA_07005 | GAOABQK02IO52T | CDS | 441759 | 897 | + | 0.284281 | |
g6291 | DLA_07006 | GAOABQK02IO52T | CDS | 442754 | 867 | - | 0.348328 | |
g6292 | DLA_07007 | GAOABQK02IO52T | CDS | 443936 | 1296 | + | 0.296296 | |
g6293 | DLA_07008 | GAOABQK02IO52T | CDS | 445389 | 702 | - | 0.324786 | |
g6294 | DLA_07009 | GAOABQK02IO52T | CDS | 446926 | 1887 | + | 0.326444 | |
g6295 | DLA_11676 | GAOABQK02IO52T | CDS | 448967 | 1152 | - | 0.283854 | |
g6296 | DLA_07010 | GAOABQK02IO52T | CDS | 450270 | 2373 | - | 0.282343 | |
g6297 | DLA_07011 | GAOABQK02IO52T | CDS | 453002 | 726 | + | 0.312672 | |
g6298 | DLA_07012 | GAOABQK02IO52T | CDS | 453969 | 1053 | - | 0.323837 | |
g6299 | DLA_07013 | GAOABQK02IO52T | CDS | 455960 | 2673 | + | 0.325103 | |
g63 | DLA_00073 | contig05409_1.exp | CDS | 155605 | 978 | - | 0.302658 | |
g630 | DLA_00697 | DDLF0038h09.f4 | CDS | 24914 | 957 | - | 0.342738 | |
g6300 | DLA_07014 | GAOABQK02IO52T | CDS | 458766 | 2121 | + | 0.30976 | |
g6301 | DLA_07015 | GAOABQK02IO52T | CDS | 461803 | 660 | - | 0.343939 | |
g6302 | DLA_11677 | GAOABQK02IO52T | CDS | 462919 | 357 | - | 0.291317 | |
g6303 | DLA_07016 | GAOABQK02IO52T | CDS | 463490 | 1251 | - | 0.253397 | |
g6304 | DLA_07018 | GAOABQK02IO52T | CDS | 465283 | 2589 | - | 0.312476 | |
g6305 | DLA_07021 | conserved eukaryotic kinase (human MVK yeast ERG12) that plays a role in the synthesis of isopentanyl pyrophosphate a common intermediate in pathways including cholesterol biosynthesis | GAOABQK02IO52T | CDS | 470082 | 1155 | + | 0.341991 |
g6306 | DLA_07022 | GAOABQK02IO52T | CDS | 471770 | 1680 | - | 0.28869 | |
g6307 | DLA_07023 | GAOABQK02IO52T | CDS | 473753 | 1464 | + | 0.295765 | |
g6308 | DLA_07025 | GAOABQK02IO52T | CDS | 475447 | 3846 | - | 0.326573 | |
g6309 | DLA_07026 | GAOABQK02IO52T | CDS | 479637 | 3696 | - | 0.325216 | |
g631 | DLA_00698 | F4PJNLW01A00V1 | CDS | 1 | 83 | - | 0.385542 | |
g6310 | DLA_07028 | GAOABQK02IO52T | CDS | 484023 | 546 | + | 0.326007 | |
g6311 | DLA_07030 | GAOABQK02IO52T | CDS | 485155 | 2169 | - | 0.339327 | |
g6312 | DLA_07031 | GAOABQK02IO52T | CDS | 488247 | 294 | + | 0.401361 | |
g6313 | DLA_07032 | GAOABQK02IO52T | CDS | 489254 | 885 | - | 0.353672 | |
g6314 | DLA_07033 | catalyzes the reaction D-glyceraldehyde 3-phosphate glycerone phosphate defects in human TPI1 are the cause of triosephosphate isomerase deficiency severe clinical disorder of glycolysis | GAOABQK02IO52T | CDS | 490529 | 777 | - | 0.365508 |
g6315 | DLA_07034 | GAOABQK02IO52T | CDS | 491546 | 1056 | + | 0.322917 | |
g6316 | DLA_07035 | GAOABQK02IO52T | CDS | 492988 | 1053 | - | 0.283951 | |
g6317 | DLA_07036 | homolog of human HMGCS1 catalyzes the reaction acetyl-CoA H2O acetoacetyl-CoA (S)-3-hydroxy-3-methylglutaryl-CoA CoA contains a predicted peroxisomal targeting signal | GAOABQK02IO52T | CDS | 495479 | 1401 | + | 0.356888 |
g6318 | DLA_07037 | GAOABQK02IO52T | CDS | 497222 | 2205 | - | 0.317914 | |
g6319 | DLA_07039 | GAOABQK02IO52T | CDS | 501910 | 1596 | - | 0.31391 | |
g632 | DLA_00700 | F4PJNLW01A00V1 | CDS | 1619 | 1938 | + | 0.31063 | |
g6320 | DLA_07040 | GAOABQK02IO52T | CDS | 503740 | 2217 | + | 0.341001 | |
g6321 | DLA_07041 | catalyzes the reaction geranylgeranyl diphosphate protein-cysteine S-geranylgeranyl-protein diphosphate | GAOABQK02IO52T | CDS | 506221 | 1083 | + | 0.34903 |
g6322 | DLA_07042 | GAOABQK02IO52T | CDS | 507413 | 5760 | - | 0.312153 | |
g6323 | DLA_07043 | GAOABQK02IO52T | CDS | 513590 | 2301 | + | 0.317253 | |
g6324 | DLA_07044 | GAOABQK02IO52T | CDS | 516261 | 2535 | + | 0.321105 | |
g6325 | DLA_07045 | GAOABQK02IO52T | CDS | 518831 | 3597 | - | 0.318599 | |
g6326 | DLA_07046 | GAOABQK02IO52T | CDS | 523045 | 1407 | + | 0.316987 | |
g6327 | DLA_07047 | underexpressed in | GAOABQK02IO52T | CDS | 524724 | 888 | + | 0.337838 |
g6328 | DLA_07048 | GAOABQK02IO52T | CDS | 525873 | 879 | + | 0.336746 | |
g6329 | DLA_07049 | GAOABQK02IO52T | CDS | 526971 | 2703 | - | 0.337403 | |
g633 | DLA_00701 | F4PJNLW01A00V1 | CDS | 3780 | 1101 | - | 0.247956 | |
g6330 | DLA_11678 | GAOABQK02IO52T | CDS | 530240 | 618 | - | 0.331715 | |
g6331 | DLA_07050 | GAOABQK02IO52T | CDS | 531352 | 918 | + | 0.339869 | |
g6332 | DLA_07051 | GAOABQK02IO52T | CDS | 532386 | 837 | + | 0.321386 | |
g6333 | DLA_07052 | GAOABQK02IO52T | CDS | 533333 | 498 | - | 0.307229 | |
g6334 | DLA_07053 | GAOABQK02IO52T | CDS | 534110 | 3546 | + | 0.319515 | |
g6335 | DLA_07054 | GAOABQK02IO52T | CDS | 537757 | 378 | - | 0.298942 | |
g6336 | DLA_07055 | GAOABQK02IO52T | CDS | 538454 | 375 | - | 0.328 | |
g6337 | DLA_07056 | GAOABQK02IO52T | CDS | 540651 | 1158 | + | 0.309154 | |
g6338 | DLA_07057 | GAOABQK02IO52T | CDS | 541977 | 474 | - | 0.2827 | |
g6339 | DLA_07058 | GAOABQK02IO52T | CDS | 542749 | 483 | + | 0.296066 | |
g634 | DLA_00702 | F4PJNLW01A00V1 | CDS | 4965 | 2502 | + | 0.278577 | |
g6340 | DLA_07059 | GAOABQK02IO52T | CDS | 543681 | 1629 | + | 0.368324 | |
g6341 | DLA_07060 | GAOABQK02IO52T | CDS | 545602 | 2247 | + | 0.336894 | |
g6342 | DLA_07061 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H4 | GAOABQK02IO52T | CDS | 548163 | 414 | + | 0.39372 |
g6343 | DLA_07062 | ortholog of S. cerevisiae URA1 and human DPYD defects in DPYD cause dihydropyrimidine dehydrogenase deficiency catalyzes the reaction 56-dihydrouracil NADP uracil NADPH H | GAOABQK02IO52T | CDS | 549158 | 3054 | + | 0.384741 |
g6344 | DLA_07063 | GAOABQK02IO52T | CDS | 552777 | 5415 | + | 0.328901 | |
g6345 | DLA_07064 | GAOABQK02IO52T | CDS | 558791 | 2451 | - | 0.314565 | |
g6346 | DLA_07065 | GAOABQK02IO52T | CDS | 561324 | 1548 | - | 0.313953 | |
g6347 | DLA_07066 | ortholog of human CRIP1 contains 1 zinc-binding LIM domain LIM domains are found in proteins with differing functions including gene expression and cytoskeleton organisation and development | GAOABQK02IO52T | CDS | 563122 | 264 | - | 0.382576 |
g6348 | DLA_07067 | GAOABQK02IO52T | CDS | 563828 | 606 | - | 0.232673 | |
g6349 | DLA_07069 | GAOABQK02IO52T | CDS | 564818 | 2496 | + | 0.314103 | |
g635 | DLA_00703 | catalyzes the reaction ATP L-glutamyl-tRNA(Gln) L-glutamine ADP phosphate L-glutaminyl-tRNA(Gln) L-glutamate | F4PJNLW01A00V1 | CDS | 7654 | 1668 | + | 0.291966 |
g6350 | DLA_07070 | GAOABQK02IO52T | CDS | 567474 | 3417 | - | 0.321042 | |
g6351 | DLA_07071 | GAOABQK02IO52T | CDS | 571269 | 531 | - | 0.335217 | |
g6352 | DLA_07072 | GAOABQK02IO52T | CDS | 572541 | 891 | + | 0.276094 | |
g6353 | DLA_07073 | GAOABQK02IO52T | CDS | 573795 | 1047 | + | 0.369628 | |
g6354 | DLA_07074 | GAOABQK02IO52T | CDS | 575157 | 1287 | + | 0.309246 | |
g6355 | DLA_07075 | GAOABQK02IO52T | CDS | 576512 | 4257 | - | 0.322293 | |
g6356 | DLA_07076 | GAOABQK02IO52T | CDS | 581262 | 1839 | - | 0.363785 | |
g6357 | DLA_07077 | GAOABQK02IO52T | CDS | 583246 | 1563 | - | 0.337172 | |
g6358 | DLA_07078 | GAOABQK02IO52T | CDS | 585242 | 423 | + | 0.288416 | |
g6359 | DLA_07079 | GAOABQK02IO52T | CDS | 586217 | 231 | + | 0.30303 | |
g636 | DLA_00704 | F4PJNLW01A00V1 | CDS | 9460 | 1839 | + | 0.256661 | |
g6360 | DLA_07080 | involved in phagocytosis and substrate adhesion controls the levels of SibA adhesion molecules at the cell surface as well as the intracellular transport and stability of the SibA protein also involved in the intracellular killing of bacteria by determining the stability and cellular amount of the sulfotransferase Kil1br bNomenclature conflict: b Do not confuse this gene with phgA encoding drainin or with the phgA locus ( | GAOABQK02IO52T | CDS | 586782 | 1893 | - | 0.368199 |
g6361 | DLA_07081 | GAOABQK02IO52T | CDS | 589090 | 270 | - | 0.296296 | |
g6362 | DLA_07082 | GAOABQK02IO52T | CDS | 589566 | 1362 | - | 0.422173 | |
g6363 | DLA_07083 | GAOABQK02IO52T | CDS | 591815 | 1098 | + | 0.32969 | |
g6364 | DLA_07084 | GAOABQK02IO52T | CDS | 593010 | 2448 | - | 0.329657 | |
g6365 | DLA_07085 | GAOABQK02IO52T | CDS | 595945 | 1101 | - | 0.315168 | |
g6366 | DLA_07086 | GAOABQK02IO52T | CDS | 600546 | 1707 | + | 0.357352 | |
g6367 | DLA_07087 | putative protein serinethreonine kinase belongs to the PAKL subfamily of protein kinases the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | GAOABQK02IO52T | CDS | 603199 | 2982 | + | 0.346412 |
g6368 | DLA_07088 | GAOABQK02IO52T | CDS | 606292 | 1755 | - | 0.283191 | |
g6369 | DLA_07089 | GAOABQK02IO52T | CDS | 609130 | 2634 | + | 0.329916 | |
g637 | DLA_00705 | F4PJNLW01A00V1 | CDS | 11526 | 2700 | + | 0.33 | |
g6370 | DLA_07090 | GAOABQK02IO52T | CDS | 612055 | 615 | + | 0.317073 | |
g6371 | DLA_07091 | GAOABQK02IO52T | CDS | 612802 | 1539 | - | 0.339181 | |
g6372 | DLA_07092 | GAOABQK02IO52T | CDS | 614911 | 2685 | + | 0.347114 | |
g6373 | DLA_07093 | GAOABQK02IO52T | CDS | 617780 | 627 | - | 0.370016 | |
g6374 | DLA_07094 | GAOABQK02IO52T | CDS | 619195 | 1515 | - | 0.305611 | |
g6375 | DLA_07095 | GAOABQK02IO52T | CDS | 621953 | 1251 | + | 0.308553 | |
g6376 | DLA_07096 | belongs to a gene family conserved in amoeba contains a putative metal-binding domain | GAOABQK02IO52T | CDS | 625710 | 1059 | + | 0.326723 |
g6377 | DLA_07097 | GAOABQK02IO52T | CDS | 627094 | 2634 | - | 0.314351 | |
g6378 | DLA_07098 | GAOABQK02IO52T | CDS | 629988 | 903 | + | 0.314507 | |
g6379 | DLA_07099 | GAOABQK02IO52T | CDS | 631298 | 1080 | - | 0.356481 | |
g638 | DLA_00706 | F4PJNLW01A00V1 | CDS | 14437 | 2826 | - | 0.314225 | |
g6380 | DLA_07100 | GAOABQK02IO52T | CDS | 632667 | 2820 | + | 0.30922 | |
g6381 | DLA_07101 | GAOABQK02IO52T | CDS | 635945 | 4212 | + | 0.328348 | |
g6382 | DLA_07102 | GAOABQK02IO52T | CDS | 640401 | 1662 | - | 0.295427 | |
g6383 | DLA_07103 | GAOABQK02IO52T | CDS | 642277 | 1752 | - | 0.304224 | |
g6384 | DLA_07105 | GAOABQK02IO52T | CDS | 644577 | 1728 | - | 0.302662 | |
g6385 | DLA_07106 | GAOABQK02IO52T | CDS | 646704 | 1536 | + | 0.314453 | |
g6386 | DLA_07107 | GAOABQK02IO52T | CDS | 648464 | 762 | - | 0.353018 | |
g6387 | DLA_07108 | GAOABQK02IO52T | CDS | 649858 | 747 | + | 0.348059 | |
g6388 | DLA_07109 | GAOABQK02IO52T | CDS | 650898 | 396 | - | 0.313131 | |
g6389 | DLA_07110 | GAOABQK02IO52T | CDS | 651734 | 1254 | + | 0.296651 | |
g639 | DLA_00707 | F4PJNLW01A00V1 | CDS | 17774 | 2130 | + | 0.349296 | |
g6390 | DLA_07111 | GAOABQK02IO52T | CDS | 653197 | 660 | - | 0.359091 | |
g6391 | DLA_07112 | GAOABQK02IO52T | CDS | 654391 | 933 | + | 0.301179 | |
g6392 | DLA_07113 | ortholog of S. cerevisiae TFB1 subunit of TFIIH and nucleotide excision repair factor 3 complexes required for nucleotide excision repair target for transcriptional activators | GAOABQK02IO52T | CDS | 655521 | 1926 | + | 0.350987 |
g6393 | DLA_07114 | putative protein serinethreonine kinase N-terminus similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase C-terminal half belongs to the peptidase C2 family contains 4 calpain III domains and has similarity to calpain-like cysteine protease | GAOABQK02IO52T | CDS | 657826 | 3318 | + | 0.347499 |
g6394 | DLA_07115 | GAOABQK02IO52T | CDS | 661516 | 1122 | - | 0.309269 | |
g6395 | DLA_07116 | GAOABQK02IO52T | CDS | 662877 | 534 | - | 0.277154 | |
g6396 | DLA_07117 | controls RNA polymerase II activity by phosphorylating the carboxy terminal domain (CTD) of the largest subunit predicted to interact with | GAOABQK02IO52T | CDS | 663556 | 1113 | + | 0.343217 |
g6397 | DLA_07118 | GAOABQK02IO52T | CDS | 664722 | 1782 | - | 0.306397 | |
g6398 | DLA_07119 | GAOABQK02IO52T | CDS | 666791 | 1806 | + | 0.295681 | |
g6399 | DLA_07121 | GAOABQK02IO52T | CDS | 668752 | 2100 | - | 0.33381 | |
g64 | DLA_00074 | contig05409_1.exp | CDS | 156736 | 1272 | - | 0.306604 | |
g640 | DLA_00708 | F4PJNLW01A00V1 | CDS | 20157 | 486 | - | 0.320988 | |
g6400 | DLA_07122 | GAOABQK02IO52T | CDS | 671553 | 909 | - | 0.349835 | |
g6401 | DLA_07123 | GAOABQK02IO52T | CDS | 673443 | 2532 | - | 0.317536 | |
g6402 | DLA_07124 | GAOABQK02IO52T | CDS | 676808 | 228 | - | 0.27193 | |
g6403 | DLA_07125 | GAOABQK02IO52T | CDS | 677804 | 2007 | + | 0.308919 | |
g6404 | DLA_07126 | GAOABQK02IO52T | CDS | 680176 | 900 | - | 0.322222 | |
g6405 | DLA_07127 | GAOABQK02IO52T | CDS | 681179 | 1026 | - | 0.302144 | |
g6406 | DLA_07128 | GAOABQK02IO52T | CDS | 683154 | 1290 | - | 0.317829 | |
g6407 | DLA_07130 | GAOABQK02IO52T | CDS | 684776 | 2007 | - | 0.310414 | |
g6408 | DLA_07132 | GAOABQK02IO52T | CDS | 687639 | 2376 | - | 0.323653 | |
g6409 | DLA_07133 | GAOABQK02IO52T | CDS | 690319 | 3717 | - | 0.379338 | |
g641 | DLA_00709 | F4PJNLW01A00V1 | CDS | 21016 | 525 | + | 0.413333 | |
g6410 | DLA_07135 | GAOABQK02IO52T | CDS | 695459 | 18697 | + | 0.365246 | |
g6411 | DLA_07136 | GAOABQK02JBK0O | CDS | 1 | 1659 | + | 0.454491 | |
g6412 | DLA_07137 | GAOABQK02JBK0O | CDS | 2690 | 2361 | + | 0.302838 | |
g6413 | DLA_07138 | GAOABQK02JBK0O | CDS | 6017 | 1473 | + | 0.300068 | |
g6414 | DLA_11679 | GAOABQK02JBK0O | CDS | 7805 | 231 | - | 0.367965 | |
g6415 | DLA_07139 | GAOABQK02JBK0O | CDS | 8235 | 486 | - | 0.351852 | |
g6416 | DLA_07140 | GAOABQK02JBK0O | CDS | 9280 | 1620 | + | 0.367284 | |
g6417 | DLA_07141 | GAOABQK02JBK0O | CDS | 11072 | 1659 | - | 0.300784 | |
g6418 | DLA_07142 | GAOABQK02JBK0O | CDS | 12995 | 2841 | - | 0.344245 | |
g6419 | DLA_07143 | GAOABQK02JBK0O | CDS | 16153 | 597 | - | 0.256281 | |
g642 | DLA_00710 | F4PJNLW01A00V1 | CDS | 21765 | 522 | - | 0.277778 | |
g6420 | DLA_07144 | GAOABQK02JBK0O | CDS | 17128 | 3264 | + | 0.32261 | |
g6421 | DLA_11680 | GAOABQK02JBK0O | CDS | 20921 | 588 | - | 0.340136 | |
g6422 | DLA_07145 | GAOABQK02JBK0O | CDS | 22326 | 543 | - | 0.279926 | |
g6423 | DLA_07146 | GAOABQK02JBK0O | CDS | 23543 | 651 | + | 0.30722 | |
g6424 | DLA_07147 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | GAOABQK02JBK0O | CDS | 24534 | 3360 | - | 0.338393 |
g6425 | DLA_07148 | GAOABQK02JBK0O | CDS | 28462 | 2439 | - | 0.299303 | |
g6426 | DLA_07149 | GAOABQK02JBK0O | CDS | 31261 | 1320 | + | 0.27197 | |
g6427 | DLA_07150 | GAOABQK02JBK0O | CDS | 32673 | 795 | - | 0.338365 | |
g6428 | DLA_07151 | GAOABQK02JBK0O | CDS | 34456 | 858 | + | 0.334499 | |
g6429 | DLA_07152 | GAOABQK02JBK0O | CDS | 35811 | 1614 | + | 0.348203 | |
g643 | DLA_00711 | F4PJNLW01A00V1 | CDS | 22496 | 918 | - | 0.302832 | |
g6430 | DLA_07154 | GAOABQK02JBK0O | CDS | 38387 | 744 | - | 0.295699 | |
g6431 | DLA_07156 | GAOABQK02JBK0O | CDS | 40849 | 585 | + | 0.34188 | |
g6432 | DLA_07157 | GAOABQK02JBK0O | CDS | 42078 | 1422 | - | 0.287623 | |
g6433 | DLA_07159 | GAOABQK02JBK0O | CDS | 45121 | 2970 | - | 0.306734 | |
g6434 | DLA_07160 | GAOABQK02JBK0O | CDS | 49233 | 1890 | + | 0.309524 | |
g6435 | DLA_07161 | GAOABQK02JBK0O | CDS | 51597 | 2976 | + | 0.302755 | |
g6436 | DLA_07162 | GAOABQK02JBK0O | CDS | 55174 | 2730 | + | 0.323077 | |
g6437 | DLA_07163 | GAOABQK02JBK0O | CDS | 58247 | 1959 | - | 0.291475 | |
g6438 | DLA_07164 | GAOABQK02JBK0O | CDS | 60708 | 1098 | + | 0.273224 | |
g6439 | DLA_07165 | GAOABQK02JBK0O | CDS | 62011 | 4239 | - | 0.313517 | |
g644 | DLA_00712 | F4PJNLW01A00V1 | CDS | 23588 | 1596 | - | 0.316416 | |
g6440 | DLA_07166 | GAOABQK02JBK0O | CDS | 67515 | 1182 | + | 0.319797 | |
g6441 | DLA_07167 | GAOABQK02JBK0O | CDS | 68748 | 1353 | - | 0.269771 | |
g6442 | DLA_07168 | GAOABQK02JBK0O | CDS | 70676 | 2202 | + | 0.349682 | |
g6443 | DLA_07169 | GAOABQK02JBK0O | CDS | 73123 | 1680 | - | 0.285119 | |
g6444 | DLA_07171 | GAOABQK02JBK0O | CDS | 76314 | 2199 | + | 0.295134 | |
g6445 | DLA_07172 | GAOABQK02JBK0O | CDS | 78619 | 2445 | - | 0.310429 | |
g6446 | DLA_07173 | GAOABQK02JBK0O | CDS | 81330 | 1440 | + | 0.301389 | |
g6447 | DLA_07174 | GAOABQK02JBK0O | CDS | 83071 | 6564 | + | 0.296009 | |
g6448 | DLA_07176 | GAOABQK02JBK0O | CDS | 90039 | 2832 | + | 0.316737 | |
g6449 | DLA_07177 | GAOABQK02JBK0O | CDS | 92958 | 1965 | - | 0.262595 | |
g645 | DLA_00713 | F4PJNLW01A00V1 | CDS | 25932 | 1755 | + | 0.317949 | |
g6450 | DLA_07178 | contains a central single transmembrane domain | GAOABQK02JBK0O | CDS | 95036 | 303 | + | 0.306931 |
g6451 | DLA_07179 | GAOABQK02JBK0O | CDS | 95836 | 1188 | + | 0.31229 | |
g6452 | DLA_07180 | catalyzes the reaction 3-methyl-2-oxobutanoate lipoamide S-(2-methylpropanoyl)-dihydrolipoamide COsub2sub E1 component of branched-chain keto acid dehydrogenase | GAOABQK02JBK0O | CDS | 97173 | 1113 | + | 0.345912 |
g6453 | DLA_07181 | GAOABQK02JBK0O | CDS | 98584 | 1656 | + | 0.286836 | |
g6454 | DLA_07182 | similar to human PRSS16 (thymus-specific serine protease) contains a putative signal peptide | GAOABQK02JBK0O | CDS | 100391 | 1476 | + | 0.307588 |
g6455 | DLA_11681 | GAOABQK02JBK0O | CDS | 102185 | 762 | + | 0.351706 | |
g6456 | DLA_07183 | GAOABQK02JBK0O | CDS | 103324 | 819 | + | 0.336996 | |
g6457 | DLA_07185 | GAOABQK02JBK0O | CDS | 105348 | 852 | + | 0.340376 | |
g6458 | DLA_07186 | GAOABQK02JBK0O | CDS | 106583 | 2280 | + | 0.320175 | |
g6459 | DLA_07188 | GAOABQK02JBK0O | CDS | 110119 | 909 | - | 0.289329 | |
g646 | DLA_00714 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | F4PJNLW01A00V1 | CDS | 28242 | 447 | + | 0.360179 |
g6460 | DLA_07189 | GAOABQK02JBK0O | CDS | 111330 | 3525 | - | 0.332482 | |
g6461 | DLA_07190 | GAOABQK02JBK0O | CDS | 115182 | 3573 | + | 0.344528 | |
g6462 | DLA_07191 | GAOABQK02JBK0O | CDS | 119124 | 1737 | + | 0.288428 | |
g6463 | DLA_07192 | GAOABQK02JBK0O | CDS | 121515 | 1545 | + | 0.301618 | |
g6464 | DLA_07193 | GAOABQK02JBK0O | CDS | 123828 | 3255 | + | 0.288786 | |
g6465 | DLA_07194 | GAOABQK02JBK0O | CDS | 128630 | 1839 | + | 0.327352 | |
g6466 | DLA_07195 | GAOABQK02JBK0O | CDS | 130705 | 501 | - | 0.315369 | |
g6467 | DLA_07196 | GAOABQK02JBK0O | CDS | 131417 | 2556 | + | 0.321205 | |
g6468 | DLA_07197 | GAOABQK02JBK0O | CDS | 134291 | 858 | - | 0.32634 | |
g6469 | DLA_07198 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | GAOABQK02JBK0O | CDS | 135234 | 3006 | - | 0.294744 |
g647 | DLA_00715 | F4PJNLW01A00V1 | CDS | 29125 | 1464 | + | 0.267076 | |
g6470 | DLA_07199 | GAOABQK02JBK0O | CDS | 138345 | 1731 | - | 0.281918 | |
g6471 | DLA_07200 | GAOABQK02JBK0O | CDS | 140210 | 798 | + | 0.265664 | |
g6472 | DLA_07201 | GAOABQK02JBK0O | CDS | 141373 | 1107 | - | 0.265583 | |
g6473 | DLA_07202 | GAOABQK02JBK0O | CDS | 142600 | 1740 | + | 0.298276 | |
g6474 | DLA_07203 | rab family small GTPase involved in vesicle fusion during endocytosis there is another rab7 homolog rab7B | GAOABQK02JEBFV | CDS | 601 | 609 | + | 0.374384 |
g6475 | DLA_07204 | GAOABQK02JEBFV | CDS | 1691 | 882 | - | 0.304989 | |
g6476 | DLA_07205 | ortholog of the H. sapiens UBLCP1 a conserved protein that contains a ubiquitin and a NLI interacting factor domain there is a second copy of this gene | GAOABQK02JEBFV | CDS | 3056 | 1143 | - | 0.293963 |
g6477 | DLA_07208 | GAOABQK02JEBFV | CDS | 5432 | 1839 | - | 0.292007 | |
g6478 | DLA_07209 | GAOABQK02JEBFV | CDS | 8723 | 291 | + | 0.32646 | |
g6479 | DLA_07211 | GAOABQK02JEBFV | CDS | 9829 | 1767 | - | 0.291454 | |
g648 | DLA_00717 | F4PJNLW01A00V1 | CDS | 31881 | 354 | - | 0.324859 | |
g6480 | DLA_11682 | GAOABQK02JEBFV | CDS | 12930 | 231 | - | 0.316017 | |
g6481 | DLA_07212 | GAOABQK02JEBFV | CDS | 13399 | 1755 | + | 0.290028 | |
g6482 | DLA_07213 | GAOABQK02JEBFV | CDS | 16894 | 1767 | - | 0.294284 | |
g6483 | DLA_07214 | GAOABQK02JEBFV | CDS | 18830 | 384 | + | 0.317708 | |
g6484 | DLA_07215 | GAOABQK02JEBFV | CDS | 20418 | 1632 | + | 0.295956 | |
g6485 | DLA_07216 | GAOABQK02JEBFV | CDS | 22114 | 996 | - | 0.318273 | |
g6486 | DLA_07218 | GAOABQK02JEBFV | CDS | 24064 | 588 | + | 0.353741 | |
g6487 | DLA_07222 | ortholog of peroxin 16 involved in import of proteins into peroxisomes mutations in human homolog cause peroxisomal disorders | GAOABQK02JEBFV | CDS | 27245 | 981 | - | 0.295617 |
g6488 | DLA_07223 | GAOABQK02JEBFV | CDS | 28796 | 2520 | + | 0.349206 | |
g6489 | DLA_07224 | GAOABQK02JEBFV | CDS | 32112 | 1551 | + | 0.348162 | |
g649 | DLA_00718 | member of the histone H2A-H2B sub-family related to the NF-YB subunit of the CCAAT-binding activator NF-Y | F4PJNLW01A00V1 | CDS | 32467 | 417 | - | 0.275779 |
g6490 | DLA_07225 | GAOABQK02JEBFV | CDS | 34277 | 1305 | + | 0.300383 | |
g6491 | DLA_07226 | GAOABQK02JEBFV | CDS | 35840 | 1401 | - | 0.294076 | |
g6492 | DLA_07227 | GAOABQK02JEBFV | CDS | 37648 | 1710 | - | 0.299415 | |
g6493 | DLA_07229 | contains one AN1-type zinc finger and one A20-type zinc finger similar to A. thaliana SAP7 (stress-associated protein) | GAOABQK02JEBFV | CDS | 41031 | 519 | + | 0.350674 |
g6494 | DLA_07230 | GAOABQK02JEBFV | CDS | 41926 | 777 | + | 0.266409 | |
g6495 | DLA_07231 | GAOABQK02JEBFV | CDS | 42982 | 984 | - | 0.341463 | |
g6496 | DLA_07233 | GAOABQK02JEBFV | CDS | 44856 | 588 | + | 0.306122 | |
g6497 | DLA_07234 | GAOABQK02JEBFV | CDS | 45755 | 2196 | - | 0.331056 | |
g6498 | DLA_07235 | GAOABQK02JEBFV | CDS | 48636 | 2055 | - | 0.331873 | |
g6499 | DLA_07236 | GAOABQK02JEBFV | CDS | 51550 | 1086 | + | 0.308471 | |
g65 | DLA_00076 | contig05409_1.exp | CDS | 158535 | 2472 | + | 0.281958 | |
g650 | DLA_00719 | F4PJNLW01A00V1 | CDS | 33208 | 1356 | + | 0.262537 | |
g6500 | DLA_07238 | GAOABQK02JEBFV | CDS | 53165 | 1764 | + | 0.295351 | |
g6501 | DLA_07239 | GAOABQK02JEBFV | CDS | 57752 | 1665 | - | 0.2997 | |
g6502 | DLA_07240 | GAOABQK02JEBFV | CDS | 59681 | 234 | + | 0.303419 | |
g6503 | DLA_07242 | GAOABQK02JEBFV | CDS | 61379 | 699 | + | 0.281831 | |
g6504 | DLA_07244 | GAOABQK02JOCCH | CDS | 760 | 765 | - | 0.347712 | |
g6505 | DLA_07245 | half transporter consisting of one ABC domain and one transmembrane domain | GAOABQK02JOCCH | CDS | 2035 | 1836 | - | 0.337146 |
g6506 | DLA_07246 | GAOABQK02JOCCH | CDS | 4360 | 4077 | - | 0.298994 | |
g6507 | DLA_07248 | GAOABQK02JOCCH | CDS | 9321 | 873 | - | 0.312715 | |
g6508 | DLA_07249 | GAOABQK02JOCCH | CDS | 10963 | 723 | + | 0.26556 | |
g6509 | DLA_07250 | GAOABQK02JOCCH | CDS | 11775 | 3129 | - | 0.317034 | |
g651 | DLA_00720 | F4PJNLW01A00V1 | CDS | 34648 | 1248 | - | 0.309295 | |
g6510 | DLA_07251 | GAOABQK02JOCCH | CDS | 15763 | 786 | - | 0.305344 | |
g6511 | DLA_07252 | GAOABQK02JOCCH | CDS | 17035 | 4353 | + | 0.295658 | |
g6512 | DLA_07253 | GAOABQK02JOCCH | CDS | 21891 | 924 | - | 0.318182 | |
g6513 | DLA_07254 | GAOABQK02JOCCH | CDS | 23299 | 3558 | - | 0.290894 | |
g6514 | DLA_07255 | GAOABQK02JOCCH | CDS | 27622 | 3234 | + | 0.28726 | |
g6515 | DLA_07257 | GAOABQK02JOCCH | CDS | 31217 | 1065 | - | 0.284507 | |
g6516 | DLA_07258 | GAOABQK02JOCCH | CDS | 32571 | 1788 | - | 0.298098 | |
g6517 | DLA_07259 | GAOABQK02JOCCH | CDS | 34653 | 1818 | - | 0.319582 | |
g6518 | DLA_07260 | GAOABQK02JOCCH | CDS | 36885 | 2748 | + | 0.218705 | |
g6519 | DLA_07261 | GAOABQK02JOCCH | CDS | 39872 | 534 | + | 0.224719 | |
g652 | DLA_00721 | F4PJNLW01A00V1 | CDS | 38734 | 642 | - | 0.32866 | |
g6520 | DLA_07262 | GAOABQK02JOCCH | CDS | 40465 | 1494 | - | 0.321285 | |
g6521 | DLA_07263 | GAOABQK02JOCCH | CDS | 42165 | 2247 | - | 0.305296 | |
g6522 | DLA_07264 | GAOABQK02JOCCH | CDS | 44662 | 1047 | - | 0.334288 | |
g6523 | DLA_11683 | GAOABQK02JOCCH | CDS | 46384 | 1023 | + | 0.346041 | |
g6524 | DLA_07265 | GAOABQK02JOCCH | CDS | 48097 | 3072 | + | 0.277995 | |
g6525 | DLA_07266 | GAOABQK02JOCCH | CDS | 51299 | 1959 | - | 0.28586 | |
g6526 | DLA_07267 | GAOABQK02JOCCH | CDS | 54609 | 621 | + | 0.347826 | |
g6527 | DLA_07268 | GAOABQK02JOCCH | CDS | 55426 | 651 | - | 0.385561 | |
g6528 | DLA_07269 | GAOABQK02JOCCH | CDS | 56989 | 1377 | + | 0.328976 | |
g6529 | DLA_07270 | GAOABQK02JOCCH | CDS | 58644 | 1905 | - | 0.290814 | |
g653 | DLA_00722 | F4PJNLW01A00V1 | CDS | 39623 | 1137 | + | 0.350923 | |
g6530 | DLA_07272 | GAOABQK02JOCCH | CDS | 61204 | 2685 | + | 0.297952 | |
g6531 | DLA_07273 | GAOABQK02JOCCH | CDS | 64478 | 1146 | - | 0.333333 | |
g6532 | DLA_07274 | GAOABQK02JOCCH | CDS | 66010 | 1539 | + | 0.271605 | |
g6533 | DLA_07275 | GAOABQK02JOCCH | CDS | 67880 | 1137 | + | 0.276165 | |
g6534 | DLA_07276 | GAOABQK02JOCCH | CDS | 69118 | 2628 | - | 0.306317 | |
g6535 | DLA_07277 | GAOABQK02JOCCH | CDS | 72776 | 2139 | + | 0.328191 | |
g6536 | DLA_07279 | GAOABQK02JOCCH | CDS | 77101 | 1803 | - | 0.36162 | |
g6537 | DLA_07280 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein involved in the metabolism of compounds that control Dictyostelium cell differentiation | GAOABQK02JOCCH | CDS | 79667 | 1893 | + | 0.384046 |
g6538 | DLA_07281 | GAOABQK02JOCCH | CDS | 81624 | 1983 | - | 0.281392 | |
g6539 | DLA_07282 | GAOABQK02JOCCH | CDS | 83909 | 2757 | + | 0.286181 | |
g654 | DLA_00723 | RrmJFtsJ ribosomal RNA methyltransferase family member well conserved heat shock proteins present in prokaryotes archaea and eukaryotes similar to S. cerevisiae MRM2 required for methylation of U(2791) in 21S rRNA | F4PJNLW01A00V1 | CDS | 40896 | 978 | + | 0.271984 |
g6540 | DLA_07283 | GAOABQK02JOCCH | CDS | 86736 | 2736 | - | 0.339547 | |
g6541 | DLA_07284 | GAOABQK02JOCCH | CDS | 89658 | 1740 | - | 0.275862 | |
g6542 | DLA_07285 | GAOABQK02JOCCH | CDS | 91462 | 1734 | - | 0.27797 | |
g6543 | DLA_07286 | GAOABQK02JOCCH | CDS | 93729 | 600 | - | 0.271667 | |
g6544 | DLA_07289 | GAOABQK02JOCCH | CDS | 96810 | 1707 | + | 0.336262 | |
g6545 | DLA_07290 | GAOABQK02JOCCH | CDS | 98656 | 954 | - | 0.301887 | |
g6546 | DLA_07291 | GAOABQK02JOCCH | CDS | 99768 | 573 | + | 0.298429 | |
g6547 | DLA_07292 | GAOABQK02JOCCH | CDS | 100471 | 261 | - | 0.390805 | |
g6548 | DLA_07293 | GAOABQK02JOCCH | CDS | 101840 | 1251 | + | 0.344524 | |
g6549 | DLA_07294 | GAOABQK02JOCCH | CDS | 103562 | 1458 | + | 0.397119 | |
g655 | DLA_00724 | F4PJNLW01A00V1 | CDS | 41961 | 2124 | - | 0.281544 | |
g6550 | DLA_07295 | GAOABQK02JOCCH | CDS | 105545 | 579 | - | 0.340242 | |
g6551 | DLA_07296 | GAOABQK02JOCCH | CDS | 106491 | 684 | + | 0.255848 | |
g6552 | DLA_07297 | GAOABQK02JOCCH | CDS | 107432 | 1428 | - | 0.338235 | |
g6553 | DLA_07299 | GAOABQK02JOCCH | CDS | 109742 | 2556 | + | 0.384977 | |
g6554 | DLA_07300 | GAOABQK02JOCCH | CDS | 112691 | 4047 | + | 0.302446 | |
g6555 | DLA_07301 | GAOABQK02JOCCH | CDS | 117808 | 3543 | + | 0.307367 | |
g6556 | DLA_07302 | GAOABQK02JOCCH | CDS | 121924 | 4038 | + | 0.312531 | |
g6557 | DLA_07303 | GAOABQK02JOCCH | CDS | 126858 | 3849 | + | 0.315666 | |
g6558 | DLA_07305 | GAOABQK02JOCCH | CDS | 131555 | 1737 | - | 0.287853 | |
g6559 | DLA_07306 | GAOABQK02JOCCH | CDS | 133604 | 852 | - | 0.287559 | |
g656 | DLA_00725 | F4PJNLW01A00V1 | CDS | 44689 | 2286 | - | 0.323272 | |
g6560 | DLA_07308 | GAOABQK02JOCCH | CDS | 135479 | 3258 | - | 0.310927 | |
g6561 | DLA_07310 | GAOABQK02JOCCH | CDS | 139703 | 2958 | + | 0.322177 | |
g6562 | DLA_07313 | GAOABQK02JOCCH | CDS | 143049 | 330 | + | 0.293939 | |
g6563 | DLA_07314 | GAOABQK02JOCCH | CDS | 147275 | 1806 | + | 0.343854 | |
g6564 | DLA_07315 | GAOABQK02JOCCH | CDS | 149496 | 1251 | + | 0.385292 | |
g6565 | DLA_07316 | GAOABQK02JOCCH | CDS | 151107 | 861 | - | 0.335656 | |
g6566 | DLA_07317 | contains 5 transmembrane domains there is a second copy of this gene | GAOABQK02JOCCH | CDS | 152486 | 705 | + | 0.339007 |
g6567 | DLA_07318 | GAOABQK02JOCCH | CDS | 153260 | 1845 | - | 0.313279 | |
g6568 | DLA_07319 | AGC group AKT family protein serinethreonine kinase similar to other metazoan AktPKB including an N-terminal PH domain homologous kinase and C-terminal regulatory domains and phosphorylation sites required for AktPKB activation | GAOABQK02JOCCH | CDS | 155446 | 1314 | + | 0.350837 |
g6569 | DLA_07320 | GAOABQK02JOCCH | CDS | 157284 | 435 | - | 0.397701 | |
g657 | DLA_00726 | F4PJNLW01A00V1 | CDS | 47753 | 474 | + | 0.350211 | |
g6570 | DLA_07321 | GAOABQK02JOCCH | CDS | 158535 | 3507 | + | 0.35586 | |
g6571 | DLA_07322 | GAOABQK02JOCCH | CDS | 162311 | 2259 | - | 0.376715 | |
g6572 | DLA_07323 | GAOABQK02JOCCH | CDS | 165347 | 573 | + | 0.317627 | |
g6573 | DLA_07324 | GAOABQK02JOCCH | CDS | 166129 | 657 | - | 0.334855 | |
g6574 | DLA_07325 | GAOABQK02JOCCH | CDS | 167381 | 663 | + | 0.378582 | |
g6575 | DLA_07326 | GAOABQK02JOCCH | CDS | 168295 | 1659 | + | 0.335744 | |
g6576 | DLA_07327 | GAOABQK02JOCCH | CDS | 170201 | 1485 | + | 0.295623 | |
g6577 | DLA_07328 | GAOABQK02JOCCH | CDS | 172029 | 4065 | - | 0.308979 | |
g6578 | DLA_07329 | GAOABQK02JOCCH | CDS | 178415 | 4065 | - | 0.310947 | |
g6579 | DLA_07330 | GAOABQK02JOCCH | CDS | 183234 | 7974 | - | 0.36318 | |
g658 | DLA_00727 | F4PJNLW01A00V1 | CDS | 48546 | 1665 | + | 0.307508 | |
g6580 | DLA_07331 | GAOABQK02JOCCH | CDS | 192371 | 531 | + | 0.310734 | |
g6581 | DLA_07332 | GAOABQK02JOCCH | CDS | 193042 | 1245 | - | 0.338956 | |
g6582 | DLA_07333 | GAOABQK02JOCCH | CDS | 194838 | 483 | + | 0.310559 | |
g6583 | DLA_07335 | GAOABQK02JOCCH | CDS | 196497 | 339 | + | 0.309735 | |
g6584 | DLA_07337 | GAOABQK02JOCCH | CDS | 198382 | 840 | + | 0.280952 | |
g6585 | DLA_07338 | GAOABQK02JOCCH | CDS | 200693 | 582 | - | 0.338488 | |
g6586 | DLA_07340 | GAOABQK02JOCCH | CDS | 202209 | 2187 | - | 0.3123 | |
g6587 | DLA_07341 | GAOABQK02JOCCH | CDS | 204753 | 912 | + | 0.392544 | |
g6588 | DLA_07342 | GAOABQK02JOCCH | CDS | 206234 | 2118 | - | 0.32814 | |
g6589 | DLA_07343 | GAOABQK02JOCCH | CDS | 208529 | 3237 | - | 0.318505 | |
g659 | DLA_00728 | F4PJNLW01A00V1 | CDS | 50300 | 1050 | - | 0.290476 | |
g6590 | DLA_07344 | GAOABQK02JOCCH | CDS | 211907 | 1029 | - | 0.3207 | |
g6591 | DLA_07345 | GAOABQK02JOCCH | CDS | 213333 | 1383 | + | 0.250181 | |
g6592 | DLA_07346 | GAOABQK02JOCCH | CDS | 214936 | 714 | - | 0.330532 | |
g6593 | DLA_07347 | GAOABQK02JOCCH | CDS | 216090 | 735 | + | 0.27483 | |
g6594 | DLA_07348 | GAOABQK02JOCCH | CDS | 217088 | 1245 | - | 0.319679 | |
g6595 | DLA_11684 | GAOABQK02JOCCH | CDS | 218411 | 1743 | + | 0.27424 | |
g6596 | DLA_07349 | GAOABQK02JOCCH | CDS | 220272 | 3489 | + | 0.273431 | |
g6597 | DLA_11685 | GAOABQK02JOCCH | CDS | 224293 | 858 | - | 0.301865 | |
g6598 | DLA_07350 | GAOABQK02JOCCH | CDS | 225609 | 1236 | - | 0.295307 | |
g6599 | DLA_07351 | GAOABQK02JOCCH | CDS | 228160 | 1170 | - | 0.315385 | |
g66 | DLA_00077 | contig05409_1.exp | CDS | 161135 | 1104 | - | 0.313406 | |
g660 | DLA_00729 | F4PJNLW01A00V1 | CDS | 51694 | 1098 | - | 0.282332 | |
g6600 | DLA_07352 | GAOABQK02JOCCH | CDS | 229712 | 750 | + | 0.354667 | |
g6601 | DLA_07353 | GAOABQK02JOCCH | CDS | 230866 | 1050 | - | 0.339048 | |
g6602 | DLA_07354 | GAOABQK02JOCCH | CDS | 232324 | 2454 | - | 0.362266 | |
g6603 | DLA_11686 | GAOABQK02JOCCH | CDS | 235577 | 954 | - | 0.389937 | |
g6604 | DLA_07355 | GAOABQK02JOCCH | CDS | 237042 | 339 | - | 0.303835 | |
g6605 | DLA_07356 | GAOABQK02JOCCH | CDS | 237571 | 867 | - | 0.306805 | |
g6606 | DLA_07357 | GAOABQK02JOCCH | CDS | 238540 | 1194 | + | 0.253769 | |
g6607 | DLA_07358 | GAOABQK02JOCCH | CDS | 240004 | 12681 | - | 0.328365 | |
g6608 | DLA_07359 | GAOABQK02JOCCH | CDS | 252875 | 2922 | - | 0.343942 | |
g6609 | DLA_07360 | GAOABQK02JOCCH | CDS | 256322 | 1389 | + | 0.339093 | |
g661 | DLA_00730 | F4PJNLW01A00V1 | CDS | 53130 | 1572 | + | 0.283715 | |
g6610 | DLA_07361 | GAOABQK02JOCCH | CDS | 258156 | 1071 | + | 0.294118 | |
g6611 | DLA_07362 | GAOABQK02JOCCH | CDS | 259714 | 1281 | - | 0.333333 | |
g6612 | DLA_07363 | GAOABQK02JOCCH | CDS | 261881 | 6459 | + | 0.343706 | |
g6613 | DLA_07364 | GAOABQK02JOCCH | CDS | 268554 | 1665 | - | 0.306306 | |
g6614 | DLA_07365 | GAOABQK02JOCCH | CDS | 270577 | 426 | - | 0.284038 | |
g6615 | DLA_07366 | GAOABQK02JOCCH | CDS | 271307 | 2067 | + | 0.351717 | |
g6616 | DLA_07367 | GAOABQK02JOCCH | CDS | 273516 | 1341 | - | 0.35123 | |
g6617 | DLA_07368 | GAOABQK02JOCCH | CDS | 276065 | 5565 | + | 0.349865 | |
g6618 | DLA_07369 | GAOABQK02JOCCH | CDS | 281782 | 3228 | - | 0.326518 | |
g6619 | DLA_07371 | GAOABQK02JOCCH | CDS | 286520 | 2859 | - | 0.335432 | |
g662 | DLA_00731 | F4PJNLW01A00V1 | CDS | 55144 | 5109 | + | 0.315717 | |
g6620 | DLA_07373 | GAOABQK02JOCCH | CDS | 290458 | 534 | + | 0.284644 | |
g6621 | DLA_07374 | GAOABQK02JOCCH | CDS | 291118 | 1125 | - | 0.369778 | |
g6622 | DLA_07375 | GAOABQK02JOCCH | CDS | 292426 | 1110 | - | 0.318919 | |
g6623 | DLA_07376 | GAOABQK02JOCCH | CDS | 293651 | 1023 | - | 0.312805 | |
g6624 | DLA_07377 | GAOABQK02JOCCH | CDS | 295220 | 423 | - | 0.321513 | |
g6625 | DLA_07378 | GAOABQK02JOCCH | CDS | 295875 | 606 | - | 0.280528 | |
g6626 | DLA_07379 | GAOABQK02JOCCH | CDS | 296728 | 1443 | + | 0.327096 | |
g6627 | DLA_07380 | GAOABQK02JOCCH | CDS | 298298 | 1572 | - | 0.326336 | |
g6628 | DLA_07381 | GAOABQK02JOCCH | CDS | 300111 | 1581 | - | 0.324478 | |
g6629 | DLA_07382 | GAOABQK02JOCCH | CDS | 301931 | 8622 | - | 0.350847 | |
g663 | DLA_00732 | F4PJNLW01A00V1 | CDS | 60841 | 852 | - | 0.319249 | |
g6630 | DLA_07383 | GAOABQK02JOCCH | CDS | 312345 | 1431 | + | 0.321454 | |
g6631 | DLA_07384 | GAOABQK02JOCCH | CDS | 313908 | 501 | - | 0.317365 | |
g6632 | DLA_07385 | GAOABQK02JOCCH | CDS | 314715 | 462 | - | 0.331169 | |
g6633 | DLA_07386 | GAOABQK02JOCCH | CDS | 315674 | 1044 | + | 0.310345 | |
g6634 | DLA_07388 | GAOABQK02JOCCH | CDS | 316735 | 426 | - | 0.302817 | |
g6635 | DLA_07389 | GAOABQK02JOCCH | CDS | 318164 | 1002 | + | 0.357285 | |
g6636 | DLA_07391 | GAOABQK02JOCCH | CDS | 319799 | 5493 | + | 0.298744 | |
g6637 | DLA_07392 | GAOABQK02JOCCH | CDS | 326514 | 807 | - | 0.322181 | |
g6638 | DLA_07393 | GAOABQK02JOCCH | CDS | 329029 | 549 | - | 0.304189 | |
g6639 | DLA_07395 | GAOABQK02JOCCH | CDS | 330331 | 3600 | + | 0.364444 | |
g664 | DLA_00733 | F4PJNLW01A00V1 | CDS | 61950 | 2313 | - | 0.279291 | |
g6640 | DLA_07396 | GAOABQK02JOCCH | CDS | 334124 | 867 | - | 0.324106 | |
g6641 | DLA_07397 | GAOABQK02JOCCH | CDS | 335204 | 921 | - | 0.273616 | |
g6642 | DLA_07398 | GAOABQK02JOCCH | CDS | 336249 | 273 | + | 0.322344 | |
g6643 | DLA_07399 | GAOABQK02JOCCH | CDS | 336816 | 723 | - | 0.318119 | |
g6644 | DLA_07400 | GAOABQK02JOCCH | CDS | 337771 | 756 | - | 0.37963 | |
g6645 | DLA_07401 | GAOABQK02JOCCH | CDS | 338999 | 327 | + | 0.302752 | |
g6646 | DLA_07402 | GAOABQK02JOCCH | CDS | 340215 | 2226 | - | 0.319407 | |
g6647 | DLA_07403 | GAOABQK02JOCCH | CDS | 343924 | 1209 | - | 0.349876 | |
g6648 | DLA_07404 | GAOABQK02JOCCH | CDS | 345395 | 348 | + | 0.258621 | |
g6649 | DLA_07405 | GAOABQK02JOCCH | CDS | 345937 | 486 | + | 0.251029 | |
g665 | DLA_00735 | F4PJNLW01A00V1 | CDS | 65491 | 1167 | + | 0.353042 | |
g6650 | DLA_07406 | GAOABQK02JOCCH | CDS | 346876 | 2601 | - | 0.306036 | |
g6651 | DLA_07408 | GAOABQK02JOCCH | CDS | 350435 | 1887 | + | 0.344462 | |
g6652 | DLA_07409 | GAOABQK02JOCCH | CDS | 352531 | 630 | - | 0.306349 | |
g6653 | DLA_07410 | GAOABQK02JOCCH | CDS | 353884 | 969 | + | 0.341589 | |
g6654 | DLA_07411 | GAOABQK02JOCCH | CDS | 354952 | 2757 | - | 0.295611 | |
g6655 | DLA_07413 | GAOABQK02JOCCH | CDS | 358428 | 1854 | + | 0.313376 | |
g6656 | DLA_07414 | GAOABQK02JOCCH | CDS | 361079 | 3303 | + | 0.328489 | |
g6657 | DLA_07415 | GAOABQK02JOCCH | CDS | 364574 | 1131 | + | 0.365164 | |
g6658 | DLA_07417 | GAOABQK02JOCCH | CDS | 366226 | 1464 | - | 0.314208 | |
g6659 | DLA_07418 | GAOABQK02JOCCH | CDS | 368041 | 744 | - | 0.337366 | |
g666 | DLA_00736 | F4PJNLW01A00V1 | CDS | 66823 | 444 | - | 0.331081 | |
g6660 | DLA_07419 | GAOABQK02JOCCH | CDS | 369780 | 1896 | - | 0.323312 | |
g6661 | DLA_07422 | GAOABQK02JOCCH | CDS | 372773 | 609 | - | 0.303777 | |
g6662 | DLA_07423 | GAOABQK02JOCCH | CDS | 374628 | 546 | - | 0.283883 | |
g6663 | DLA_07424 | GAOABQK02JOCCH | CDS | 376389 | 1104 | - | 0.380435 | |
g6664 | DLA_07425 | GAOABQK02JOCCH | CDS | 378435 | 1008 | - | 0.3125 | |
g6665 | DLA_07426 | GAOABQK02JOCCH | CDS | 379642 | 2760 | + | 0.292754 | |
g6666 | DLA_07427 | GAOABQK02JOCCH | CDS | 382585 | 747 | - | 0.349398 | |
g6667 | DLA_07428 | GAOABQK02JOCCH | CDS | 383578 | 390 | - | 0.34359 | |
g6668 | DLA_07429 | GAOABQK02JOCCH | CDS | 388992 | 606 | + | 0.244224 | |
g6669 | DLA_11687 | GAOABQK02JOCCH | CDS | 390115 | 552 | + | 0.293478 | |
g667 | DLA_00737 | F4PJNLW01A00V1 | CDS | 67871 | 738 | - | 0.390244 | |
g6670 | DLA_07430 | GAOABQK02JOCCH | CDS | 391397 | 2022 | - | 0.329377 | |
g6671 | DLA_07431 | GAOABQK02JOCCH | CDS | 393899 | 2295 | - | 0.334205 | |
g6672 | DLA_07432 | GAOABQK02JOCCH | CDS | 397149 | 2121 | - | 0.320603 | |
g6673 | DLA_07433 | GAOABQK02JOCCH | CDS | 399799 | 2340 | - | 0.336752 | |
g6674 | DLA_07435 | GAOABQK02JOCCH | CDS | 403183 | 3987 | + | 0.346627 | |
g6675 | DLA_07436 | GAOABQK02JOCCH | CDS | 407743 | 1149 | + | 0.366406 | |
g6676 | DLA_07437 | GAOABQK02JOCCH | CDS | 409143 | 885 | - | 0.327684 | |
g6677 | DLA_11688 | GAOABQK02JOCCH | CDS | 410178 | 936 | - | 0.275641 | |
g6678 | DLA_07438 | GAOABQK02JOCCH | CDS | 413316 | 432 | - | 0.333333 | |
g6679 | DLA_07439 | GAOABQK02JOCCH | CDS | 414241 | 1386 | - | 0.368687 | |
g668 | DLA_00738 | F4PJNLW01A00V1 | CDS | 69380 | 1170 | + | 0.298291 | |
g6680 | DLA_07440 | GAOABQK02JOCCH | CDS | 416128 | 900 | + | 0.377778 | |
g6681 | DLA_07441 | GAOABQK02JOCCH | CDS | 417275 | 1857 | + | 0.339257 | |
g6682 | DLA_07442 | GAOABQK02JOCCH | CDS | 419533 | 474 | + | 0.295359 | |
g6683 | DLA_07443 | GAOABQK02JOCCH | CDS | 420845 | 3360 | - | 0.332738 | |
g6684 | DLA_07444 | GAOABQK02JOCCH | CDS | 425342 | 411 | + | 0.304136 | |
g6685 | DLA_07445 | GAOABQK02JOCCH | CDS | 426048 | 2004 | - | 0.313872 | |
g6686 | DLA_07446 | GAOABQK02JOCCH | CDS | 428514 | 2859 | - | 0.317943 | |
g6687 | DLA_07447 | GAOABQK02JOCCH | CDS | 431732 | 1089 | - | 0.372819 | |
g6688 | DLA_07448 | GAOABQK02JOCCH | CDS | 433357 | 1290 | + | 0.302326 | |
g6689 | DLA_07449 | GAOABQK02JOCCH | CDS | 434842 | 1197 | - | 0.314954 | |
g669 | DLA_00739 | F4PJNLW01A00V1 | CDS | 70760 | 3471 | - | 0.312014 | |
g6690 | DLA_07450 | similar to aquaporin family of water-channel proteins expressed in prespore cells | GAOABQK02JOCCH | CDS | 436199 | 825 | - | 0.386667 |
g6691 | DLA_07452 | GAOABQK02JOCCH | CDS | 437931 | 624 | + | 0.323718 | |
g6692 | DLA_07453 | GAOABQK02JOCCH | CDS | 439283 | 2997 | - | 0.340007 | |
g6693 | DLA_07454 | GAOABQK02JOCCH | CDS | 443607 | 885 | + | 0.319774 | |
g6694 | DLA_07455 | GAOABQK02JOCCH | CDS | 444715 | 1041 | - | 0.306436 | |
g6695 | DLA_07456 | GAOABQK02JOCCH | CDS | 446164 | 1017 | - | 0.321534 | |
g6696 | DLA_07457 | GAOABQK02JOCCH | CDS | 447460 | 1428 | + | 0.27381 | |
g6697 | DLA_07458 | GAOABQK02JOCCH | CDS | 449198 | 2064 | - | 0.33188 | |
g6698 | DLA_07459 | GAOABQK02JOCCH | CDS | 451732 | 909 | + | 0.326733 | |
g6699 | DLA_07460 | GAOABQK02JOCCH | CDS | 452924 | 1515 | - | 0.29571 | |
g67 | DLA_00078 | component of the RNA polymerase I complex ortholog of S. cerevisiae RPA135 | contig05409_1.exp | CDS | 162866 | 3342 | - | 0.3462 |
g670 | DLA_00740 | F4PJNLW01A00V1 | CDS | 74728 | 1353 | + | 0.350333 | |
g6700 | DLA_07461 | GAOABQK02JOCCH | CDS | 454566 | 906 | + | 0.252759 | |
g6701 | DLA_07462 | GAOABQK02JOCCH | CDS | 455668 | 993 | - | 0.326284 | |
g6702 | DLA_07463 | GAOABQK02JOCCH | CDS | 457011 | 684 | + | 0.254386 | |
g6703 | DLA_07464 | GAOABQK02JOCCH | CDS | 458009 | 558 | - | 0.31362 | |
g6704 | DLA_07465 | GAOABQK02JOCCH | CDS | 459234 | 1173 | - | 0.329923 | |
g6705 | DLA_07466 | ortholog of human APOA1BP S. pombe mug182 | GAOABQK02JOCCH | CDS | 460852 | 987 | - | 0.35461 |
g6706 | DLA_07468 | GAOABQK02JOCCH | CDS | 462640 | 657 | - | 0.342466 | |
g6707 | DLA_07469 | GAOABQK02JOCCH | CDS | 464173 | 951 | + | 0.336488 | |
g6708 | DLA_07470 | GAOABQK02JOCCH | CDS | 465219 | 1446 | + | 0.331259 | |
g6709 | DLA_07471 | GAOABQK02JOCCH | CDS | 466788 | 552 | - | 0.286232 | |
g671 | DLA_00741 | F4PJNLW01A00V1 | CDS | 76363 | 5484 | - | 0.30434 | |
g6710 | DLA_07472 | GAOABQK02JOCCH | CDS | 467845 | 2673 | - | 0.329592 | |
g6711 | DLA_07474 | GAOABQK02JOCCH | CDS | 471109 | 7059 | - | 0.374982 | |
g6712 | DLA_07475 | GAOABQK02JOCCH | CDS | 478671 | 2856 | + | 0.290966 | |
g6713 | DLA_07478 | GAOABQK02JOCCH | CDS | 483707 | 303 | + | 0.287129 | |
g6714 | DLA_07479 | GAOABQK02JOCCH | CDS | 484033 | 447 | - | 0.259508 | |
g6715 | DLA_07480 | GAOABQK02JOCCH | CDS | 484720 | 2208 | - | 0.275815 | |
g6716 | DLA_07481 | GAOABQK02JOCCH | CDS | 487529 | 2154 | - | 0.327298 | |
g6717 | DLA_07482 | GAOABQK02JOCCH | CDS | 490199 | 2037 | - | 0.361807 | |
g6718 | DLA_07483 | ortholog of peroxin 4 a peroxisomal ubiquitin conjugating enzyme required for peroxisomal matrix protein import and peroxisome biogenesis | GAOABQK02JOCCH | CDS | 492752 | 678 | - | 0.306785 |
g6719 | DLA_07484 | GAOABQK02JOCCH | CDS | 493773 | 855 | + | 0.297076 | |
g672 | DLA_11447 | F4PJNLW01A00V1 | CDS | 81977 | 1602 | - | 0.318352 | |
g6720 | DLA_07485 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GAOABQK02JOCCH | CDS | 494830 | 1011 | - | 0.318497 |
g6721 | DLA_07486 | GAOABQK02JOCCH | CDS | 496650 | 3603 | - | 0.34277 | |
g6722 | DLA_07487 | GAOABQK02JOCCH | CDS | 501224 | 5244 | + | 0.345728 | |
g6723 | DLA_07488 | GAOABQK02JOCCH | CDS | 506545 | 918 | - | 0.299564 | |
g6724 | DLA_07489 | GAOABQK02JOCCH | CDS | 507907 | 1743 | - | 0.353987 | |
g6725 | DLA_07491 | GAOABQK02JOCCH | CDS | 510968 | 2076 | - | 0.338632 | |
g6726 | DLA_07492 | GAOABQK02JOCCH | CDS | 513442 | 261 | + | 0.329502 | |
g6727 | DLA_07493 | GAOABQK02JOCCH | CDS | 514738 | 2802 | - | 0.350107 | |
g6728 | DLA_07494 | GAOABQK02JOCCH | CDS | 519675 | 282 | + | 0.336879 | |
g6729 | DLA_07495 | GAOABQK02JOCCH | CDS | 520324 | 3249 | + | 0.284395 | |
g673 | DLA_00742 | F4PJNLW01A00V1 | CDS | 83911 | 1125 | + | 0.304889 | |
g6730 | DLA_07496 | GAOABQK02JOCCH | CDS | 524480 | 3012 | + | 0.281208 | |
g6731 | DLA_07497 | GAOABQK02JOCCH | CDS | 527724 | 1686 | - | 0.281139 | |
g6732 | DLA_07498 | GAOABQK02JOCCH | CDS | 530184 | 588 | + | 0.370748 | |
g6733 | DLA_07499 | GAOABQK02JOCCH | CDS | 531146 | 531 | - | 0.303201 | |
g6734 | DLA_07500 | GAOABQK02JOCCH | CDS | 532191 | 1329 | - | 0.34161 | |
g6735 | DLA_07501 | GAOABQK02JOCCH | CDS | 534441 | 861 | - | 0.341463 | |
g6736 | DLA_07502 | GAOABQK02JOCCH | CDS | 536088 | 1155 | + | 0.31342 | |
g6737 | DLA_07503 | GAOABQK02JOCCH | CDS | 537620 | 3087 | - | 0.308066 | |
g6738 | DLA_07504 | GAOABQK02JOCCH | CDS | 541359 | 639 | - | 0.334898 | |
g6739 | DLA_07505 | GAOABQK02JOCCH | CDS | 542233 | 1338 | - | 0.316143 | |
g674 | DLA_00743 | F4PJNLW01A00V1 | CDS | 85489 | 1101 | - | 0.326975 | |
g6740 | DLA_07506 | GAOABQK02JOCCH | CDS | 544248 | 2379 | + | 0.337537 | |
g6741 | DLA_07507 | GAOABQK02JOCCH | CDS | 546798 | 1653 | - | 0.30732 | |
g6742 | DLA_07508 | GAOABQK02JOCCH | CDS | 548672 | 879 | + | 0.343572 | |
g6743 | DLA_07509 | GAOABQK02JOCCH | CDS | 550102 | 879 | - | 0.34471 | |
g6744 | DLA_07510 | GAOABQK02JOCCH | CDS | 552770 | 2706 | - | 0.36031 | |
g6745 | DLA_07511 | GAOABQK02JOCCH | CDS | 556022 | 1062 | - | 0.304143 | |
g6746 | DLA_07512 | GAOABQK02JOCCH | CDS | 558615 | 492 | - | 0.365854 | |
g6747 | DLA_07513 | GAOABQK02JOCCH | CDS | 559473 | 1011 | + | 0.333333 | |
g6748 | DLA_07514 | GAOABQK02JOCCH | CDS | 560934 | 2172 | - | 0.351289 | |
g6749 | DLA_07515 | GAOABQK02JOCCH | CDS | 564907 | 1167 | + | 0.337618 | |
g675 | DLA_00744 | F4PJNLW01A00V1 | CDS | 86826 | 717 | + | 0.331939 | |
g6750 | DLA_07516 | GAOABQK02JOCCH | CDS | 566237 | 573 | - | 0.294939 | |
g6751 | DLA_07517 | GAOABQK02JOCCH | CDS | 567413 | 1461 | + | 0.365503 | |
g6752 | DLA_07519 | GAOABQK02JOCCH | CDS | 569846 | 8064 | - | 0.352679 | |
g6753 | DLA_07521 | GAOABQK02JOCCH | CDS | 581627 | 1803 | + | 0.36051 | |
g6754 | DLA_07522 | GAOABQK02JOCCH | CDS | 584352 | 1605 | + | 0.338318 | |
g6755 | DLA_07523 | GAOABQK02JOCCH | CDS | 586643 | 1677 | + | 0.319022 | |
g6756 | DLA_07524 | GAOABQK02JOCCH | CDS | 588961 | 2115 | - | 0.336643 | |
g6757 | DLA_07525 | GAOABQK02JOCCH | CDS | 595310 | 516 | - | 0.337209 | |
g6758 | DLA_07526 | GAOABQK02JOCCH | CDS | 596046 | 1362 | + | 0.31351 | |
g6759 | DLA_07528 | GAOABQK02JOCCH | CDS | 597731 | 2229 | - | 0.368775 | |
g676 | DLA_00745 | F4PJNLW01A00V1 | CDS | 87632 | 1698 | - | 0.312721 | |
g6760 | DLA_07530 | GAOABQK02JOCCH | CDS | 601599 | 1413 | + | 0.300778 | |
g6761 | DLA_07531 | GAOABQK02JOCCH | CDS | 603442 | 267 | + | 0.322097 | |
g6762 | DLA_07532 | GAOABQK02JOCCH | CDS | 603884 | 1425 | - | 0.304561 | |
g6763 | DLA_07534 | GAOABQK02JOCCH | CDS | 605634 | 567 | - | 0.308642 | |
g6764 | DLA_07535 | GAOABQK02JOCCH | CDS | 606288 | 3144 | - | 0.326654 | |
g6765 | DLA_07536 | GAOABQK02JOCCH | CDS | 609612 | 819 | + | 0.252747 | |
g6766 | DLA_07538 | catalyzes the reaction UDP-glucose UDP-galactose expressed in prespore cells | GAOABQK02JOCCH | CDS | 610615 | 1101 | - | 0.360581 |
g6767 | DLA_07539 | GAOABQK02JOCCH | CDS | 612594 | 942 | - | 0.323779 | |
g6768 | DLA_07540 | GAOABQK02JOCCH | CDS | 613883 | 3288 | - | 0.314173 | |
g6769 | DLA_07541 | GAOABQK02JOCCH | CDS | 617478 | 2157 | + | 0.320352 | |
g677 | DLA_00746 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | F4PJNLW01A00V1 | CDS | 89633 | 792 | - | 0.301768 |
g6770 | DLA_07542 | GAOABQK02JOCCH | CDS | 619823 | 381 | - | 0.293963 | |
g6771 | DLA_07543 | GAOABQK02JOCCH | CDS | 620905 | 738 | + | 0.311653 | |
g6772 | DLA_07544 | GAOABQK02JOCCH | CDS | 621947 | 570 | + | 0.352632 | |
g6773 | DLA_07545 | GAOABQK02JOCCH | CDS | 622703 | 1878 | + | 0.3541 | |
g6774 | DLA_07546 | GAOABQK02JOCCH | CDS | 624963 | 573 | + | 0.312391 | |
g6775 | DLA_07547 | GAOABQK02JOCCH | CDS | 625765 | 420 | - | 0.280952 | |
g6776 | DLA_07548 | GAOABQK02JOCCH | CDS | 626390 | 576 | + | 0.289931 | |
g6777 | DLA_07549 | GAOABQK02JOCCH | CDS | 627098 | 894 | - | 0.332215 | |
g6778 | DLA_07550 | GAOABQK02JOCCH | CDS | 628320 | 1191 | + | 0.320739 | |
g6779 | DLA_07552 | full transporter consisting of two ABC domains and two transmembrane domains there is a second copy of this gene | GAOABQK02JOCCH | CDS | 630530 | 4362 | - | 0.357863 |
g678 | DLA_00748 | F4PJNLW01A00V1 | CDS | 91087 | 7068 | - | 0.317629 | |
g6780 | DLA_07554 | GAOABQK02JOCCH | CDS | 635615 | 267 | - | 0.28839 | |
g6781 | DLA_07556 | GAOABQK02JOCCH | CDS | 636441 | 1938 | - | 0.329205 | |
g6782 | DLA_07557 | colocalizes with clathrin spots suggesting involvement in endocytosis does not localize to pseudopods in wild type in SCAR depleted mutants WASP replaces the functions of SCAR and localizes to pseudopods | GAOABQK02JOCCH | CDS | 638591 | 1218 | + | 0.426108 |
g6783 | DLA_07558 | catalyzes the reaction N-D-ribosylpurine Hsub2subO purine D-ribose | GAOABQK02JOCCH | CDS | 640398 | 1764 | + | 0.365646 |
g6784 | DLA_07559 | GAOABQK02JOCCH | CDS | 642356 | 573 | + | 0.321117 | |
g6785 | DLA_07560 | very similar to the H. sapiens tumor protein p53-inducible protein 3 (TP53I3) belongs to the broader superfamily of zinc-dependent alcohol dehydrogenases | GAOABQK02JOCCH | CDS | 643131 | 1005 | - | 0.351244 |
g6786 | DLA_07562 | GAOABQK02JOCCH | CDS | 644436 | 1110 | - | 0.311712 | |
g6787 | DLA_07563 | GAOABQK02JOCCH | CDS | 646686 | 3858 | - | 0.369881 | |
g6788 | DLA_07564 | GAOABQK02JOCCH | CDS | 650995 | 1587 | - | 0.333963 | |
g6789 | DLA_07565 | GAOABQK02JOCCH | CDS | 652815 | 3417 | - | 0.347381 | |
g679 | DLA_00749 | F4PJNLW01A00V1 | CDS | 98677 | 858 | + | 0.342657 | |
g6790 | DLA_07568 | GAOABQK02JOCCH | CDS | 658160 | 2007 | + | 0.286996 | |
g6791 | DLA_07569 | GAOABQK02JOCCH | CDS | 660363 | 1011 | + | 0.297725 | |
g6792 | DLA_07570 | GAOABQK02JOCCH | CDS | 661524 | 474 | - | 0.308017 | |
g6793 | DLA_07571 | GAOABQK02JOCCH | CDS | 662693 | 4017 | - | 0.326612 | |
g6794 | DLA_07572 | GAOABQK02JOCCH | CDS | 667015 | 3837 | - | 0.309096 | |
g6795 | DLA_07573 | GAOABQK02JOCCH | CDS | 671476 | 4077 | - | 0.31739 | |
g6796 | DLA_07574 | GAOABQK02JOCCH | CDS | 675831 | 4104 | - | 0.334552 | |
g6797 | DLA_07575 | GAOABQK02JOCCH | CDS | 680387 | 3117 | + | 0.343279 | |
g6798 | DLA_07576 | GAOABQK02JOCCH | CDS | 683653 | 969 | - | 0.330237 | |
g6799 | DLA_07578 | GAOABQK02JOCCH | CDS | 685364 | 771 | + | 0.304799 | |
g68 | DLA_00079 | contig05409_1.exp | CDS | 166524 | 825 | + | 0.304242 | |
g680 | DLA_00750 | F4PJNLW01A00V1 | CDS | 99661 | 993 | - | 0.352467 | |
g6800 | DLA_07579 | GAOABQK02JOCCH | CDS | 688379 | 1458 | + | 0.364198 | |
g6801 | DLA_07580 | GAOABQK02JOCCH | CDS | 690343 | 342 | - | 0.292398 | |
g6802 | DLA_07581 | GAOABQK02JOCCH | CDS | 690898 | 4530 | - | 0.368653 | |
g6803 | DLA_07582 | GAOABQK02JOCCH | CDS | 695808 | 2931 | - | 0.297168 | |
g6804 | DLA_07583 | GAOABQK02JOCCH | CDS | 698998 | 4560 | + | 0.334868 | |
g6805 | DLA_07584 | GAOABQK02JOCCH | CDS | 703635 | 1395 | - | 0.314695 | |
g6806 | DLA_07585 | GAOABQK02JOCCH | CDS | 705181 | 1095 | - | 0.408219 | |
g6807 | DLA_07586 | GAOABQK02JOCCH | CDS | 706659 | 690 | + | 0.304348 | |
g6808 | DLA_07587 | GAOABQK02JOCCH | CDS | 707510 | 2346 | - | 0.349531 | |
g6809 | DLA_07588 | GAOABQK02JOCCH | CDS | 710286 | 2079 | - | 0.326118 | |
g681 | DLA_00751 | F4PJNLW01A00V1 | CDS | 101167 | 666 | + | 0.348348 | |
g6810 | DLA_07589 | GAOABQK02JOCCH | CDS | 714750 | 2040 | + | 0.240196 | |
g6811 | DLA_07591 | GAOABQK02JOCCH | CDS | 717644 | 1812 | + | 0.275386 | |
g6812 | DLA_07592 | GAOABQK02JOCCH | CDS | 719832 | 4098 | - | 0.363836 | |
g6813 | DLA_11689 | GAOABQK02JOCCH | CDS | 724837 | 1344 | - | 0.365327 | |
g6814 | DLA_07593 | GAOABQK02JOCCH | CDS | 726605 | 1503 | - | 0.345975 | |
g6815 | DLA_07594 | GAOABQK02JOCCH | CDS | 728528 | 210 | - | 0.285714 | |
g6816 | DLA_07595 | GAOABQK02JOCCH | CDS | 729101 | 2610 | + | 0.34023 | |
g6817 | DLA_07597 | GAOABQK02JOCCH | CDS | 732920 | 1836 | - | 0.392702 | |
g6818 | DLA_07598 | GAOABQK02JOCCH | CDS | 735519 | 810 | + | 0.317284 | |
g6819 | DLA_07599 | GAOABQK02JOCCH | CDS | 736947 | 1446 | + | 0.379668 | |
g682 | DLA_00752 | F4PJNLW01A00V1 | CDS | 102369 | 1788 | + | 0.362975 | |
g6820 | DLA_07600 | GAOABQK02JOCCH | CDS | 738626 | 2859 | - | 0.308849 | |
g6821 | DLA_07601 | GAOABQK02JOCCH | CDS | 742310 | 1890 | + | 0.367725 | |
g6822 | DLA_11690 | GAOABQK02JOCCH | CDS | 744371 | 1479 | - | 0.363759 | |
g6823 | DLA_07602 | GAOABQK02JOCCH | CDS | 746286 | 1221 | - | 0.320229 | |
g6824 | DLA_07603 | GAOABQK02JOCCH | CDS | 748276 | 321 | - | 0.314642 | |
g6825 | DLA_07604 | GAOABQK02JOCCH | CDS | 749009 | 396 | + | 0.29798 | |
g6826 | DLA_07605 | similar to coiled-coil domain containing protein 43 (CCDC43) contains two predicted coiled-coil domains | GAOABQK02JOCCH | CDS | 749931 | 666 | - | 0.298799 |
g6827 | DLA_07606 | GAOABQK02JOCCH | CDS | 750878 | 1497 | - | 0.342685 | |
g6828 | DLA_07607 | GAOABQK02JOCCH | CDS | 753247 | 1410 | + | 0.324113 | |
g6829 | DLA_07608 | GAOABQK02JOCCH | CDS | 755101 | 1083 | - | 0.358264 | |
g683 | DLA_00753 | F4PJNLW01A00V1 | CDS | 104591 | 912 | - | 0.423246 | |
g6830 | DLA_07609 | GAOABQK02JOCCH | CDS | 756599 | 474 | - | 0.419831 | |
g6831 | DLA_07610 | GAOABQK02JOCCH | CDS | 757796 | 291 | + | 0.340206 | |
g6832 | DLA_07611 | GAOABQK02JOCCH | CDS | 758339 | 1497 | - | 0.321977 | |
g6833 | DLA_07612 | GAOABQK02JOCCH | CDS | 759986 | 1695 | - | 0.373451 | |
g6834 | DLA_07613 | GAOABQK02JOCCH | CDS | 762084 | 654 | + | 0.304281 | |
g6835 | DLA_07614 | GAOABQK02JOCCH | CDS | 762955 | 3699 | - | 0.333333 | |
g6836 | DLA_07615 | GAOABQK02JOCCH | CDS | 767057 | 3144 | - | 0.374682 | |
g6837 | DLA_07617 | GAOABQK02JOCCH | CDS | 771336 | 1071 | + | 0.331466 | |
g6838 | DLA_07620 | GAOABQK02JOCCH | CDS | 773463 | 1722 | + | 0.271777 | |
g6839 | DLA_07621 | GAOABQK02JOCCH | CDS | 775507 | 6165 | + | 0.323114 | |
g684 | DLA_00754 | F4PJNLW01A00V1 | CDS | 105851 | 828 | - | 0.262077 | |
g6840 | DLA_07622 | GAOABQK02JOCCH | CDS | 782658 | 975 | + | 0.265641 | |
g6841 | DLA_07624 | GAOABQK02JOCCH | CDS | 784612 | 1059 | + | 0.324835 | |
g6842 | DLA_07625 | GAOABQK02JOCCH | CDS | 785902 | 2406 | + | 0.309643 | |
g6843 | DLA_07626 | GAOABQK02JOCCH | CDS | 788486 | 1056 | - | 0.327652 | |
g6844 | DLA_07628 | GAOABQK02JOCCH | CDS | 790410 | 2037 | - | 0.305842 | |
g6845 | DLA_07630 | GAOABQK02JOCCH | CDS | 792941 | 1722 | - | 0.290941 | |
g6846 | DLA_07631 | GAOABQK02JOCCH | CDS | 795642 | 1263 | + | 0.326207 | |
g6847 | DLA_07632 | GAOABQK02JOCCH | CDS | 797187 | 420 | - | 0.285714 | |
g6848 | DLA_07633 | GAOABQK02JOCCH | CDS | 798148 | 1809 | + | 0.310669 | |
g6849 | DLA_07634 | GAOABQK02JOCCH | CDS | 800425 | 231 | + | 0.363636 | |
g685 | DLA_00755 | F4PJNLW01A00V1 | CDS | 106754 | 1449 | + | 0.289165 | |
g6850 | DLA_07635 | GAOABQK02JOCCH | CDS | 800717 | 549 | + | 0.35337 | |
g6851 | DLA_07636 | GAOABQK02JOCCH | CDS | 801411 | 492 | - | 0.339431 | |
g6852 | DLA_07637 | GAOABQK02JOCCH | CDS | 802160 | 1809 | + | 0.317855 | |
g6853 | DLA_07638 | GAOABQK02JOCCH | CDS | 804618 | 2301 | - | 0.295524 | |
g6854 | DLA_07639 | GAOABQK02JOCCH | CDS | 807287 | 2367 | + | 0.269117 | |
g6855 | DLA_07641 | GAOABQK02JOCCH | CDS | 809961 | 984 | + | 0.311992 | |
g6856 | DLA_07642 | GAOABQK02JOCCH | CDS | 811111 | 1539 | + | 0.296946 | |
g6857 | DLA_07643 | GAOABQK02JOCCH | CDS | 812714 | 6405 | - | 0.340515 | |
g6858 | DLA_07645 | GAOABQK02JOCCH | CDS | 820122 | 2751 | + | 0.338059 | |
g6859 | DLA_07646 | GAOABQK02JOCCH | CDS | 823009 | 1197 | - | 0.299916 | |
g686 | DLA_00757 | F4PJNLW01A00V1 | CDS | 108444 | 1512 | - | 0.39418 | |
g6860 | DLA_07647 | GAOABQK02JOCCH | CDS | 824529 | 915 | + | 0.330055 | |
g6861 | DLA_07649 | GAOABQK02JOCCH | CDS | 826555 | 1818 | + | 0.309131 | |
g6862 | DLA_07650 | GAOABQK02JOCCH | CDS | 828753 | 1836 | - | 0.351307 | |
g6863 | DLA_07651 | GAOABQK02JOCCH | CDS | 830831 | 2820 | - | 0.322695 | |
g6864 | DLA_07652 | GAOABQK02JOCCH | CDS | 833819 | 2640 | + | 0.311742 | |
g6865 | DLA_07654 | GAOABQK02JOCCH | CDS | 837671 | 1131 | + | 0.312113 | |
g6866 | DLA_07655 | GAOABQK02JOCCH | CDS | 839143 | 2553 | + | 0.302781 | |
g6867 | DLA_07656 | GAOABQK02JOCCH | CDS | 842319 | 1398 | - | 0.344063 | |
g6868 | DLA_07657 | GAOABQK02JOCCH | CDS | 844040 | 1149 | - | 0.375979 | |
g6869 | DLA_07658 | GAOABQK02JOCCH | CDS | 845551 | 1203 | - | 0.294264 | |
g687 | DLA_00758 | F4PJNLW01A00V1 | CDS | 111311 | 2625 | + | 0.34781 | |
g6870 | DLA_07662 | GAOABQK02JOCCH | CDS | 848642 | 1800 | - | 0.260556 | |
g6871 | DLA_07663 | GAOABQK02JOCCH | CDS | 852785 | 1560 | - | 0.271154 | |
g6872 | DLA_07666 | GAOABQK02JOCCH | CDS | 856241 | 894 | - | 0.253915 | |
g6873 | DLA_07667 | GAOABQK02JOCCH | CDS | 857310 | 2301 | - | 0.262495 | |
g6874 | DLA_07669 | GAOABQK02JOCCH | CDS | 862314 | 672 | + | 0.297619 | |
g6875 | DLA_07670 | GAOABQK02JOCCH | CDS | 863277 | 1884 | + | 0.289809 | |
g6876 | DLA_07671 | GAOABQK02JOCCH | CDS | 865389 | 1530 | + | 0.295425 | |
g6877 | DLA_07672 | GAOABQK02JOCCH | CDS | 868441 | 1995 | + | 0.337343 | |
g6878 | DLA_07673 | GAOABQK02JOCCH | CDS | 870609 | 849 | + | 0.316843 | |
g6879 | DLA_07674 | GAOABQK02JOCCH | CDS | 871578 | 2889 | - | 0.301488 | |
g688 | DLA_00759 | F4PJNLW01A00V1 | CDS | 114128 | 3147 | - | 0.288529 | |
g6880 | DLA_11691 | GAOABQK02JOCCH | CDS | 875207 | 210 | + | 0.333333 | |
g6881 | DLA_07675 | GAOABQK02JOCCH | CDS | 875703 | 1035 | + | 0.354589 | |
g6882 | DLA_07676 | GAOABQK02JOCCH | CDS | 876856 | 1569 | + | 0.3174 | |
g6883 | DLA_07677 | GAOABQK02JOCCH | CDS | 880767 | 1194 | + | 0.326633 | |
g6884 | DLA_07678 | Band 4.1 contains the FERM domain found in a number of cytoskeletal-associated proteins and involved in the linkage of cytoplasmic proteins to the membrane | GAOABQK02JOCCH | CDS | 882447 | 1389 | - | 0.318934 |
g6885 | DLA_07681 | GLQOFTK02FH5TG | CDS | 1853 | 2370 | - | 0.412658 | |
g6886 | DLA_07682 | GLQOFTK02FH5TG | CDS | 4995 | 1023 | + | 0.307918 | |
g6887 | DLA_07683 | GLQOFTK02FH5TG | CDS | 6135 | 795 | - | 0.291824 | |
g6888 | DLA_07684 | GLQOFTK02FH5TG | CDS | 7080 | 1533 | - | 0.283105 | |
g6889 | DLA_07685 | GLQOFTK02FH5TG | CDS | 8846 | 2778 | - | 0.302736 | |
g689 | DLA_00761 | F4PJNLW01A00V1 | CDS | 118427 | 1425 | + | 0.327719 | |
g6890 | DLA_07686 | GLQOFTK02FH5TG | CDS | 11930 | 786 | - | 0.349873 | |
g6891 | DLA_07687 | GLQOFTK02FH5TG | CDS | 13232 | 609 | - | 0.316913 | |
g6892 | DLA_07688 | GLQOFTK02FH5TG | CDS | 14234 | 1314 | + | 0.255708 | |
g6893 | DLA_07689 | GLQOFTK02FH5TG | CDS | 15683 | 1479 | - | 0.284652 | |
g6894 | DLA_07690 | GLQOFTK02FH5TG | CDS | 19522 | 1401 | + | 0.33262 | |
g6895 | DLA_11692 | GLQOFTK02FH5TG | CDS | 21876 | 954 | + | 0.305031 | |
g6896 | DLA_07691 | GLQOFTK02FH5TG | CDS | 23014 | 1419 | + | 0.347428 | |
g6897 | DLA_07692 | GLQOFTK02FH5TG | CDS | 24610 | 693 | - | 0.326118 | |
g6898 | DLA_07693 | GLQOFTK02FH5TG | CDS | 25999 | 3165 | - | 0.304897 | |
g6899 | DLA_07694 | GLQOFTK02FH5TG | CDS | 29301 | 3255 | - | 0.288479 | |
g69 | DLA_00080 | contig05409_1.exp | CDS | 167452 | 2208 | - | 0.27808 | |
g690 | DLA_00762 | F4PJNLW01A00V1 | CDS | 120103 | 282 | - | 0.368794 | |
g6900 | DLA_07695 | GLQOFTK02FH5TG | CDS | 32872 | 462 | + | 0.322511 | |
g6901 | DLA_07696 | GLQOFTK02FH5TG | CDS | 33525 | 1086 | - | 0.298343 | |
g6902 | DLA_07697 | GLQOFTK02FH5TG | CDS | 35293 | 1161 | + | 0.329888 | |
g6903 | DLA_07698 | GLQOFTK02FH5TG | CDS | 36662 | 2406 | - | 0.375727 | |
g6904 | DLA_07699 | GLQOFTK02FH5TG | CDS | 39781 | 2802 | + | 0.29586 | |
g6905 | DLA_07700 | GLQOFTK02FH5TG | CDS | 42878 | 591 | - | 0.314721 | |
g6906 | DLA_07701 | GLQOFTK02FH5TG | CDS | 43842 | 1752 | - | 0.277397 | |
g6907 | DLA_07702 | GLQOFTK02FH5TG | CDS | 46924 | 774 | + | 0.268734 | |
g6908 | DLA_07703 | GLQOFTK02FH5TG | CDS | 47920 | 3033 | + | 0.338609 | |
g6909 | DLA_07705 | GLQOFTK02FH5TG | CDS | 51342 | 663 | - | 0.26546 | |
g691 | DLA_00763 | F4PJNLW01A00V1 | CDS | 120597 | 2127 | + | 0.332863 | |
g6910 | DLA_07706 | GLQOFTK02FH5TG | CDS | 52915 | 1503 | + | 0.342648 | |
g6911 | DLA_07707 | GLQOFTK02FH5TG | CDS | 54997 | 1104 | + | 0.326087 | |
g6912 | DLA_07708 | GLQOFTK02FH5TG | CDS | 56325 | 366 | - | 0.401639 | |
g6913 | DLA_07709 | GLQOFTK02FH5TG | CDS | 57378 | 1998 | + | 0.325826 | |
g6914 | DLA_07710 | GLQOFTK02FH5TG | CDS | 59516 | 2574 | - | 0.289044 | |
g6915 | DLA_07711 | GLQOFTK02FH5TG | CDS | 62523 | 1221 | - | 0.269451 | |
g6916 | DLA_07713 | GLQOFTK02FH5TG | CDS | 64083 | 3045 | - | 0.299836 | |
g6917 | DLA_07714 | GLQOFTK02FH5TG | CDS | 67516 | 1473 | - | 0.325187 | |
g6918 | DLA_07716 | GLQOFTK02FH5TG | CDS | 69545 | 3681 | + | 0.30182 | |
g6919 | DLA_07717 | GLQOFTK02FH5TG | CDS | 73488 | 1623 | + | 0.321627 | |
g692 | DLA_00764 | F4PJNLW01A00V1 | CDS | 123009 | 1257 | + | 0.412888 | |
g6920 | DLA_07718 | GLQOFTK02FH5TG | CDS | 75446 | 885 | + | 0.293785 | |
g6921 | DLA_07719 | GLQOFTK02FH5TG | CDS | 76451 | 4755 | - | 0.320715 | |
g6922 | DLA_07720 | GLQOFTK02FH5TG | CDS | 81498 | 2283 | - | 0.272449 | |
g6923 | DLA_07721 | GLQOFTK02FH5TG | CDS | 84388 | 2478 | + | 0.317191 | |
g6924 | DLA_07722 | GLQOFTK02FH5TG | CDS | 87054 | 804 | + | 0.30597 | |
g6925 | DLA_07723 | GLQOFTK02FH5TG | CDS | 88135 | 1224 | - | 0.269608 | |
g6926 | DLA_07724 | GLQOFTK02FH5TG | CDS | 89491 | 309 | + | 0.275081 | |
g6927 | DLA_07725 | GLQOFTK02FH5TG | CDS | 89928 | 1617 | - | 0.337044 | |
g6928 | DLA_07726 | GLQOFTK02FH5TG | CDS | 91993 | 2859 | + | 0.359916 | |
g6929 | DLA_11693 | GLQOFTK02FH5TG | CDS | 95960 | 2934 | + | 0.316633 | |
g693 | DLA_00765 | F4PJNLW01A00V1 | CDS | 124627 | 1254 | + | 0.357257 | |
g6930 | DLA_07727 | GLQOFTK02FH5TG | CDS | 99251 | 1437 | + | 0.281837 | |
g6931 | DLA_07728 | GLQOFTK02FH5TG | CDS | 101211 | 945 | + | 0.277249 | |
g6932 | DLA_07729 | GLQOFTK02FH5TG | CDS | 102202 | 711 | - | 0.305204 | |
g6933 | DLA_07730 | GLQOFTK02FH5TG | CDS | 103350 | 1941 | - | 0.320453 | |
g6934 | DLA_07732 | GLQOFTK02FH5TG | CDS | 105789 | 1641 | - | 0.285192 | |
g6935 | DLA_07733 | GLQOFTK02FH5TG | CDS | 107567 | 3393 | - | 0.336281 | |
g6936 | DLA_07734 | GLQOFTK02FH5TG | CDS | 111631 | 792 | - | 0.421717 | |
g6937 | DLA_04686 | GLQOFTK02FH5TG | CDS | 112858 | 411 | - | 0.29927 | |
g6938 | DLA_07736 | GLQOFTK02FH5TG | CDS | 113643 | 1098 | + | 0.325137 | |
g6939 | DLA_07737 | GLQOFTK02FH5TG | CDS | 115079 | 567 | - | 0.37037 | |
g694 | DLA_00766 | F4PJNLW01A00V1 | CDS | 125928 | 1743 | - | 0.292599 | |
g6940 | DLA_07738 | GLQOFTK02FH5TG | CDS | 116003 | 1692 | - | 0.298463 | |
g6941 | DLA_07739 | GLQOFTK02FH5TG | CDS | 117917 | 1092 | + | 0.338828 | |
g6942 | DLA_07740 | putative protein serinethreonine kinase the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 119247 | 2916 | + | 0.315844 |
g6943 | DLA_07742 | belongs to the POT (proton-dependent oligopeptide transport) family contains 12 putative transmembrane domains | GLQOFTK02FH5TG | CDS | 123038 | 1920 | + | 0.331771 |
g6944 | DLA_11694 | GLQOFTK02FH5TG | CDS | 125162 | 408 | - | 0.276961 | |
g6945 | DLA_07743 | GLQOFTK02FH5TG | CDS | 126283 | 699 | - | 0.274678 | |
g6946 | DLA_07744 | GLQOFTK02FH5TG | CDS | 127258 | 2967 | - | 0.285811 | |
g6947 | DLA_07745 | GLQOFTK02FH5TG | CDS | 131271 | 654 | + | 0.310398 | |
g6948 | DLA_07746 | GLQOFTK02FH5TG | CDS | 133532 | 600 | + | 0.333333 | |
g6949 | DLA_07747 | GLQOFTK02FH5TG | CDS | 134378 | 354 | + | 0.268362 | |
g695 | DLA_00767 | F4PJNLW01A00V1 | CDS | 127817 | 5166 | - | 0.392373 | |
g6950 | DLA_07748 | GLQOFTK02FH5TG | CDS | 134949 | 351 | - | 0.299145 | |
g6951 | DLA_07749 | GLQOFTK02FH5TG | CDS | 135633 | 474 | + | 0.297468 | |
g6952 | DLA_07750 | GLQOFTK02FH5TG | CDS | 136273 | 2754 | - | 0.327161 | |
g6953 | DLA_07751 | GLQOFTK02FH5TG | CDS | 139461 | 2937 | - | 0.345591 | |
g6954 | DLA_07752 | GLQOFTK02FH5TG | CDS | 143222 | 4212 | - | 0.340456 | |
g6955 | DLA_07753 | highly similar to PRS involved in nucleotide histidine and tryptophan biosynthesis | GLQOFTK02FH5TG | CDS | 148168 | 957 | + | 0.366771 |
g6956 | DLA_07754 | belongs to the substrate carrier proteins that are involved in energy transferbrbr bCommunity annotation:b Overview of the | GLQOFTK02FH5TG | CDS | 149346 | 1002 | + | 0.353293 |
g6957 | DLA_07755 | GLQOFTK02FH5TG | CDS | 150469 | 1818 | - | 0.309131 | |
g6958 | DLA_07756 | GLQOFTK02FH5TG | CDS | 152472 | 1140 | - | 0.307018 | |
g6959 | DLA_07757 | GLQOFTK02FH5TG | CDS | 154096 | 336 | - | 0.300595 | |
g696 | DLA_00769 | F4PJNLW01A00V1 | CDS | 134290 | 240 | + | 0.304167 | |
g6960 | DLA_07758 | GLQOFTK02FH5TG | CDS | 155458 | 1305 | - | 0.324904 | |
g6961 | DLA_07759 | GLQOFTK02FH5TG | CDS | 157252 | 1926 | - | 0.346314 | |
g6962 | DLA_07760 | GLQOFTK02FH5TG | CDS | 159480 | 2742 | + | 0.310357 | |
g6963 | DLA_07761 | GLQOFTK02FH5TG | CDS | 162248 | 3084 | - | 0.308366 | |
g6964 | DLA_07762 | GLQOFTK02FH5TG | CDS | 165978 | 2784 | - | 0.368175 | |
g6965 | DLA_07763 | GLQOFTK02FH5TG | CDS | 169365 | 1272 | + | 0.323899 | |
g6966 | DLA_07764 | GLQOFTK02FH5TG | CDS | 170711 | 2202 | - | 0.368756 | |
g6967 | DLA_07765 | GLQOFTK02FH5TG | CDS | 173393 | 885 | + | 0.362712 | |
g6968 | DLA_07766 | GLQOFTK02FH5TG | CDS | 174550 | 3987 | - | 0.318786 | |
g6969 | DLA_07767 | GLQOFTK02FH5TG | CDS | 179062 | 2796 | - | 0.363019 | |
g697 | DLA_00770 | F4PJNLW01A00V1 | CDS | 134815 | 678 | + | 0.336283 | |
g6970 | DLA_07768 | GLQOFTK02FH5TG | CDS | 182247 | 1566 | - | 0.302682 | |
g6971 | DLA_07771 | highly similar to | GLQOFTK02FH5TG | CDS | 184944 | 1680 | - | 0.347619 |
g6972 | DLA_07772 | GLQOFTK02FH5TG | CDS | 187147 | 627 | - | 0.341308 | |
g6973 | DLA_07773 | GLQOFTK02FH5TG | CDS | 188226 | 3966 | - | 0.314423 | |
g6974 | DLA_07774 | GLQOFTK02FH5TG | CDS | 192719 | 681 | + | 0.33627 | |
g6975 | DLA_07775 | GLQOFTK02FH5TG | CDS | 194059 | 1857 | + | 0.403339 | |
g6976 | DLA_07776 | GLQOFTK02FH5TG | CDS | 196053 | 2202 | + | 0.297457 | |
g6977 | DLA_07777 | GLQOFTK02FH5TG | CDS | 198422 | 954 | - | 0.389937 | |
g6978 | DLA_07778 | GLQOFTK02FH5TG | CDS | 199915 | 789 | + | 0.302915 | |
g6979 | DLA_07779 | GLQOFTK02FH5TG | CDS | 201197 | 456 | + | 0.39693 | |
g698 | DLA_00771 | F4PJNLW01A00V1 | CDS | 136270 | 7062 | + | 0.323421 | |
g6980 | DLA_07780 | GLQOFTK02FH5TG | CDS | 201859 | 1221 | + | 0.336609 | |
g6981 | DLA_07781 | GLQOFTK02FH5TG | CDS | 203126 | 2628 | - | 0.317732 | |
g6982 | DLA_07782 | GLQOFTK02FH5TG | CDS | 206005 | 633 | - | 0.328594 | |
g6983 | DLA_07783 | GLQOFTK02FH5TG | CDS | 207004 | 1563 | - | 0.319898 | |
g6984 | DLA_07784 | GLQOFTK02FH5TG | CDS | 208738 | 2853 | + | 0.33123 | |
g6985 | DLA_07786 | GLQOFTK02FH5TG | CDS | 212046 | 747 | + | 0.298527 | |
g6986 | DLA_07787 | GLQOFTK02FH5TG | CDS | 213367 | 1623 | + | 0.358595 | |
g6987 | DLA_07789 | GLQOFTK02FH5TG | CDS | 215316 | 690 | + | 0.276812 | |
g6988 | DLA_11695 | GLQOFTK02FH5TG | CDS | 216687 | 1467 | + | 0.361282 | |
g6989 | DLA_07790 | GLQOFTK02FH5TG | CDS | 218356 | 2607 | + | 0.335251 | |
g699 | DLA_00772 | F4PJNLW01A00V1 | CDS | 143489 | 1716 | - | 0.320513 | |
g6990 | DLA_07792 | GLQOFTK02FH5TG | CDS | 221945 | 1668 | - | 0.311151 | |
g6991 | DLA_07793 | GLQOFTK02FH5TG | CDS | 223961 | 1251 | - | 0.294964 | |
g6992 | DLA_07794 | GLQOFTK02FH5TG | CDS | 225458 | 534 | + | 0.327715 | |
g6993 | DLA_07795 | GLQOFTK02FH5TG | CDS | 226617 | 3459 | + | 0.33449 | |
g6994 | DLA_07796 | GLQOFTK02FH5TG | CDS | 230727 | 2295 | + | 0.344662 | |
g6995 | DLA_07797 | GLQOFTK02FH5TG | CDS | 233421 | 2916 | + | 0.351509 | |
g6996 | DLA_07798 | GLQOFTK02FH5TG | CDS | 237749 | 666 | + | 0.315315 | |
g6997 | DLA_07799 | GLQOFTK02FH5TG | CDS | 238572 | 1332 | - | 0.292793 | |
g6998 | DLA_07800 | GLQOFTK02FH5TG | CDS | 240209 | 1164 | - | 0.302406 | |
g6999 | DLA_07801 | GLQOFTK02FH5TG | CDS | 241685 | 1479 | - | 0.387424 | |
g7 | DLA_00008 | contig05409_1.exp | CDS | 13806 | 10869 | - | 0.308584 | |
g70 | DLA_00081 | contig05409_1.exp | CDS | 169936 | 618 | - | 0.322006 | |
g700 | DLA_00773 | ortholog of vitellogenic carboxypeptidase a conserved serine carboxypeptidase expressed in mosquito ovaries contains a predicted signal peptide | F4PJNLW01A00V1 | CDS | 145541 | 1521 | - | 0.332676 |
g7000 | DLA_07802 | GLQOFTK02FH5TG | CDS | 243440 | 1278 | + | 0.271518 | |
g7001 | DLA_07803 | GLQOFTK02FH5TG | CDS | 245100 | 426 | - | 0.352113 | |
g7002 | DLA_07804 | GLQOFTK02FH5TG | CDS | 246435 | 1239 | - | 0.292978 | |
g7003 | DLA_07806 | GLQOFTK02FH5TG | CDS | 250685 | 1536 | - | 0.277995 | |
g7004 | DLA_07807 | GLQOFTK02FH5TG | CDS | 252306 | 1518 | - | 0.276021 | |
g7005 | DLA_07808 | GLQOFTK02FH5TG | CDS | 254104 | 2106 | + | 0.332384 | |
g7006 | DLA_07809 | GLQOFTK02FH5TG | CDS | 256365 | 1926 | - | 0.34839 | |
g7007 | DLA_07810 | GLQOFTK02FH5TG | CDS | 258610 | 975 | + | 0.328205 | |
g7008 | DLA_07811 | GLQOFTK02FH5TG | CDS | 261033 | 2460 | + | 0.34878 | |
g7009 | DLA_07812 | GLQOFTK02FH5TG | CDS | 263926 | 1068 | - | 0.367978 | |
g701 | DLA_00774 | F4PJNLW01A00V1 | CDS | 147285 | 1170 | - | 0.298291 | |
g7010 | DLA_07813 | GLQOFTK02FH5TG | CDS | 265802 | 2601 | + | 0.331411 | |
g7011 | DLA_07814 | GLQOFTK02FH5TG | CDS | 269937 | 6186 | + | 0.35257 | |
g7012 | DLA_07815 | GLQOFTK02FH5TG | CDS | 276321 | 2337 | - | 0.344031 | |
g7013 | DLA_07816 | GLQOFTK02FH5TG | CDS | 279781 | 1254 | + | 0.296651 | |
g7014 | DLA_07817 | GLQOFTK02FH5TG | CDS | 281784 | 1071 | + | 0.272642 | |
g7015 | DLA_07818 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family kinase activity stimulated by hyperosmolarity and heat shock there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 283213 | 2583 | - | 0.342238 |
g7016 | DLA_07821 | GLQOFTK02FH5TG | CDS | 291583 | 3063 | + | 0.316683 | |
g7017 | DLA_11696 | GLQOFTK02FH5TG | CDS | 294959 | 1113 | + | 0.330638 | |
g7018 | DLA_07822 | GLQOFTK02FH5TG | CDS | 297080 | 3927 | + | 0.330278 | |
g7019 | DLA_07824 | GLQOFTK02FH5TG | CDS | 301627 | 330 | + | 0.315152 | |
g702 | DLA_00775 | F4PJNLW01A00V1 | CDS | 149037 | 1473 | + | 0.30482 | |
g7020 | DLA_07825 | GLQOFTK02FH5TG | CDS | 302318 | 2499 | - | 0.341337 | |
g7021 | DLA_07828 | GLQOFTK02FH5TG | CDS | 307902 | 528 | - | 0.304924 | |
g7022 | DLA_07829 | GLQOFTK02FH5TG | CDS | 308701 | 6111 | - | 0.308624 | |
g7023 | DLA_07830 | GLQOFTK02FH5TG | CDS | 315928 | 1398 | + | 0.31402 | |
g7024 | DLA_07831 | GLQOFTK02FH5TG | CDS | 318028 | 471 | - | 0.305732 | |
g7025 | DLA_07832 | GLQOFTK02FH5TG | CDS | 318840 | 1098 | + | 0.312386 | |
g7026 | DLA_11697 | GLQOFTK02FH5TG | CDS | 320418 | 1623 | + | 0.332101 | |
g7027 | DLA_07833 | GLQOFTK02FH5TG | CDS | 322482 | 1929 | - | 0.396579 | |
g7028 | DLA_07835 | GLQOFTK02FH5TG | CDS | 325328 | 3099 | + | 0.31849 | |
g7029 | DLA_07837 | GLQOFTK02FH5TG | CDS | 329404 | 1482 | - | 0.307018 | |
g703 | DLA_00776 | F4PJNLW01A00V1 | CDS | 151130 | 1470 | + | 0.364626 | |
g7030 | DLA_07838 | GLQOFTK02FH5TG | CDS | 331396 | 2919 | + | 0.373416 | |
g7031 | DLA_07840 | GLQOFTK02FH5TG | CDS | 335226 | 1401 | + | 0.325482 | |
g7032 | DLA_07842 | GLQOFTK02FH5TG | CDS | 339584 | 1338 | + | 0.302691 | |
g7033 | DLA_07843 | putative ortholog of S. cerevisiae VPS54 component of the GARP (Golgi-associated retrograde protein) complex | GLQOFTK02FH5TG | CDS | 342096 | 2652 | + | 0.290347 |
g7034 | DLA_07844 | protein component of the small (40S) ribosomal subunit highly expressed in vegetative cells and in early development | GLQOFTK02FH5TG | CDS | 344908 | 801 | - | 0.406991 |
g7035 | DLA_07845 | GLQOFTK02FH5TG | CDS | 346146 | 921 | - | 0.274701 | |
g7036 | DLA_07847 | GLQOFTK02FH5TG | CDS | 348329 | 1116 | - | 0.291219 | |
g7037 | DLA_07848 | GLQOFTK02FH5TG | CDS | 349717 | 480 | - | 0.314583 | |
g7038 | DLA_07849 | GLQOFTK02FH5TG | CDS | 350657 | 831 | - | 0.277978 | |
g7039 | DLA_07850 | GLQOFTK02FH5TG | CDS | 352010 | 2667 | + | 0.31871 | |
g704 | DLA_00777 | F4PJNLW01A00V1 | CDS | 152799 | 327 | + | 0.327217 | |
g7040 | DLA_07851 | GLQOFTK02FH5TG | CDS | 354757 | 918 | - | 0.296296 | |
g7041 | DLA_07852 | GLQOFTK02FH5TG | CDS | 355920 | 1548 | + | 0.339793 | |
g7042 | DLA_07856 | GLQOFTK02FH5TG | CDS | 361063 | 1422 | + | 0.317862 | |
g7043 | DLA_07857 | GLQOFTK02FH5TG | CDS | 364491 | 1200 | + | 0.3075 | |
g7044 | DLA_11698 | GLQOFTK02FH5TG | CDS | 366332 | 1524 | + | 0.340551 | |
g7045 | DLA_07858 | belongs to the villingelsolin family contains 5 gelsolin-like repeats and one villin headpiece domain | GLQOFTK02FH5TG | CDS | 367957 | 2499 | + | 0.343337 |
g7046 | DLA_07859 | ortholog of ATP-dependent RNA helicase DDX1 contains an SPRY domain which is of unknown function | GLQOFTK02FH5TG | CDS | 370624 | 3510 | + | 0.329345 |
g7047 | DLA_07861 | ortholog of Rad51 which is involved in activation of homologous recombination and double-strand break repair and interacts with XRCC3 there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 374463 | 1044 | - | 0.376437 |
g7048 | DLA_07862 | GLQOFTK02FH5TG | CDS | 375847 | 1008 | + | 0.293651 | |
g7049 | DLA_07864 | GLQOFTK02FH5TG | CDS | 377191 | 960 | + | 0.30625 | |
g705 | DLA_00778 | F4PJNLW01A00V1 | CDS | 153474 | 432 | - | 0.298611 | |
g7050 | DLA_07865 | GLQOFTK02FH5TG | CDS | 378481 | 951 | + | 0.28286 | |
g7051 | DLA_07866 | GLQOFTK02FH5TG | CDS | 379973 | 588 | - | 0.227891 | |
g7052 | DLA_07867 | GLQOFTK02FH5TG | CDS | 381329 | 2187 | - | 0.296296 | |
g7053 | DLA_07869 | GLQOFTK02FH5TG | CDS | 385293 | 5196 | - | 0.343341 | |
g7054 | DLA_07870 | GLQOFTK02FH5TG | CDS | 391023 | 1128 | + | 0.31383 | |
g7055 | DLA_11699 | GLQOFTK02FH5TG | CDS | 392288 | 462 | - | 0.279221 | |
g7056 | DLA_07871 | GLQOFTK02FH5TG | CDS | 392990 | 1512 | - | 0.421296 | |
g7057 | DLA_07873 | GLQOFTK02FH5TG | CDS | 395388 | 1587 | + | 0.328292 | |
g7058 | DLA_07874 | GLQOFTK02FH5TG | CDS | 397075 | 2931 | - | 0.293074 | |
g7059 | DLA_07875 | GLQOFTK02FH5TG | CDS | 400463 | 828 | + | 0.293478 | |
g706 | DLA_00779 | ortholog of the putative tumor suppressor candidate 4 protein (TUSC4) the nitrogen permease regulator 2 (NPR2) family of regulators are involved in post-translational control of nitrogen permease | F4PJNLW01A00V1 | CDS | 154243 | 1182 | - | 0.327411 |
g7060 | DLA_07876 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | GLQOFTK02FH5TG | CDS | 401492 | 1173 | - | 0.341006 |
g7061 | DLA_07877 | GLQOFTK02FH5TG | CDS | 402856 | 3843 | - | 0.334634 | |
g7062 | DLA_07878 | GLQOFTK02FH5TG | CDS | 407406 | 591 | - | 0.314721 | |
g7063 | DLA_07880 | GLQOFTK02FH5TG | CDS | 409112 | 1239 | - | 0.346247 | |
g7064 | DLA_07882 | GLQOFTK02FH5TG | CDS | 411408 | 2643 | + | 0.360953 | |
g7065 | DLA_07885 | GLQOFTK02FH5TG | CDS | 415383 | 849 | - | 0.335689 | |
g7066 | DLA_07886 | GLQOFTK02FH5TG | CDS | 416723 | 6294 | + | 0.335399 | |
g7067 | DLA_07887 | GLQOFTK02FH5TG | CDS | 423232 | 1470 | - | 0.336735 | |
g7068 | DLA_07888 | putative RNA helicase involved in the second step of RNA splicing ortholog of human ASCC3L1 and yeast BRR2 | GLQOFTK02FH5TG | CDS | 424895 | 6555 | + | 0.344012 |
g7069 | DLA_07889 | GLQOFTK02FH5TG | CDS | 431745 | 1041 | + | 0.302594 | |
g707 | DLA_11448 | F4PJNLW01A00V1 | CDS | 155658 | 453 | - | 0.452539 | |
g7070 | DLA_07890 | GLQOFTK02FH5TG | CDS | 432977 | 330 | + | 0.363636 | |
g7071 | DLA_07891 | GLQOFTK02FH5TG | CDS | 433993 | 429 | - | 0.314685 | |
g7072 | DLA_07892 | component of the U4U6-U5 snRNP complex human PRP3 interacts with PRP4 | GLQOFTK02FH5TG | CDS | 434949 | 1572 | + | 0.314885 |
g7073 | DLA_07893 | GLQOFTK02FH5TG | CDS | 437192 | 1782 | + | 0.360831 | |
g7074 | DLA_07894 | GLQOFTK02FH5TG | CDS | 439223 | 1578 | + | 0.378327 | |
g7075 | DLA_07895 | GLQOFTK02FH5TG | CDS | 441355 | 3612 | + | 0.357143 | |
g7076 | DLA_07896 | GLQOFTK02FH5TG | CDS | 445167 | 624 | - | 0.285256 | |
g7077 | DLA_11700 | GLQOFTK02FH5TG | CDS | 446102 | 486 | + | 0.226337 | |
g7078 | DLA_07897 | GLQOFTK02FH5TG | CDS | 448023 | 765 | + | 0.334641 | |
g7079 | DLA_07898 | GLQOFTK02FH5TG | CDS | 449014 | 7215 | - | 0.360776 | |
g708 | DLA_00780 | F4PJNLW01A00V1 | CDS | 156871 | 2907 | + | 0.325421 | |
g7080 | DLA_07899 | GLQOFTK02FH5TG | CDS | 457132 | 4641 | + | 0.36393 | |
g7081 | DLA_07901 | GLQOFTK02FH5TG | CDS | 462198 | 714 | - | 0.305322 | |
g7082 | DLA_07902 | GLQOFTK02FH5TG | CDS | 463673 | 576 | - | 0.319444 | |
g7083 | DLA_07903 | GLQOFTK02FH5TG | CDS | 464589 | 636 | - | 0.31761 | |
g7084 | DLA_07904 | GLQOFTK02FH5TG | CDS | 465512 | 2028 | - | 0.345168 | |
g7085 | DLA_07906 | GLQOFTK02FH5TG | CDS | 468236 | 3894 | + | 0.28942 | |
g7086 | DLA_07908 | GLQOFTK02FH5TG | CDS | 472270 | 1821 | - | 0.29709 | |
g7087 | DLA_07910 | GLQOFTK02FH5TG | CDS | 474332 | 1572 | + | 0.344148 | |
g7088 | DLA_07913 | GLQOFTK02FH5TG | CDS | 476795 | 915 | + | 0.285246 | |
g7089 | DLA_07914 | GLQOFTK02FH5TG | CDS | 478409 | 303 | + | 0.323432 | |
g709 | DLA_00781 | F4PJNLW01A00V1 | CDS | 159971 | 3423 | - | 0.315221 | |
g7090 | DLA_07916 | GLQOFTK02FH5TG | CDS | 478983 | 489 | + | 0.282209 | |
g7091 | DLA_07917 | GLQOFTK02FH5TG | CDS | 479590 | 1134 | - | 0.298942 | |
g7092 | DLA_07918 | putative pseudogene similar to coactosin contains an ADF (actin depolymerisation factorcofilin-like) domain there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 480954 | 1023 | - | 0.347019 |
g7093 | DLA_07919 | belongs to a family of conserved mammalian HCaRG (hypertension-related calcium-regulated gene) proteins | GLQOFTK02FH5TG | CDS | 483033 | 603 | - | 0.3267 |
g7094 | DLA_07920 | GLQOFTK02FH5TG | CDS | 484278 | 1554 | + | 0.332046 | |
g7095 | DLA_07921 | similar to the THAP domain in the mammalian THAP domain-containing protein 4 underexpressed in | GLQOFTK02FH5TG | CDS | 486165 | 483 | - | 0.31677 |
g7096 | DLA_07922 | GLQOFTK02FH5TG | CDS | 486806 | 492 | + | 0.339431 | |
g7097 | DLA_07923 | GLQOFTK02FH5TG | CDS | 487583 | 1089 | - | 0.312213 | |
g7098 | DLA_07924 | GLQOFTK02FH5TG | CDS | 489001 | 2274 | + | 0.317942 | |
g7099 | DLA_07925 | GLQOFTK02FH5TG | CDS | 491751 | 504 | - | 0.339286 | |
g71 | DLA_00082 | contig05409_1.exp | CDS | 170810 | 906 | - | 0.248344 | |
g710 | DLA_00782 | F4PJNLW01A00V1 | CDS | 163745 | 399 | - | 0.390977 | |
g7100 | DLA_07926 | GLQOFTK02FH5TG | CDS | 492610 | 585 | + | 0.294017 | |
g7101 | DLA_07928 | GLQOFTK02FH5TG | CDS | 493642 | 1347 | + | 0.361544 | |
g7102 | DLA_07929 | GLQOFTK02FH5TG | CDS | 495086 | 1566 | - | 0.277139 | |
g7103 | DLA_07930 | GLQOFTK02FH5TG | CDS | 496861 | 1425 | + | 0.320702 | |
g7104 | DLA_07932 | GLQOFTK02FH5TG | CDS | 498907 | 2385 | + | 0.315304 | |
g7105 | DLA_07933 | GLQOFTK02FH5TG | CDS | 501508 | 3135 | + | 0.304625 | |
g7106 | DLA_07934 | GLQOFTK02FH5TG | CDS | 505658 | 1608 | + | 0.284826 | |
g7107 | DLA_07935 | GLQOFTK02FH5TG | CDS | 507679 | 1062 | - | 0.297552 | |
g7108 | DLA_07936 | GLQOFTK02FH5TG | CDS | 510032 | 1293 | + | 0.300077 | |
g7109 | DLA_07937 | GLQOFTK02FH5TG | CDS | 512890 | 336 | + | 0.35119 | |
g711 | DLA_00783 | F4PJNLW01A00V1 | CDS | 164811 | 894 | + | 0.369128 | |
g7110 | DLA_07938 | GLQOFTK02FH5TG | CDS | 515468 | 1161 | - | 0.281654 | |
g7111 | DLA_07939 | GLQOFTK02FH5TG | CDS | 516807 | 477 | + | 0.297694 | |
g7112 | DLA_07940 | GLQOFTK02FH5TG | CDS | 517488 | 2871 | - | 0.31348 | |
g7113 | DLA_07942 | GLQOFTK02FH5TG | CDS | 520886 | 1692 | + | 0.349291 | |
g7114 | DLA_11701 | GLQOFTK02FH5TG | CDS | 522823 | 501 | + | 0.387226 | |
g7115 | DLA_07943 | GLQOFTK02FH5TG | CDS | 523828 | 918 | + | 0.286492 | |
g7116 | DLA_07944 | GLQOFTK02FH5TG | CDS | 524816 | 1245 | - | 0.353414 | |
g7117 | DLA_07945 | GLQOFTK02FH5TG | CDS | 526254 | 1326 | - | 0.294872 | |
g7118 | DLA_07946 | GLQOFTK02FH5TG | CDS | 530737 | 2652 | + | 0.328431 | |
g7119 | DLA_07947 | GLQOFTK02FH5TG | CDS | 533740 | 2316 | + | 0.355786 | |
g712 | DLA_00784 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPB10 | F4PJNLW01A00V1 | CDS | 165886 | 207 | - | 0.31401 |
g7120 | DLA_07948 | GLQOFTK02FH5TG | CDS | 536331 | 3279 | + | 0.351632 | |
g7121 | DLA_07951 | GLQOFTK02FH5TG | CDS | 540723 | 1026 | + | 0.307992 | |
g7122 | DLA_07952 | GLQOFTK02FH5TG | CDS | 541931 | 2778 | - | 0.364651 | |
g7123 | DLA_07953 | GLQOFTK02FH5TG | CDS | 544957 | 549 | + | 0.289617 | |
g7124 | DLA_11702 | GLQOFTK02FH5TG | CDS | 545898 | 408 | + | 0.262255 | |
g7125 | DLA_07954 | GLQOFTK02FH5TG | CDS | 546516 | 1935 | - | 0.315762 | |
g7126 | DLA_07955 | GLQOFTK02FH5TG | CDS | 549187 | 531 | - | 0.308851 | |
g7127 | DLA_07956 | GLQOFTK02FH5TG | CDS | 549915 | 1044 | - | 0.33908 | |
g7128 | DLA_07957 | GLQOFTK02FH5TG | CDS | 551338 | 405 | + | 0.31358 | |
g7129 | DLA_07958 | GLQOFTK02FH5TG | CDS | 551849 | 1209 | - | 0.315136 | |
g713 | DLA_00785 | F4PJNLW01A00V1 | CDS | 167363 | 1281 | + | 0.323966 | |
g7130 | DLA_07959 | GLQOFTK02FH5TG | CDS | 553267 | 1290 | + | 0.322481 | |
g7131 | DLA_07960 | GLQOFTK02FH5TG | CDS | 555889 | 756 | + | 0.304233 | |
g7132 | DLA_07962 | GLQOFTK02FH5TG | CDS | 557061 | 4722 | - | 0.366158 | |
g7133 | DLA_07963 | GLQOFTK02FH5TG | CDS | 562162 | 1206 | - | 0.31592 | |
g7134 | DLA_07964 | GLQOFTK02FH5TG | CDS | 563924 | 363 | - | 0.30854 | |
g7135 | DLA_07965 | GLQOFTK02FH5TG | CDS | 564483 | 2160 | + | 0.327778 | |
g7136 | DLA_07966 | GLQOFTK02FH5TG | CDS | 567020 | 600 | - | 0.34 | |
g7137 | DLA_11703 | GLQOFTK02FH5TG | CDS | 569441 | 3072 | + | 0.333008 | |
g7138 | DLA_07967 | GLQOFTK02FH5TG | CDS | 573321 | 1563 | + | 0.289827 | |
g7139 | DLA_07968 | GLQOFTK02FH5TG | CDS | 575114 | 330 | + | 0.30303 | |
g714 | DLA_00786 | F4PJNLW01A00V1 | CDS | 168705 | 1512 | - | 0.342593 | |
g7140 | DLA_07969 | GLQOFTK02FH5TG | CDS | 575598 | 1110 | + | 0.328829 | |
g7141 | DLA_07970 | GLQOFTK02FH5TG | CDS | 576836 | 618 | + | 0.305825 | |
g7142 | DLA_07971 | GLQOFTK02FH5TG | CDS | 577825 | 1185 | - | 0.299578 | |
g7143 | DLA_07973 | GLQOFTK02FH5TG | CDS | 580542 | 771 | + | 0.325551 | |
g7144 | DLA_07974 | GLQOFTK02FH5TG | CDS | 581617 | 600 | + | 0.321667 | |
g7145 | DLA_07975 | GLQOFTK02FH5TG | CDS | 582475 | 1227 | + | 0.320293 | |
g7146 | DLA_07976 | GLQOFTK02FH5TG | CDS | 583863 | 1821 | - | 0.298737 | |
g7147 | DLA_07977 | GLQOFTK02FH5TG | CDS | 585807 | 957 | - | 0.338558 | |
g7148 | DLA_07978 | GLQOFTK02FH5TG | CDS | 587193 | 2544 | + | 0.355739 | |
g7149 | DLA_07979 | GLQOFTK02FH5TG | CDS | 589921 | 4734 | - | 0.320237 | |
g715 | DLA_00787 | F4PJNLW01A00V1 | CDS | 170363 | 2574 | - | 0.378399 | |
g7150 | DLA_07980 | GLQOFTK02FH5TG | CDS | 595236 | 804 | + | 0.317164 | |
g7151 | DLA_07981 | GLQOFTK02FH5TG | CDS | 596350 | 801 | + | 0.31211 | |
g7152 | DLA_07983 | GLQOFTK02FH5TG | CDS | 597442 | 789 | + | 0.264892 | |
g7153 | DLA_07984 | GLQOFTK02FH5TG | CDS | 598463 | 1527 | + | 0.275704 | |
g7154 | DLA_07985 | GLQOFTK02FH5TG | CDS | 600275 | 1380 | - | 0.313768 | |
g7155 | DLA_07986 | GLQOFTK02FH5TG | CDS | 601976 | 5955 | - | 0.358858 | |
g7156 | DLA_07987 | GLQOFTK02FH5TG | CDS | 609153 | 1371 | + | 0.301969 | |
g7157 | DLA_07988 | GLQOFTK02FH5TG | CDS | 610898 | 1047 | + | 0.312321 | |
g7158 | DLA_11704 | GLQOFTK02FH5TG | CDS | 612941 | 207 | - | 0.338164 | |
g7159 | DLA_07989 | GLQOFTK02FH5TG | CDS | 613874 | 477 | + | 0.385744 | |
g716 | DLA_11449 | F4PJNLW01A00V1 | CDS | 173362 | 1539 | + | 0.332684 | |
g7160 | DLA_07991 | GLQOFTK02FH5TG | CDS | 614661 | 2460 | + | 0.342276 | |
g7161 | DLA_07992 | GLQOFTK02FH5TG | CDS | 617621 | 3918 | + | 0.360898 | |
g7162 | DLA_07993 | GLQOFTK02FH5TG | CDS | 622406 | 5154 | + | 0.386496 | |
g7163 | DLA_07994 | GLQOFTK02FH5TG | CDS | 627631 | 3921 | - | 0.31191 | |
g7164 | DLA_07995 | GLQOFTK02FH5TG | CDS | 631778 | 744 | - | 0.319892 | |
g7165 | DLA_07996 | GLQOFTK02FH5TG | CDS | 632631 | 3159 | + | 0.312757 | |
g7166 | DLA_07997 | GLQOFTK02FH5TG | CDS | 636543 | 4971 | - | 0.356468 | |
g7167 | DLA_07998 | GLQOFTK02FH5TG | CDS | 642697 | 237 | + | 0.379747 | |
g7168 | DLA_07999 | GLQOFTK02FH5TG | CDS | 643499 | 882 | - | 0.339002 | |
g7169 | DLA_08000 | GLQOFTK02FH5TG | CDS | 644830 | 6462 | - | 0.33844 | |
g717 | DLA_00788 | F4PJNLW01A00V1 | CDS | 175851 | 861 | + | 0.326365 | |
g7170 | DLA_08002 | GLQOFTK02FH5TG | CDS | 652700 | 324 | + | 0.287037 | |
g7171 | DLA_08004 | GLQOFTK02FH5TG | CDS | 654798 | 1743 | + | 0.309237 | |
g7172 | DLA_08005 | GLQOFTK02FH5TG | CDS | 656563 | 1311 | - | 0.309687 | |
g7173 | DLA_08006 | GLQOFTK02FH5TG | CDS | 658058 | 294 | - | 0.316327 | |
g7174 | DLA_08007 | ortholog of SURF1 encoding a factor involved in the biogenesis of cytochrome c oxidase mutated in Leigh syndrome there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 658747 | 741 | - | 0.325236 |
g7175 | DLA_08008 | similar to human RWDD1 S. cerevisiae GIR2 S. cerevisiae GIR2 binds to and regulates the expression of GTP-binding protein DRG2 there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 659863 | 702 | + | 0.311966 |
g7176 | DLA_08009 | GLQOFTK02FH5TG | CDS | 660856 | 1470 | - | 0.359184 | |
g7177 | DLA_08010 | carries out carboyxl methylation of cleaved eukaryotic proteins that terminate in a CaaX motif such as NE81 (lmnB) there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 662531 | 711 | - | 0.331927 |
g7178 | DLA_08011 | GLQOFTK02FH5TG | CDS | 663633 | 2505 | + | 0.31976 | |
g7179 | DLA_08012 | GLQOFTK02FH5TG | CDS | 666329 | 2289 | + | 0.300131 | |
g718 | DLA_00790 | F4PJNLW01A00V1 | CDS | 177891 | 606 | - | 0.334983 | |
g7180 | DLA_08013 | GLQOFTK02FH5TG | CDS | 669179 | 2037 | - | 0.329897 | |
g7181 | DLA_08014 | GLQOFTK02FH5TG | CDS | 671623 | 978 | + | 0.287321 | |
g7182 | DLA_08015 | GLQOFTK02FH5TG | CDS | 672958 | 1659 | - | 0.3044 | |
g7183 | DLA_08016 | GLQOFTK02FH5TG | CDS | 674860 | 456 | + | 0.285088 | |
g7184 | DLA_08017 | GLQOFTK02FH5TG | CDS | 675771 | 1635 | - | 0.299694 | |
g7185 | DLA_08018 | GLQOFTK02FH5TG | CDS | 677622 | 1713 | - | 0.345593 | |
g7186 | DLA_08019 | GLQOFTK02FH5TG | CDS | 679903 | 2898 | + | 0.316425 | |
g7187 | DLA_08021 | GLQOFTK02FH5TG | CDS | 683896 | 3252 | + | 0.289668 | |
g7188 | DLA_11705 | GLQOFTK02FH5TG | CDS | 688090 | 4086 | + | 0.318649 | |
g7189 | DLA_08022 | GLQOFTK02FH5TG | CDS | 692803 | 363 | + | 0.327824 | |
g719 | DLA_00791 | F4PJNLW01A00V1 | CDS | 178857 | 1383 | - | 0.336226 | |
g7190 | DLA_08023 | GLQOFTK02FH5TG | CDS | 693356 | 2370 | - | 0.310549 | |
g7191 | DLA_08024 | GLQOFTK02FH5TG | CDS | 696397 | 279 | + | 0.268817 | |
g7192 | DLA_08025 | GLQOFTK02FH5TG | CDS | 697036 | 702 | + | 0.358974 | |
g7193 | DLA_08026 | GLQOFTK02FH5TG | CDS | 698052 | 2301 | - | 0.328553 | |
g7194 | DLA_08027 | GLQOFTK02FH5TG | CDS | 700530 | 915 | + | 0.261202 | |
g7195 | DLA_08029 | homolog of human HMGCS1 catalyzes the reaction acetyl-CoA H2O acetoacetyl-CoA (S)-3-hydroxy-3-methylglutaryl-CoA CoA contains a predicted peroxisomal targeting signal | GLQOFTK02FH5TG | CDS | 701909 | 1398 | - | 0.389127 |
g7196 | DLA_08030 | GLQOFTK02FH5TG | CDS | 704660 | 282 | - | 0.322695 | |
g7197 | DLA_08031 | GLQOFTK02FH5TG | CDS | 705248 | 1230 | + | 0.295122 | |
g7198 | DLA_08032 | GLQOFTK02FH5TG | CDS | 706717 | 1734 | - | 0.316032 | |
g7199 | DLA_08033 | GLQOFTK02FH5TG | CDS | 708754 | 549 | + | 0.278689 | |
g72 | DLA_00083 | contig05409_1.exp | CDS | 171875 | 1356 | - | 0.338496 | |
g720 | DLA_00792 | Ca2-binding protein with chaperone activity in the endoplasmic reticulum plays a role in phagocytosis | F4PJNLW01A00V1 | CDS | 180508 | 1608 | - | 0.393657 |
g7200 | DLA_08035 | GLQOFTK02FH5TG | CDS | 709649 | 996 | - | 0.320281 | |
g7201 | DLA_08036 | GLQOFTK02FH5TG | CDS | 711273 | 3213 | + | 0.348895 | |
g7202 | DLA_08037 | GLQOFTK02FH5TG | CDS | 714928 | 1077 | + | 0.359331 | |
g7203 | DLA_08038 | GLQOFTK02FH5TG | CDS | 716163 | 2421 | - | 0.319703 | |
g7204 | DLA_11706 | GLQOFTK02FH5TG | CDS | 718809 | 1005 | - | 0.334328 | |
g7205 | DLA_08039 | GLQOFTK02FH5TG | CDS | 720195 | 1467 | + | 0.290389 | |
g7206 | DLA_08040 | GLQOFTK02FH5TG | CDS | 722028 | 927 | + | 0.326861 | |
g7207 | DLA_08041 | GLQOFTK02FH5TG | CDS | 722990 | 381 | + | 0.283465 | |
g7208 | DLA_08042 | GLQOFTK02FH5TG | CDS | 724502 | 1299 | - | 0.292533 | |
g7209 | DLA_08043 | GLQOFTK02FH5TG | CDS | 725921 | 288 | + | 0.295139 | |
g721 | DLA_00793 | ortholog of MON2 in S. cerevisiae MON2 plays a a role in endocytosis and vacuole integrity | F4PJNLW01A00V1 | CDS | 182489 | 5205 | + | 0.360807 |
g7210 | DLA_08045 | GLQOFTK02FH5TG | CDS | 726784 | 1431 | + | 0.292802 | |
g7211 | DLA_08046 | GLQOFTK02FH5TG | CDS | 728467 | 2109 | - | 0.348032 | |
g7212 | DLA_08048 | GLQOFTK02FH5TG | CDS | 731330 | 741 | - | 0.390013 | |
g7213 | DLA_08049 | GLQOFTK02FH5TG | CDS | 732300 | 1326 | - | 0.28733 | |
g7214 | DLA_08050 | GLQOFTK02FH5TG | CDS | 734142 | 933 | - | 0.330118 | |
g7215 | DLA_08051 | half transporter consisting of one ABC domain and one transmembrane domain | GLQOFTK02FH5TG | CDS | 735269 | 2055 | - | 0.349878 |
g7216 | DLA_08052 | contains eight transmembrane domains there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 738361 | 3552 | - | 0.37134 |
g7217 | DLA_08053 | GLQOFTK02FH5TG | CDS | 742825 | 5442 | - | 0.34932 | |
g7218 | DLA_08056 | GLQOFTK02FH5TG | CDS | 749644 | 639 | + | 0.306729 | |
g7219 | DLA_08057 | GLQOFTK02FH5TG | CDS | 750982 | 2772 | - | 0.344517 | |
g722 | DLA_00794 | F4PJNLW01A00V1 | CDS | 188088 | 2253 | + | 0.340879 | |
g7220 | DLA_08058 | GLQOFTK02FH5TG | CDS | 754465 | 1008 | - | 0.327381 | |
g7221 | DLA_08061 | GLQOFTK02FH5TG | CDS | 756670 | 2181 | - | 0.358551 | |
g7222 | DLA_08062 | GLQOFTK02FH5TG | CDS | 759231 | 1590 | + | 0.284906 | |
g7223 | DLA_08063 | GLQOFTK02FH5TG | CDS | 761123 | 462 | - | 0.411255 | |
g7224 | DLA_08064 | GLQOFTK02FH5TG | CDS | 762109 | 2898 | + | 0.359213 | |
g7225 | DLA_08065 | GLQOFTK02FH5TG | CDS | 765139 | 999 | + | 0.37037 | |
g7226 | DLA_08066 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | GLQOFTK02FH5TG | CDS | 766604 | 615 | + | 0.331707 |
g7227 | DLA_08067 | GLQOFTK02FH5TG | CDS | 767556 | 585 | + | 0.278632 | |
g7228 | DLA_08068 | GLQOFTK02FH5TG | CDS | 768512 | 978 | - | 0.274029 | |
g7229 | DLA_11707 | similar to TNRC4 (TriNucleotide Repeat Containing 4 protein) and Bruno-like proteins contains 3 RRM domains | GLQOFTK02FH5TG | CDS | 770131 | 1062 | + | 0.335217 |
g723 | DLA_00796 | F4PJNLW01A00V1 | CDS | 190893 | 4350 | + | 0.355632 | |
g7230 | DLA_08069 | contains two predicted transmembrane domains one at amino terminus and one at carboxyl terminus | GLQOFTK02FH5TG | CDS | 772852 | 2967 | + | 0.375463 |
g7231 | DLA_08070 | GLQOFTK02FH5TG | CDS | 776119 | 1698 | + | 0.30742 | |
g7232 | DLA_08071 | GLQOFTK02FH5TG | CDS | 778934 | 3300 | - | 0.311212 | |
g7233 | DLA_08072 | belongs to the synaptotagmin family contains a predicted signal sequence and a transmembrane domain | GLQOFTK02FH5TG | CDS | 782841 | 519 | + | 0.346821 |
g7234 | DLA_08073 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 783751 | 1683 | - | 0.361854 |
g7235 | DLA_08074 | GLQOFTK02FH5TG | CDS | 785757 | 4005 | + | 0.321598 | |
g7236 | DLA_11708 | GLQOFTK02FH5TG | CDS | 790372 | 4023 | + | 0.311956 | |
g7237 | DLA_08075 | GLQOFTK02FH5TG | CDS | 794907 | 4074 | + | 0.32327 | |
g7238 | DLA_08076 | GLQOFTK02FH5TG | CDS | 799601 | 630 | + | 0.266667 | |
g7239 | DLA_08077 | GLQOFTK02FH5TG | CDS | 800598 | 1068 | + | 0.268727 | |
g724 | DLA_00797 | F4PJNLW01A00V1 | CDS | 195634 | 4053 | + | 0.303726 | |
g7240 | DLA_11709 | GLQOFTK02FH5TG | CDS | 802107 | 648 | + | 0.285494 | |
g7241 | DLA_08079 | GLQOFTK02FH5TG | CDS | 803514 | 900 | + | 0.352222 | |
g7242 | DLA_08080 | GLQOFTK02FH5TG | CDS | 804525 | 231 | + | 0.316017 | |
g7243 | DLA_08081 | GLQOFTK02FH5TG | CDS | 804964 | 879 | - | 0.354949 | |
g7244 | DLA_08082 | GLQOFTK02FH5TG | CDS | 806202 | 2307 | + | 0.326831 | |
g7245 | DLA_08083 | GLQOFTK02FH5TG | CDS | 808644 | 717 | + | 0.319386 | |
g7246 | DLA_08084 | GLQOFTK02FH5TG | CDS | 809568 | 1560 | - | 0.274359 | |
g7247 | DLA_08085 | GLQOFTK02FH5TG | CDS | 811394 | 1674 | - | 0.350657 | |
g7248 | DLA_08086 | GLQOFTK02FH5TG | CDS | 813627 | 3159 | + | 0.369104 | |
g7249 | DLA_08087 | GLQOFTK02FH5TG | CDS | 816982 | 1239 | + | 0.306699 | |
g725 | DLA_00798 | F4PJNLW01A00V1 | CDS | 200058 | 3948 | + | 0.323961 | |
g7250 | DLA_08089 | GLQOFTK02FH5TG | CDS | 818320 | 984 | - | 0.336382 | |
g7251 | DLA_08090 | GLQOFTK02FH5TG | CDS | 819524 | 1608 | + | 0.333955 | |
g7252 | DLA_08091 | GLQOFTK02FH5TG | CDS | 821282 | 789 | + | 0.278834 | |
g7253 | DLA_08092 | GLQOFTK02FH5TG | CDS | 822315 | 933 | - | 0.310825 | |
g7254 | DLA_08093 | GLQOFTK02FH5TG | CDS | 826051 | 330 | + | 0.315152 | |
g7255 | DLA_08096 | GLQOFTK02FH5TG | CDS | 826740 | 5268 | - | 0.34814 | |
g7256 | DLA_08097 | GLQOFTK02FH5TG | CDS | 833383 | 405 | - | 0.308642 | |
g7257 | DLA_08098 | CAZy family GT2 catalyzes the reaction UDP-glucose (14-beta-D-glucosyl)n UDP (14-beta-D-glucosyl)n1 | GLQOFTK02FH5TG | CDS | 834154 | 3237 | - | 0.371023 |
g7258 | DLA_08101 | GLQOFTK02FH5TG | CDS | 840371 | 2235 | - | 0.359284 | |
g7259 | DLA_08102 | GLQOFTK02FH5TG | CDS | 842937 | 654 | - | 0.328746 | |
g726 | DLA_00799 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | F4PJNLW01A00V1 | CDS | 204635 | 3465 | - | 0.361039 |
g7260 | DLA_08103 | GLQOFTK02FH5TG | CDS | 844783 | 2106 | + | 0.347578 | |
g7261 | DLA_08105 | ortholog of the human SLC25A3 and S. cerevisiae MIR1 which transports inorganic phosphate from the cytosol to the mitochondrion matrix brbr bCommunity annotation:b Overview of the | GLQOFTK02FH5TG | CDS | 847818 | 936 | + | 0.354701 |
g7262 | DLA_08106 | GLQOFTK02FH5TG | CDS | 848935 | 1452 | - | 0.365014 | |
g7263 | DLA_08107 | GLQOFTK02FH5TG | CDS | 850673 | 3012 | + | 0.323705 | |
g7264 | DLA_08109 | GLQOFTK02FH5TG | CDS | 853818 | 744 | + | 0.295699 | |
g7265 | DLA_08110 | phosphorylates NAD to NADP | GLQOFTK02FH5TG | CDS | 854853 | 1323 | - | 0.31746 |
g7266 | DLA_11710 | GLQOFTK02FH5TG | CDS | 856730 | 435 | - | 0.31954 | |
g7267 | DLA_08111 | GLQOFTK02FH5TG | CDS | 857463 | 636 | + | 0.294025 | |
g7268 | DLA_08112 | CAZy family GT3 catalyzes the reaction UDP-glucose (14-alpha-D-glucosyl)(n) UDP (14-alpha-D-glucosyl)(n1) | GLQOFTK02FH5TG | CDS | 858164 | 2364 | - | 0.357445 |
g7269 | DLA_08115 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 861910 | 1713 | - | 0.304729 |
g727 | DLA_00800 | F4PJNLW01A00V1 | CDS | 208293 | 360 | - | 0.291667 | |
g7270 | DLA_08116 | AGC group AKT family protein serinethreonine kinase similar to other metazoan AktPKB including an N-terminal PH domain homologous kinase and C-terminal regulatory domains and phosphorylation sites required for AktPKB activation | GLQOFTK02FH5TG | CDS | 864074 | 2313 | - | 0.378729 |
g7271 | DLA_08117 | GLQOFTK02FH5TG | CDS | 867166 | 987 | + | 0.33536 | |
g7272 | DLA_08120 | GLQOFTK02FH5TG | CDS | 869478 | 4377 | + | 0.323966 | |
g7273 | DLA_08122 | GLQOFTK02FH5TG | CDS | 874083 | 435 | + | 0.252874 | |
g7274 | DLA_08124 | GLQOFTK02FH5TG | CDS | 874999 | 3279 | + | 0.343092 | |
g7275 | DLA_08125 | GLQOFTK02FH5TG | CDS | 878474 | 2520 | - | 0.329365 | |
g7276 | DLA_08126 | GLQOFTK02FH5TG | CDS | 881547 | 2613 | + | 0.347876 | |
g7277 | DLA_08127 | GLQOFTK02FH5TG | CDS | 884360 | 879 | - | 0.274175 | |
g7278 | DLA_08128 | GLQOFTK02FH5TG | CDS | 885407 | 2181 | - | 0.302155 | |
g7279 | DLA_08129 | GLQOFTK02FH5TG | CDS | 887702 | 1632 | - | 0.300858 | |
g728 | DLA_00801 | F4PJNLW01A00V1 | CDS | 209082 | 876 | + | 0.297945 | |
g7280 | DLA_08130 | GLQOFTK02FH5TG | CDS | 889945 | 807 | + | 0.298637 | |
g7281 | DLA_08131 | GLQOFTK02FH5TG | CDS | 890942 | 1773 | - | 0.338973 | |
g7282 | DLA_08132 | GLQOFTK02FH5TG | CDS | 893738 | 330 | - | 0.242424 | |
g7283 | DLA_08133 | GLQOFTK02FH5TG | CDS | 894541 | 1524 | + | 0.324803 | |
g7284 | DLA_08136 | GLQOFTK02FH5TG | CDS | 897408 | 486 | + | 0.31893 | |
g7285 | DLA_08138 | GLQOFTK02FH5TG | CDS | 898525 | 1047 | + | 0.311366 | |
g7286 | DLA_08139 | GLQOFTK02FH5TG | CDS | 899635 | 3267 | - | 0.326599 | |
g7287 | DLA_08140 | GLQOFTK02FH5TG | CDS | 903111 | 1119 | + | 0.287757 | |
g7288 | DLA_08141 | GLQOFTK02FH5TG | CDS | 904404 | 1536 | + | 0.32487 | |
g7289 | DLA_08142 | GLQOFTK02FH5TG | CDS | 905957 | 903 | - | 0.310078 | |
g729 | DLA_00802 | F4PJNLW01A00V1 | CDS | 212215 | 1983 | + | 0.348462 | |
g7290 | DLA_08143 | GLQOFTK02FH5TG | CDS | 907211 | 1212 | + | 0.282178 | |
g7291 | DLA_08144 | GLQOFTK02FH5TG | CDS | 908615 | 2283 | - | 0.385458 | |
g7292 | DLA_08145 | similar to aquaporin family of water-channel proteins expressed in prespore cells | GLQOFTK02FH5TG | CDS | 911786 | 825 | + | 0.398788 |
g7293 | DLA_08146 | GLQOFTK02FH5TG | CDS | 912727 | 1815 | + | 0.323416 | |
g7294 | DLA_08147 | GLQOFTK02FH5TG | CDS | 914666 | 2397 | + | 0.314977 | |
g7295 | DLA_08149 | GLQOFTK02FH5TG | CDS | 918533 | 1356 | - | 0.295723 | |
g7296 | DLA_08150 | GLQOFTK02FH5TG | CDS | 920479 | 1599 | - | 0.305191 | |
g7297 | DLA_11711 | GLQOFTK02FH5TG | CDS | 922476 | 906 | - | 0.278146 | |
g7298 | DLA_08151 | conditional processive motor protein that can move over long distances along F-actin without disassociating processiveness depends on high physiological Mgsup2sup concentrations | GLQOFTK02FH5TG | CDS | 923504 | 6678 | - | 0.33528 |
g7299 | DLA_08152 | GLQOFTK02FH5TG | CDS | 930661 | 1569 | + | 0.278521 | |
g73 | DLA_00084 | contig05409_1.exp | CDS | 173780 | 2514 | + | 0.356404 | |
g730 | DLA_00803 | F4PJNLW01A00V1 | CDS | 214464 | 1044 | - | 0.360153 | |
g7300 | DLA_08153 | full transporter consisting of two ABC domains and two transmembrane domains there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 932302 | 4476 | - | 0.358356 |
g7301 | DLA_08154 | similar to acid sphingomyelinase which hydrolyze the phosphodiester bond in sphingomyelin to form ceramide | GLQOFTK02FH5TG | CDS | 937515 | 1329 | + | 0.334086 |
g7302 | DLA_08156 | GLQOFTK02FH5TG | CDS | 939557 | 624 | + | 0.350962 | |
g7303 | DLA_08158 | GLQOFTK02FH5TG | CDS | 940952 | 345 | - | 0.284058 | |
g7304 | DLA_08160 | GLQOFTK02FH5TG | CDS | 941776 | 375 | + | 0.408 | |
g7305 | DLA_08161 | similar to MAD2 and REV7 there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 942332 | 600 | + | 0.326667 |
g7306 | DLA_08162 | GLQOFTK02FH5TG | CDS | 943298 | 582 | - | 0.298969 | |
g7307 | DLA_08163 | GLQOFTK02FH5TG | CDS | 945122 | 2166 | + | 0.388735 | |
g7308 | DLA_08164 | GLQOFTK02FH5TG | CDS | 947412 | 822 | - | 0.298054 | |
g7309 | DLA_08165 | similar to the cofilin phosphatase slingshot and to other dual-specificity phosphatasesbr there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 948410 | 1101 | + | 0.322434 |
g731 | DLA_11450 | F4PJNLW01A00V1 | CDS | 215990 | 360 | + | 0.308333 | |
g7310 | DLA_08166 | GLQOFTK02FH5TG | CDS | 949551 | 765 | - | 0.296732 | |
g7311 | DLA_08167 | GLQOFTK02FH5TG | CDS | 950417 | 6909 | - | 0.345202 | |
g7312 | DLA_08168 | GLQOFTK02FH5TG | CDS | 957709 | 2355 | + | 0.293843 | |
g7313 | DLA_08169 | GLQOFTK02FH5TG | CDS | 960361 | 1518 | - | 0.350461 | |
g7314 | DLA_08170 | component of the RNA polymerase I complex ortholog of S. cerevisiae RPA43 | GLQOFTK02FH5TG | CDS | 962349 | 963 | + | 0.298027 |
g7315 | DLA_08171 | GLQOFTK02FH5TG | CDS | 963580 | 3531 | + | 0.324554 | |
g7316 | DLA_08173 | GLQOFTK02FH5TG | CDS | 968897 | 6009 | + | 0.328008 | |
g7317 | DLA_08174 | GLQOFTK02FH5TG | CDS | 975303 | 897 | - | 0.299889 | |
g7318 | DLA_08175 | GLQOFTK02FH5TG | CDS | 976719 | 1563 | + | 0.385797 | |
g7319 | DLA_08177 | GLQOFTK02FH5TG | CDS | 979251 | 3837 | + | 0.346625 | |
g732 | DLA_00804 | F4PJNLW01A00V1 | CDS | 216545 | 2196 | + | 0.338798 | |
g7320 | DLA_08178 | GLQOFTK02FH5TG | CDS | 983465 | 483 | - | 0.331263 | |
g7321 | DLA_08180 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | GLQOFTK02FH5TG | CDS | 984926 | 483 | - | 0.325052 |
g7322 | DLA_08182 | GLQOFTK02FH5TG | CDS | 986706 | 2640 | - | 0.338636 | |
g7323 | DLA_08183 | GLQOFTK02FH5TG | CDS | 989588 | 1059 | - | 0.283286 | |
g7324 | DLA_08184 | GLQOFTK02FH5TG | CDS | 991272 | 678 | + | 0.342183 | |
g7325 | DLA_08185 | GLQOFTK02FH5TG | CDS | 992004 | 3723 | - | 0.295192 | |
g7326 | DLA_08186 | GLQOFTK02FH5TG | CDS | 996205 | 1680 | - | 0.293452 | |
g7327 | DLA_08187 | GLQOFTK02FH5TG | CDS | 998342 | 945 | - | 0.33545 | |
g7328 | DLA_08190 | GLQOFTK02FH5TG | CDS | 1002502 | 2196 | - | 0.295537 | |
g7329 | DLA_08191 | GLQOFTK02FH5TG | CDS | 1004800 | 1815 | - | 0.352617 | |
g733 | DLA_00805 | F4PJNLW01A00V1 | CDS | 218912 | 471 | - | 0.271762 | |
g7330 | DLA_11712 | GLQOFTK02FH5TG | CDS | 1007236 | 1923 | + | 0.292252 | |
g7331 | DLA_08192 | GLQOFTK02FH5TG | CDS | 1009391 | 2154 | + | 0.302693 | |
g7332 | DLA_08193 | GLQOFTK02FH5TG | CDS | 1012010 | 4275 | + | 0.34386 | |
g7333 | DLA_08194 | GLQOFTK02FH5TG | CDS | 1017215 | 1266 | + | 0.28515 | |
g7334 | DLA_08195 | GLQOFTK02FH5TG | CDS | 1018729 | 1275 | - | 0.337255 | |
g7335 | DLA_08196 | GLQOFTK02FH5TG | CDS | 1020217 | 1299 | + | 0.341032 | |
g7336 | DLA_08197 | GLQOFTK02FH5TG | CDS | 1021755 | 246 | - | 0.304878 | |
g7337 | DLA_08198 | GLQOFTK02FH5TG | CDS | 1023849 | 2184 | + | 0.292582 | |
g7338 | DLA_08199 | GLQOFTK02FH5TG | CDS | 1026386 | 714 | - | 0.270308 | |
g7339 | DLA_08201 | GLQOFTK02FH5TG | CDS | 1028324 | 642 | + | 0.336449 | |
g734 | DLA_00806 | F4PJNLW01A00V1 | CDS | 219784 | 3666 | + | 0.29078 | |
g7340 | DLA_08203 | GLQOFTK02FH5TG | CDS | 1029915 | 3885 | + | 0.324582 | |
g7341 | DLA_08205 | GLQOFTK02FH5TG | CDS | 1034587 | 987 | - | 0.344478 | |
g7342 | DLA_08206 | GLQOFTK02FH5TG | CDS | 1036092 | 1260 | + | 0.292064 | |
g7343 | DLA_08207 | GLQOFTK02FH5TG | CDS | 1037849 | 1668 | + | 0.360911 | |
g7344 | DLA_08208 | GLQOFTK02FH5TG | CDS | 1039642 | 2334 | - | 0.334619 | |
g7345 | DLA_08209 | GLQOFTK02FH5TG | CDS | 1042040 | 1194 | + | 0.376047 | |
g7346 | DLA_08210 | similar to syntaxin 1 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GLQOFTK02FH5TG | CDS | 1043861 | 1017 | + | 0.281219 |
g7347 | DLA_08211 | GLQOFTK02FH5TG | CDS | 1045164 | 2544 | - | 0.363994 | |
g7348 | DLA_08212 | GLQOFTK02FH5TG | CDS | 1048648 | 1383 | - | 0.333333 | |
g7349 | DLA_08213 | GLQOFTK02FH5TG | CDS | 1050209 | 537 | + | 0.266294 | |
g735 | DLA_00807 | F4PJNLW01A00V1 | CDS | 223542 | 6822 | - | 0.340369 | |
g7350 | DLA_08215 | GLQOFTK02FH5TG | CDS | 1050959 | 2487 | + | 0.318054 | |
g7351 | DLA_08217 | GLQOFTK02FH5TG | CDS | 1053919 | 264 | - | 0.386364 | |
g7352 | DLA_08218 | GLQOFTK02FH5TG | CDS | 1055095 | 567 | + | 0.328042 | |
g7353 | DLA_08219 | GLQOFTK02FH5TG | CDS | 1055676 | 2877 | - | 0.333333 | |
g7354 | DLA_08221 | GLQOFTK02FH5TG | CDS | 1059195 | 312 | - | 0.285256 | |
g7355 | DLA_08222 | GLQOFTK02FH5TG | CDS | 1059649 | 1869 | - | 0.29374 | |
g7356 | DLA_08223 | GLQOFTK02FH5TG | CDS | 1062412 | 555 | + | 0.428829 | |
g7357 | DLA_08224 | STE20PAK protein kinase required for normal chemotaxis contains PAK-boxP21-Rho-binding (CRIB) domain and pleckstrin homology (PH) domain | GLQOFTK02FH5TG | CDS | 1063318 | 1470 | + | 0.383673 |
g7358 | DLA_08225 | GLQOFTK02FH5TG | CDS | 1065115 | 1101 | + | 0.35604 | |
g7359 | DLA_08226 | GLQOFTK02FH5TG | CDS | 1066569 | 6324 | + | 0.347407 | |
g736 | DLA_00808 | similar to COG8 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | F4PJNLW01A00V1 | CDS | 231513 | 2127 | + | 0.29055 |
g7360 | DLA_08227 | GLQOFTK02FH5TG | CDS | 1073085 | 2037 | - | 0.303387 | |
g7361 | DLA_11713 | GLQOFTK02FH5TG | CDS | 1075611 | 210 | - | 0.271429 | |
g7362 | DLA_08228 | GLQOFTK02FH5TG | CDS | 1075918 | 1857 | + | 0.301562 | |
g7363 | DLA_08229 | GLQOFTK02FH5TG | CDS | 1077951 | 987 | - | 0.426545 | |
g7364 | DLA_08230 | GLQOFTK02FH5TG | CDS | 1080251 | 720 | - | 0.326389 | |
g7365 | DLA_08232 | GLQOFTK02FH5TG | CDS | 1081300 | 3945 | + | 0.315082 | |
g7366 | DLA_08233 | GLQOFTK02FH5TG | CDS | 1085528 | 2229 | - | 0.328398 | |
g7367 | DLA_08234 | GLQOFTK02FH5TG | CDS | 1088033 | 474 | + | 0.28481 | |
g7368 | DLA_08235 | GLQOFTK02FH5TG | CDS | 1089007 | 984 | + | 0.362805 | |
g7369 | DLA_08236 | GLQOFTK02FH5TG | CDS | 1090261 | 2121 | + | 0.359736 | |
g737 | DLA_00809 | F4PJNLW01A00V1 | CDS | 234799 | 387 | + | 0.374677 | |
g7370 | DLA_08237 | GLQOFTK02FH5TG | CDS | 1092599 | 1764 | + | 0.307823 | |
g7371 | DLA_08239 | EIF3S7 and S. pombe Moe1 ortholog the eukaryotic initiation factor zeta subunit in human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | GLQOFTK02FH5TG | CDS | 1094826 | 1605 | + | 0.358878 |
g7372 | DLA_08240 | GLQOFTK02FH5TG | CDS | 1096751 | 1893 | + | 0.325938 | |
g7373 | DLA_08241 | GLQOFTK02FH5TG | CDS | 1098823 | 843 | - | 0.302491 | |
g7374 | DLA_08242 | GLQOFTK02FH5TG | CDS | 1100166 | 3105 | + | 0.345894 | |
g7375 | DLA_08243 | GLQOFTK02FH5TG | CDS | 1103714 | 1398 | - | 0.345494 | |
g7376 | DLA_08247 | GLQOFTK02FH5TG | CDS | 1107166 | 4839 | + | 0.356892 | |
g7377 | DLA_08250 | GLQOFTK02FH5TG | CDS | 1114069 | 714 | + | 0.329132 | |
g7378 | DLA_08251 | GLQOFTK02FH5TG | CDS | 1114892 | 1305 | - | 0.264368 | |
g7379 | DLA_08252 | GLQOFTK02FH5TG | CDS | 1117238 | 1086 | + | 0.380295 | |
g738 | DLA_00811 | F4PJNLW01A00V1 | CDS | 235608 | 1470 | + | 0.308163 | |
g7380 | DLA_08253 | GLQOFTK02FH5TG | CDS | 1118900 | 423 | + | 0.323877 | |
g7381 | DLA_08254 | GLQOFTK02FH5TG | CDS | 1119608 | 2541 | + | 0.299488 | |
g7382 | DLA_08255 | GLQOFTK02FH5TG | CDS | 1122408 | 1620 | - | 0.312346 | |
g7383 | DLA_08256 | GLQOFTK02FH5TG | CDS | 1124384 | 2478 | - | 0.32042 | |
g7384 | DLA_08257 | GLQOFTK02FH5TG | CDS | 1127993 | 420 | + | 0.292857 | |
g7385 | DLA_08258 | similar to Homo sapiens transcription factor Dp-2 (E2F dimerization partner 2) which binds to E2F to activate the expression of cell cycle-regulated genes (SwissProt Q14188) | GLQOFTK02FH5TG | CDS | 1128678 | 1578 | - | 0.294043 |
g7386 | DLA_08259 | GLQOFTK02FH5TG | CDS | 1130733 | 1926 | + | 0.38162 | |
g7387 | DLA_08261 | GLQOFTK02FH5TG | CDS | 1133522 | 1056 | + | 0.354167 | |
g7388 | DLA_11714 | GLQOFTK02FH5TG | CDS | 1134972 | 948 | + | 0.333333 | |
g7389 | DLA_08262 | GLQOFTK02FH5TG | CDS | 1136649 | 4692 | + | 0.340793 | |
g739 | DLA_00812 | F4PJNLW01A00V1 | CDS | 237137 | 1650 | - | 0.306667 | |
g7390 | DLA_08263 | NRAMP family protein similar to bacterial manganese transport protein mntH contains 12 transmembrane domains involved in iron homeostasis and resistance to pathogenic bacteria | GLQOFTK02FH5TG | CDS | 1141470 | 1635 | - | 0.313761 |
g7391 | DLA_08264 | GLQOFTK02FH5TG | CDS | 1143655 | 2562 | + | 0.325527 | |
g7392 | DLA_08265 | GLQOFTK02FH5TG | CDS | 1146410 | 468 | + | 0.309829 | |
g7393 | DLA_08266 | GLQOFTK02FH5TG | CDS | 1147055 | 1536 | - | 0.350911 | |
g7394 | DLA_08267 | GLQOFTK02FH5TG | CDS | 1149952 | 1446 | + | 0.393499 | |
g7395 | DLA_08268 | GLQOFTK02FH5TG | CDS | 1151925 | 3015 | + | 0.330017 | |
g7396 | DLA_08269 | GLQOFTK02FH5TG | CDS | 1155232 | 447 | - | 0.306488 | |
g7397 | DLA_08270 | GLQOFTK02FH5TG | CDS | 1157325 | 4005 | + | 0.358302 | |
g7398 | DLA_08271 | GLQOFTK02FH5TG | CDS | 1162259 | 4167 | + | 0.340533 | |
g7399 | DLA_08272 | GLQOFTK02FH5TG | CDS | 1166649 | 282 | - | 0.304965 | |
g74 | DLA_00085 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases there is a second copy of this gene | contig05409_1.exp | CDS | 177081 | 1011 | - | 0.328388 |
g740 | DLA_00814 | similar to human EXOSC6 and S. pombe mtr3 which are components of the exosome a 3'-5' exoribonuclease complex involved in RNA processing | F4PJNLW01A00V1 | CDS | 239231 | 822 | + | 0.310219 |
g7400 | DLA_08273 | GLQOFTK02FH5TG | CDS | 1167205 | 4845 | + | 0.321362 | |
g7401 | DLA_08274 | GLQOFTK02FH5TG | CDS | 1172341 | 765 | - | 0.339869 | |
g7402 | DLA_08275 | GLQOFTK02FH5TG | CDS | 1173475 | 3729 | - | 0.320729 | |
g7403 | DLA_08277 | GLQOFTK02FH5TG | CDS | 1177519 | 2268 | - | 0.330247 | |
g7404 | DLA_08278 | GLQOFTK02FH5TG | CDS | 1180029 | 3123 | - | 0.317964 | |
g7405 | DLA_08279 | GLQOFTK02FH5TG | CDS | 1183503 | 2982 | - | 0.319249 | |
g7406 | DLA_08280 | GLQOFTK02FH5TG | CDS | 1186792 | 7824 | + | 0.32362 | |
g7407 | DLA_08281 | GLQOFTK02FH5TG | CDS | 1194955 | 3114 | - | 0.309891 | |
g7408 | DLA_08282 | GLQOFTK02FH5TG | CDS | 1198386 | 2802 | - | 0.324054 | |
g7409 | DLA_08284 | GLQOFTK02FH5TG | CDS | 1201676 | 7860 | + | 0.326463 | |
g741 | DLA_00815 | F4PJNLW01A00V1 | CDS | 240411 | 1833 | - | 0.29569 | |
g7410 | DLA_08285 | GLQOFTK02FH5TG | CDS | 1209860 | 3183 | - | 0.332077 | |
g7411 | DLA_08286 | GLQOFTK02FH5TG | CDS | 1213731 | 1203 | + | 0.334996 | |
g7412 | DLA_08287 | GLQOFTK02FH5TG | CDS | 1215296 | 3237 | - | 0.331789 | |
g7413 | DLA_08288 | GLQOFTK02FH5TG | CDS | 1219781 | 249 | + | 0.325301 | |
g7414 | DLA_08289 | GLQOFTK02FH5TG | CDS | 1220504 | 540 | - | 0.288889 | |
g7415 | DLA_08290 | GLQOFTK02FH5TG | CDS | 1221324 | 1890 | - | 0.295238 | |
g7416 | DLA_08291 | GLQOFTK02FH5TG | CDS | 1223408 | 1836 | - | 0.333333 | |
g7417 | DLA_08293 | GLQOFTK02FH5TG | CDS | 1225700 | 1260 | + | 0.375397 | |
g7418 | DLA_08294 | GLQOFTK02FH5TG | CDS | 1227701 | 1629 | - | 0.303254 | |
g7419 | DLA_08295 | GLQOFTK02FH5TG | CDS | 1229535 | 1950 | - | 0.351795 | |
g742 | DLA_00816 | F4PJNLW01A00V1 | CDS | 242340 | 1851 | - | 0.311723 | |
g7420 | DLA_08296 | GLQOFTK02FH5TG | CDS | 1231695 | 1026 | + | 0.322612 | |
g7421 | DLA_08297 | GLQOFTK02FH5TG | CDS | 1232883 | 528 | - | 0.344697 | |
g7422 | DLA_08298 | GLQOFTK02FH5TG | CDS | 1233693 | 1164 | + | 0.32646 | |
g7423 | DLA_08299 | GLQOFTK02FH5TG | CDS | 1235258 | 1386 | + | 0.401876 | |
g7424 | DLA_08300 | GLQOFTK02FH5TG | CDS | 1236840 | 1608 | - | 0.299129 | |
g7425 | DLA_08302 | GLQOFTK02FH5TG | CDS | 1238702 | 426 | - | 0.298122 | |
g7426 | DLA_08303 | GLQOFTK02FH5TG | CDS | 1239451 | 510 | + | 0.280392 | |
g7427 | DLA_08304 | GLQOFTK02FH5TG | CDS | 1240059 | 579 | - | 0.321244 | |
g7428 | DLA_08306 | GLQOFTK02FH5TG | CDS | 1241843 | 330 | + | 0.357576 | |
g7429 | DLA_08308 | GLQOFTK02FH5TG | CDS | 1243703 | 258 | + | 0.294574 | |
g743 | DLA_00817 | F4PJNLW01A00V1 | CDS | 244268 | 1881 | - | 0.310473 | |
g7430 | DLA_08309 | GLQOFTK02FH5TG | CDS | 1244453 | 2094 | - | 0.330946 | |
g7431 | DLA_08310 | GLQOFTK02FH5TG | CDS | 1247341 | 840 | - | 0.333333 | |
g7432 | DLA_08311 | GLQOFTK02FH5TG | CDS | 1249103 | 324 | + | 0.342593 | |
g7433 | DLA_08312 | GLQOFTK02FH5TG | CDS | 1249771 | 1671 | - | 0.351287 | |
g7434 | DLA_08313 | GLQOFTK02FH5TG | CDS | 1251930 | 1500 | - | 0.29 | |
g7435 | DLA_08315 | GLQOFTK02FH5TG | CDS | 1254296 | 393 | + | 0.335878 | |
g7436 | DLA_08316 | wealky similar to acid ceramidase which catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine | GLQOFTK02FH5TG | CDS | 1254788 | 1299 | - | 0.357198 |
g7437 | DLA_08318 | half transporter consisting of one ABC domain and one transmembrane domain | GLQOFTK02FH5TG | CDS | 1257547 | 1872 | + | 0.369124 |
g7438 | DLA_08319 | STE20PAKA protein kinase involved in the regulation of the cytoskeleton during chemotaxis and required for cytokinesis contains PAK-boxP21-Rho-binding (CRIB) domain found in the WASP C-terminal | GLQOFTK02FH5TG | CDS | 1260149 | 3315 | + | 0.355656 |
g7439 | DLA_08320 | GLQOFTK02FH5TG | CDS | 1263935 | 2562 | + | 0.302888 | |
g744 | DLA_00819 | F4PJNLW01A00V1 | CDS | 247009 | 1746 | - | 0.338488 | |
g7440 | DLA_08321 | GLQOFTK02FH5TG | CDS | 1266769 | 720 | - | 0.301389 | |
g7441 | DLA_08322 | GLQOFTK02FH5TG | CDS | 1268406 | 1125 | - | 0.347556 | |
g7442 | DLA_08325 | GLQOFTK02FH5TG | CDS | 1271620 | 1125 | - | 0.329778 | |
g7443 | DLA_08326 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | GLQOFTK02FH5TG | CDS | 1273568 | 3420 | - | 0.355263 |
g7444 | DLA_11715 | GLQOFTK02FH5TG | CDS | 1277332 | 849 | - | 0.366313 | |
g7445 | DLA_08327 | GLQOFTK02FH5TG | CDS | 1278694 | 2976 | - | 0.325941 | |
g7446 | DLA_08328 | GLQOFTK02FH5TG | CDS | 1282838 | 579 | - | 0.316062 | |
g7447 | DLA_08329 | GLQOFTK02FH5TG | CDS | 1283458 | 645 | - | 0.337985 | |
g7448 | DLA_08330 | GLQOFTK02FH5TG | CDS | 1284360 | 639 | - | 0.316119 | |
g7449 | DLA_08331 | GLQOFTK02FH5TG | CDS | 1285584 | 2055 | + | 0.279805 | |
g745 | DLA_00820 | catalyzes the reaction GTP oxaloacetate GDP phosphoenolpyruvate COsub2sub in gluconeogenesis and the TCA cycle | F4PJNLW01A00V1 | CDS | 249191 | 1887 | + | 0.397986 |
g7450 | DLA_08332 | GLQOFTK02FH5TG | CDS | 1287718 | 4320 | - | 0.336343 | |
g7451 | DLA_08334 | GLQOFTK02FH5TG | CDS | 1292420 | 909 | + | 0.30253 | |
g7452 | DLA_08335 | GLQOFTK02FH5TG | CDS | 1293598 | 1518 | + | 0.296443 | |
g7453 | DLA_08336 | GLQOFTK02FH5TG | CDS | 1295281 | 2235 | - | 0.280537 | |
g7454 | DLA_08337 | similar to uncharacterized eukaryotic proteins of the DUF1909 (4F5) family | GLQOFTK02FH5TG | CDS | 1298314 | 231 | + | 0.34632 |
g7455 | DLA_08338 | GLQOFTK02FH5TG | CDS | 1299161 | 1983 | - | 0.312658 | |
g7456 | DLA_08340 | GLQOFTK02FH5TG | CDS | 1301682 | 3168 | - | 0.308081 | |
g7457 | DLA_08341 | GLQOFTK02FH5TG | CDS | 1305207 | 990 | + | 0.259596 | |
g7458 | DLA_08342 | GLQOFTK02FH5TG | CDS | 1306303 | 201 | - | 0.278607 | |
g7459 | DLA_08344 | GLQOFTK02FH5TG | CDS | 1308098 | 1155 | + | 0.290043 | |
g746 | DLA_00821 | F4PJNLW01A00V1 | CDS | 251425 | 1431 | - | 0.34102 | |
g7460 | DLA_08345 | member of the Dyp-type peroxidase family lacking a typical heme-binding region does not appear to be present in higher organisms there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 1309398 | 1965 | + | 0.281425 |
g7461 | DLA_08347 | GLQOFTK02FH5TG | CDS | 1312027 | 6075 | - | 0.320823 | |
g7462 | DLA_08348 | GLQOFTK02FH5TG | CDS | 1318823 | 1131 | + | 0.335102 | |
g7463 | DLA_08349 | GLQOFTK02FH5TG | CDS | 1320351 | 1209 | - | 0.30273 | |
g7464 | DLA_08350 | GLQOFTK02FH5TG | CDS | 1321705 | 2667 | - | 0.303337 | |
g7465 | DLA_08351 | component of the RNA polymerase III complex ortholog of S. cerevisiae RPC25 and H. sapiens RPC8 there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 1325158 | 903 | - | 0.320044 |
g7466 | DLA_08353 | GLQOFTK02FH5TG | CDS | 1327222 | 2046 | - | 0.273216 | |
g7467 | DLA_08354 | GLQOFTK02FH5TG | CDS | 1329625 | 1353 | - | 0.300074 | |
g7468 | DLA_08355 | GLQOFTK02FH5TG | CDS | 1331142 | 2745 | - | 0.286339 | |
g7469 | DLA_08356 | GLQOFTK02FH5TG | CDS | 1335202 | 1944 | - | 0.308128 | |
g747 | DLA_00822 | F4PJNLW01A00V1 | CDS | 253903 | 207 | - | 0.318841 | |
g7470 | DLA_08357 | GLQOFTK02FH5TG | CDS | 1338085 | 3267 | - | 0.329966 | |
g7471 | DLA_08358 | GLQOFTK02FH5TG | CDS | 1342002 | 1641 | - | 0.366849 | |
g7472 | DLA_08359 | ortholog of the DNA primase large subunit of the DNA polymerase alpha-primase complex required for the initiation of DNA replication | GLQOFTK02FH5TG | CDS | 1344065 | 1356 | + | 0.314897 |
g7473 | DLA_08361 | GLQOFTK02FH5TG | CDS | 1345636 | 555 | - | 0.282883 | |
g7474 | DLA_08363 | GLQOFTK02FH5TG | CDS | 1346313 | 2133 | - | 0.283638 | |
g7475 | DLA_08365 | GLQOFTK02FH5TG | CDS | 1349218 | 11601 | - | 0.325403 | |
g7476 | DLA_08366 | GLQOFTK02FH5TG | CDS | 1361359 | 420 | + | 0.340476 | |
g7477 | DLA_08367 | GLQOFTK02FH5TG | CDS | 1362404 | 2241 | - | 0.339134 | |
g7478 | DLA_08370 | GLQOFTK02FH5TG | CDS | 1365797 | 1965 | - | 0.322137 | |
g7479 | DLA_08371 | GLQOFTK02FH5TG | CDS | 1367923 | 717 | - | 0.297071 | |
g748 | DLA_00823 | F4PJNLW01A00V1 | CDS | 255007 | 1323 | + | 0.269085 | |
g7480 | DLA_08372 | GLQOFTK02FH5TG | CDS | 1369269 | 1503 | + | 0.338656 | |
g7481 | DLA_08373 | GLQOFTK02FH5TG | CDS | 1371132 | 966 | - | 0.295031 | |
g7482 | DLA_08374 | belongs to the RAS-like GTPase superfamily ortholog of human OLA1 | GLQOFTK02FH5TG | CDS | 1372750 | 1134 | + | 0.349206 |
g7483 | DLA_08375 | catalyzes the reaction Hsub2subO dCTP NH3 dUTP in de novo biosynthesis of pyrimidine deoxyribonucleotides | GLQOFTK02FH5TG | CDS | 1374165 | 513 | - | 0.319688 |
g7484 | DLA_08376 | GLQOFTK02FH5TG | CDS | 1376110 | 2082 | + | 0.371278 | |
g7485 | DLA_08377 | GLQOFTK02FH5TG | CDS | 1379973 | 3231 | + | 0.374807 | |
g7486 | DLA_08378 | GLQOFTK02FH5TG | CDS | 1383522 | 3045 | + | 0.314286 | |
g7487 | DLA_11716 | GLQOFTK02FH5TG | CDS | 1386767 | 387 | - | 0.325581 | |
g7488 | DLA_08379 | GLQOFTK02FH5TG | CDS | 1387197 | 726 | - | 0.290634 | |
g7489 | DLA_08380 | GLQOFTK02FH5TG | CDS | 1388042 | 1035 | - | 0.308213 | |
g749 | DLA_00824 | ortholog of the human G6PD defects in G6PD cause chronic non-spherocytic hemolytic anemia (CNSHA) catalyzes the reaction D-glucose 6-phosphate NADPsupsup D-glucono-15-lactone 6-phosphate NADPH Hsupsup there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 256464 | 1536 | - | 0.373047 |
g7490 | DLA_08381 | GLQOFTK02FH5TG | CDS | 1389806 | 3186 | - | 0.278406 | |
g7491 | DLA_08382 | GLQOFTK02FH5TG | CDS | 1393825 | 1614 | - | 0.276952 | |
g7492 | DLA_08384 | GLQOFTK02FH5TG | CDS | 1396338 | 306 | + | 0.372549 | |
g7493 | DLA_08385 | GLQOFTK02FH5TG | CDS | 1396968 | 297 | + | 0.447811 | |
g7494 | DLA_08386 | GLQOFTK02FH5TG | CDS | 1397307 | 1236 | + | 0.38754 | |
g7495 | DLA_08387 | GLQOFTK02FH5TG | CDS | 1398713 | 942 | - | 0.267516 | |
g7496 | DLA_08388 | GLQOFTK02FH5TG | CDS | 1400396 | 483 | - | 0.337474 | |
g7497 | DLA_08389 | GLQOFTK02FH5TG | CDS | 1401005 | 1611 | - | 0.267536 | |
g7498 | DLA_11717 | GLQOFTK02FH5TG | CDS | 1403137 | 438 | - | 0.276256 | |
g7499 | DLA_08390 | GLQOFTK02FH5TG | CDS | 1404152 | 11397 | + | 0.347899 | |
g75 | DLA_00086 | contig05409_1.exp | CDS | 178641 | 390 | - | 0.274359 | |
g750 | DLA_00826 | F4PJNLW01A00V1 | CDS | 258630 | 1767 | + | 0.359932 | |
g7500 | DLA_08392 | GLQOFTK02FH5TG | CDS | 1416334 | 1764 | + | 0.278912 | |
g7501 | DLA_08393 | GLQOFTK02FH5TG | CDS | 1418499 | 2343 | + | 0.278703 | |
g7502 | DLA_08394 | GLQOFTK02FH5TG | CDS | 1421527 | 294 | + | 0.340136 | |
g7503 | DLA_08395 | GLQOFTK02FH5TG | CDS | 1422203 | 1176 | + | 0.37415 | |
g7504 | DLA_08396 | similar to S. cerevisiae Lgs1 a putative GTPase involved in 60S ribosomal subunit biogenesis | GLQOFTK02FH5TG | CDS | 1424073 | 2001 | + | 0.337331 |
g7505 | DLA_08398 | GLQOFTK02FH5TG | CDS | 1426528 | 1038 | - | 0.345857 | |
g7506 | DLA_08399 | GLQOFTK02FH5TG | CDS | 1427682 | 1758 | - | 0.287258 | |
g7507 | DLA_11718 | GLQOFTK02FH5TG | CDS | 1431546 | 1509 | + | 0.228628 | |
g7508 | DLA_08400 | GLQOFTK02FH5TG | CDS | 1433870 | 1965 | + | 0.248855 | |
g7509 | DLA_08403 | GLQOFTK02FH5TG | CDS | 1436204 | 3498 | - | 0.333905 | |
g751 | DLA_00827 | F4PJNLW01A00V1 | CDS | 260892 | 825 | + | 0.273939 | |
g7510 | DLA_08405 | GLQOFTK02FH5TG | CDS | 1440231 | 771 | - | 0.299611 | |
g7511 | DLA_08406 | GLQOFTK02FH5TG | CDS | 1441488 | 396 | + | 0.340909 | |
g7512 | DLA_08407 | GLQOFTK02FH5TG | CDS | 1442202 | 1704 | + | 0.33216 | |
g7513 | DLA_08408 | GLQOFTK02FH5TG | CDS | 1444081 | 3882 | - | 0.340804 | |
g7514 | DLA_08409 | GLQOFTK02FH5TG | CDS | 1448206 | 2724 | - | 0.310206 | |
g7515 | DLA_08410 | GLQOFTK02FH5TG | CDS | 1451510 | 642 | + | 0.32866 | |
g7516 | DLA_08411 | GLQOFTK02FH5TG | CDS | 1453541 | 675 | + | 0.29037 | |
g7517 | DLA_08412 | GLQOFTK02FH5TG | CDS | 1455062 | 906 | - | 0.315673 | |
g7518 | DLA_08413 | GLQOFTK02FH5TG | CDS | 1456324 | 1779 | + | 0.29511 | |
g7519 | DLA_08414 | GLQOFTK02FH5TG | CDS | 1458224 | 1761 | + | 0.273708 | |
g752 | DLA_00828 | F4PJNLW01A00V1 | CDS | 262490 | 1920 | + | 0.411458 | |
g7520 | DLA_11719 | GLQOFTK02FH5TG | CDS | 1460087 | 1734 | + | 0.267013 | |
g7521 | DLA_08415 | GLQOFTK02FH5TG | CDS | 1461897 | 1737 | + | 0.280944 | |
g7522 | DLA_08416 | TFIIE large subunit involved in recruitment of RNA polymerase II to the promoter activation of TFIIH and promoter opening there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 1463757 | 1254 | + | 0.315789 |
g7523 | DLA_08417 | GLQOFTK02FH5TG | CDS | 1465188 | 645 | - | 0.350388 | |
g7524 | DLA_08418 | GLQOFTK02FH5TG | CDS | 1465994 | 1224 | - | 0.285948 | |
g7525 | DLA_08419 | GLQOFTK02FH5TG | CDS | 1467414 | 1674 | + | 0.272999 | |
g7526 | DLA_08420 | GLQOFTK02FH5TG | CDS | 1469302 | 2112 | + | 0.358428 | |
g7527 | DLA_08421 | GLQOFTK02FH5TG | CDS | 1471758 | 1278 | + | 0.273083 | |
g7528 | DLA_08422 | phosphorylates 1D-myo-inositol 3456-tetrakisphosphate to 1D-myo-inositol 13456-pentakisphosphate | GLQOFTK02FH5TG | CDS | 1473227 | 987 | - | 0.276596 |
g7529 | DLA_08423 | GLQOFTK02FH5TG | CDS | 1474460 | 1920 | - | 0.295312 | |
g753 | DLA_00829 | putative ortholog of H. sapiens SHOC2 also known as Ras-binding protein Sur-8 | F4PJNLW01A00V1 | CDS | 264836 | 1536 | + | 0.350911 |
g7530 | DLA_08424 | GLQOFTK02FH5TG | CDS | 1476483 | 993 | + | 0.257805 | |
g7531 | DLA_08425 | GLQOFTK02FH5TG | CDS | 1477524 | 1950 | - | 0.314359 | |
g7532 | DLA_08426 | GLQOFTK02FH5TG | CDS | 1479839 | 2241 | - | 0.337349 | |
g7533 | DLA_08427 | GLQOFTK02FH5TG | CDS | 1483060 | 3141 | + | 0.323464 | |
g7534 | DLA_08428 | GLQOFTK02FH5TG | CDS | 1486544 | 204 | - | 0.377451 | |
g7535 | DLA_08429 | GLQOFTK02FH5TG | CDS | 1487264 | 1770 | - | 0.29435 | |
g7536 | DLA_08430 | GLQOFTK02FH5TG | CDS | 1489317 | 438 | + | 0.328767 | |
g7537 | DLA_08431 | GLQOFTK02FH5TG | CDS | 1489928 | 447 | + | 0.297539 | |
g7538 | DLA_08432 | GLQOFTK02FH5TG | CDS | 1490583 | 486 | - | 0.306584 | |
g7539 | DLA_08433 | there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 1491296 | 2943 | + | 0.321441 |
g754 | DLA_00830 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | F4PJNLW01A00V1 | CDS | 266491 | 2316 | - | 0.324698 |
g7540 | DLA_08434 | catalyzes the reaction: CTP phosphatidate diphosphate CDP-diacylglycerol provides CDP-diacylglycerol an important precursor for the synthesis of phospholipids contains 8 putative transmembrane domains | GLQOFTK02FH5TG | CDS | 1495102 | 1347 | + | 0.309577 |
g7541 | DLA_08435 | GLQOFTK02FH5TG | CDS | 1497102 | 1614 | - | 0.345105 | |
g7542 | DLA_08436 | GLQOFTK02FH5TG | CDS | 1499543 | 1359 | + | 0.299485 | |
g7543 | DLA_08437 | GLQOFTK02FH5TG | CDS | 1501490 | 3495 | + | 0.313591 | |
g7544 | DLA_08438 | GLQOFTK02FH5TG | CDS | 1505223 | 1965 | - | 0.325191 | |
g7545 | DLA_08439 | GLQOFTK02FH5TG | CDS | 1507594 | 3453 | - | 0.29945 | |
g7546 | DLA_08440 | GLQOFTK02FH5TG | CDS | 1511682 | 309 | - | 0.288026 | |
g7547 | DLA_08441 | GLQOFTK02FH5TG | CDS | 1513159 | 600 | + | 0.213333 | |
g7548 | DLA_08442 | GLQOFTK02FH5TG | CDS | 1514144 | 597 | + | 0.39866 | |
g7549 | DLA_08443 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide | GLQOFTK02FH5TG | CDS | 1515238 | 642 | + | 0.336449 |
g755 | DLA_00831 | F4PJNLW01A00V1 | CDS | 269332 | 1707 | - | 0.326303 | |
g7550 | DLA_08444 | GLQOFTK02FH5TG | CDS | 1515984 | 2223 | + | 0.253261 | |
g7551 | DLA_08445 | GLQOFTK02FH5TG | CDS | 1518238 | 1248 | - | 0.298077 | |
g7552 | DLA_08446 | GLQOFTK02FH5TG | CDS | 1519740 | 336 | + | 0.366071 | |
g7553 | DLA_08448 | GLQOFTK02FH5TG | CDS | 1520992 | 774 | + | 0.338501 | |
g7554 | DLA_11720 | GLQOFTK02FH5TG | CDS | 1522176 | 315 | + | 0.32381 | |
g7555 | DLA_08449 | GLQOFTK02FH5TG | CDS | 1522546 | 585 | + | 0.34188 | |
g7556 | DLA_08450 | GLQOFTK02FH5TG | CDS | 1524579 | 1722 | + | 0.252033 | |
g7557 | DLA_08452 | GLQOFTK02FH5TG | CDS | 1526661 | 1251 | - | 0.219824 | |
g7558 | DLA_08453 | GLQOFTK02FH5TG | CDS | 1528443 | 1062 | + | 0.332392 | |
g7559 | DLA_08454 | GLQOFTK02FH5TG | CDS | 1529803 | 975 | + | 0.267692 | |
g756 | DLA_00833 | F4PJNLW01A00V1 | CDS | 271654 | 753 | - | 0.361222 | |
g7560 | DLA_08455 | GLQOFTK02FH5TG | CDS | 1530851 | 4974 | - | 0.271009 | |
g7561 | DLA_08456 | GLQOFTK02FJ5LP | CDS | 2 | 2500 | + | 0.3856 | |
g7562 | DLA_08458 | GLQOFTK02G2F2O | CDS | 121 | 1536 | - | 0.342448 | |
g7563 | DLA_08459 | GLQOFTK02G2F2O | CDS | 2117 | 2343 | + | 0.293641 | |
g7564 | DLA_08460 | GLQOFTK02G2F2O | CDS | 4919 | 1695 | - | 0.321534 | |
g7565 | DLA_08461 | GLQOFTK02G2F2O | CDS | 7014 | 1107 | + | 0.266486 | |
g7566 | DLA_08462 | GLQOFTK02G2F2O | CDS | 8848 | 1590 | - | 0.31195 | |
g7567 | DLA_08463 | GLQOFTK02G2F2O | CDS | 11165 | 3903 | + | 0.320266 | |
g7568 | DLA_08466 | GLQOFTK02G2F2O | CDS | 15174 | 735 | - | 0.246258 | |
g7569 | DLA_08467 | GLQOFTK02G2F2O | CDS | 19070 | 741 | - | 0.296896 | |
g757 | DLA_00834 | F4PJNLW01A00V1 | CDS | 272712 | 912 | - | 0.246711 | |
g7570 | DLA_08468 | GLQOFTK02G2F2O | CDS | 20743 | 1446 | + | 0.267635 | |
g7571 | DLA_08469 | GLQOFTK02G2F2O | CDS | 22723 | 1053 | - | 0.266857 | |
g7572 | DLA_11721 | GLQOFTK02G2F2O | CDS | 25460 | 204 | - | 0.323529 | |
g7573 | DLA_08470 | GLQOFTK02G2F2O | CDS | 26876 | 1050 | - | 0.270476 | |
g7574 | DLA_08472 | GLQOFTK02G2F2O | CDS | 28835 | 396 | - | 0.229798 | |
g7575 | DLA_08473 | GLQOFTK02G2F2O | CDS | 29823 | 1461 | + | 0.285421 | |
g7576 | DLA_08474 | GLQOFTK02G2F2O | CDS | 31480 | 675 | - | 0.371852 | |
g7577 | DLA_08476 | GLQOFTK02G2F2O | CDS | 34103 | 501 | - | 0.289421 | |
g7578 | DLA_08478 | GLQOFTK02G2F2O | CDS | 36274 | 1053 | - | 0.276353 | |
g7579 | DLA_08479 | GLQOFTK02G2F2O | CDS | 38228 | 576 | + | 0.295139 | |
g758 | DLA_00835 | F4PJNLW01A00V1 | CDS | 273958 | 909 | - | 0.330033 | |
g7580 | DLA_08480 | GLQOFTK02G2F2O | CDS | 38971 | 1050 | - | 0.272381 | |
g7581 | DLA_11722 | GLQOFTK02G2F2O | CDS | 40381 | 801 | + | 0.274657 | |
g7582 | DLA_08481 | GLQOFTK02G2F2O | CDS | 41243 | 786 | + | 0.260814 | |
g7583 | DLA_08482 | GLQOFTK02G2F2O | CDS | 42360 | 1053 | - | 0.272555 | |
g7584 | DLA_08484 | GLQOFTK02G2F2O | CDS | 44418 | 1671 | + | 0.333333 | |
g7585 | DLA_08485 | GLQOFTK02G2F2O | CDS | 46273 | 1152 | + | 0.295139 | |
g7586 | DLA_08487 | GLQOFTK02G2F2O | CDS | 48067 | 2085 | + | 0.278177 | |
g7587 | DLA_08488 | GLQOFTK02G2F2O | CDS | 50354 | 5013 | - | 0.324556 | |
g7588 | DLA_08489 | GLQOFTK02G2F2O | CDS | 56666 | 828 | - | 0.295894 | |
g7589 | DLA_08490 | GLQOFTK02G2F2O | CDS | 57793 | 525 | + | 0.272381 | |
g759 | DLA_00836 | F4PJNLW01A00V1 | CDS | 275234 | 381 | - | 0.291339 | |
g7590 | DLA_08491 | GLQOFTK02G2F2O | CDS | 58393 | 2388 | - | 0.322446 | |
g7591 | DLA_08493 | GLQOFTK02G2F2O | CDS | 63296 | 1386 | + | 0.37013 | |
g7592 | DLA_08494 | GLQOFTK02G2F2O | CDS | 65134 | 1248 | - | 0.314103 | |
g7593 | DLA_08495 | GLQOFTK02G2F2O | CDS | 66544 | 1296 | + | 0.358796 | |
g7594 | DLA_08497 | GLQOFTK02G2F2O | CDS | 68849 | 3240 | - | 0.335802 | |
g7595 | DLA_08498 | GLQOFTK02G2F2O | CDS | 72615 | 3561 | + | 0.344285 | |
g7596 | DLA_08499 | GLQOFTK02G2F2O | CDS | 76661 | 1476 | - | 0.319106 | |
g7597 | DLA_08502 | GLQOFTK02G2F2O | CDS | 79282 | 2178 | + | 0.332874 | |
g7598 | DLA_08503 | GLQOFTK02G2F2O | CDS | 81854 | 1635 | - | 0.29052 | |
g7599 | DLA_11723 | GLQOFTK02G2F2O | CDS | 84638 | 459 | + | 0.324619 | |
g76 | DLA_00088 | contig05409_1.exp | CDS | 179466 | 888 | + | 0.334459 | |
g760 | DLA_00837 | F4PJNLW01A00V1 | CDS | 275914 | 1620 | + | 0.307407 | |
g7600 | DLA_08504 | GLQOFTK02G2F2O | CDS | 85331 | 2091 | + | 0.286944 | |
g7601 | DLA_08505 | GLQOFTK02G2F2O | CDS | 87509 | 1578 | - | 0.338403 | |
g7602 | DLA_08506 | GLQOFTK02G2F2O | CDS | 89225 | 2895 | + | 0.334715 | |
g7603 | DLA_11724 | GLQOFTK02G2F2O | CDS | 92327 | 378 | + | 0.28836 | |
g7604 | DLA_08507 | GLQOFTK02G2F2O | CDS | 93078 | 1074 | + | 0.301676 | |
g7605 | DLA_08508 | GLQOFTK02G2F2O | CDS | 94411 | 465 | - | 0.337634 | |
g7606 | DLA_08510 | GLQOFTK02G2F2O | CDS | 95344 | 1983 | + | 0.30358 | |
g7607 | DLA_08511 | GLQOFTK02G2F2O | CDS | 97545 | 897 | - | 0.352285 | |
g7608 | DLA_08512 | GLQOFTK02G2F2O | CDS | 98912 | 651 | + | 0.291859 | |
g7609 | DLA_08513 | GLQOFTK02G2F2O | CDS | 99678 | 1227 | - | 0.360228 | |
g761 | DLA_00838 | F4PJNLW01A00V1 | CDS | 277567 | 1449 | - | 0.310559 | |
g7610 | DLA_11725 | GLQOFTK02G2F2O | CDS | 102233 | 687 | + | 0.330422 | |
g7611 | DLA_08514 | GLQOFTK02G2F2O | CDS | 103110 | 2076 | + | 0.308767 | |
g7612 | DLA_08515 | GLQOFTK02G2F2O | CDS | 105408 | 1311 | - | 0.356979 | |
g7613 | DLA_08516 | GLQOFTK02G2F2O | CDS | 107113 | 717 | + | 0.294282 | |
g7614 | DLA_08517 | GLQOFTK02G2F2O | CDS | 108115 | 1812 | - | 0.3234 | |
g7615 | DLA_08519 | GLQOFTK02G2F2O | CDS | 114555 | 1650 | - | 0.302424 | |
g7616 | DLA_08520 | GLQOFTK02G2F2O | CDS | 116587 | 567 | - | 0.280423 | |
g7617 | DLA_08521 | GLQOFTK02G2F2O | CDS | 118207 | 2454 | - | 0.368378 | |
g7618 | DLA_08522 | GLQOFTK02G2F2O | CDS | 121750 | 1038 | - | 0.314066 | |
g7619 | DLA_08523 | GLQOFTK02G2F2O | CDS | 123368 | 948 | + | 0.372363 | |
g762 | DLA_11451 | F4PJNLW01A00V1 | CDS | 279080 | 1206 | + | 0.313433 | |
g7620 | DLA_08524 | GLQOFTK02G2F2O | CDS | 124723 | 3159 | + | 0.3346 | |
g7621 | DLA_08525 | GLQOFTK02G2F2O | CDS | 128029 | 2262 | - | 0.284262 | |
g7622 | DLA_08526 | GLQOFTK02G2F2O | CDS | 130616 | 1599 | - | 0.273296 | |
g7623 | DLA_08527 | GLQOFTK02G2F2O | CDS | 132797 | 2373 | + | 0.347661 | |
g7624 | DLA_08528 | GLQOFTK02G2F2O | CDS | 135623 | 1311 | - | 0.285278 | |
g7625 | DLA_08529 | highly similar to mammalian puromycin-sensitive aminopeptidase belonging to the peptidase M1 family (metallopeptidases) contains a peptidase M1 domain including a zinc-binding site | GLQOFTK02G2F2O | CDS | 139243 | 2667 | - | 0.347957 |
g7626 | DLA_08530 | GLQOFTK02G2F2O | CDS | 142508 | 924 | + | 0.300866 | |
g7627 | DLA_08531 | GLQOFTK02G2F2O | CDS | 143813 | 1113 | + | 0.36478 | |
g7628 | DLA_11726 | GLQOFTK02G2F2O | CDS | 145413 | 1512 | + | 0.277116 | |
g7629 | DLA_08532 | half transporter consisting of one ABC domain and one transmembrane domain | GLQOFTK02G2F2O | CDS | 146959 | 2214 | - | 0.349142 |
g763 | DLA_00839 | F4PJNLW01A00V1 | CDS | 280717 | 828 | + | 0.285024 | |
g7630 | DLA_08533 | GLQOFTK02G2F2O | CDS | 149375 | 270 | + | 0.322222 | |
g7631 | DLA_08534 | central component of the U4U6-U5 snRNP complex contains the PRO8NT PROCN PRO C-terminal and Mov34MPNPAD-1 domains found in pre-mRNA splicing factors of the PRO8 family | GLQOFTK02G2F2O | CDS | 149914 | 6996 | + | 0.384791 |
g7632 | DLA_08535 | GLQOFTK02G2F2O | CDS | 157051 | 663 | - | 0.257919 | |
g7633 | DLA_08536 | GLQOFTK02G2F2O | CDS | 158322 | 2430 | + | 0.290123 | |
g7634 | DLA_11727 | GLQOFTK02G2F2O | CDS | 161245 | 1026 | + | 0.339181 | |
g7635 | DLA_08537 | GLQOFTK02G2F2O | CDS | 162390 | 1383 | - | 0.334779 | |
g7636 | DLA_08539 | GLQOFTK02G2F2O | CDS | 164236 | 867 | + | 0.297578 | |
g7637 | DLA_08541 | GLQOFTK02G2F2O | CDS | 165894 | 4134 | + | 0.332608 | |
g7638 | DLA_11728 | GLQOFTK02G2F2O | CDS | 171015 | 825 | + | 0.301818 | |
g7639 | DLA_08542 | GLQOFTK02G2F2O | CDS | 172154 | 2055 | + | 0.296837 | |
g764 | DLA_00841 | F4PJNLW01A00V1 | CDS | 282447 | 306 | - | 0.294118 | |
g7640 | DLA_08543 | GLQOFTK02G2F2O | CDS | 174255 | 1686 | - | 0.336299 | |
g7641 | DLA_08544 | GLQOFTK02G2F2O | CDS | 176418 | 1617 | + | 0.294372 | |
g7642 | DLA_08545 | GLQOFTK02G2F2O | CDS | 178133 | 3213 | - | 0.323374 | |
g7643 | DLA_08546 | GLQOFTK02G2F2O | CDS | 183857 | 1197 | - | 0.355054 | |
g7644 | DLA_08547 | GLQOFTK02G2F2O | CDS | 185737 | 1284 | + | 0.314642 | |
g7645 | DLA_08548 | GLQOFTK02G2F2O | CDS | 187112 | 1056 | - | 0.326705 | |
g7646 | DLA_08550 | GLQOFTK02G2F2O | CDS | 188693 | 1848 | + | 0.308442 | |
g7647 | DLA_08551 | GLQOFTK02G2F2O | CDS | 190745 | 348 | - | 0.316092 | |
g7648 | DLA_08552 | GLQOFTK02G2F2O | CDS | 191176 | 834 | - | 0.335731 | |
g7649 | DLA_08553 | GLQOFTK02G2F2O | CDS | 192510 | 2517 | - | 0.357569 | |
g765 | DLA_00842 | F4PJNLW01A00V1 | CDS | 283616 | 396 | + | 0.363636 | |
g7650 | DLA_08555 | GLQOFTK02G2F2O | CDS | 196825 | 810 | - | 0.332099 | |
g7651 | DLA_11729 | GLQOFTK02G2F2O | CDS | 198101 | 918 | + | 0.324619 | |
g7652 | DLA_08556 | GLQOFTK02G2F2O | CDS | 199318 | 1431 | + | 0.310273 | |
g7653 | DLA_08557 | GLQOFTK02G2F2O | CDS | 200961 | 600 | - | 0.291667 | |
g7654 | DLA_11730 | GLQOFTK02G2F2O | CDS | 201761 | 3231 | - | 0.314144 | |
g7655 | DLA_08558 | GLQOFTK02G2F2O | CDS | 205992 | 1665 | - | 0.263063 | |
g7656 | DLA_11731 | GLQOFTK02G2F2O | CDS | 210334 | 600 | - | 0.293333 | |
g7657 | DLA_08559 | GLQOFTK02G2F2O | CDS | 211103 | 3228 | - | 0.316605 | |
g7658 | DLA_08561 | GLQOFTK02G2F2O | CDS | 215043 | 1401 | + | 0.359743 | |
g7659 | DLA_08562 | GLQOFTK02G2F2O | CDS | 216682 | 540 | - | 0.344444 | |
g766 | DLA_00843 | F4PJNLW01A00V1 | CDS | 284519 | 1326 | - | 0.293364 | |
g7660 | DLA_08564 | GLQOFTK02G2F2O | CDS | 218083 | 2028 | - | 0.336292 | |
g7661 | DLA_08565 | GLQOFTK02G2F2O | CDS | 220668 | 1914 | - | 0.367816 | |
g7662 | DLA_08566 | GLQOFTK02G2F2O | CDS | 223228 | 930 | + | 0.310753 | |
g7663 | DLA_08568 | GLQOFTK02G2F2O | CDS | 225980 | 1332 | + | 0.338589 | |
g7664 | DLA_08569 | GLQOFTK02G2F2O | CDS | 227457 | 696 | - | 0.265805 | |
g7665 | DLA_08570 | GLQOFTK02G2F2O | CDS | 228435 | 321 | + | 0.352025 | |
g7666 | DLA_08571 | GLQOFTK02G2F2O | CDS | 229400 | 3729 | + | 0.335747 | |
g7667 | DLA_08572 | GLQOFTK02G2F2O | CDS | 233474 | 732 | - | 0.331967 | |
g7668 | DLA_08574 | GLQOFTK02G2F2O | CDS | 235170 | 4119 | + | 0.315125 | |
g7669 | DLA_08576 | GLQOFTK02G2F2O | CDS | 239572 | 900 | - | 0.28 | |
g767 | DLA_00844 | F4PJNLW01A00V1 | CDS | 285946 | 957 | + | 0.345873 | |
g7670 | DLA_08577 | GLQOFTK02G2F2O | CDS | 242159 | 921 | - | 0.322476 | |
g7671 | DLA_08578 | GLQOFTK02G2F2O | CDS | 243157 | 360 | - | 0.327778 | |
g7672 | DLA_08579 | GLQOFTK02G2F2O | CDS | 244749 | 357 | + | 0.282913 | |
g7673 | DLA_08580 | GLQOFTK02G2F2O | CDS | 246143 | 1617 | + | 0.31107 | |
g7674 | DLA_08582 | GLQOFTK02G2F2O | CDS | 248651 | 351 | + | 0.253561 | |
g7675 | DLA_08583 | GLQOFTK02G2F2O | CDS | 249431 | 432 | + | 0.31713 | |
g7676 | DLA_08584 | GLQOFTK02G2F2O | CDS | 250493 | 426 | - | 0.276995 | |
g7677 | DLA_08585 | GLQOFTK02G2F2O | CDS | 251569 | 1548 | + | 0.324289 | |
g7678 | DLA_08586 | GLQOFTK02G2F2O | CDS | 253171 | 6300 | - | 0.329524 | |
g7679 | DLA_08587 | GLQOFTK02G2F2O | CDS | 260354 | 4086 | - | 0.320607 | |
g768 | DLA_00846 | F4PJNLW01A00V1 | CDS | 287419 | 987 | - | 0.331307 | |
g7680 | DLA_08588 | GLQOFTK02G2F2O | CDS | 264928 | 4056 | - | 0.337032 | |
g7681 | DLA_08589 | GLQOFTK02G2F2O | CDS | 269530 | 4002 | - | 0.327336 | |
g7682 | DLA_08590 | GLQOFTK02G2F2O | CDS | 274055 | 2502 | - | 0.338129 | |
g7683 | DLA_08592 | GLQOFTK02G2F2O | CDS | 277666 | 1203 | - | 0.284289 | |
g7684 | DLA_08593 | GLQOFTK02G2F2O | CDS | 280896 | 1041 | + | 0.331412 | |
g7685 | DLA_08594 | GLQOFTK02G2F2O | CDS | 282148 | 4089 | - | 0.32942 | |
g7686 | DLA_08595 | GLQOFTK02G2F2O | CDS | 286649 | 4146 | - | 0.310902 | |
g7687 | DLA_08598 | GLQOFTK02G2F2O | CDS | 292903 | 2943 | - | 0.305471 | |
g7688 | DLA_08599 | GLQOFTK02G2F2O | CDS | 296484 | 4050 | - | 0.31679 | |
g7689 | DLA_08600 | GLQOFTK02G2F2O | CDS | 301331 | 1173 | - | 0.319693 | |
g769 | DLA_00847 | F4PJNLW01A00V1 | CDS | 288983 | 5649 | + | 0.355815 | |
g7690 | DLA_08601 | GLQOFTK02G2F2O | CDS | 302809 | 1521 | + | 0.315582 | |
g7691 | DLA_08602 | GLQOFTK02G2F2O | CDS | 304650 | 6945 | + | 0.324694 | |
g7692 | DLA_08603 | GLQOFTK02G2F2O | CDS | 312314 | 678 | + | 0.346608 | |
g7693 | DLA_08606 | GLQOFTK02G2F2O | CDS | 313796 | 672 | + | 0.394345 | |
g7694 | DLA_08607 | GLQOFTK02G2F2O | CDS | 315208 | 672 | + | 0.397321 | |
g7695 | DLA_08608 | GLQOFTK02G2F2O | CDS | 316850 | 672 | + | 0.394345 | |
g7696 | DLA_08609 | controls the topological state of DNA by transient double-strand breakage and subsequent rejoining of DNA strands this is predicted to be a nuclear topoisomerase II | GLQOFTK02G2F2O | CDS | 317745 | 4539 | - | 0.352941 |
g7697 | DLA_08610 | GLQOFTK02G2F2O | CDS | 322741 | 1179 | + | 0.319762 | |
g7698 | DLA_08611 | GLQOFTK02G2F2O | CDS | 324300 | 822 | + | 0.333333 | |
g7699 | DLA_08612 | GLQOFTK02G2F2O | CDS | 325595 | 2148 | + | 0.346369 | |
g77 | DLA_00089 | contig05409_1.exp | CDS | 180412 | 684 | - | 0.252924 | |
g770 | DLA_00848 | F4PJNLW01A00V1 | CDS | 294833 | 375 | - | 0.277333 | |
g7700 | DLA_08615 | GLQOFTK02G2F2O | CDS | 328717 | 2313 | + | 0.344142 | |
g7701 | DLA_08618 | GLQOFTK02G2F2O | CDS | 332555 | 3444 | + | 0.305459 | |
g7702 | DLA_08619 | GLQOFTK02G2F2O | CDS | 336146 | 495 | - | 0.311111 | |
g7703 | DLA_08620 | GLQOFTK02G2F2O | CDS | 337995 | 6435 | + | 0.343745 | |
g7704 | DLA_08622 | GLQOFTK02G2F2O | CDS | 345797 | 234 | + | 0.286325 | |
g7705 | DLA_08623 | GLQOFTK02G2F2O | CDS | 346500 | 477 | + | 0.259958 | |
g7706 | DLA_08624 | GLQOFTK02G2F2O | CDS | 347129 | 831 | - | 0.276775 | |
g7707 | DLA_08626 | utilizes the methyl donor S-adenosyl-L-methionine to catalyze the site-specific 2'-hydroxyl methylation of ribose moieties in pre-ribosomal RNA | GLQOFTK02G2F2O | CDS | 349605 | 999 | - | 0.429429 |
g7708 | DLA_08627 | GLQOFTK02G2F2O | CDS | 351215 | 996 | - | 0.368474 | |
g7709 | DLA_11732 | GLQOFTK02G2F2O | CDS | 352794 | 306 | - | 0.395425 | |
g771 | DLA_00849 | F4PJNLW01A00V1 | CDS | 295345 | 558 | - | 0.284946 | |
g7710 | DLA_11733 | GLQOFTK02G2F2O | CDS | 353599 | 198 | - | 0.272727 | |
g7711 | DLA_08628 | similar to the mammalian CD9 antigen contains a tetraspanin and 4 putative transmembrane domains | GLQOFTK02G2F2O | CDS | 354701 | 681 | + | 0.352423 |
g7712 | DLA_08629 | GLQOFTK02G2F2O | CDS | 355717 | 2370 | + | 0.348101 | |
g7713 | DLA_08630 | GLQOFTK02G2F2O | CDS | 358254 | 3864 | + | 0.336698 | |
g7714 | DLA_08632 | GLQOFTK02G2F2O | CDS | 362992 | 1401 | - | 0.320485 | |
g7715 | DLA_08633 | GLQOFTK02G2F2O | CDS | 365135 | 4098 | - | 0.32162 | |
g7716 | DLA_08634 | GLQOFTK02G2F2O | CDS | 369837 | 2043 | + | 0.297602 | |
g7717 | DLA_08636 | GLQOFTK02G2F2O | CDS | 372435 | 1083 | + | 0.313019 | |
g7718 | DLA_08637 | GLQOFTK02G2F2O | CDS | 374164 | 2229 | - | 0.349933 | |
g7719 | DLA_11734 | GLQOFTK02G2F2O | CDS | 376628 | 942 | - | 0.301486 | |
g772 | DLA_00850 | F4PJNLW01A00V1 | CDS | 296003 | 1506 | + | 0.286189 | |
g7720 | DLA_08638 | GLQOFTK02G2F2O | CDS | 377895 | 1539 | - | 0.2859 | |
g7721 | DLA_08639 | GLQOFTK02G2F2O | CDS | 380620 | 1179 | + | 0.345208 | |
g7722 | DLA_08641 | GLQOFTK02G2F2O | CDS | 382113 | 876 | + | 0.27169 | |
g7723 | DLA_11735 | GLQOFTK02G2F2O | CDS | 383287 | 288 | + | 0.350694 | |
g7724 | DLA_08642 | GLQOFTK02G2F2O | CDS | 383694 | 4512 | - | 0.359043 | |
g7725 | DLA_11736 | GLQOFTK02G2F2O | CDS | 389027 | 1224 | - | 0.353758 | |
g7726 | DLA_08643 | GLQOFTK02G2F2O | CDS | 391355 | 4086 | - | 0.311552 | |
g7727 | DLA_08644 | GLQOFTK02G2F2O | CDS | 396299 | 3969 | - | 0.322247 | |
g7728 | DLA_08645 | GLQOFTK02G2F2O | CDS | 401058 | 4053 | - | 0.325931 | |
g7729 | DLA_11737 | GLQOFTK02G2F2O | CDS | 405904 | 234 | - | 0.380342 | |
g773 | DLA_00851 | ortholog of S. cerevisiae and H. sapiens EMG1 involved in 40S ribosome biogenesis | F4PJNLW01A00V1 | CDS | 297802 | 978 | - | 0.322086 |
g7730 | DLA_08646 | GLQOFTK02G2F2O | CDS | 407578 | 261 | - | 0.35249 | |
g7731 | DLA_08647 | GLQOFTK02G2F2O | CDS | 408323 | 1794 | + | 0.30825 | |
g7732 | DLA_08648 | GLQOFTK02G2F2O | CDS | 410654 | 1920 | - | 0.280208 | |
g7733 | DLA_08650 | GLQOFTK02G2F2O | CDS | 413889 | 1443 | - | 0.358281 | |
g7734 | DLA_08651 | GLQOFTK02G2F2O | CDS | 415454 | 1563 | - | 0.370441 | |
g7735 | DLA_08652 | GLQOFTK02G2F2O | CDS | 417413 | 387 | + | 0.377261 | |
g7736 | DLA_08653 | GLQOFTK02G2F2O | CDS | 418053 | 945 | - | 0.283598 | |
g7737 | DLA_08654 | GLQOFTK02G2F2O | CDS | 419526 | 1137 | + | 0.288478 | |
g7738 | DLA_08655 | GLQOFTK02G2F2O | CDS | 421308 | 1755 | - | 0.361254 | |
g7739 | DLA_11738 | GLQOFTK02G2F2O | CDS | 423147 | 240 | + | 0.308333 | |
g774 | DLA_00852 | similar to human LMAN1 (lectin mannose-binding protein 1) belongs to the legume-like lectin family contains 1 predicted transmembrane domain similar to D. purpureum protein | F4PJNLW01A00V1 | CDS | 299268 | 1593 | + | 0.327056 |
g7740 | DLA_11739 | member of a new lysozyme class there is a second copy of this gene | GLQOFTK02G2F2O | CDS | 423794 | 852 | - | 0.369718 |
g7741 | DLA_08656 | GLQOFTK02G2F2O | CDS | 425482 | 1005 | + | 0.337313 | |
g7742 | DLA_08657 | GLQOFTK02G2F2O | CDS | 427080 | 1161 | - | 0.328165 | |
g7743 | DLA_08658 | GLQOFTK02G2F2O | CDS | 428650 | 1686 | - | 0.291222 | |
g7744 | DLA_08659 | GLQOFTK02G2F2O | CDS | 430417 | 1089 | - | 0.337006 | |
g7745 | DLA_08660 | GLQOFTK02G2F2O | CDS | 431663 | 1128 | - | 0.332447 | |
g7746 | DLA_08661 | GLQOFTK02G2F2O | CDS | 433203 | 2652 | + | 0.334465 | |
g7747 | DLA_08662 | conserved protein mainly among fungi and plants | GLQOFTK02G2F2O | CDS | 436087 | 2898 | + | 0.333333 |
g7748 | DLA_08663 | GLQOFTK02G2F2O | CDS | 439272 | 1941 | + | 0.296754 | |
g7749 | DLA_08664 | GLQOFTK02G2F2O | CDS | 441430 | 2250 | - | 0.296444 | |
g775 | DLA_00854 | F4PJNLW01A00V1 | CDS | 303099 | 306 | - | 0.261438 | |
g7750 | DLA_08666 | catalyzes the reaction ATP L-tryptophan tRNATrp AMP diphosphate L-tryptophan-tRNAThr similar to bacterial tryptophan-tRNA ligases | GLQOFTK02G2F2O | CDS | 444155 | 1617 | - | 0.313544 |
g7751 | DLA_08668 | GLQOFTK02G2F2O | CDS | 446051 | 936 | + | 0.319444 | |
g7752 | DLA_08669 | GLQOFTK02G2F2O | CDS | 447431 | 915 | - | 0.28306 | |
g7753 | DLA_08670 | GLQOFTK02G2F2O | CDS | 448934 | 2043 | - | 0.358297 | |
g7754 | DLA_08672 | GLQOFTK02G2F2O | CDS | 452174 | 1539 | + | 0.389864 | |
g7755 | DLA_08674 | GLQOFTK02G2F2O | CDS | 455474 | 5547 | - | 0.348116 | |
g7756 | DLA_08675 | GLQOFTK02G2F2O | CDS | 461658 | 1083 | + | 0.33795 | |
g7757 | DLA_11740 | GLQOFTK02G2F2O | CDS | 462800 | 588 | + | 0.297619 | |
g7758 | DLA_08676 | GLQOFTK02G2F2O | CDS | 463871 | 1437 | + | 0.322895 | |
g7759 | DLA_08677 | GLQOFTK02G2F2O | CDS | 465366 | 948 | - | 0.287975 | |
g776 | DLA_00855 | F4PJNLW01A00V1 | CDS | 303707 | 1491 | + | 0.315225 | |
g7760 | DLA_08678 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | GLQOFTK02G2F2O | CDS | 466621 | 3690 | - | 0.304336 |
g7761 | DLA_08679 | GLQOFTK02G2F2O | CDS | 470447 | 1743 | + | 0.279403 | |
g7762 | DLA_08680 | GLQOFTK02G2F2O | CDS | 472264 | 4284 | - | 0.336835 | |
g7763 | DLA_08681 | GLQOFTK02G2F2O | CDS | 476830 | 1227 | - | 0.231459 | |
g7764 | DLA_08682 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | GLQOFTK02G2F2O | CDS | 478161 | 1740 | - | 0.356322 |
g7765 | DLA_08683 | GLQOFTK02G2F2O | CDS | 480228 | 1548 | + | 0.29199 | |
g7766 | DLA_08684 | member of the TKL (tyrosine kinase-like) group of protein kinases contains filamin repeat similar to ABP120 | GLQOFTK02G2F2O | CDS | 482933 | 4218 | + | 0.336415 |
g7767 | DLA_08685 | GLQOFTK02G2F2O | CDS | 487671 | 573 | + | 0.26178 | |
g7768 | DLA_08686 | GLQOFTK02G2F2O | CDS | 488882 | 768 | + | 0.321615 | |
g7769 | DLA_08687 | GLQOFTK02G2F2O | CDS | 489736 | 1656 | - | 0.288043 | |
g777 | DLA_00856 | F4PJNLW01A00V1 | CDS | 305305 | 3129 | + | 0.286353 | |
g7770 | DLA_08688 | GLQOFTK02G2F2O | CDS | 491561 | 1971 | - | 0.333841 | |
g7771 | DLA_11741 | GLQOFTK02G2F2O | CDS | 493936 | 309 | - | 0.352751 | |
g7772 | DLA_08689 | GLQOFTK02G2F2O | CDS | 494507 | 585 | + | 0.317949 | |
g7773 | DLA_08690 | GLQOFTK02G2F2O | CDS | 495240 | 753 | - | 0.371846 | |
g7774 | DLA_08691 | GLQOFTK02G2F2O | CDS | 496310 | 2664 | - | 0.311937 | |
g7775 | DLA_11742 | GLQOFTK02G2F2O | CDS | 499125 | 711 | - | 0.367089 | |
g7776 | DLA_08692 | GLQOFTK02G2F2O | CDS | 500237 | 903 | - | 0.312292 | |
g7777 | DLA_08693 | contains a signal peptide a PA14 (anthrax protection antigen) domain 4 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | GLQOFTK02G2F2O | CDS | 502389 | 2082 | - | 0.352546 |
g7778 | DLA_08694 | GLQOFTK02G2F2O | CDS | 506550 | 1257 | + | 0.35004 | |
g7779 | DLA_08695 | eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase putative protein serinethreonine kinase contains two kinase domains and a HisRS domain N-terminal kinase domain related to STE group C-terminal kinase domain related to GCN2 subfamily | GLQOFTK02G2F2O | CDS | 508309 | 6072 | + | 0.339427 |
g778 | DLA_00858 | F4PJNLW01A00V1 | CDS | 308752 | 1359 | - | 0.303164 | |
g7780 | DLA_08696 | ortholog of the mammalian C15orf15 gene and the S. cerevisiae RLP24 protein which is involved in the biogenesis of the 60S ribosomal subunit and at the end of biogenesis is likely to be exchanged for its ribosomal homologue rpl24 | GLQOFTK02G2F2O | CDS | 514511 | 516 | - | 0.286822 |
g7781 | DLA_08697 | GLQOFTK02G2F2O | CDS | 515375 | 2706 | + | 0.307834 | |
g7782 | DLA_08698 | GLQOFTK02G2F2O | CDS | 518191 | 678 | + | 0.266962 | |
g7783 | DLA_08699 | GLQOFTK02G2F2O | CDS | 518968 | 2958 | - | 0.331643 | |
g7784 | DLA_08700 | putative protein serinethreonine kinase similar to yeast CDC5 Drosophila polo and mammalian PLK which play a role in mitosis and localize to the centrosomes | GLQOFTK02G2F2O | CDS | 522616 | 2478 | - | 0.315174 |
g7785 | DLA_08701 | GLQOFTK02G2F2O | CDS | 526126 | 1215 | - | 0.291358 | |
g7786 | DLA_08702 | GLQOFTK02G2F2O | CDS | 527605 | 957 | + | 0.318704 | |
g7787 | DLA_08703 | GLQOFTK02G2F2O | CDS | 529119 | 1506 | + | 0.293493 | |
g7788 | DLA_08704 | contains one VWFA domain and one copine domain copines are phospholipid-binding proteins | GLQOFTK02G2F2O | CDS | 530931 | 843 | - | 0.345196 |
g7789 | DLA_08705 | GLQOFTK02G2F2O | CDS | 532470 | 1620 | + | 0.287037 | |
g779 | DLA_00859 | F4PJNLW01A00V1 | CDS | 310297 | 1461 | + | 0.299795 | |
g7790 | DLA_08706 | GLQOFTK02G2F2O | CDS | 534393 | 732 | + | 0.315574 | |
g7791 | DLA_08707 | ortholog of H. sapiens SLC25A28 and D. reiro SLC25A37 involved in iron transport across the mitochondrial membranebrbr bCommunity annotation:b Overview of the | GLQOFTK02G2F2O | CDS | 535504 | 897 | - | 0.375697 |
g7792 | DLA_08709 | GLQOFTK02G2F2O | CDS | 537114 | 936 | + | 0.286325 | |
g7793 | DLA_08711 | GLQOFTK02G2F2O | CDS | 538241 | 2769 | - | 0.340195 | |
g7794 | DLA_08712 | GLQOFTK02G2F2O | CDS | 541218 | 1539 | - | 0.348278 | |
g7795 | DLA_08715 | GLQOFTK02G2F2O | CDS | 543174 | 1359 | + | 0.331126 | |
g7796 | DLA_08716 | GLQOFTK02G2F2O | CDS | 551080 | 1302 | + | 0.293395 | |
g7797 | DLA_08717 | GLQOFTK02G2F2O | CDS | 552613 | 375 | - | 0.197333 | |
g7798 | DLA_08718 | GLQOFTK02G2F2O | CDS | 553106 | 5211 | - | 0.333525 | |
g7799 | DLA_08719 | GLQOFTK02G2F2O | CDS | 558957 | 822 | + | 0.294404 | |
g78 | DLA_00090 | contig05409_1.exp | CDS | 181469 | 825 | - | 0.278788 | |
g780 | DLA_00860 | F4PJNLW01A00V1 | CDS | 311798 | 1473 | + | 0.281738 | |
g7800 | DLA_08720 | GLQOFTK02G2F2O | CDS | 560087 | 462 | + | 0.339827 | |
g7801 | DLA_11743 | GLQOFTK02G2F2O | CDS | 560704 | 849 | - | 0.292108 | |
g7802 | DLA_08721 | GLQOFTK02G2F2O | CDS | 561961 | 1017 | - | 0.273353 | |
g7803 | DLA_08722 | GLQOFTK02G2F2O | CDS | 563464 | 2481 | + | 0.347844 | |
g7804 | DLA_08724 | GLQOFTK02G2F2O | CDS | 566835 | 1533 | - | 0.303327 | |
g7805 | DLA_08725 | GLQOFTK02G2F2O | CDS | 569310 | 228 | - | 0.289474 | |
g7806 | DLA_08726 | GLQOFTK02G2F2O | CDS | 569809 | 831 | - | 0.330927 | |
g7807 | DLA_08727 | GLQOFTK02G2F2O | CDS | 571012 | 612 | - | 0.328431 | |
g7808 | DLA_08728 | GLQOFTK02G2F2O | CDS | 571786 | 318 | + | 0.308176 | |
g7809 | DLA_08729 | GLQOFTK02G2F2O | CDS | 572190 | 2460 | - | 0.311789 | |
g781 | DLA_00861 | F4PJNLW01A00V1 | CDS | 313355 | 942 | + | 0.283439 | |
g7810 | DLA_08730 | GLQOFTK02G2F2O | CDS | 574896 | 2790 | + | 0.318638 | |
g7811 | DLA_08731 | GLQOFTK02G2F2O | CDS | 577853 | 399 | + | 0.295739 | |
g7812 | DLA_08732 | protein serinethreonine phosphatase required for chemotaxis and development suppresses the | GLQOFTK02G2F2O | CDS | 578711 | 918 | - | 0.360566 |
g7813 | DLA_08733 | similar to A. thaliana short chain specific acyl-Coa oxidase ACX4 which catalyzes the first step of peroxisomal fatty acid beta-oxidation | GLQOFTK02G2F2O | CDS | 580237 | 1260 | + | 0.340476 |
g7814 | DLA_08734 | GLQOFTK02G2F2O | CDS | 582484 | 405 | + | 0.31358 | |
g7815 | DLA_08735 | GLQOFTK02G2F2O | CDS | 583700 | 1905 | - | 0.344357 | |
g7816 | DLA_08737 | GLQOFTK02G2F2O | CDS | 586205 | 3159 | + | 0.297246 | |
g7817 | DLA_08740 | GLQOFTK02G2F2O | CDS | 590105 | 1329 | - | 0.303236 | |
g7818 | DLA_08741 | GLQOFTK02G2F2O | CDS | 592181 | 1263 | - | 0.272367 | |
g7819 | DLA_08743 | GLQOFTK02G2F2O | CDS | 596995 | 627 | + | 0.341308 | |
g782 | DLA_11452 | F4PJNLW01A00V1 | CDS | 315214 | 459 | + | 0.300654 | |
g7820 | DLA_08744 | GLQOFTK02G2F2O | CDS | 598627 | 3354 | - | 0.31932 | |
g7821 | DLA_11744 | GLQOFTK02G2F2O | CDS | 602511 | 819 | - | 0.252747 | |
g7822 | DLA_08745 | GLQOFTK02G2F2O | CDS | 605989 | 1704 | - | 0.363263 | |
g7823 | DLA_08746 | GLQOFTK02G2F2O | CDS | 607928 | 1089 | + | 0.344353 | |
g7824 | DLA_08747 | GLQOFTK02G2F2O | CDS | 609504 | 597 | - | 0.289782 | |
g7825 | DLA_08748 | GLQOFTK02G2F2O | CDS | 610453 | 708 | - | 0.336158 | |
g7826 | DLA_08749 | GLQOFTK02G2F2O | CDS | 612457 | 747 | + | 0.491299 | |
g7827 | DLA_08750 | GLQOFTK02G2F2O | CDS | 614105 | 2568 | + | 0.332555 | |
g7828 | DLA_08751 | GLQOFTK02G2F2O | CDS | 617420 | 1011 | + | 0.301681 | |
g7829 | DLA_08752 | highly similar to PRS involved in nucleotide histidine and tryptophan biosynthesis | GLQOFTK02G2F2O | CDS | 621182 | 1023 | + | 0.319648 |
g783 | DLA_00862 | F4PJNLW01A00V1 | CDS | 316270 | 3633 | + | 0.289017 | |
g7830 | DLA_08753 | GLQOFTK02G2F2O | CDS | 622378 | 2643 | + | 0.317064 | |
g7831 | DLA_08754 | GLQOFTK02G2F2O | CDS | 625079 | 1128 | - | 0.340426 | |
g7832 | DLA_08755 | GLQOFTK02G2F2O | CDS | 626381 | 510 | - | 0.303922 | |
g7833 | DLA_08756 | similar to S. cerevisiae nonhistone chromosomal protein 6A and B (NCP6A and NCP6B) and mammalian HMGB2 contains a single HMG12 box | GLQOFTK02G2F2O | CDS | 627361 | 447 | - | 0.369128 |
g7834 | DLA_08757 | GLQOFTK02G2F2O | CDS | 628504 | 1059 | + | 0.281398 | |
g7835 | DLA_08758 | GLQOFTK02G2F2O | CDS | 629599 | 1941 | - | 0.381247 | |
g7836 | DLA_08759 | GLQOFTK02G2F2O | CDS | 632056 | 390 | + | 0.335897 | |
g7837 | DLA_08760 | GLQOFTK02G2F2O | CDS | 632731 | 498 | - | 0.285141 | |
g7838 | DLA_08761 | GLQOFTK02G2F2O | CDS | 633393 | 1452 | + | 0.310606 | |
g7839 | DLA_08763 | SNF2 family protein similar to human SMARCA4 putative regulator of chromatin | GLQOFTK02G2F2O | CDS | 635822 | 6768 | + | 0.346927 |
g784 | DLA_00863 | F4PJNLW01A00V1 | CDS | 320436 | 1503 | + | 0.298071 | |
g7840 | DLA_08765 | GLQOFTK02G2F2O | CDS | 643221 | 558 | - | 0.274194 | |
g7841 | DLA_08766 | GLQOFTK02G2F2O | CDS | 644019 | 561 | + | 0.297683 | |
g7842 | DLA_08767 | GLQOFTK02G2F2O | CDS | 644639 | 798 | - | 0.327068 | |
g7843 | DLA_08768 | GLQOFTK02G2F2O | CDS | 645756 | 249 | + | 0.281125 | |
g7844 | DLA_08769 | GLQOFTK02G2F2O | CDS | 646214 | 756 | - | 0.330688 | |
g7845 | DLA_08771 | GLQOFTK02G2F2O | CDS | 647480 | 1437 | + | 0.316632 | |
g7846 | DLA_08772 | ortholog of the H subunit of vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes the H subunit is part of the V1 subunit | GLQOFTK02G2F2O | CDS | 649239 | 1350 | - | 0.326667 |
g7847 | DLA_08773 | GLQOFTK02G2F2O | CDS | 651260 | 1851 | + | 0.386818 | |
g7848 | DLA_08774 | GLQOFTK02G2F2O | CDS | 653650 | 2829 | - | 0.324143 | |
g7849 | DLA_08779 | catalyzes the conversion of nicotinic acid (NA) to NA mononucleotide (NaMN) which elevates cellular NAD levels and prevent oxidative stress | GLQOFTK02G2F2O | CDS | 660088 | 1782 | + | 0.342873 |
g785 | DLA_00864 | F4PJNLW01A00V1 | CDS | 322040 | 351 | - | 0.307692 | |
g7850 | DLA_08780 | GLQOFTK02G2F2O | CDS | 661902 | 1584 | - | 0.282828 | |
g7851 | DLA_08781 | GLQOFTK02G2F2O | CDS | 663754 | 2451 | + | 0.298246 | |
g7852 | DLA_08782 | GLQOFTK02G2F2O | CDS | 666409 | 594 | - | 0.333333 | |
g7853 | DLA_11745 | GLQOFTK02G2F2O | CDS | 667794 | 531 | + | 0.299435 | |
g7854 | DLA_08783 | GLQOFTK02G2F2O | CDS | 668764 | 801 | + | 0.300874 | |
g7855 | DLA_08785 | GLQOFTK02G2F2O | CDS | 670727 | 1965 | - | 0.332824 | |
g7856 | DLA_08786 | GLQOFTK02G2F2O | CDS | 673152 | 1272 | + | 0.28695 | |
g7857 | DLA_08787 | GLQOFTK02G2F2O | CDS | 674567 | 849 | - | 0.290931 | |
g7858 | DLA_08788 | very conserved protein among bacteria and fungi zinc-binding ADH's are dimeric or tetrameric enzymes that bind two atoms of zinc per subunit | GLQOFTK02G2F2O | CDS | 676596 | 969 | + | 0.335397 |
g7859 | DLA_08789 | GLQOFTK02G2F2O | CDS | 677672 | 360 | + | 0.283333 | |
g786 | DLA_00865 | F4PJNLW01A00V1 | CDS | 322782 | 3009 | - | 0.378863 | |
g7860 | DLA_08790 | P-type ATPase (E1-E2) highly similar to human ATP8A1 believed to be involved in the transport of aminophospholipids | GLQOFTK02G2F2O | CDS | 678460 | 3597 | - | 0.352238 |
g7861 | DLA_08791 | GLQOFTK02G2F2O | CDS | 683085 | 438 | + | 0.267123 | |
g7862 | DLA_08792 | GLQOFTK02G2F2O | CDS | 684076 | 1326 | - | 0.315988 | |
g7863 | DLA_08793 | GLQOFTK02G2F2O | CDS | 686012 | 2763 | + | 0.352153 | |
g7864 | DLA_08794 | GLQOFTK02G2F2O | CDS | 689100 | 945 | + | 0.402116 | |
g7865 | DLA_08796 | GLQOFTK02G2F2O | CDS | 690856 | 537 | + | 0.422719 | |
g7866 | DLA_08797 | GLQOFTK02G2F2O | CDS | 691785 | 1575 | - | 0.274921 | |
g7867 | DLA_08798 | GLQOFTK02G2F2O | CDS | 693761 | 687 | - | 0.320233 | |
g7868 | DLA_08799 | GLQOFTK02G2F2O | CDS | 694721 | 870 | - | 0.264368 | |
g7869 | DLA_08800 | GLQOFTK02G2F2O | CDS | 695813 | 1893 | - | 0.325938 | |
g787 | DLA_00866 | F4PJNLW01A00V1 | CDS | 326549 | 1014 | + | 0.361933 | |
g7870 | DLA_08801 | GLQOFTK02G2F2O | CDS | 698383 | 792 | + | 0.335859 | |
g7871 | DLA_08802 | GLQOFTK02G2F2O | CDS | 699340 | 3039 | - | 0.303389 | |
g7872 | DLA_08803 | GLQOFTK02G2F2O | CDS | 703812 | 1278 | - | 0.311424 | |
g7873 | DLA_08805 | GLQOFTK02G2F2O | CDS | 706922 | 1329 | + | 0.313017 | |
g7874 | DLA_08806 | GLQOFTK02G2F2O | CDS | 708527 | 894 | - | 0.317673 | |
g7875 | DLA_08807 | GLQOFTK02G2F2O | CDS | 710380 | 1500 | - | 0.32 | |
g7876 | DLA_08808 | GLQOFTK02G2F2O | CDS | 711974 | 741 | + | 0.296896 | |
g7877 | DLA_08810 | GLQOFTK02G2F2O | CDS | 713075 | 1005 | - | 0.304478 | |
g7878 | DLA_08811 | GLQOFTK02G2F2O | CDS | 715505 | 1989 | + | 0.305178 | |
g7879 | DLA_08812 | GLQOFTK02G2F2O | CDS | 717784 | 663 | - | 0.292609 | |
g788 | DLA_00867 | F4PJNLW01A00V1 | CDS | 328013 | 1314 | - | 0.331811 | |
g7880 | DLA_08813 | GLQOFTK02G2F2O | CDS | 718630 | 3813 | + | 0.33648 | |
g7881 | DLA_08814 | GLQOFTK02G2F2O | CDS | 722919 | 3381 | + | 0.339545 | |
g7882 | DLA_08815 | GLQOFTK02G2F2O | CDS | 726857 | 2244 | + | 0.291444 | |
g7883 | DLA_08816 | catalyzes the reaction 2'-deoxyribonucleoside diphosphate thioredoxin disulfide Hsub2subO ribonucleoside diphosphate reduced thioredoxin there is a second copy of this gene | GLQOFTK02G2F2O | CDS | 729424 | 1017 | + | 0.331367 |
g7884 | DLA_08817 | GLQOFTK02G2F2O | CDS | 730782 | 2313 | - | 0.348033 | |
g7885 | DLA_08818 | ortholog of the human SDCCAG10 (Serologically Defined Colon Cancer Antigen 10) PPIase is an enzyme that accelerates protein folding by catalyzing the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | GLQOFTK02G2F2O | CDS | 733366 | 1332 | - | 0.284535 |
g7886 | DLA_08819 | GLQOFTK02G2F2O | CDS | 735619 | 1674 | + | 0.267622 | |
g7887 | DLA_08820 | GLQOFTK02G2F2O | CDS | 737416 | 6120 | - | 0.315523 | |
g7888 | DLA_08821 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum there is a second copy of this gene | GLQOFTK02G2F2O | CDS | 743900 | 351 | + | 0.276353 |
g7889 | DLA_08822 | GLQOFTK02G2F2O | CDS | 744495 | 780 | - | 0.284615 | |
g789 | DLA_00868 | F4PJNLW01A00V1 | CDS | 329642 | 2184 | + | 0.325092 | |
g7890 | DLA_08823 | GLQOFTK02G2F2O | CDS | 745863 | 1323 | + | 0.306122 | |
g7891 | DLA_08824 | GLQOFTK02G2F2O | CDS | 747422 | 1713 | - | 0.286632 | |
g7892 | DLA_08825 | GLQOFTK02G2F2O | CDS | 749498 | 1536 | + | 0.326172 | |
g7893 | DLA_08826 | GLQOFTK02G2F2O | CDS | 751253 | 1227 | - | 0.252649 | |
g7894 | DLA_08827 | GLQOFTK02G2F2O | CDS | 752990 | 1113 | - | 0.32345 | |
g7895 | DLA_08828 | GLQOFTK02G2F2O | CDS | 754400 | 1569 | + | 0.328872 | |
g7896 | DLA_08829 | GLQOFTK02G2F2O | CDS | 756179 | 1017 | - | 0.306785 | |
g7897 | DLA_08830 | GLQOFTK02G2F2O | CDS | 757478 | 531 | + | 0.286252 | |
g7898 | DLA_08831 | GLQOFTK02G2F2O | CDS | 758333 | 510 | - | 0.294118 | |
g7899 | DLA_08832 | GLQOFTK02G2F2O | CDS | 759035 | 1548 | + | 0.286176 | |
g79 | DLA_00091 | contig05409_1.exp | CDS | 182507 | 588 | + | 0.285714 | |
g790 | DLA_00869 | F4PJNLW01A00V1 | CDS | 332134 | 2709 | - | 0.323736 | |
g7900 | DLA_08833 | GLQOFTK02G2F2O | CDS | 760784 | 1527 | + | 0.261297 | |
g7901 | DLA_08834 | GLQOFTK02G2F2O | CDS | 763422 | 1233 | + | 0.30738 | |
g7902 | DLA_08835 | GLQOFTK02G2F2O | CDS | 764983 | 1413 | + | 0.250531 | |
g7903 | DLA_08836 | GLQOFTK02G2F2O | CDS | 766445 | 1557 | - | 0.302505 | |
g7904 | DLA_08838 | GLQOFTK02G2F2O | CDS | 769033 | 960 | + | 0.277083 | |
g7905 | DLA_08839 | GLQOFTK02G2F2O | CDS | 770238 | 402 | - | 0.233831 | |
g7906 | DLA_08840 | GLQOFTK02G2F2O | CDS | 770863 | 648 | - | 0.280864 | |
g7907 | DLA_08841 | GLQOFTK02G2F2O | CDS | 772452 | 3525 | - | 0.255035 | |
g7908 | DLA_08842 | GLQOFTK02G2F2O | CDS | 776140 | 3462 | - | 0.238879 | |
g7909 | DLA_08843 | GLQOFTK02G2F2O | CDS | 779995 | 1656 | + | 0.300121 | |
g791 | DLA_00870 | F4PJNLW01A00V1 | CDS | 335427 | 1572 | - | 0.370865 | |
g7910 | DLA_08844 | GLQOFTK02G2F2O | CDS | 782240 | 672 | + | 0.318452 | |
g7911 | DLA_08845 | GLQOFTK02G2F2O | CDS | 783209 | 1515 | - | 0.30231 | |
g7912 | DLA_08847 | GLQOFTK02G2F2O | CDS | 786791 | 219 | + | 0.315068 | |
g7913 | DLA_08848 | GLQOFTK02G2F2O | CDS | 789256 | 1440 | - | 0.243056 | |
g7914 | DLA_08849 | GLQOFTK02G2F2O | CDS | 790904 | 1209 | - | 0.249793 | |
g7915 | DLA_08850 | GLQOFTK02G2F2O | CDS | 792283 | 651 | - | 0.247312 | |
g7916 | DLA_08851 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases there is a second copy of this gene | GLQOFTK02G2F2O | CDS | 793088 | 993 | - | 0.293051 |
g7917 | DLA_08852 | GLQOFTK02G2F2O | CDS | 794471 | 1509 | + | 0.296223 | |
g7918 | DLA_08853 | similar to TBCK in human fly and worm TBC domain-containing proteins in yeast are GTPase activator proteins unlikely to function as a kinase as it does not contain a catalytic aspartate | GLQOFTK02G2F2O | CDS | 795994 | 2850 | - | 0.265614 |
g7919 | DLA_08854 | GLQOFTK02G2F2O | CDS | 799070 | 1746 | + | 0.250859 | |
g792 | DLA_00871 | conserved protein similar to yeast CWC22 an essential putative spliceosomal component | F4PJNLW01A00V1 | CDS | 337487 | 2142 | - | 0.352007 |
g7920 | DLA_08855 | GLQOFTK02G2F2O | CDS | 800830 | 1533 | - | 0.254403 | |
g7921 | DLA_08856 | GLQOFTK02G2F2O | CDS | 802448 | 918 | - | 0.29085 | |
g7922 | DLA_11746 | GLQOFTK02G2F2O | CDS | 803533 | 888 | + | 0.27027 | |
g7923 | DLA_08857 | GLQOFTK02G2F2O | CDS | 804563 | 1752 | + | 0.304224 | |
g7924 | DLA_08859 | GLQOFTK02G2F2O | CDS | 807298 | 1602 | + | 0.320225 | |
g7925 | DLA_08860 | GLQOFTK02G2F2O | CDS | 809097 | 4932 | + | 0.305556 | |
g7926 | DLA_08861 | GLQOFTK02G2F2O | CDS | 815513 | 4200 | + | 0.338095 | |
g7927 | DLA_08862 | GLQOFTK02G2F2O | CDS | 820104 | 1335 | + | 0.292135 | |
g7928 | DLA_08864 | involved in cytokinesis stabilizes actin filaments expressed in pstAB cells and in upper cup during culmination | GLQOFTK02G2F2O | CDS | 822640 | 2499 | + | 0.335334 |
g7929 | DLA_08865 | GLQOFTK02G2F2O | CDS | 826240 | 741 | + | 0.265857 | |
g793 | DLA_00872 | F4PJNLW01A00V1 | CDS | 339945 | 1755 | - | 0.317379 | |
g7930 | DLA_08866 | GLQOFTK02G2F2O | CDS | 827195 | 1722 | + | 0.292102 | |
g7931 | DLA_11747 | GLQOFTK02G2F2O | CDS | 829043 | 1239 | + | 0.326877 | |
g7932 | DLA_08867 | GLQOFTK02G2F2O | CDS | 830460 | 5121 | + | 0.343292 | |
g7933 | DLA_08868 | GLQOFTK02G2F2O | CDS | 836080 | 1020 | + | 0.366667 | |
g7934 | DLA_08869 | GLQOFTK02G2F2O | CDS | 837751 | 234 | + | 0.25641 | |
g7935 | DLA_08870 | similar to human TTC39C matches PFAM outer membrane protein IML2 mitochondrialtetratricopeptide repeat protein 39 | GLQOFTK02G2F2O | CDS | 838424 | 1563 | + | 0.319898 |
g7936 | DLA_08871 | GLQOFTK02G2F2O | CDS | 840428 | 2337 | + | 0.286264 | |
g7937 | DLA_08872 | GLQOFTK02G2F2O | CDS | 843089 | 1449 | - | 0.327812 | |
g7938 | DLA_11748 | GLQOFTK02G2F2O | CDS | 844633 | 888 | - | 0.310811 | |
g7939 | DLA_08873 | GLQOFTK02G2F2O | CDS | 845720 | 2619 | - | 0.316915 | |
g794 | DLA_00874 | F4PJNLW01A00V1 | CDS | 343306 | 312 | - | 0.294872 | |
g7940 | DLA_08874 | GLQOFTK02G2F2O | CDS | 849908 | 561 | + | 0.292335 | |
g7941 | DLA_08875 | GLQOFTK02G2F2O | CDS | 850971 | 3771 | - | 0.319279 | |
g7942 | DLA_08876 | GLQOFTK02G2F2O | CDS | 855523 | 3186 | + | 0.293471 | |
g7943 | DLA_08878 | GLQOFTK02G2F2O | CDS | 860405 | 1803 | + | 0.246811 | |
g7944 | DLA_11749 | GLQOFTK02G2F2O | CDS | 862629 | 1761 | + | 0.28109 | |
g7945 | DLA_08879 | GLQOFTK02G2F2O | CDS | 864567 | 6342 | - | 0.40492 | |
g7946 | DLA_08880 | GLQOFTK02G2F2O | CDS | 871744 | 3843 | - | 0.349206 | |
g7947 | DLA_08881 | GLQOFTK02G2F2O | CDS | 875862 | 555 | + | 0.27027 | |
g7948 | DLA_08882 | GLQOFTK02G2F2O | CDS | 876534 | 357 | - | 0.280112 | |
g7949 | DLA_08883 | GLQOFTK02G2F2O | CDS | 877695 | 2925 | + | 0.316239 | |
g795 | DLA_00875 | F4PJNLW01A00V1 | CDS | 344010 | 1749 | + | 0.321326 | |
g7950 | DLA_08884 | GLQOFTK02G2F2O | CDS | 881161 | 2064 | - | 0.327519 | |
g7951 | DLA_08885 | GLQOFTK02G2F2O | CDS | 883845 | 1668 | + | 0.340528 | |
g7952 | DLA_08887 | GLQOFTK02G2F2O | CDS | 885853 | 288 | - | 0.402778 | |
g7953 | DLA_08888 | GLQOFTK02G2F2O | CDS | 886835 | 1737 | + | 0.35118 | |
g7954 | DLA_08889 | GLQOFTK02G2F2O | CDS | 889012 | 1677 | - | 0.297555 | |
g7955 | DLA_08892 | GLQOFTK02G2F2O | CDS | 893468 | 1689 | + | 0.348727 | |
g7956 | DLA_08893 | GLQOFTK02G2F2O | CDS | 895338 | 1335 | - | 0.276405 | |
g7957 | DLA_11750 | GLQOFTK02G2F2O | CDS | 896852 | 591 | - | 0.296108 | |
g7958 | DLA_11751 | GLQOFTK02G2F2O | CDS | 897546 | 207 | - | 0.280193 | |
g7959 | DLA_08894 | similar to metazoan cyclin H predicted to interact with cyclin-dependent kinase | GLQOFTK02G2F2O | CDS | 898007 | 1032 | + | 0.297481 |
g796 | DLA_00876 | F4PJNLW01A00V1 | CDS | 345844 | 1503 | - | 0.323353 | |
g7960 | DLA_08895 | GLQOFTK02G2F2O | CDS | 899403 | 897 | + | 0.337793 | |
g7961 | DLA_08896 | GLQOFTK02G2F2O | CDS | 900856 | 1836 | + | 0.376362 | |
g7962 | DLA_08897 | GLQOFTK02G2F2O | CDS | 904325 | 1542 | + | 0.371595 | |
g7963 | DLA_08898 | GLQOFTK02G2F2O | CDS | 906086 | 780 | + | 0.355128 | |
g7964 | DLA_08899 | GLQOFTK02G2F2O | CDS | 907053 | 468 | + | 0.316239 | |
g7965 | DLA_08900 | GLQOFTK02G2F2O | CDS | 908478 | 1134 | + | 0.386243 | |
g7966 | DLA_08901 | GLQOFTK02G2F2O | CDS | 909785 | 1512 | - | 0.297619 | |
g7967 | DLA_08902 | GLQOFTK02G2F2O | CDS | 911415 | 444 | - | 0.353604 | |
g7968 | DLA_08903 | GLQOFTK02G2F2O | CDS | 912588 | 1515 | - | 0.277228 | |
g7969 | DLA_11752 | GLQOFTK02G2F2O | CDS | 914235 | 1491 | - | 0.274313 | |
g797 | DLA_00877 | F4PJNLW01A00V1 | CDS | 347714 | 684 | + | 0.346491 | |
g7970 | DLA_08904 | GLQOFTK02G2F2O | CDS | 915796 | 1491 | - | 0.295775 | |
g7971 | DLA_08905 | GLQOFTK02G2F2O | CDS | 917351 | 1467 | - | 0.301295 | |
g7972 | DLA_08906 | GLQOFTK02G2F2O | CDS | 919062 | 522 | - | 0.329502 | |
g7973 | DLA_08907 | GLQOFTK02G2F2O | CDS | 919966 | 2409 | - | 0.347862 | |
g7974 | DLA_08908 | GLQOFTK02G2F2O | CDS | 923298 | 1680 | - | 0.311905 | |
g7975 | DLA_08909 | contains a SAM (and some other nucleotide) binding motif similar to bacterial and eukaryotic methyltransferases | GLQOFTK02G2F2O | CDS | 925501 | 837 | + | 0.334528 |
g7976 | DLA_08910 | GLQOFTK02G2F2O | CDS | 926441 | 2172 | - | 0.354512 | |
g7977 | DLA_08911 | GLQOFTK02G2F2O | CDS | 929162 | 1878 | + | 0.367945 | |
g7978 | DLA_08912 | GLQOFTK02G2F2O | CDS | 931370 | 1170 | + | 0.322222 | |
g7979 | DLA_08913 | GLQOFTK02G2F2O | CDS | 932814 | 2109 | - | 0.333333 | |
g798 | DLA_00879 | F4PJNLW01A00V1 | CDS | 349371 | 1707 | + | 0.369654 | |
g7980 | DLA_08914 | GLQOFTK02G2F2O | CDS | 935326 | 4251 | - | 0.336627 | |
g7981 | DLA_08915 | GLQOFTK02G2F2O | CDS | 939838 | 3336 | - | 0.358513 | |
g7982 | DLA_08916 | GLQOFTK02G2F2O | CDS | 943714 | 1146 | - | 0.36562 | |
g7983 | DLA_08917 | GLQOFTK02G2F2O | CDS | 945378 | 2232 | - | 0.358871 | |
g7984 | DLA_08918 | GLQOFTK02G2F2O | CDS | 948441 | 780 | - | 0.289744 | |
g7985 | DLA_08921 | GLQOFTK02G2F2O | CDS | 950355 | 2844 | - | 0.297468 | |
g7986 | DLA_08922 | homolog of A. thaliana CPI1 (cycloeucalenol cycloisomerase) contains 6 putative transmembrane domains converts pentacyclic cyclopropyl sterols to tetracyclic sterols | GLQOFTK02G2F2O | CDS | 953598 | 819 | + | 0.373626 |
g7987 | DLA_08923 | GLQOFTK02G2F2O | CDS | 954719 | 609 | + | 0.320197 | |
g7988 | DLA_08924 | GLQOFTK02G2F2O | CDS | 955583 | 810 | - | 0.298765 | |
g7989 | DLA_08925 | GLQOFTK02G2F2O | CDS | 956513 | 468 | - | 0.33547 | |
g799 | DLA_00880 | F4PJNLW01A00V1 | CDS | 351586 | 1113 | + | 0.362983 | |
g7990 | DLA_08926 | GLQOFTK02G2F2O | CDS | 957376 | 3219 | + | 0.325878 | |
g7991 | DLA_08927 | GLQOFTK02G2F2O | CDS | 960624 | 1485 | - | 0.317172 | |
g7992 | DLA_08928 | GLQOFTK02G2F2O | CDS | 962515 | 1332 | + | 0.307808 | |
g7993 | DLA_08929 | GLQOFTK02G2F2O | CDS | 964526 | 489 | + | 0.286299 | |
g7994 | DLA_08930 | GLQOFTK02G2F2O | CDS | 965215 | 1638 | - | 0.277167 | |
g7995 | DLA_08931 | GLQOFTK02G2F2O | CDS | 966963 | 2268 | - | 0.33157 | |
g7996 | DLA_08933 | GLQOFTK02G2F2O | CDS | 971067 | 483 | + | 0.341615 | |
g7997 | DLA_08934 | GLQOFTK02G2F2O | CDS | 971889 | 615 | - | 0.266667 | |
g7998 | DLA_08937 | GLQOFTK02G2F2O | CDS | 973031 | 843 | - | 0.290629 | |
g7999 | DLA_08938 | GLQOFTK02G2F2O | CDS | 974020 | 804 | + | 0.30597 | |
g8 | DLA_00009 | contig05409_1.exp | CDS | 25008 | 4176 | - | 0.302203 | |
g80 | DLA_00092 | contig05409_1.exp | CDS | 183140 | 951 | - | 0.311251 | |
g800 | DLA_00881 | F4PJNLW01A00V1 | CDS | 352956 | 1179 | + | 0.357082 | |
g8000 | DLA_08939 | GLQOFTK02G2F2O | CDS | 974961 | 2694 | - | 0.305865 | |
g8001 | DLA_08941 | GLQOFTK02G2F2O | CDS | 978534 | 1260 | + | 0.30873 | |
g8002 | DLA_08942 | GLQOFTK02G2F2O | CDS | 979925 | 4008 | - | 0.314371 | |
g8003 | DLA_08943 | GLQOFTK02G2F2O | CDS | 984334 | 4503 | - | 0.321785 | |
g8004 | DLA_08947 | GLQOFTK02G2F2O | CDS | 990434 | 1506 | - | 0.377822 | |
g8005 | DLA_08949 | GLQOFTK02G2F2O | CDS | 993441 | 3792 | - | 0.309599 | |
g8006 | DLA_08950 | GLQOFTK02G2F2O | CDS | 997438 | 1734 | + | 0.320069 | |
g8007 | DLA_08951 | GLQOFTK02G2F2O | CDS | 999306 | 1638 | + | 0.305861 | |
g8008 | DLA_08952 | GLQOFTK02G2F2O | CDS | 1001307 | 984 | + | 0.318089 | |
g8009 | DLA_08953 | GLQOFTK02G2F2O | CDS | 1002468 | 2010 | - | 0.352736 | |
g801 | DLA_00882 | F4PJNLW01A00V1 | CDS | 354324 | 738 | - | 0.310298 | |
g8010 | DLA_08954 | GLQOFTK02G2F2O | CDS | 1004749 | 729 | + | 0.268861 | |
g8011 | DLA_08956 | GLQOFTK02G2F2O | CDS | 1006138 | 4821 | - | 0.32068 | |
g8012 | DLA_08958 | GLQOFTK02G2F2O | CDS | 1011394 | 1464 | + | 0.327869 | |
g8013 | DLA_08959 | GLQOFTK02G2F2O | CDS | 1013272 | 393 | + | 0.318066 | |
g8014 | DLA_08960 | GLQOFTK02G2F2O | CDS | 1014012 | 1542 | + | 0.289883 | |
g8015 | DLA_08961 | GLQOFTK02G2F2O | CDS | 1015965 | 1074 | + | 0.304469 | |
g8016 | DLA_08962 | GLQOFTK02G2F2O | CDS | 1017121 | 774 | - | 0.313953 | |
g8017 | DLA_08963 | GLQOFTK02G2F2O | CDS | 1018092 | 1710 | + | 0.293567 | |
g8018 | DLA_08964 | GLQOFTK02G2F2O | CDS | 1020275 | 1617 | + | 0.273964 | |
g8019 | DLA_08966 | GLQOFTK02G2F2O | CDS | 1023427 | 1794 | - | 0.299889 | |
g802 | DLA_00883 | F4PJNLW01A00V1 | CDS | 355603 | 249 | + | 0.293173 | |
g8020 | DLA_08967 | GLQOFTK02G2F2O | CDS | 1025290 | 1581 | - | 0.297913 | |
g8021 | DLA_08968 | GLQOFTK02G2F2O | CDS | 1027247 | 3393 | - | 0.344533 | |
g8022 | DLA_08969 | GLQOFTK02G2F2O | CDS | 1031019 | 4545 | + | 0.355116 | |
g8023 | DLA_08970 | GLQOFTK02G2F2O | CDS | 1035651 | 4326 | - | 0.312529 | |
g8024 | DLA_08971 | ortholog of the mammalian V-type proton ATPase 16 kDa proteolipid subunit the proton-conducting pore forming subunit of the vacuolar ATP synthase that generates an acidic environment in several intracellular compartments V-ATPases consist of peripheral (V1) and membrane integral (V0) heteromultimeric complexes this protein is part of the V0 complex | GLQOFTK02G2F2O | CDS | 1040637 | 549 | - | 0.384335 |
g8025 | DLA_08972 | GLQOFTK02G2F2O | CDS | 1042257 | 540 | + | 0.353704 | |
g8026 | DLA_08974 | similar to metazoan cyclin C predicted to interact with cyclin-dependent kinase | GLQOFTK02G2F2O | CDS | 1043323 | 768 | + | 0.303385 |
g8027 | DLA_08975 | GLQOFTK02G2F2O | CDS | 1044359 | 1173 | - | 0.344416 | |
g8028 | DLA_08976 | GLQOFTK02G2F2O | CDS | 1046221 | 942 | + | 0.33121 | |
g8029 | DLA_08977 | GLQOFTK02G2F2O | CDS | 1047583 | 1470 | + | 0.37551 | |
g803 | DLA_00884 | F4PJNLW01A00V1 | CDS | 356279 | 2874 | + | 0.376479 | |
g8030 | DLA_08978 | GLQOFTK02G2F2O | CDS | 1049209 | 2526 | + | 0.31829 | |
g8031 | DLA_11753 | GLQOFTK02G2F2O | CDS | 1052072 | 519 | + | 0.298651 | |
g8032 | DLA_08979 | GLQOFTK02G2F2O | CDS | 1052648 | 3534 | - | 0.344086 | |
g8033 | DLA_11754 | GLQOFTK02G2F2O | CDS | 1056701 | 4302 | - | 0.255463 | |
g8034 | DLA_08980 | GLQOFTK02G2F2O | CDS | 1062585 | 1437 | - | 0.25261 | |
g8035 | DLA_08983 | GLQOFTK02G2F2O | CDS | 1065259 | 3750 | - | 0.3568 | |
g8036 | DLA_08984 | GLQOFTK02G2F2O | CDS | 1070067 | 3414 | + | 0.323374 | |
g8037 | DLA_08985 | GLQOFTK02G2F2O | CDS | 1074135 | 4110 | + | 0.317275 | |
g8038 | DLA_08988 | GLQOFTK02G2F2O | CDS | 1078982 | 483 | + | 0.341615 | |
g8039 | DLA_08989 | GLQOFTK02G2F2O | CDS | 1079768 | 303 | + | 0.339934 | |
g804 | DLA_00885 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane regulated by the MADS-box transcription factor SrfA during development brbr bCommunity annotation:b Overview of the | F4PJNLW01A00V1 | CDS | 359397 | 1071 | - | 0.349206 |
g8040 | DLA_08990 | GLQOFTK02G2F2O | CDS | 1081373 | 483 | + | 0.345756 | |
g8041 | DLA_08991 | GLQOFTK02G2F2O | CDS | 1082217 | 4113 | + | 0.311451 | |
g8042 | DLA_08992 | GLQOFTK02G2F2O | CDS | 1086848 | 2697 | - | 0.319614 | |
g8043 | DLA_08993 | GLQOFTK02G2F2O | CDS | 1090129 | 1023 | + | 0.302053 | |
g8044 | DLA_08994 | GLQOFTK02G2F2O | CDS | 1091389 | 516 | + | 0.356589 | |
g8045 | DLA_08995 | GLQOFTK02G2F2O | CDS | 1092241 | 1770 | - | 0.423729 | |
g8046 | DLA_11755 | GLQOFTK02G2F2O | CDS | 1094749 | 1848 | - | 0.293831 | |
g8047 | DLA_08996 | GLQOFTK02G2F2O | CDS | 1097062 | 1173 | + | 0.337596 | |
g8048 | DLA_08997 | GLQOFTK02G2F2O | CDS | 1098377 | 1674 | - | 0.308841 | |
g8049 | DLA_08998 | GLQOFTK02G2F2O | CDS | 1100752 | 609 | + | 0.334975 | |
g805 | DLA_00886 | F4PJNLW01A00V1 | CDS | 361091 | 987 | - | 0.368794 | |
g8050 | DLA_08999 | GLQOFTK02G2F2O | CDS | 1102070 | 897 | - | 0.352285 | |
g8051 | DLA_09000 | GLQOFTK02G2F2O | CDS | 1103132 | 576 | - | 0.34375 | |
g8052 | DLA_09001 | GLQOFTK02G2F2O | CDS | 1104053 | 5091 | + | 0.327244 | |
g8053 | DLA_09002 | GLQOFTK02G2F2O | CDS | 1109332 | 2130 | + | 0.33615 | |
g8054 | DLA_09003 | GLQOFTK02G2F2O | CDS | 1111845 | 564 | - | 0.308511 | |
g8055 | DLA_09004 | GLQOFTK02G2F2O | CDS | 1112596 | 1602 | - | 0.329588 | |
g8056 | DLA_09005 | paxillin homolog containing 4 highly conserved LIM domains and 4 paxillin LD domains involved in adhesion culmination and cell sorting slug formation and migration and endocytosis | GLQOFTK02G2F2O | CDS | 1115110 | 1695 | + | 0.369322 |
g8057 | DLA_09006 | GLQOFTK02G2F2O | CDS | 1117246 | 1077 | + | 0.345404 | |
g8058 | DLA_09007 | GLQOFTK02G2F2O | CDS | 1119173 | 3498 | + | 0.281304 | |
g8059 | DLA_09008 | GLQOFTK02G2F2O | CDS | 1123168 | 2013 | - | 0.286637 | |
g806 | DLA_11453 | F4PJNLW01A00V1 | CDS | 362755 | 603 | - | 0.313433 | |
g8060 | DLA_09009 | GLQOFTK02G2F2O | CDS | 1125492 | 2442 | + | 0.320639 | |
g8061 | DLA_09010 | GLQOFTK02G2F2O | CDS | 1128020 | 939 | - | 0.297125 | |
g8062 | DLA_09011 | GLQOFTK02G2F2O | CDS | 1129169 | 1056 | + | 0.279356 | |
g8063 | DLA_09012 | GLQOFTK02G2F2O | CDS | 1130318 | 7722 | - | 0.303419 | |
g8064 | DLA_09014 | GLQOFTK02G2F2O | CDS | 1138840 | 1788 | + | 0.319911 | |
g8065 | DLA_09015 | GLQOFTK02G2F2O | CDS | 1140800 | 651 | - | 0.236559 | |
g8066 | DLA_09016 | GLQOFTK02G2F2O | CDS | 1141972 | 4200 | + | 0.307143 | |
g8067 | DLA_09017 | GLQOFTK02G2F2O | CDS | 1146772 | 1470 | - | 0.290476 | |
g8068 | DLA_09018 | GLQOFTK02G2F2O | CDS | 1150003 | 2154 | + | 0.305942 | |
g8069 | DLA_09019 | GLQOFTK02G2F2O | CDS | 1152180 | 2337 | - | 0.296106 | |
g807 | DLA_00887 | F4PJNLW01A00V1 | CDS | 364301 | 1164 | + | 0.361684 | |
g8070 | DLA_09020 | GLQOFTK02G2F2O | CDS | 1155058 | 672 | + | 0.354167 | |
g8071 | DLA_09021 | GLQOFTK02G2F2O | CDS | 1155993 | 552 | + | 0.311594 | |
g8072 | DLA_09022 | GLQOFTK02G2F2O | CDS | 1157651 | 3978 | + | 0.302916 | |
g8073 | DLA_09023 | GLQOFTK02G2F2O | CDS | 1161799 | 2151 | - | 0.317527 | |
g8074 | DLA_09025 | GLQOFTK02G2F2O | CDS | 1165350 | 720 | - | 0.286111 | |
g8075 | DLA_09026 | GLQOFTK02G2F2O | CDS | 1166312 | 897 | - | 0.305463 | |
g8076 | DLA_09027 | GLQOFTK02G2F2O | CDS | 1167491 | 3087 | + | 0.295432 | |
g8077 | DLA_09028 | GLQOFTK02G2F2O | CDS | 1171541 | 1416 | + | 0.336158 | |
g8078 | DLA_09029 | GLQOFTK02G2F2O | CDS | 1173056 | 2673 | - | 0.30303 | |
g8079 | DLA_09030 | GLQOFTK02G2F2O | CDS | 1176074 | 4551 | + | 0.320809 | |
g808 | DLA_00888 | F4PJNLW01A00V1 | CDS | 365640 | 1284 | + | 0.285826 | |
g8080 | DLA_09031 | GLQOFTK02G2F2O | CDS | 1181099 | 1800 | - | 0.314444 | |
g8081 | DLA_09032 | GLQOFTK02G2F2O | CDS | 1183592 | 609 | + | 0.313629 | |
g8082 | DLA_09033 | GLQOFTK02G2F2O | CDS | 1184396 | 1389 | - | 0.314615 | |
g8083 | DLA_09034 | GLQOFTK02G2F2O | CDS | 1186328 | 3687 | + | 0.308652 | |
g8084 | DLA_09035 | GLQOFTK02G2F2O | CDS | 1190466 | 687 | + | 0.423581 | |
g8085 | DLA_09036 | GLQOFTK02G2F2O | CDS | 1191341 | 969 | - | 0.273478 | |
g8086 | DLA_09037 | GLQOFTK02G2F2O | CDS | 1192492 | 888 | + | 0.261261 | |
g8087 | DLA_09038 | GLQOFTK02G2F2O | CDS | 1193408 | 1725 | - | 0.275362 | |
g8088 | DLA_09039 | GLQOFTK02G2F2O | CDS | 1195390 | 1353 | - | 0.317073 | |
g8089 | DLA_09040 | GLQOFTK02G2F2O | CDS | 1197379 | 1353 | + | 0.313378 | |
g809 | DLA_00889 | catalyzes the reaction ATP L-arginine tRNAArg AMP diphosphate L-arginyl-tRNAArg | F4PJNLW01A00V1 | CDS | 367096 | 1872 | - | 0.367521 |
g8090 | DLA_09041 | GLQOFTK02G2F2O | CDS | 1198915 | 2142 | - | 0.340803 | |
g8091 | DLA_09042 | GLQOFTK02G2F2O | CDS | 1201457 | 1188 | + | 0.349327 | |
g8092 | DLA_09043 | GLQOFTK02G2F2O | CDS | 1202860 | 1071 | - | 0.344538 | |
g8093 | DLA_09045 | GLQOFTK02G2F2O | CDS | 1204449 | 1662 | - | 0.323706 | |
g8094 | DLA_09046 | GLQOFTK02G2F2O | CDS | 1206218 | 3084 | + | 0.319066 | |
g8095 | DLA_09047 | GLQOFTK02G2F2O | CDS | 1209724 | 1788 | + | 0.315996 | |
g8096 | DLA_09049 | GLQOFTK02G2F2O | CDS | 1211680 | 1524 | + | 0.286745 | |
g8097 | DLA_09050 | GLQOFTK02G2F2O | CDS | 1213624 | 3660 | + | 0.312022 | |
g8098 | DLA_09051 | GLQOFTK02G2F2O | CDS | 1217994 | 1659 | - | 0.374925 | |
g8099 | DLA_09052 | GLQOFTK02G2F2O | CDS | 1220399 | 549 | + | 0.264117 | |
g81 | DLA_00093 | contig05409_1.exp | CDS | 184719 | 1416 | + | 0.34887 | |
g810 | DLA_00890 | similar to mammalian NIT1 there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 369236 | 939 | + | 0.339723 |
g8100 | DLA_09053 | GLQOFTK02G2F2O | CDS | 1221193 | 1047 | - | 0.282713 | |
g8101 | DLA_09055 | GLQOFTK02G2F2O | CDS | 1224498 | 207 | + | 0.323671 | |
g8102 | DLA_09056 | GLQOFTK02G2F2O | CDS | 1224914 | 2379 | - | 0.274065 | |
g8103 | DLA_09057 | GLQOFTK02G2F2O | CDS | 1227643 | 1662 | + | 0.337545 | |
g8104 | DLA_09058 | GLQOFTK02G2F2O | CDS | 1229588 | 11298 | - | 0.325633 | |
g8105 | DLA_09059 | GLQOFTK02G2F2O | CDS | 1241546 | 807 | + | 0.339529 | |
g8106 | DLA_09060 | GLQOFTK02G2F2O | CDS | 1242751 | 777 | - | 0.292149 | |
g8107 | DLA_09062 | GLQOFTK02G2F2O | CDS | 1244469 | 1113 | + | 0.287511 | |
g8108 | DLA_09063 | GLQOFTK02G2F2O | CDS | 1245728 | 2325 | - | 0.32086 | |
g8109 | DLA_11756 | GLQOFTK02G2F2O | CDS | 1248595 | 873 | + | 0.357388 | |
g811 | DLA_00891 | F4PJNLW01A00V1 | CDS | 370322 | 1446 | - | 0.301521 | |
g8110 | DLA_09064 | GLQOFTK02G2F2O | CDS | 1249687 | 2730 | + | 0.295238 | |
g8111 | DLA_09065 | GLQOFTK02G2F2O | CDS | 1252809 | 5997 | + | 0.31399 | |
g8112 | DLA_09067 | GLQOFTK02G2F2O | CDS | 1259607 | 627 | + | 0.350877 | |
g8113 | DLA_11757 | GLQOFTK02G2F2O | CDS | 1260990 | 393 | + | 0.284987 | |
g8114 | DLA_09068 | GLQOFTK02G2F2O | CDS | 1262182 | 918 | + | 0.282135 | |
g8115 | DLA_09069 | GLQOFTK02G2F2O | CDS | 1263595 | 5070 | + | 0.289152 | |
g8116 | DLA_09071 | GLQOFTK02G2F2O | CDS | 1269775 | 924 | + | 0.306277 | |
g8117 | DLA_09072 | GLQOFTK02G2F2O | CDS | 1271159 | 933 | + | 0.299035 | |
g8118 | DLA_09073 | GLQOFTK02G2F2O | CDS | 1273030 | 936 | + | 0.301282 | |
g8119 | DLA_09074 | GLQOFTK02G2F2O | CDS | 1274567 | 621 | + | 0.309179 | |
g812 | DLA_00892 | F4PJNLW01A00V1 | CDS | 372454 | 2172 | + | 0.371547 | |
g8120 | DLA_09075 | GLQOFTK02G2F2O | CDS | 1275429 | 8724 | + | 0.321756 | |
g8121 | DLA_09076 | GLQOFTK02G2F2O | CDS | 1288437 | 813 | + | 0.314883 | |
g8122 | DLA_09077 | GLQOFTK02G2F2O | CDS | 1289445 | 720 | + | 0.356944 | |
g8123 | DLA_09078 | GLQOFTK02G2F2O | CDS | 1290791 | 1539 | + | 0.345679 | |
g8124 | DLA_09079 | GLQOFTK02G2F2O | CDS | 1292438 | 8142 | - | 0.318226 | |
g8125 | DLA_09080 | GLQOFTK02G2F2O | CDS | 1301942 | 1179 | + | 0.339271 | |
g8126 | DLA_09081 | GLQOFTK02G2F2O | CDS | 1303559 | 2313 | - | 0.312581 | |
g8127 | DLA_09082 | GLQOFTK02G2F2O | CDS | 1306430 | 4071 | - | 0.317858 | |
g8128 | DLA_09083 | GLQOFTK02G2F2O | CDS | 1310832 | 897 | - | 0.331104 | |
g8129 | DLA_09084 | GLQOFTK02G2F2O | CDS | 1311974 | 4071 | - | 0.313437 | |
g813 | DLA_00893 | F4PJNLW01A00V1 | CDS | 374770 | 1014 | - | 0.306706 | |
g8130 | DLA_09085 | GLQOFTK02G2F2O | CDS | 1316396 | 3207 | - | 0.347053 | |
g8131 | DLA_09086 | GLQOFTK02G2F2O | CDS | 1319801 | 1362 | + | 0.360499 | |
g8132 | DLA_09087 | GLQOFTK02G2F2O | CDS | 1321342 | 666 | + | 0.333333 | |
g8133 | DLA_09088 | GLQOFTK02G2F2O | CDS | 1322253 | 1530 | + | 0.350327 | |
g8134 | DLA_09089 | GLQOFTK02G2F2O | CDS | 1323808 | 2049 | - | 0.285505 | |
g8135 | DLA_09090 | GLQOFTK02G2F2O | CDS | 1326089 | 342 | - | 0.295322 | |
g8136 | DLA_09091 | GLQOFTK02G2F2O | CDS | 1326646 | 1752 | + | 0.347032 | |
g8137 | DLA_09092 | GLQOFTK02G2F2O | CDS | 1328555 | 1377 | - | 0.378359 | |
g8138 | DLA_09093 | GLQOFTK02G2F2O | CDS | 1330808 | 2268 | + | 0.29806 | |
g8139 | DLA_09094 | GLQOFTK02G2F2O | CDS | 1333218 | 2367 | - | 0.365019 | |
g814 | DLA_00894 | F4PJNLW01A00V1 | CDS | 376260 | 1614 | + | 0.282528 | |
g8140 | DLA_09096 | GLQOFTK02G2F2O | CDS | 1336716 | 2637 | - | 0.361016 | |
g8141 | DLA_09097 | GLQOFTK02G2F2O | CDS | 1340582 | 1710 | + | 0.339766 | |
g8142 | DLA_09098 | GLQOFTK02G2F2O | CDS | 1342634 | 1581 | - | 0.379507 | |
g8143 | DLA_09100 | GLQOFTK02G2F2O | CDS | 1346133 | 1419 | + | 0.384778 | |
g8144 | DLA_09101 | GLQOFTK02G2F2O | CDS | 1347893 | 537 | - | 0.294227 | |
g8145 | DLA_09102 | GLQOFTK02G2F2O | CDS | 1349469 | 1095 | + | 0.344292 | |
g8146 | DLA_09103 | GLQOFTK02G2F2O | CDS | 1350921 | 555 | + | 0.311712 | |
g8147 | DLA_09104 | GLQOFTK02G2F2O | CDS | 1351706 | 3204 | - | 0.35206 | |
g8148 | DLA_09105 | GLQOFTK02G2F2O | CDS | 1355252 | 504 | + | 0.335317 | |
g8149 | DLA_09106 | GLQOFTK02G2F2O | CDS | 1356264 | 666 | + | 0.318318 | |
g815 | DLA_00895 | F4PJNLW01A00V1 | CDS | 377913 | 1767 | - | 0.281834 | |
g8150 | DLA_09107 | GLQOFTK02G2F2O | CDS | 1357056 | 2331 | - | 0.305877 | |
g8151 | DLA_09109 | GLQOFTK02G2F2O | CDS | 1360135 | 2316 | + | 0.327288 | |
g8152 | DLA_09110 | GLQOFTK02G2F2O | CDS | 1362915 | 2703 | + | 0.344062 | |
g8153 | DLA_09111 | GLQOFTK02G2F2O | CDS | 1365823 | 912 | - | 0.310307 | |
g8154 | DLA_09112 | GLQOFTK02G2F2O | CDS | 1366943 | 1623 | - | 0.266174 | |
g8155 | DLA_09114 | GLQOFTK02G2F2O | CDS | 1369393 | 2067 | + | 0.311079 | |
g8156 | DLA_09115 | probable ortholog of H. sapiens and S. cerevisiae HAT1 a subunit of the HAT1HAT2 histone acetyltransferase complex | GLQOFTK02G2F2O | CDS | 1371691 | 1284 | - | 0.298287 |
g8157 | DLA_11758 | GLQOFTK02G2F2O | CDS | 1373224 | 894 | - | 0.315436 | |
g8158 | DLA_09116 | GLQOFTK02G2F2O | CDS | 1374986 | 1686 | + | 0.322657 | |
g8159 | DLA_09117 | GLQOFTK02G2F2O | CDS | 1377780 | 1236 | - | 0.282362 | |
g816 | DLA_00896 | F4PJNLW01A00V1 | CDS | 380056 | 1344 | - | 0.28869 | |
g8160 | DLA_09118 | GLQOFTK02G2F2O | CDS | 1379715 | 2157 | + | 0.351414 | |
g8161 | DLA_09119 | GLQOFTK02G2F2O | CDS | 1382129 | 1722 | - | 0.281649 | |
g8162 | DLA_09120 | GLQOFTK02G2F2O | CDS | 1385113 | 918 | - | 0.25817 | |
g8163 | DLA_11759 | GLQOFTK02G2F2O | CDS | 1386210 | 1713 | - | 0.286632 | |
g8164 | DLA_09121 | GLQOFTK02G2F2O | CDS | 1388009 | 2127 | - | 0.288199 | |
g8165 | DLA_09124 | GLQOFTK02G2F2O | CDS | 1390924 | 984 | - | 0.355691 | |
g8166 | DLA_09125 | GLQOFTK02G2F2O | CDS | 1393596 | 1257 | - | 0.287192 | |
g8167 | DLA_09126 | GLQOFTK02G2F2O | CDS | 1397480 | 600 | + | 0.283333 | |
g8168 | DLA_09127 | GLQOFTK02G2F2O | CDS | 1399214 | 4746 | + | 0.340076 | |
g8169 | DLA_09128 | GLQOFTK02G2F2O | CDS | 1404659 | 345 | - | 0.269565 | |
g817 | DLA_00897 | F4PJNLW01A00V1 | CDS | 381894 | 1473 | + | 0.281059 | |
g8170 | DLA_09129 | similar to Plasmodium falciparum CRT which confers resistance to chloroquine contains 10 predicted transmembrane domains | GLQOFTK02G2F2O | CDS | 1405204 | 1359 | - | 0.359088 |
g8171 | DLA_09130 | GLQOFTK02G2F2O | CDS | 1407348 | 1002 | + | 0.314371 | |
g8172 | DLA_09131 | GLQOFTK02G2F2O | CDS | 1408735 | 1002 | - | 0.364271 | |
g8173 | DLA_09132 | GLQOFTK02G2F2O | CDS | 1410239 | 717 | + | 0.312413 | |
g8174 | DLA_09133 | GLQOFTK02G2F2O | CDS | 1411444 | 1947 | + | 0.349255 | |
g8175 | DLA_09134 | GLQOFTK02G2F2O | CDS | 1413536 | 1362 | + | 0.323054 | |
g8176 | DLA_09135 | GLQOFTK02G2F2O | CDS | 1414967 | 1032 | - | 0.378876 | |
g8177 | DLA_09136 | GLQOFTK02G2F2O | CDS | 1416202 | 1329 | - | 0.369451 | |
g8178 | DLA_09137 | GLQOFTK02G2F2O | CDS | 1418403 | 783 | + | 0.37931 | |
g8179 | DLA_09138 | GLQOFTK02G2F2O | CDS | 1419401 | 1467 | + | 0.334697 | |
g818 | DLA_00898 | F4PJNLW01A00V1 | CDS | 383940 | 1785 | + | 0.285714 | |
g8180 | DLA_09139 | GLQOFTK02G2F2O | CDS | 1421646 | 999 | + | 0.271271 | |
g8181 | DLA_11760 | GLQOFTK02G2F2O | CDS | 1423034 | 651 | + | 0.316436 | |
g8182 | DLA_11761 | GLQOFTK02G2F2O | CDS | 1423843 | 729 | + | 0.303155 | |
g8183 | DLA_09140 | GLQOFTK02G2F2O | CDS | 1425168 | 861 | + | 0.262485 | |
g8184 | DLA_09141 | GLQOFTK02G2F2O | CDS | 1426132 | 2628 | - | 0.303272 | |
g8185 | DLA_09142 | GLQOFTK02G2F2O | CDS | 1428900 | 1686 | - | 0.320285 | |
g8186 | DLA_09143 | GLQOFTK02G2F2O | CDS | 1431060 | 2193 | - | 0.286822 | |
g8187 | DLA_09144 | GLQOFTK02G2F2O | CDS | 1433522 | 1791 | + | 0.292016 | |
g8188 | DLA_09145 | GLQOFTK02G2F2O | CDS | 1435363 | 507 | + | 0.2643 | |
g8189 | DLA_09146 | GLQOFTK02G2F2O | CDS | 1435921 | 843 | - | 0.313167 | |
g819 | DLA_00899 | F4PJNLW01A00V1 | CDS | 386130 | 1767 | + | 0.284097 | |
g8190 | DLA_09147 | GLQOFTK02G2F2O | CDS | 1437035 | 3114 | + | 0.279383 | |
g8191 | DLA_09148 | GLQOFTK02G2F2O | CDS | 1440382 | 351 | + | 0.390313 | |
g8192 | DLA_11762 | GLQOFTK02G2F2O | CDS | 1441126 | 801 | - | 0.360799 | |
g8193 | DLA_09149 | GLQOFTK02G2F2O | CDS | 1442493 | 750 | - | 0.345333 | |
g8194 | DLA_09150 | GLQOFTK02G2F2O | CDS | 1443790 | 2769 | + | 0.327555 | |
g8195 | DLA_09151 | GLQOFTK02G2F2O | CDS | 1447365 | 1158 | - | 0.363558 | |
g8196 | DLA_09153 | CAZy family GT10 some proteins in the GT10 family help form the basis of blood group antigens | GLQOFTK02G2F2O | CDS | 1449431 | 1875 | + | 0.312533 |
g8197 | DLA_09154 | GLQOFTK02G2F2O | CDS | 1451518 | 3885 | - | 0.351351 | |
g8198 | DLA_09155 | GLQOFTK02G2F2O | CDS | 1456584 | 1122 | + | 0.356506 | |
g8199 | DLA_09156 | GLQOFTK02G2F2O | CDS | 1457812 | 429 | + | 0.240093 | |
g82 | DLA_00094 | contig05409_1.exp | CDS | 186440 | 2235 | - | 0.365101 | |
g820 | DLA_11454 | F4PJNLW01A00V1 | CDS | 388492 | 1764 | + | 0.287415 | |
g8200 | DLA_09157 | GLQOFTK02G2F2O | CDS | 1458427 | 1947 | - | 0.313303 | |
g8201 | DLA_09158 | GLQOFTK02G2F2O | CDS | 1460727 | 951 | + | 0.354364 | |
g8202 | DLA_09159 | GLQOFTK02G2F2O | CDS | 1462004 | 300 | - | 0.326667 | |
g8203 | DLA_09160 | GLQOFTK02G2F2O | CDS | 1462741 | 1167 | + | 0.358183 | |
g8204 | DLA_09161 | GLQOFTK02G2F2O | CDS | 1464176 | 636 | - | 0.272013 | |
g8205 | DLA_09162 | GLQOFTK02G2F2O | CDS | 1465055 | 1026 | - | 0.318713 | |
g8206 | DLA_09163 | GLQOFTK02G2F2O | CDS | 1466961 | 1149 | + | 0.344648 | |
g8207 | DLA_09164 | GLQOFTK02G2F2O | CDS | 1468422 | 987 | - | 0.314083 | |
g8208 | DLA_09165 | GLQOFTK02G2F2O | CDS | 1469798 | 651 | - | 0.345622 | |
g8209 | DLA_09166 | GLQOFTK02G2F2O | CDS | 1471038 | 1674 | + | 0.359618 | |
g821 | DLA_00900 | F4PJNLW01A00V1 | CDS | 390582 | 1542 | + | 0.365759 | |
g8210 | DLA_09167 | GLQOFTK02G2F2O | CDS | 1473044 | 1626 | + | 0.357934 | |
g8211 | DLA_09168 | GLQOFTK02G2F2O | CDS | 1475155 | 621 | - | 0.294686 | |
g8212 | DLA_09169 | GLQOFTK02G2F2O | CDS | 1476097 | 1428 | + | 0.320728 | |
g8213 | DLA_09170 | protein serinethreonine kinase GSK family member of the CMGC kinase group essential for cell specification activated by CAR3 through ZAK1 (prespore-) and inhibited by CAR4 (prestalk-) signalling | GLQOFTK02G2F2O | CDS | 1477962 | 1386 | - | 0.330447 |
g8214 | DLA_09171 | GLQOFTK02G2F2O | CDS | 1480397 | 1470 | + | 0.321769 | |
g8215 | DLA_09172 | GLQOFTK02G2F2O | CDS | 1482132 | 1758 | - | 0.289534 | |
g8216 | DLA_09173 | GLQOFTK02G2F2O | CDS | 1484286 | 2007 | - | 0.317389 | |
g8217 | DLA_09174 | GLQOFTK02G2F2O | CDS | 1486442 | 1482 | - | 0.342105 | |
g8218 | DLA_09175 | GLQOFTK02G2F2O | CDS | 1490003 | 1221 | - | 0.329238 | |
g8219 | DLA_09176 | GLQOFTK02G2F2O | CDS | 1491858 | 1620 | - | 0.288889 | |
g822 | DLA_00901 | F4PJNLW01A00V1 | CDS | 392243 | 1842 | + | 0.286645 | |
g8220 | DLA_09178 | GLQOFTK02G2F2O | CDS | 1494405 | 1410 | + | 0.38227 | |
g8221 | DLA_09179 | GLQOFTK02G2F2O | CDS | 1495968 | 1854 | - | 0.30205 | |
g8222 | DLA_09180 | GLQOFTK02G2F2O | CDS | 1497995 | 1833 | - | 0.27605 | |
g8223 | DLA_09181 | GLQOFTK02G2F2O | CDS | 1499846 | 396 | - | 0.343434 | |
g8224 | DLA_09182 | GLQOFTK02G2F2O | CDS | 1500435 | 1836 | - | 0.30719 | |
g8225 | DLA_09183 | GLQOFTK02G2F2O | CDS | 1502323 | 1827 | - | 0.296661 | |
g8226 | DLA_09184 | GLQOFTK02G2F2O | CDS | 1504448 | 561 | - | 0.342246 | |
g8227 | DLA_09185 | GLQOFTK02G2F2O | CDS | 1505895 | 1569 | - | 0.387508 | |
g8228 | DLA_09186 | GLQOFTK02G2F2O | CDS | 1508579 | 981 | + | 0.397554 | |
g8229 | DLA_09187 | GLQOFTK02G2F2O | CDS | 1510146 | 3015 | + | 0.330348 | |
g823 | DLA_00903 | F4PJNLW01A00V1 | CDS | 394407 | 1482 | - | 0.283401 | |
g8230 | DLA_09188 | GLQOFTK02G2F2O | CDS | 1514699 | 4404 | + | 0.334923 | |
g8231 | DLA_09189 | GLQOFTK02G2F2O | CDS | 1520088 | 3552 | + | 0.33277 | |
g8232 | DLA_09192 | GLQOFTK02G2F2O | CDS | 1524966 | 5232 | + | 0.331804 | |
g8233 | DLA_09193 | GLQOFTK02G2F2O | CDS | 1531001 | 3183 | - | 0.318567 | |
g8234 | DLA_09194 | GLQOFTK02G2F2O | CDS | 1535183 | 2334 | + | 0.393316 | |
g8235 | DLA_09195 | GLQOFTK02G2F2O | CDS | 1538873 | 2289 | + | 0.349498 | |
g8236 | DLA_11763 | GLQOFTK02G2F2O | CDS | 1541296 | 1422 | + | 0.331927 | |
g8237 | DLA_09196 | GLQOFTK02G2F2O | CDS | 1542945 | 2700 | + | 0.295926 | |
g8238 | DLA_09199 | GLQOFTK02G2F2O | CDS | 1547185 | 1107 | + | 0.399277 | |
g8239 | DLA_09201 | GLQOFTK02G2F2O | CDS | 1549525 | 279 | + | 0.333333 | |
g824 | DLA_00904 | F4PJNLW01A00V1 | CDS | 396372 | 1326 | + | 0.340875 | |
g8240 | DLA_09202 | GLQOFTK02G2F2O | CDS | 1550528 | 924 | + | 0.299784 | |
g8241 | DLA_09203 | GLQOFTK02G2F2O | CDS | 1551729 | 1740 | - | 0.300575 | |
g8242 | DLA_09204 | GLQOFTK02G2F2O | CDS | 1554878 | 231 | - | 0.354978 | |
g8243 | DLA_09205 | GLQOFTK02G2F2O | CDS | 1555688 | 3324 | + | 0.337545 | |
g8244 | DLA_09206 | GLQOFTK02G2F2O | CDS | 1560139 | 615 | + | 0.347967 | |
g8245 | DLA_09207 | GLQOFTK02G2F2O | CDS | 1561446 | 399 | - | 0.318296 | |
g8246 | DLA_09208 | GLQOFTK02G2F2O | CDS | 1562122 | 1695 | + | 0.314454 | |
g8247 | DLA_09209 | GLQOFTK02G2F2O | CDS | 1564293 | 1893 | + | 0.342842 | |
g8248 | DLA_09210 | GLQOFTK02G2F2O | CDS | 1566643 | 300 | + | 0.303333 | |
g8249 | DLA_09211 | GLQOFTK02G2F2O | CDS | 1567199 | 714 | - | 0.313726 | |
g825 | DLA_00905 | F4PJNLW01A00V1 | CDS | 397716 | 2379 | - | 0.34174 | |
g8250 | DLA_09212 | GLQOFTK02G2F2O | CDS | 1568149 | 1248 | + | 0.334135 | |
g8251 | DLA_09213 | GLQOFTK02G2F2O | CDS | 1569720 | 1044 | - | 0.332375 | |
g8252 | DLA_09214 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | GLQOFTK02G2F2O | CDS | 1571019 | 504 | + | 0.331349 |
g8253 | DLA_09215 | GLQOFTK02G2F2O | CDS | 1571680 | 1434 | - | 0.286611 | |
g8254 | DLA_11764 | GLQOFTK02G2F2O | CDS | 1573785 | 312 | - | 0.339744 | |
g8255 | DLA_09216 | GLQOFTK02G2F2O | CDS | 1574683 | 1560 | - | 0.298718 | |
g8256 | DLA_09217 | GLQOFTK02G2F2O | CDS | 1576594 | 1587 | + | 0.336484 | |
g8257 | DLA_11765 | GLQOFTK02G2F2O | CDS | 1578296 | 1905 | - | 0.276115 | |
g8258 | DLA_09218 | GLQOFTK02G2F2O | CDS | 1580676 | 4380 | - | 0.324886 | |
g8259 | DLA_09219 | GLQOFTK02G2F2O | CDS | 1585321 | 2085 | - | 0.316547 | |
g826 | DLA_00906 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers br bNomenclature conflict:b Do not confuse this gene with clc also known as clcA encoding the clathrin light chain | F4PJNLW01A00V1 | CDS | 400235 | 2616 | - | 0.365443 |
g8260 | DLA_09220 | GLQOFTK02G2F2O | CDS | 1587895 | 2181 | + | 0.331499 | |
g8261 | DLA_09221 | GLQOFTK02G2F2O | CDS | 1591695 | 1860 | + | 0.374731 | |
g8262 | DLA_09222 | GLQOFTK02G2F2O | CDS | 1594177 | 1920 | + | 0.298958 | |
g8263 | DLA_09223 | GLQOFTK02G2F2O | CDS | 1596345 | 243 | - | 0.251029 | |
g8264 | DLA_09224 | contains a SAM (and some other nucleotide) binding motif similar to bacterial and eukaryotic methyltransferases | GLQOFTK02G2F2O | CDS | 1596703 | 765 | - | 0.333333 |
g8265 | DLA_09225 | GLQOFTK02G2F2O | CDS | 1598320 | 4455 | + | 0.356004 | |
g8266 | DLA_09226 | GLQOFTK02G2F2O | CDS | 1602972 | 1272 | - | 0.29717 | |
g8267 | DLA_09227 | GLQOFTK02G2F2O | CDS | 1604847 | 1932 | + | 0.3147 | |
g8268 | DLA_09228 | GLQOFTK02G2F2O | CDS | 1606931 | 1467 | - | 0.314928 | |
g8269 | DLA_09229 | GLQOFTK02G2F2O | CDS | 1608785 | 2298 | + | 0.329417 | |
g827 | DLA_00907 | F4PJNLW01A00V1 | CDS | 403659 | 1371 | + | 0.391685 | |
g8270 | DLA_09231 | GLQOFTK02G2F2O | CDS | 1611946 | 522 | + | 0.293103 | |
g8271 | DLA_09232 | GLQOFTK02G2F2O | CDS | 1612664 | 2262 | + | 0.28603 | |
g8272 | DLA_09233 | GLQOFTK02G2F2O | CDS | 1614980 | 1542 | - | 0.274968 | |
g8273 | DLA_09234 | GLQOFTK02G2F2O | CDS | 1617316 | 1968 | + | 0.303862 | |
g8274 | DLA_09235 | GLQOFTK02G2F2O | CDS | 1619539 | 408 | - | 0.311274 | |
g8275 | DLA_09236 | GLQOFTK02G2F2O | CDS | 1620628 | 591 | + | 0.333333 | |
g8276 | DLA_09237 | GLQOFTK02G2F2O | CDS | 1621778 | 1089 | - | 0.285583 | |
g8277 | DLA_11766 | GLQOFTK02G2F2O | CDS | 1623178 | 1323 | - | 0.284958 | |
g8278 | DLA_09238 | a very conserved protein known as G10 protein or BUD31 which in human is suggested to be a nuclear transcription factor and in S. pombe and S. cerevisiae has been shown to be a splicing factor | GLQOFTK02G2F2O | CDS | 1624905 | 432 | + | 0.31713 |
g8279 | DLA_09239 | GLQOFTK02G2F2O | CDS | 1625818 | 789 | - | 0.313055 | |
g828 | DLA_00908 | F4PJNLW01A00V1 | CDS | 405482 | 3894 | - | 0.357473 | |
g8280 | DLA_09241 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family contains a C2 domain (Ca2-dependent membrane-targeting module) an ankyrin repeat region and a SAM (Sterile alpha motif) domain | GLQOFTK02G2F2O | CDS | 1628524 | 2817 | + | 0.334398 |
g8281 | DLA_09242 | GLQOFTK02G2F2O | CDS | 1631895 | 1335 | + | 0.31985 | |
g8282 | DLA_09243 | GLQOFTK02G2F2O | CDS | 1633357 | 2259 | + | 0.35591 | |
g8283 | DLA_09244 | GLQOFTK02G2F2O | CDS | 1635776 | 1272 | + | 0.338836 | |
g8284 | DLA_09245 | GLQOFTK02G2F2O | CDS | 1637354 | 1575 | + | 0.292698 | |
g8285 | DLA_09246 | GLQOFTK02G2F2O | CDS | 1639007 | 4404 | - | 0.33356 | |
g8286 | DLA_09247 | GLQOFTK02G2F2O | CDS | 1644479 | 3021 | + | 0.345581 | |
g8287 | DLA_09248 | GLQOFTK02G2F2O | CDS | 1647617 | 1485 | - | 0.309764 | |
g8288 | DLA_09249 | GLQOFTK02G2F2O | CDS | 1649732 | 444 | + | 0.31982 | |
g8289 | DLA_09250 | GLQOFTK02G2F2O | CDS | 1650615 | 1218 | + | 0.394089 | |
g829 | DLA_00909 | F4PJNLW01A00V1 | CDS | 409957 | 3246 | + | 0.379544 | |
g8290 | DLA_09251 | GLQOFTK02G2F2O | CDS | 1652050 | 867 | - | 0.372549 | |
g8291 | DLA_09252 | GLQOFTK02G2F2O | CDS | 1653627 | 3138 | + | 0.336201 | |
g8292 | DLA_11767 | GLQOFTK02G2F2O | CDS | 1657691 | 744 | + | 0.330645 | |
g8293 | DLA_09253 | GLQOFTK02G2F2O | CDS | 1659090 | 2172 | + | 0.354972 | |
g8294 | DLA_09255 | GLQOFTK02G2F2O | CDS | 1662828 | 1920 | + | 0.308854 | |
g8295 | DLA_09256 | GLQOFTK02G2F2O | CDS | 1665654 | 1830 | + | 0.285792 | |
g8296 | DLA_09257 | GLQOFTK02G2F2O | CDS | 1667785 | 3975 | + | 0.318239 | |
g8297 | DLA_09258 | GLQOFTK02G2F2O | CDS | 1671893 | 1326 | - | 0.342383 | |
g8298 | DLA_09259 | GLQOFTK02G2F2O | CDS | 1673495 | 3150 | + | 0.334603 | |
g8299 | DLA_09260 | GLQOFTK02G2F2O | CDS | 1676780 | 2481 | - | 0.406288 | |
g83 | DLA_00095 | contig05409_1.exp | CDS | 189619 | 3597 | + | 0.350014 | |
g830 | DLA_00910 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | F4PJNLW01A00V1 | CDS | 413597 | 1302 | + | 0.361751 |
g8300 | DLA_09262 | GLQOFTK02G2F2O | CDS | 1681161 | 243 | + | 0.279835 | |
g8301 | DLA_09263 | GLQOFTK02G2F2O | CDS | 1681686 | 522 | - | 0.295019 | |
g8302 | DLA_09264 | GLQOFTK02G2F2O | CDS | 1682483 | 1542 | - | 0.274319 | |
g8303 | DLA_09265 | GLQOFTK02G2F2O | CDS | 1686095 | 1056 | - | 0.265152 | |
g8304 | DLA_09267 | GLQOFTK02G2F2O | CDS | 1687538 | 399 | - | 0.300752 | |
g8305 | DLA_09269 | GLQOFTK02G2F2O | CDS | 1688948 | 753 | + | 0.347942 | |
g8306 | DLA_09270 | GLQOFTK02G2F2O | CDS | 1689898 | 972 | - | 0.323045 | |
g8307 | DLA_09271 | GLQOFTK02G2F2O | CDS | 1691165 | 1062 | - | 0.299435 | |
g8308 | DLA_11768 | GLQOFTK02G2F2O | CDS | 1692433 | 864 | - | 0.355324 | |
g8309 | DLA_09272 | GLQOFTK02G2F2O | CDS | 1696533 | 432 | - | 0.30787 | |
g831 | DLA_00911 | F4PJNLW01A00V1 | CDS | 415447 | 2505 | - | 0.390818 | |
g8310 | DLA_09273 | GLQOFTK02G2F2O | CDS | 1697483 | 894 | - | 0.296421 | |
g8311 | DLA_09275 | GLQOFTK02G2F2O | CDS | 1699520 | 576 | + | 0.378472 | |
g8312 | DLA_09276 | GLQOFTK02G2F2O | CDS | 1700128 | 474 | + | 0.35654 | |
g8313 | DLA_09278 | GLQOFTK02G2F2O | CDS | 1702627 | 2088 | + | 0.319444 | |
g8314 | DLA_09279 | GLQOFTK02G2F2O | CDS | 1704788 | 1659 | - | 0.315853 | |
g8315 | DLA_09280 | GLQOFTK02G2F2O | CDS | 1706839 | 684 | - | 0.321637 | |
g8316 | DLA_09281 | GLQOFTK02G2F2O | CDS | 1707875 | 1017 | + | 0.292035 | |
g8317 | DLA_09283 | GLQOFTK02G2F2O | CDS | 1709191 | 1902 | + | 0.330705 | |
g8318 | DLA_09284 | GLQOFTK02G2F2O | CDS | 1711213 | 2031 | - | 0.310684 | |
g8319 | DLA_09285 | GLQOFTK02G2F2O | CDS | 1714267 | 1797 | + | 0.342237 | |
g832 | DLA_00912 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 418405 | 1833 | + | 0.355701 |
g8320 | DLA_09286 | GLQOFTK02G2F2O | CDS | 1716564 | 1545 | - | 0.324919 | |
g8321 | DLA_09287 | GLQOFTK02G2F2O | CDS | 1719930 | 1263 | + | 0.325416 | |
g8322 | DLA_09288 | GLQOFTK02G2F2O | CDS | 1721538 | 837 | + | 0.357228 | |
g8323 | DLA_09289 | GLQOFTK02G2F2O | CDS | 1722481 | 1926 | + | 0.306334 | |
g8324 | DLA_09290 | GLQOFTK02G2F2O | CDS | 1725034 | 2640 | + | 0.351894 | |
g8325 | DLA_09291 | GLQOFTK02G2F2O | CDS | 1728283 | 471 | + | 0.29724 | |
g8326 | DLA_09292 | GLQOFTK02G2F2O | CDS | 1729218 | 1128 | - | 0.283688 | |
g8327 | DLA_09293 | GLQOFTK02G2F2O | CDS | 1730494 | 543 | + | 0.305709 | |
g8328 | DLA_09294 | GLQOFTK02G2F2O | CDS | 1731320 | 1677 | - | 0.335122 | |
g8329 | DLA_09295 | GLQOFTK02G2F2O | CDS | 1733326 | 516 | - | 0.364341 | |
g833 | DLA_00913 | ortholog of the trafficking protein particle complex subunit 10 part of the multisubunit TRAPP (transport protein particle) complex there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 420669 | 3933 | + | 0.33969 |
g8330 | DLA_09296 | GLQOFTK02G2F2O | CDS | 1734419 | 2460 | + | 0.335366 | |
g8331 | DLA_09297 | GLQOFTK02G2F2O | CDS | 1737039 | 750 | - | 0.313333 | |
g8332 | DLA_09299 | GLQOFTK02G2F2O | CDS | 1738581 | 777 | + | 0.256113 | |
g8333 | DLA_09300 | GLQOFTK02G2F2O | CDS | 1739580 | 3417 | - | 0.352063 | |
g8334 | DLA_09301 | GLQOFTK02G2F2O | CDS | 1743321 | 3546 | - | 0.324027 | |
g8335 | DLA_09302 | GLQOFTK02G2F2O | CDS | 1747435 | 1935 | - | 0.339535 | |
g8336 | DLA_09303 | GLQOFTK02G2F2O | CDS | 1751444 | 525 | - | 0.312381 | |
g8337 | DLA_09304 | GLQOFTK02G2F2O | CDS | 1752145 | 1977 | - | 0.352049 | |
g8338 | DLA_09305 | GLQOFTK02G2F2O | CDS | 1754582 | 807 | + | 0.301115 | |
g8339 | DLA_09307 | GLQOFTK02G2F2O | CDS | 1755732 | 1512 | - | 0.337302 | |
g834 | DLA_00914 | F4PJNLW01A00V1 | CDS | 424736 | 3198 | - | 0.258286 | |
g8340 | DLA_09308 | GLQOFTK02G2F2O | CDS | 1758073 | 627 | + | 0.298246 | |
g8341 | DLA_09309 | GLQOFTK02G2F2O | CDS | 1758767 | 801 | - | 0.348315 | |
g8342 | DLA_09310 | GLQOFTK02G2F2O | CDS | 1759887 | 2610 | - | 0.318391 | |
g8343 | DLA_09311 | GLQOFTK02G2F2O | CDS | 1763200 | 1443 | - | 0.301455 | |
g8344 | DLA_09312 | GLQOFTK02G2F2O | CDS | 1765763 | 2766 | + | 0.39154 | |
g8345 | DLA_09313 | GLQOFTK02G2F2O | CDS | 1768797 | 723 | - | 0.301521 | |
g8346 | DLA_09314 | GLQOFTK02G2F2O | CDS | 1769998 | 2472 | + | 0.336165 | |
g8347 | DLA_09315 | GLQOFTK02G2F2O | CDS | 1772731 | 363 | - | 0.264463 | |
g8348 | DLA_09316 | GLQOFTK02G2F2O | CDS | 1773632 | 1650 | - | 0.384848 | |
g8349 | DLA_09317 | GLQOFTK02G2F2O | CDS | 1775471 | 933 | + | 0.327974 | |
g835 | DLA_00916 | F4PJNLW01A00V1 | CDS | 428746 | 1794 | - | 0.375697 | |
g8350 | DLA_09318 | GLQOFTK02G2F2O | CDS | 1777168 | 405 | + | 0.325926 | |
g8351 | DLA_09319 | similar to budding yeast Sar1 a 21 kDa GTP- binding protein involved in vesicular transport between the endoplasmic reticulum and the Golgi | GLQOFTK02G2F2O | CDS | 1778348 | 594 | + | 0.291246 |
g8352 | DLA_09320 | GLQOFTK02G2F2O | CDS | 1779183 | 876 | + | 0.300228 | |
g8353 | DLA_09321 | GLQOFTK02G2F2O | CDS | 1780188 | 693 | - | 0.359307 | |
g8354 | DLA_09322 | GLQOFTK02G2F2O | CDS | 1781328 | 900 | + | 0.346667 | |
g8355 | DLA_09323 | GLQOFTK02G2F2O | CDS | 1782674 | 3042 | + | 0.325115 | |
g8356 | DLA_11769 | GLQOFTK02G2F2O | CDS | 1786130 | 1542 | + | 0.263943 | |
g8357 | DLA_09324 | GLQOFTK02G2F2O | CDS | 1787804 | 918 | - | 0.330065 | |
g8358 | DLA_09325 | GLQOFTK02G2F2O | CDS | 1789120 | 621 | - | 0.278583 | |
g8359 | DLA_09326 | GLQOFTK02G2F2O | CDS | 1790208 | 3306 | + | 0.340895 | |
g836 | DLA_11455 | F4PJNLW01A00V1 | CDS | 432399 | 2580 | + | 0.324419 | |
g8360 | DLA_09327 | GLQOFTK02G2F2O | CDS | 1793796 | 999 | + | 0.283283 | |
g8361 | DLA_11770 | GLQOFTK02G2F2O | CDS | 1795125 | 609 | + | 0.325123 | |
g8362 | DLA_11771 | GLQOFTK02G2F2O | CDS | 1796070 | 783 | + | 0.309068 | |
g8363 | DLA_09328 | GLQOFTK02G2F2O | CDS | 1797586 | 969 | + | 0.324045 | |
g8364 | DLA_09330 | GLQOFTK02G2F2O | CDS | 1798823 | 975 | - | 0.301538 | |
g8365 | DLA_09331 | GLQOFTK02G2F2O | CDS | 1799937 | 1503 | - | 0.328011 | |
g8366 | DLA_09332 | GLQOFTK02G2F2O | CDS | 1801663 | 588 | - | 0.270408 | |
g8367 | DLA_09333 | GLQOFTK02G2F2O | CDS | 1802337 | 1683 | + | 0.325015 | |
g8368 | DLA_09334 | GLQOFTK02G2F2O | CDS | 1804605 | 483 | + | 0.337474 | |
g8369 | DLA_09335 | GLQOFTK02G2F2O | CDS | 1805721 | 216 | + | 0.384259 | |
g837 | DLA_00917 | F4PJNLW01A00V1 | CDS | 435856 | 2655 | + | 0.369492 | |
g8370 | DLA_09336 | GLQOFTK02G2F2O | CDS | 1806183 | 2058 | + | 0.31827 | |
g8371 | DLA_09337 | GLQOFTK02G2F2O | CDS | 1808455 | 708 | - | 0.282486 | |
g8372 | DLA_09339 | GLQOFTK02G2F2O | CDS | 1809776 | 324 | - | 0.404321 | |
g8373 | DLA_09340 | GLQOFTK02G2F2O | CDS | 1810366 | 909 | - | 0.325633 | |
g8374 | DLA_09341 | GLQOFTK02G2F2O | CDS | 1811831 | 4878 | + | 0.341328 | |
g8375 | DLA_09342 | GLQOFTK02G2F2O | CDS | 1816908 | 1617 | - | 0.372913 | |
g8376 | DLA_09343 | GLQOFTK02G2F2O | CDS | 1819206 | 396 | - | 0.318182 | |
g8377 | DLA_09344 | GLQOFTK02G2F2O | CDS | 1821038 | 591 | - | 0.351946 | |
g8378 | DLA_09345 | GLQOFTK02G2F2O | CDS | 1822001 | 1047 | - | 0.298949 | |
g8379 | DLA_09346 | GLQOFTK02G2F2O | CDS | 1823415 | 573 | + | 0.195462 | |
g838 | DLA_00918 | phosphoinositide phosphatase with low specific activity compared to other known phosphoinositide phosphatases can dephosphorylate several phosphoinositide substrates with a preference for PI(5)P constitutively expressed putative ortholog of H. sapiens EPM2A involved in myoclonic epilepsy of Lafora | F4PJNLW01A00V1 | CDS | 439027 | 657 | - | 0.316591 |
g8380 | DLA_09347 | GLQOFTK02G2F2O | CDS | 1824326 | 1353 | + | 0.317073 | |
g8381 | DLA_09348 | GLQOFTK02G2F2O | CDS | 1825849 | 1035 | - | 0.319807 | |
g8382 | DLA_09349 | GLQOFTK02G2F2O | CDS | 1827121 | 2289 | + | 0.315422 | |
g8383 | DLA_09350 | GLQOFTK02G2F2O | CDS | 1830734 | 1791 | + | 0.335567 | |
g8384 | DLA_09351 | GLQOFTK02G2F2O | CDS | 1833059 | 1260 | - | 0.384921 | |
g8385 | DLA_09352 | GLQOFTK02G2F2O | CDS | 1834905 | 669 | + | 0.38565 | |
g8386 | DLA_09353 | GLQOFTK02G2F2O | CDS | 1835892 | 1062 | + | 0.356874 | |
g8387 | DLA_09354 | GLQOFTK02G2F2O | CDS | 1837045 | 534 | - | 0.26779 | |
g8388 | DLA_09356 | GLQOFTK02G2F2O | CDS | 1837983 | 696 | + | 0.29454 | |
g8389 | DLA_09358 | GLQOFTK02G2F2O | CDS | 1839516 | 1446 | + | 0.347856 | |
g839 | DLA_00919 | F4PJNLW01A00V1 | CDS | 439803 | 591 | - | 0.302876 | |
g8390 | DLA_09359 | GLQOFTK02G2F2O | CDS | 1841378 | 2946 | + | 0.347251 | |
g8391 | DLA_09360 | GLQOFTK02G2F2O | CDS | 1844853 | 831 | - | 0.292419 | |
g8392 | DLA_09361 | GLQOFTK02G2F2O | CDS | 1846184 | 1938 | - | 0.30031 | |
g8393 | DLA_09362 | weakly similar to niban protein a marker for renal carcinogenesisbr bCommunity annotation:b DDB_G0267786 appears to be cell-cycle regulated expressed in late G2 at the same time when virtually all S-phase and M-phase specific genes are active (see graph on wiki page). The gene is slightly overexpressed in the rblA disruptant (15-fold) but appears primarily regulated by at present unknown Rb-independent mechanisms. No ortholog of DDB_G0267786 is recognizable in yeast. Harry MacWilliams August 2010br | GLQOFTK02G2F2O | CDS | 1849012 | 1614 | + | 0.357497 |
g8394 | DLA_09363 | GLQOFTK02G2F2O | CDS | 1851292 | 792 | + | 0.364899 | |
g8395 | DLA_09364 | GLQOFTK02G2F2O | CDS | 1852220 | 222 | - | 0.225225 | |
g8396 | DLA_09365 | GLQOFTK02G2F2O | CDS | 1852909 | 447 | - | 0.317673 | |
g8397 | DLA_09366 | GLQOFTK02G2F2O | CDS | 1853927 | 819 | + | 0.326007 | |
g8398 | DLA_09367 | GLQOFTK02G2F2O | CDS | 1855033 | 1767 | + | 0.299943 | |
g8399 | DLA_09368 | GLQOFTK02G2F2O | CDS | 1857156 | 342 | - | 0.342105 | |
g84 | DLA_00097 | contig05409_1.exp | CDS | 193755 | 1533 | - | 0.315068 | |
g840 | DLA_11456 | F4PJNLW01A00V1 | CDS | 440657 | 1554 | + | 0.301158 | |
g8400 | DLA_09369 | GLQOFTK02G2F2O | CDS | 1857713 | 2004 | + | 0.299401 | |
g8401 | DLA_09370 | GLQOFTK02G2F2O | CDS | 1859940 | 1521 | + | 0.342538 | |
g8402 | DLA_09371 | GLQOFTK02G2F2O | CDS | 1861905 | 1116 | - | 0.331541 | |
g8403 | DLA_09372 | GLQOFTK02G2F2O | CDS | 1864027 | 1155 | + | 0.316883 | |
g8404 | DLA_09373 | GLQOFTK02G2F2O | CDS | 1865531 | 1281 | + | 0.323185 | |
g8405 | DLA_09374 | GLQOFTK02G2F2O | CDS | 1867535 | 615 | - | 0.302439 | |
g8406 | DLA_09375 | GLQOFTK02G2F2O | CDS | 1868353 | 1449 | - | 0.282954 | |
g8407 | DLA_09376 | GLQOFTK02G2F2O | CDS | 1869902 | 426 | - | 0.262911 | |
g8408 | DLA_09377 | GLQOFTK02G2F2O | CDS | 1870716 | 1308 | + | 0.315749 | |
g8409 | DLA_09378 | GLQOFTK02G2F2O | CDS | 1872185 | 1212 | - | 0.29538 | |
g841 | DLA_00920 | F4PJNLW01A00V1 | CDS | 442743 | 3303 | + | 0.340599 | |
g8410 | DLA_09379 | GLQOFTK02G2F2O | CDS | 1873560 | 3123 | + | 0.365354 | |
g8411 | DLA_09380 | GLQOFTK02G2F2O | CDS | 1876839 | 2823 | - | 0.307474 | |
g8412 | DLA_09381 | GLQOFTK02G2F2O | CDS | 1880032 | 2088 | - | 0.357759 | |
g8413 | DLA_09382 | GLQOFTK02G2F2O | CDS | 1884044 | 3234 | + | 0.316636 | |
g8414 | DLA_09383 | GLQOFTK02G2F2O | CDS | 1888250 | 1143 | + | 0.339458 | |
g8415 | DLA_09384 | GLQOFTK02G2F2O | CDS | 1889693 | 288 | - | 0.256944 | |
g8416 | DLA_09385 | GLQOFTK02G2F2O | CDS | 1890456 | 453 | + | 0.335541 | |
g8417 | DLA_09386 | GLQOFTK02G2F2O | CDS | 1891326 | 1098 | - | 0.37796 | |
g8418 | DLA_09387 | catalyzes the reaction L-methionine thioredoxin disulfide H2O L-methionine (S)-S-oxide thioredoxin functions as a repair enzyme for proteins that have been inactivated by oxidation | GLQOFTK02G2F2O | CDS | 1892943 | 504 | + | 0.333333 |
g8419 | DLA_09388 | GLQOFTK02G2F2O | CDS | 1893580 | 1980 | - | 0.29899 | |
g842 | DLA_00921 | F4PJNLW01A00V1 | CDS | 446407 | 3276 | + | 0.320513 | |
g8420 | DLA_09390 | the kinase domain is similar to mammalian stress-induced STK and OSR1 (oxidative stress responsive 1) kinases and other STE20-like kinasesbrbr bCommunity annotation:b Fray1 and Fray2 represent the FRAY-subfamily of Ste20-like kinases in D. discoideum (see | GLQOFTK02G2F2O | CDS | 1897895 | 3102 | + | 0.356222 |
g8421 | DLA_09391 | GLQOFTK02G2F2O | CDS | 1901520 | 1383 | + | 0.310918 | |
g8422 | DLA_09392 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | GLQOFTK02G2F2O | CDS | 1903144 | 759 | + | 0.332016 |
g8423 | DLA_09393 | GLQOFTK02G2F2O | CDS | 1904298 | 1455 | + | 0.358076 | |
g8424 | DLA_09394 | GLQOFTK02G2F2O | CDS | 1905841 | 1863 | + | 0.27912 | |
g8425 | DLA_09395 | GLQOFTK02G2F2O | CDS | 1907965 | 546 | - | 0.342491 | |
g8426 | DLA_09396 | GLQOFTK02G2F2O | CDS | 1908786 | 483 | + | 0.341615 | |
g8427 | DLA_09397 | GLQOFTK02G2F2O | CDS | 1909450 | 2268 | + | 0.322751 | |
g8428 | DLA_09398 | GLQOFTK02G2F2O | CDS | 1911833 | 2367 | - | 0.291086 | |
g8429 | DLA_09400 | GLQOFTK02G2F2O | CDS | 1914880 | 492 | - | 0.264228 | |
g843 | DLA_00923 | F4PJNLW01A00V1 | CDS | 450368 | 1644 | + | 0.379562 | |
g8430 | DLA_09401 | GLQOFTK02G2F2O | CDS | 1915881 | 780 | - | 0.319231 | |
g8431 | DLA_09402 | GLQOFTK02G2F2O | CDS | 1916763 | 1656 | + | 0.289855 | |
g8432 | DLA_09403 | GLQOFTK02G2F2O | CDS | 1918655 | 1152 | - | 0.269965 | |
g8433 | DLA_09404 | GLQOFTK02G2F2O | CDS | 1920380 | 1725 | + | 0.313623 | |
g8434 | DLA_09405 | GLQOFTK02G2F2O | CDS | 1922424 | 7155 | - | 0.361845 | |
g8435 | DLA_09406 | ortholog of ZPR1 a eukaryotic zinc finger protein | GLQOFTK02G2F2O | CDS | 1930055 | 1440 | - | 0.358333 |
g8436 | DLA_09407 | has a BAR domain at the N terminus and a DNAJ heat shock N-terminal domain at the carboxyl domain shares a short region of similarity with plant auxilin-like protein a heat shock protein binding | GLQOFTK02G2F2O | CDS | 1931999 | 2160 | + | 0.332407 |
g8437 | DLA_09408 | GLQOFTK02G2F2O | CDS | 1934579 | 1977 | + | 0.367729 | |
g8438 | DLA_09409 | GLQOFTK02G2F2O | CDS | 1936897 | 486 | + | 0.27572 | |
g8439 | DLA_09411 | GLQOFTK02G2F2O | CDS | 1938214 | 945 | - | 0.265608 | |
g844 | DLA_00924 | F4PJNLW01A00V1 | CDS | 452710 | 810 | - | 0.264198 | |
g8440 | DLA_09412 | GLQOFTK02G2F2O | CDS | 1939429 | 4191 | + | 0.321403 | |
g8441 | DLA_09413 | GLQOFTK02G2F2O | CDS | 1943754 | 720 | - | 0.308333 | |
g8442 | DLA_09414 | GLQOFTK02G2F2O | CDS | 1944715 | 3000 | - | 0.352333 | |
g8443 | DLA_09415 | GLQOFTK02G2F2O | CDS | 1948145 | 2280 | + | 0.309211 | |
g8444 | DLA_09416 | GLQOFTK02G2F2O | CDS | 1950826 | 1854 | - | 0.334412 | |
g8445 | DLA_09417 | GLQOFTK02G2F2O | CDS | 1953233 | 4416 | + | 0.330163 | |
g8446 | DLA_11772 | GLQOFTK02G2F2O | CDS | 1958051 | 3507 | - | 0.289421 | |
g8447 | DLA_09418 | GLQOFTK02G2F2O | CDS | 1961723 | 678 | - | 0.309735 | |
g8448 | DLA_09419 | GLQOFTK02G2F2O | CDS | 1962710 | 1416 | - | 0.301554 | |
g8449 | DLA_09421 | GLQOFTK02G2F2O | CDS | 1964463 | 540 | - | 0.309259 | |
g845 | DLA_00925 | F4PJNLW01A00V1 | CDS | 453911 | 4515 | - | 0.341085 | |
g8450 | DLA_09422 | GLQOFTK02G2F2O | CDS | 1965361 | 1293 | + | 0.317092 | |
g8451 | DLA_09423 | belongs to the methyltransferase superfamily AML1 family similar to human N6AMT2 S. cerevisiae AML1 | GLQOFTK02G2F2O | CDS | 1966691 | 618 | - | 0.288026 |
g8452 | DLA_09424 | GLQOFTK02G2F2O | CDS | 1967909 | 936 | + | 0.360043 | |
g8453 | DLA_09425 | GLQOFTK02G2F2O | CDS | 1968942 | 945 | - | 0.298413 | |
g8454 | DLA_11773 | GLQOFTK02G2F2O | CDS | 1970343 | 1752 | + | 0.28653 | |
g8455 | DLA_09426 | GLQOFTK02G2F2O | CDS | 1972603 | 2385 | + | 0.288889 | |
g8456 | DLA_09427 | GLQOFTK02G2F2O | CDS | 1975087 | 6162 | - | 0.314833 | |
g8457 | DLA_09428 | GLQOFTK02G2F2O | CDS | 1983835 | 1182 | - | 0.318105 | |
g8458 | DLA_09429 | GLQOFTK02G2F2O | CDS | 1985291 | 1002 | + | 0.322355 | |
g8459 | DLA_09430 | protein component of the small (40S) ribosomal subunit ribosomal protein S18 homolog | GLQOFTK02G2F2O | CDS | 1986423 | 456 | + | 0.388158 |
g846 | DLA_00926 | F4PJNLW01A00V1 | CDS | 459261 | 1626 | + | 0.353014 | |
g8460 | DLA_09431 | GLQOFTK02G2F2O | CDS | 1987483 | 3312 | + | 0.302838 | |
g8461 | DLA_09432 | GLQOFTK02G2F2O | CDS | 1991204 | 2175 | + | 0.333333 | |
g8462 | DLA_09433 | GLQOFTK02G2F2O | CDS | 1993768 | 675 | - | 0.340741 | |
g8463 | DLA_09434 | GLQOFTK02G2F2O | CDS | 1994982 | 2067 | + | 0.311563 | |
g8464 | DLA_09435 | GLQOFTK02G2F2O | CDS | 1997725 | 5733 | + | 0.329147 | |
g8465 | DLA_09436 | GLQOFTK02G2F2O | CDS | 2005191 | 1206 | + | 0.327529 | |
g8466 | DLA_09437 | GLQOFTK02G2F2O | CDS | 2007616 | 2796 | + | 0.308655 | |
g8467 | DLA_09439 | catalyzes the reaction ATP L-aspartate tRNAAsp AMP diphosphate L-aspartyl-tRNAAsp | GLQOFTK02G2F2O | CDS | 2010760 | 1707 | + | 0.357938 |
g8468 | DLA_09441 | GLQOFTK02G2F2O | CDS | 2013677 | 252 | + | 0.313492 | |
g8469 | DLA_09442 | GLQOFTK02G2F2O | CDS | 2014170 | 309 | - | 0.38835 | |
g847 | DLA_00927 | F4PJNLW01A00V1 | CDS | 461092 | 1266 | + | 0.300948 | |
g8470 | DLA_09443 | one of two identical H4 proteins (other is | GLQOFTK02G2F2O | CDS | 2015054 | 309 | + | 0.375405 |
g8471 | DLA_09444 | GLQOFTK02G2F2O | CDS | 2015723 | 1248 | + | 0.307692 | |
g8472 | DLA_09445 | GLQOFTK02G2F2O | CDS | 2017278 | 5043 | + | 0.340274 | |
g8473 | DLA_09446 | GLQOFTK02G2F2O | CDS | 2022424 | 954 | - | 0.27044 | |
g8474 | DLA_09447 | GLQOFTK02G2F2O | CDS | 2023625 | 2490 | + | 0.317671 | |
g8475 | DLA_09448 | GLQOFTK02G2F2O | CDS | 2026378 | 564 | - | 0.274823 | |
g8476 | DLA_09449 | GLQOFTK02G2F2O | CDS | 2027604 | 663 | + | 0.27451 | |
g8477 | DLA_09450 | SNARE protein interacts with AP180 (clmA) which retrieves Vamp7B from the contractile vacuole | GLQOFTK02G2F2O | CDS | 2028516 | 690 | + | 0.291304 |
g8478 | DLA_09451 | homolog of human Sphk1 phosphorylates sphinganine to sphinganine 1-phosphate | GLQOFTK02G2F2O | CDS | 2029787 | 1752 | + | 0.31621 |
g8479 | DLA_09454 | GLQOFTK02GEI5A | CDS | 37 | 927 | - | 0.305286 | |
g848 | DLA_00928 | F4PJNLW01A00V1 | CDS | 462535 | 369 | - | 0.319783 | |
g8480 | DLA_09455 | GLQOFTK02GEI5A | CDS | 1894 | 1584 | - | 0.285985 | |
g8481 | DLA_09457 | GLQOFTK02GEI5A | CDS | 5485 | 480 | + | 0.239583 | |
g8482 | DLA_09458 | GLQOFTK02GEI5A | CDS | 6097 | 1251 | - | 0.293365 | |
g8483 | DLA_09459 | GLQOFTK02GEI5A | CDS | 7450 | 1320 | - | 0.258333 | |
g8484 | DLA_09460 | GLQOFTK02GEI5A | CDS | 8849 | 2172 | - | 0.288674 | |
g8485 | DLA_09461 | GLQOFTK02GEI5A | CDS | 11123 | 456 | - | 0.243421 | |
g8486 | DLA_09462 | GLQOFTK02GHM7A | CDS | 754 | 2646 | + | 0.247166 | |
g8487 | DLA_09463 | conserved hypothetical protein contains 13 predicted transmembrane domains and a partial endonucleaseexonucleasephosphatase domain | GLQOFTK02GHM7A | CDS | 3851 | 2106 | - | 0.311016 |
g8488 | DLA_09464 | GLQOFTK02GHM7A | CDS | 6402 | 942 | + | 0.291932 | |
g8489 | DLA_09465 | GLQOFTK02GHM7A | CDS | 7456 | 1404 | - | 0.274929 | |
g849 | DLA_00929 | F4PJNLW01A00V1 | CDS | 464441 | 2265 | - | 0.349669 | |
g8490 | DLA_09466 | GLQOFTK02GHM7A | CDS | 9539 | 1077 | - | 0.36026 | |
g8491 | DLA_09467 | GLQOFTK02GHM7A | CDS | 11524 | 360 | + | 0.266667 | |
g8492 | DLA_09468 | partial ORF2 of tRNA-specific non-long terminal repeat retrotransposon TRE3-D refer to Genbank AF135841 for partial consensus element | GLQOFTK02GHM7A | CDS | 12666 | 1182 | - | 0.370558 |
g8493 | DLA_09471 | GLQOFTK02GHM7A | CDS | 15793 | 339 | + | 0.315634 | |
g8494 | DLA_09472 | GLQOFTK02GHM7A | CDS | 17342 | 1032 | + | 0.263566 | |
g8495 | DLA_11774 | GLQOFTK02GHM7A | CDS | 18934 | 222 | + | 0.396396 | |
g8496 | DLA_09473 | GLQOFTK02GHM7A | CDS | 19362 | 1143 | + | 0.382327 | |
g8497 | DLA_11775 | GLQOFTK02GHM7A | CDS | 20955 | 1182 | + | 0.26819 | |
g8498 | DLA_09474 | GLQOFTK02GHM7A | CDS | 22762 | 285 | - | 0.319298 | |
g8499 | DLA_09475 | GLQOFTK02GHM7A | CDS | 23339 | 1143 | - | 0.35783 | |
g85 | DLA_11431 | contig05409_1.exp | CDS | 195949 | 1239 | - | 0.329298 | |
g850 | DLA_00930 | F4PJNLW01A00V1 | CDS | 467822 | 369 | - | 0.303523 | |
g8500 | DLA_09476 | GLQOFTK02GHM7A | CDS | 25245 | 1185 | + | 0.295359 | |
g8501 | DLA_09478 | GLQOFTK02GHM7A | CDS | 27802 | 1296 | + | 0.334877 | |
g8502 | DLA_09479 | GLQOFTK02GHM7A | CDS | 29273 | 558 | + | 0.299283 | |
g8503 | DLA_09480 | GLQOFTK02GHM7A | CDS | 30013 | 1167 | - | 0.27078 | |
g8504 | DLA_09481 | GLQOFTK02GHM7A | CDS | 32770 | 300 | + | 0.296667 | |
g8505 | DLA_09482 | ortholog of H. sapiens DDX52 and S. cerevisiae ROK1 (Rescuer Of Kem1) ROK1 required for 18S rRNA synthesis | GLQOFTK02GHM7A | CDS | 33431 | 1893 | - | 0.277866 |
g8506 | DLA_09483 | GLQOFTK02GHM7A | CDS | 35572 | 666 | + | 0.247748 | |
g8507 | DLA_11776 | catalyzes the reaction L-serine pyruvate NHsub3sub | GLQOFTK02GHM7A | CDS | 36898 | 1047 | + | 0.346705 |
g8508 | DLA_09484 | GLQOFTK02GHM7A | CDS | 38320 | 2019 | + | 0.301139 | |
g8509 | DLA_09485 | GLQOFTK02GHM7A | CDS | 40990 | 7914 | + | 0.321203 | |
g851 | DLA_00931 | F4PJNLW01A00V1 | CDS | 469670 | 831 | + | 0.345367 | |
g8510 | DLA_09486 | GLQOFTK02GHM7A | CDS | 49108 | 1653 | - | 0.273442 | |
g8511 | DLA_09487 | GLQOFTK02GHM7A | CDS | 50846 | 1086 | - | 0.286372 | |
g8512 | DLA_09488 | GLQOFTK02GHM7A | CDS | 52561 | 1395 | + | 0.306093 | |
g8513 | DLA_09489 | GLQOFTK02GHM7A | CDS | 54286 | 642 | - | 0.327103 | |
g8514 | DLA_09490 | GLQOFTK02GHM7A | CDS | 55254 | 1857 | - | 0.333872 | |
g8515 | DLA_09491 | GLQOFTK02GHM7A | CDS | 58164 | 2499 | + | 0.292917 | |
g8516 | DLA_09492 | GLQOFTK02GHM7A | CDS | 60770 | 798 | - | 0.275689 | |
g8517 | DLA_09493 | GLQOFTK02GHM7A | CDS | 62185 | 2979 | + | 0.325948 | |
g8518 | DLA_09494 | GLQOFTK02GHM7A | CDS | 65353 | 1881 | - | 0.320043 | |
g8519 | DLA_09495 | GLQOFTK02GHM7A | CDS | 67461 | 948 | + | 0.291139 | |
g852 | DLA_00932 | F4PJNLW01A00V1 | CDS | 470736 | 10092 | + | 0.339279 | |
g8520 | DLA_09497 | GLQOFTK02GHM7A | CDS | 68836 | 5745 | + | 0.343777 | |
g8521 | DLA_09498 | similar to the eukaryotic transmembrane protein 85 (TMEM85) contains two putative transmembrane domains | GLQOFTK02GHM7A | CDS | 75271 | 579 | - | 0.29361 |
g8522 | DLA_09499 | putative protein serinethreonine kinase similar to the kinase domains of AAK1 (AP2 associated kinase) and BMP-inducible protein kinase (BIKe) | GLQOFTK02GHM7A | CDS | 76238 | 2130 | + | 0.302817 |
g8523 | DLA_09500 | GLQOFTK02GHM7A | CDS | 78474 | 1224 | - | 0.308824 | |
g8524 | DLA_09501 | GLQOFTK02GHM7A | CDS | 80367 | 1527 | - | 0.337917 | |
g8525 | DLA_09502 | GLQOFTK02GHM7A | CDS | 82102 | 771 | - | 0.267185 | |
g8526 | DLA_09503 | GLQOFTK02GHM7A | CDS | 82967 | 3201 | - | 0.294283 | |
g8527 | DLA_09505 | GLQOFTK02GHM7A | CDS | 86804 | 7434 | + | 0.309927 | |
g8528 | DLA_09507 | GLQOFTK02GHM7A | CDS | 94367 | 747 | - | 0.287818 | |
g8529 | DLA_09508 | GLQOFTK02GHM7A | CDS | 95714 | 978 | + | 0.322086 | |
g853 | DLA_00933 | catalyzes the reaction Nsub2sub-acetyl-L-ornithine 2-oxoglutarate N-acetyl-L-glutamate 5-semialdehyde L-glutamate | F4PJNLW01A00V1 | CDS | 481206 | 1332 | - | 0.354354 |
g8530 | DLA_09509 | GLQOFTK02GHM7A | CDS | 96832 | 471 | - | 0.326964 | |
g8531 | DLA_09510 | GLQOFTK02GHM7A | CDS | 98002 | 2253 | + | 0.377275 | |
g8532 | DLA_11777 | GLQOFTK02GHM7A | CDS | 100570 | 1755 | - | 0.279772 | |
g8533 | DLA_11778 | GLQOFTK02GHM7A | CDS | 102375 | 1779 | - | 0.277684 | |
g8534 | DLA_09511 | GLQOFTK02GHM7A | CDS | 104188 | 4017 | - | 0.287279 | |
g8535 | DLA_09514 | GLQOFTK02GHM7A | CDS | 110678 | 1734 | + | 0.291234 | |
g8536 | DLA_09515 | GLQOFTK02GHM7A | CDS | 112936 | 978 | - | 0.275051 | |
g8537 | DLA_09516 | GLQOFTK02GHM7A | CDS | 114096 | 1206 | + | 0.313433 | |
g8538 | DLA_09518 | GLQOFTK02GHM7A | CDS | 116414 | 3102 | + | 0.293682 | |
g8539 | DLA_09519 | GLQOFTK02GHM7A | CDS | 119842 | 2667 | - | 0.262467 | |
g854 | DLA_00934 | F4PJNLW01A00V1 | CDS | 482667 | 663 | - | 0.374057 | |
g8540 | DLA_09521 | GLQOFTK02GHM7A | CDS | 123442 | 1371 | + | 0.364697 | |
g8541 | DLA_09522 | GLQOFTK02GHM7A | CDS | 124846 | 435 | - | 0.324138 | |
g8542 | DLA_09523 | GLQOFTK02GHM7A | CDS | 125680 | 1917 | + | 0.340115 | |
g8543 | DLA_09524 | GLQOFTK02GHM7A | CDS | 127751 | 1023 | - | 0.347019 | |
g8544 | DLA_09525 | GLQOFTK02GHM7A | CDS | 129088 | 1419 | + | 0.293164 | |
g8545 | DLA_09527 | GLQOFTK02GHM7A | CDS | 131447 | 2031 | + | 0.300837 | |
g8546 | DLA_09529 | GLQOFTK02GHM7A | CDS | 134809 | 402 | + | 0.308458 | |
g8547 | DLA_09530 | GLQOFTK02GHM7A | CDS | 135261 | 2247 | - | 0.352915 | |
g8548 | DLA_09532 | GLQOFTK02GHM7A | CDS | 138992 | 3324 | + | 0.286402 | |
g8549 | DLA_09533 | GLQOFTK02GHM7A | CDS | 142400 | 813 | - | 0.305043 | |
g855 | DLA_00935 | F4PJNLW01A00V1 | CDS | 483602 | 570 | + | 0.308772 | |
g8550 | DLA_09534 | GLQOFTK02GHM7A | CDS | 143275 | 984 | - | 0.336382 | |
g8551 | DLA_09535 | GLQOFTK02GHM7A | CDS | 144790 | 1197 | - | 0.279031 | |
g8552 | DLA_09536 | GLQOFTK02GHM7A | CDS | 146266 | 1326 | - | 0.304676 | |
g8553 | DLA_09537 | GLQOFTK02GHM7A | CDS | 148256 | 843 | + | 0.393832 | |
g8554 | DLA_09538 | GLQOFTK02GHM7A | CDS | 149349 | 1038 | + | 0.315992 | |
g8555 | DLA_09539 | catalyzes the reaction isocitrate NADP 2-oxoglutarate CO2 NADPH | GLQOFTK02GHM7A | CDS | 150554 | 1308 | - | 0.348624 |
g8556 | DLA_09540 | GLQOFTK02GHM7A | CDS | 152126 | 555 | - | 0.338739 | |
g8557 | DLA_09541 | GLQOFTK02GHM7A | CDS | 153460 | 531 | - | 0.3258 | |
g8558 | DLA_11779 | GLQOFTK02GHM7A | CDS | 154270 | 270 | + | 0.277778 | |
g8559 | DLA_09542 | GLQOFTK02GHM7A | CDS | 154695 | 609 | - | 0.330049 | |
g856 | DLA_00936 | F4PJNLW01A00V1 | CDS | 484234 | 2835 | - | 0.31358 | |
g8560 | DLA_09543 | GLQOFTK02GHM7A | CDS | 155870 | 1362 | + | 0.314978 | |
g8561 | DLA_09544 | GLQOFTK02GHM7A | CDS | 158007 | 2088 | + | 0.331418 | |
g8562 | DLA_09545 | GLQOFTK02GHM7A | CDS | 160375 | 585 | + | 0.28547 | |
g8563 | DLA_09546 | GLQOFTK02GHM7A | CDS | 161055 | 843 | + | 0.246738 | |
g8564 | DLA_09547 | GLQOFTK02GHM7A | CDS | 162001 | 3615 | + | 0.333333 | |
g8565 | DLA_09548 | GLQOFTK02GHM7A | CDS | 165844 | 1842 | + | 0.320304 | |
g8566 | DLA_09550 | GLQOFTK02GHM7A | CDS | 168204 | 1461 | - | 0.314853 | |
g8567 | DLA_09552 | GLQOFTK02GHM7A | CDS | 172544 | 1035 | + | 0.348792 | |
g8568 | DLA_09553 | GLQOFTK02GHM7A | CDS | 173753 | 2601 | - | 0.285275 | |
g8569 | DLA_09554 | GLQOFTK02GHM7A | CDS | 176826 | 1656 | - | 0.327899 | |
g857 | DLA_00937 | F4PJNLW01A00V1 | CDS | 487333 | 2793 | + | 0.368779 | |
g8570 | DLA_09555 | GLQOFTK02GHM7A | CDS | 178742 | 798 | - | 0.323308 | |
g8571 | DLA_09556 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | GLQOFTK02GHM7A | CDS | 179980 | 3096 | + | 0.347222 |
g8572 | DLA_09557 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | GLQOFTK02GHM7A | CDS | 183164 | 2592 | - | 0.297839 |
g8573 | DLA_09558 | GLQOFTK02GHM7A | CDS | 186489 | 3087 | + | 0.329446 | |
g8574 | DLA_09559 | GLQOFTK02GHM7A | CDS | 190078 | 2403 | + | 0.363296 | |
g8575 | DLA_11780 | NAD-dependent deacetylase Sirutin 2 family protein that regulate various biological processes by deacetylating histones and other target proteins nuclear protein expressed in pstA and pstO cells in the slug and to the apical disc upper and lower cups in the culminant (similar expression pattern as sir2B) | GLQOFTK02GHM7A | CDS | 192810 | 1011 | + | 0.293769 |
g8576 | DLA_09560 | GLQOFTK02GHM7A | CDS | 194349 | 4242 | + | 0.329562 | |
g8577 | DLA_09561 | GLQOFTK02GHM7A | CDS | 198919 | 1011 | - | 0.358061 | |
g8578 | DLA_09562 | GLQOFTK02GHM7A | CDS | 200094 | 1404 | + | 0.301994 | |
g8579 | DLA_09563 | GLQOFTK02GHM7A | CDS | 201572 | 957 | + | 0.276907 | |
g858 | DLA_00938 | F4PJNLW01A00V1 | CDS | 490212 | 684 | - | 0.282164 | |
g8580 | DLA_09564 | GLQOFTK02GHM7A | CDS | 203153 | 1074 | + | 0.354749 | |
g8581 | DLA_09565 | GLQOFTK02GHM7A | CDS | 205126 | 1794 | + | 0.348383 | |
g8582 | DLA_09566 | GLQOFTK02GHM7A | CDS | 210109 | 417 | - | 0.342926 | |
g8583 | DLA_09571 | GLQOFTK02GHM7A | CDS | 212049 | 6114 | + | 0.319267 | |
g8584 | DLA_09572 | GLQOFTK02GHM7A | CDS | 218698 | 1647 | + | 0.371585 | |
g8585 | DLA_09573 | GLQOFTK02GHM7A | CDS | 220727 | 894 | + | 0.337808 | |
g8586 | DLA_09575 | GLQOFTK02GHM7A | CDS | 223926 | 2124 | + | 0.348399 | |
g8587 | DLA_09577 | belongs to the methyltransferase superfamily ortholog of human WBSCR22 an uncharacterized methyltransferase associated with Williams-Beuren syndrome | GLQOFTK02GHM7A | CDS | 226810 | 960 | - | 0.355208 |
g8588 | DLA_09579 | GLQOFTK02GHM7A | CDS | 228486 | 1752 | + | 0.301941 | |
g8589 | DLA_09580 | half transporter consisting of one ABC domain and one transmembrane domain | GLQOFTK02GHM7A | CDS | 230667 | 2187 | + | 0.321445 |
g859 | DLA_00940 | F4PJNLW01A00V1 | CDS | 491788 | 6873 | + | 0.295941 | |
g8590 | DLA_09581 | GLQOFTK02GHM7A | CDS | 235612 | 3405 | + | 0.325404 | |
g8591 | DLA_09582 | GLQOFTK02GHM7A | CDS | 239071 | 5457 | - | 0.316841 | |
g8592 | DLA_09583 | GLQOFTK02GHM7A | CDS | 245422 | 492 | - | 0.252033 | |
g8593 | DLA_09585 | GLQOFTK02GHM7A | CDS | 246755 | 4185 | + | 0.314934 | |
g8594 | DLA_09586 | GLQOFTK02GHM7A | CDS | 251508 | 717 | + | 0.313808 | |
g8595 | DLA_09587 | GLQOFTK02GHM7A | CDS | 252353 | 1893 | + | 0.34654 | |
g8596 | DLA_09588 | GLQOFTK02GHM7A | CDS | 254418 | 1764 | + | 0.360544 | |
g8597 | DLA_09589 | GLQOFTK02GHM7A | CDS | 256496 | 2496 | - | 0.306891 | |
g8598 | DLA_09590 | GLQOFTK02GHM7A | CDS | 259672 | 1491 | - | 0.357478 | |
g8599 | DLA_09591 | CAZy family GT49 similar to vertebrate acetylglucosaminyltransferase-like protein (LARGE) essential for development | GLQOFTK02GHM7A | CDS | 261513 | 1170 | + | 0.323932 |
g86 | DLA_00098 | contig05409_1.exp | CDS | 197357 | 2535 | + | 0.313215 | |
g860 | DLA_00941 | F4PJNLW01A00V1 | CDS | 500057 | 6390 | + | 0.291549 | |
g8600 | DLA_09592 | GLQOFTK02GHM7A | CDS | 263144 | 447 | - | 0.239374 | |
g8601 | DLA_09593 | GLQOFTK02GHM7A | CDS | 263656 | 1479 | - | 0.3286 | |
g8602 | DLA_09595 | GLQOFTK02GHM7A | CDS | 268083 | 720 | - | 0.258333 | |
g8603 | DLA_09596 | GLQOFTK02GHM7A | CDS | 269579 | 1653 | + | 0.356927 | |
g8604 | DLA_09597 | GLQOFTK02GHM7A | CDS | 271420 | 627 | - | 0.368421 | |
g8605 | DLA_09598 | GLQOFTK02GHM7A | CDS | 273072 | 1167 | + | 0.297344 | |
g8606 | DLA_09599 | GLQOFTK02GHM7A | CDS | 274613 | 2397 | - | 0.361702 | |
g8607 | DLA_09600 | catalyzes the reaction homocysteine L-serine Hsub2subO cystathionine | GLQOFTK02GHM7A | CDS | 278164 | 1494 | + | 0.382865 |
g8608 | DLA_09601 | GLQOFTK02GHM7A | CDS | 279919 | 3174 | - | 0.371456 | |
g8609 | DLA_09602 | GLQOFTK02GHM7A | CDS | 283717 | 822 | + | 0.36618 | |
g861 | DLA_00942 | F4PJNLW01A00V1 | CDS | 506676 | 2997 | - | 0.331999 | |
g8610 | DLA_09603 | GLQOFTK02GHM7A | CDS | 284611 | 2928 | - | 0.27903 | |
g8611 | DLA_09604 | GLQOFTK02GHM7A | CDS | 288917 | 213 | + | 0.356808 | |
g8612 | DLA_09605 | GLQOFTK02GHM7A | CDS | 289302 | 549 | - | 0.313297 | |
g8613 | DLA_09607 | contains a signal peptide a PA14 (anthrax protection antigen) domain 4 Dictyostelium (CTDC) repeats and a C-terminal transmembrane domain | GLQOFTK02GHM7A | CDS | 290704 | 2058 | - | 0.360058 |
g8614 | DLA_09608 | GLQOFTK02GHM7A | CDS | 294096 | 2796 | + | 0.323677 | |
g8615 | DLA_09609 | GLQOFTK02GHM7A | CDS | 297031 | 2145 | - | 0.332401 | |
g8616 | DLA_11781 | GLQOFTK02GHM7A | CDS | 299412 | 594 | + | 0.267677 | |
g8617 | DLA_09610 | GLQOFTK02GHM7A | CDS | 300345 | 3561 | + | 0.33221 | |
g8618 | DLA_09612 | GLQOFTK02GHM7A | CDS | 305556 | 1260 | + | 0.351587 | |
g8619 | DLA_09613 | GLQOFTK02GHM7A | CDS | 307094 | 2970 | + | 0.313131 | |
g862 | DLA_00943 | F4PJNLW01A00V1 | CDS | 510412 | 966 | + | 0.350932 | |
g8620 | DLA_09614 | GLQOFTK02GHM7A | CDS | 310950 | 7086 | + | 0.309342 | |
g8621 | DLA_09615 | fatty acid synthases catalyze the formation of long-chain fatty acids from acetyl-CoA malonyl-CoA and NADPH. This multifunctional protein has several catalytic activities and an acyl carrier protein | GLQOFTK02GHM7A | CDS | 319222 | 7071 | + | 0.305473 |
g8622 | DLA_09616 | GLQOFTK02GHM7A | CDS | 326437 | 1686 | + | 0.299525 | |
g8623 | DLA_09617 | GLQOFTK02GHM7A | CDS | 328363 | 1137 | - | 0.28584 | |
g8624 | DLA_09618 | GLQOFTK02GHM7A | CDS | 329990 | 2130 | + | 0.358216 | |
g8625 | DLA_09619 | GLQOFTK02GHM7A | CDS | 332217 | 3981 | - | 0.331826 | |
g8626 | DLA_09620 | GLQOFTK02GHM7A | CDS | 336697 | 2094 | + | 0.379656 | |
g8627 | DLA_09621 | GLQOFTK02GHM7A | CDS | 338919 | 1860 | - | 0.346774 | |
g8628 | DLA_09622 | GLQOFTK02GHM7A | CDS | 340924 | 834 | - | 0.266187 | |
g8629 | DLA_09623 | similar to D. purpureum protein contains 5 predicted transmembrane domains | GLQOFTK02GHM7A | CDS | 343225 | 759 | - | 0.305665 |
g863 | DLA_00945 | F4PJNLW01A00V1 | CDS | 512443 | 837 | + | 0.297491 | |
g8630 | DLA_09624 | GLQOFTK02GHM7A | CDS | 344176 | 2403 | - | 0.324594 | |
g8631 | DLA_09625 | GLQOFTK02GHM7A | CDS | 346876 | 324 | + | 0.25 | |
g8632 | DLA_11782 | GLQOFTK02GHM7A | CDS | 347313 | 1491 | - | 0.309859 | |
g8633 | DLA_09626 | GLQOFTK02GHM7A | CDS | 349150 | 3288 | - | 0.327251 | |
g8634 | DLA_09627 | GLQOFTK02GHM7A | CDS | 352969 | 867 | + | 0.312572 | |
g8635 | DLA_09628 | GLQOFTK02GHM7A | CDS | 354334 | 981 | - | 0.367992 | |
g8636 | DLA_09629 | GLQOFTK02GHM7A | CDS | 355574 | 1437 | - | 0.320807 | |
g8637 | DLA_09630 | GLQOFTK02GHM7A | CDS | 357355 | 885 | + | 0.322034 | |
g8638 | DLA_09631 | GLQOFTK02GHM7A | CDS | 358343 | 960 | - | 0.370833 | |
g8639 | DLA_09632 | GLQOFTK02GHM7A | CDS | 359995 | 1083 | - | 0.373038 | |
g864 | DLA_00947 | F4PJNLW01A00V1 | CDS | 513891 | 819 | + | 0.285714 | |
g8640 | DLA_09634 | GLQOFTK02GHM7A | CDS | 361786 | 996 | - | 0.348394 | |
g8641 | DLA_09635 | GLQOFTK02GHM7A | CDS | 362954 | 1293 | + | 0.311678 | |
g8642 | DLA_09636 | GLQOFTK02GHM7A | CDS | 364469 | 450 | + | 0.351111 | |
g8643 | DLA_09637 | GLQOFTK02GHM7A | CDS | 365333 | 4689 | + | 0.326082 | |
g8644 | DLA_09638 | GLQOFTK02GHM7A | CDS | 370185 | 1284 | - | 0.315421 | |
g8645 | DLA_09639 | GLQOFTK02GHM7A | CDS | 371661 | 1761 | + | 0.319137 | |
g8646 | DLA_09640 | GLQOFTK02GHM7A | CDS | 373668 | 984 | - | 0.344512 | |
g8647 | DLA_09641 | GLQOFTK02GHM7A | CDS | 375317 | 336 | - | 0.220238 | |
g8648 | DLA_09642 | GLQOFTK02GHM7A | CDS | 375878 | 1143 | + | 0.286089 | |
g8649 | DLA_09643 | GLQOFTK02GHM7A | CDS | 377074 | 3840 | - | 0.341667 | |
g865 | DLA_00948 | F4PJNLW01A00V1 | CDS | 515333 | 1656 | + | 0.347826 | |
g8650 | DLA_09645 | GLQOFTK02GHM7A | CDS | 382314 | 1803 | - | 0.384359 | |
g8651 | DLA_09646 | GLQOFTK02GHM7A | CDS | 386557 | 1548 | + | 0.399225 | |
g8652 | DLA_09647 | GLQOFTK02GHM7A | CDS | 389024 | 693 | - | 0.300144 | |
g8653 | DLA_09648 | GLQOFTK02GHM7A | CDS | 389885 | 792 | + | 0.281566 | |
g8654 | DLA_09649 | GLQOFTK02GHM7A | CDS | 390870 | 5502 | + | 0.320247 | |
g8655 | DLA_09650 | GLQOFTK02GHM7A | CDS | 396742 | 495 | - | 0.418182 | |
g8656 | DLA_09651 | similar to CDK1 and CDK2 cell cycle CAK (CDK-activating kinase) kinases predicted to activate SG2 cyclins cyclin A B and D | GLQOFTK02GHM7A | CDS | 398221 | 876 | - | 0.381279 |
g8657 | DLA_09652 | GLQOFTK02GHM7A | CDS | 399591 | 2358 | - | 0.305344 | |
g8658 | DLA_09653 | GLQOFTK02GHM7A | CDS | 402528 | 2721 | + | 0.338111 | |
g8659 | DLA_09654 | GLQOFTK02GHM7A | CDS | 405729 | 552 | + | 0.277174 | |
g866 | DLA_00950 | F4PJNLW01A00V1 | CDS | 517473 | 261 | - | 0.302682 | |
g8660 | DLA_09655 | GLQOFTK02GHM7A | CDS | 406521 | 1956 | + | 0.32362 | |
g8661 | DLA_09656 | GLQOFTK02GHM7A | CDS | 409042 | 2538 | + | 0.297084 | |
g8662 | DLA_09657 | GLQOFTK02GHM7A | CDS | 411737 | 558 | - | 0.34767 | |
g8663 | DLA_09658 | GLQOFTK02GHM7A | CDS | 412464 | 3243 | - | 0.271354 | |
g8664 | DLA_09659 | GLQOFTK02GHM7A | CDS | 416237 | 432 | + | 0.293981 | |
g8665 | DLA_09660 | GLQOFTK02GHM7A | CDS | 417215 | 3471 | - | 0.362432 | |
g8666 | DLA_09661 | ortholog of S. cerevisiae RRS1 an essential protein that binds ribosomal protein L11 and is required for nuclear export of the 60S pre-ribosomal subunit during ribosome biogenesis mouse homolog shows altered expression in Huntington's disease model mice | GLQOFTK02GHM7A | CDS | 421534 | 975 | + | 0.341538 |
g8667 | DLA_09662 | GLQOFTK02GHM7A | CDS | 423219 | 1770 | + | 0.317514 | |
g8668 | DLA_09663 | GLQOFTK02GHM7A | CDS | 425522 | 207 | - | 0.328502 | |
g8669 | DLA_09664 | GLQOFTK02GHM7A | CDS | 426267 | 5121 | + | 0.359695 | |
g867 | DLA_00951 | F4PJNLW01A00V1 | CDS | 518095 | 1188 | - | 0.361111 | |
g8670 | DLA_09666 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains an N-terminal transmembrane domain that might be a signal sequence | GLQOFTK02GHM7A | CDS | 431790 | 1008 | + | 0.335317 |
g8671 | DLA_09667 | GLQOFTK02GHM7A | CDS | 432963 | 318 | - | 0.31761 | |
g8672 | DLA_09668 | GLQOFTK02GHM7A | CDS | 433903 | 1545 | - | 0.348867 | |
g8673 | DLA_09669 | GLQOFTK02GHM7A | CDS | 436114 | 1023 | + | 0.292278 | |
g8674 | DLA_09670 | GLQOFTK02GHM7A | CDS | 437318 | 1056 | - | 0.314394 | |
g8675 | DLA_09672 | GLQOFTK02GHM7A | CDS | 440164 | 2031 | - | 0.36583 | |
g8676 | DLA_09673 | GLQOFTK02GHM7A | CDS | 442530 | 618 | + | 0.228155 | |
g8677 | DLA_09674 | GLQOFTK02GHM7A | CDS | 443306 | 807 | - | 0.294919 | |
g8678 | DLA_09675 | GLQOFTK02GHM7A | CDS | 444330 | 474 | - | 0.297468 | |
g8679 | DLA_09676 | GLQOFTK02GHM7A | CDS | 445403 | 2091 | - | 0.345289 | |
g868 | DLA_00952 | component of the RNA polymerase III complex has similarity to H. sapiens RPC5 and S. cerevisiae RPC37 | F4PJNLW01A00V1 | CDS | 519855 | 1971 | - | 0.369863 |
g8680 | DLA_09677 | GLQOFTK02GHM7A | CDS | 448178 | 2967 | + | 0.317155 | |
g8681 | DLA_09678 | GLQOFTK02GHM7A | CDS | 451365 | 2946 | - | 0.348608 | |
g8682 | DLA_11783 | GLQOFTK02GHM7A | CDS | 455056 | 708 | - | 0.322034 | |
g8683 | DLA_09679 | GLQOFTK02GHM7A | CDS | 455956 | 2016 | + | 0.288194 | |
g8684 | DLA_09680 | GLQOFTK02GHM7A | CDS | 458214 | 1929 | - | 0.350959 | |
g8685 | DLA_09681 | GLQOFTK02GHM7A | CDS | 461208 | 912 | + | 0.35636 | |
g8686 | DLA_09682 | GLQOFTK02GHM7A | CDS | 462627 | 2409 | + | 0.350353 | |
g8687 | DLA_09683 | GLQOFTK02GHM7A | CDS | 465515 | 3981 | + | 0.363728 | |
g8688 | DLA_09684 | orthlog of the human SBDS protein which is mutated in a majority of patients with Shwachman-Bodian-Diamond syndrome localizes to the pseudopodia in cAMP gradient | GLQOFTK02GHM7A | CDS | 469868 | 885 | + | 0.303955 |
g8689 | DLA_09685 | members of this family are membrane proteins involved in long chain fatty acid elongation systems that produce 26-carbon precursors for ceramide and sphingolipid synthesis contains 7 putative transmembrane domains | GLQOFTK02GHM7A | CDS | 471216 | 882 | - | 0.334467 |
g869 | DLA_00954 | F4PJNLW01A00V1 | CDS | 522511 | 3792 | + | 0.336234 | |
g8690 | DLA_09686 | very similar to the H. sapiens PISD a mitochondrial proenzyme that is cleaved into a phosphatidylserine decarboxylase alpha and beta chain contains one putative transmembrane domain | GLQOFTK02GHM7A | CDS | 472847 | 1269 | + | 0.321513 |
g8691 | DLA_09687 | GLQOFTK02GHM7A | CDS | 474391 | 2313 | + | 0.320796 | |
g8692 | DLA_09688 | GLQOFTK02GHM7A | CDS | 476886 | 1662 | + | 0.288809 | |
g8693 | DLA_09689 | GLQOFTK02GHM7A | CDS | 478603 | 1416 | - | 0.344633 | |
g8694 | DLA_09690 | GLQOFTK02GHM7A | CDS | 481147 | 285 | + | 0.333333 | |
g8695 | DLA_09691 | GLQOFTK02GHM7A | CDS | 481830 | 1944 | - | 0.360082 | |
g8696 | DLA_09692 | GLQOFTK02GHM7A | CDS | 484410 | 1380 | + | 0.299275 | |
g8697 | DLA_09693 | GLQOFTK02GHM7A | CDS | 486437 | 894 | + | 0.420582 | |
g8698 | DLA_09694 | GLQOFTK02GHM7A | CDS | 487590 | 1074 | - | 0.286778 | |
g8699 | DLA_09695 | GLQOFTK02GHM7A | CDS | 489002 | 3639 | - | 0.335532 | |
g87 | DLA_00099 | contig05409_1.exp | CDS | 199998 | 1878 | - | 0.309372 | |
g870 | DLA_00955 | F4PJNLW01A00V1 | CDS | 526863 | 3900 | + | 0.317949 | |
g8700 | DLA_09696 | GLQOFTK02GHM7A | CDS | 493617 | 4632 | - | 0.360967 | |
g8701 | DLA_09697 | GLQOFTK02GHM7A | CDS | 498917 | 1710 | + | 0.287719 | |
g8702 | DLA_09698 | GLQOFTK02GHM7A | CDS | 501076 | 1680 | - | 0.288095 | |
g8703 | DLA_09699 | GLQOFTK02GHM7A | CDS | 503067 | 1062 | + | 0.310734 | |
g8704 | DLA_09700 | GLQOFTK02GHM7A | CDS | 504242 | 1575 | + | 0.309841 | |
g8705 | DLA_09701 | GLQOFTK02GHM7A | CDS | 505848 | 3387 | - | 0.327428 | |
g8706 | DLA_09702 | GLQOFTK02GHM7A | CDS | 510025 | 2067 | + | 0.385583 | |
g8707 | DLA_09703 | GLQOFTK02GHM7A | CDS | 512228 | 1707 | - | 0.280023 | |
g8708 | DLA_09704 | GLQOFTK02GHM7A | CDS | 514445 | 1374 | - | 0.368996 | |
g8709 | DLA_09705 | GLQOFTK02GHM7A | CDS | 516768 | 1248 | + | 0.318109 | |
g871 | DLA_11457 | F4PJNLW01A00V1 | CDS | 531095 | 1464 | + | 0.29918 | |
g8710 | DLA_09706 | GLQOFTK02GHM7A | CDS | 518181 | 4470 | - | 0.337584 | |
g8711 | DLA_09707 | GLQOFTK02GHM7A | CDS | 523192 | 3249 | - | 0.281625 | |
g8712 | DLA_09708 | GLQOFTK02GHM7A | CDS | 526843 | 1746 | + | 0.352806 | |
g8713 | DLA_09709 | GLQOFTK02GHM7A | CDS | 528742 | 1308 | - | 0.279817 | |
g8714 | DLA_09710 | component of the counting factor complex which includes CF60 CF50 CF45-1 and CtnA (countin) | GLQOFTK02GHM7A | CDS | 530240 | 777 | - | 0.425997 |
g8715 | DLA_09711 | GLQOFTK02GHM7A | CDS | 531422 | 1476 | - | 0.339431 | |
g8716 | DLA_09712 | similar to the H. sapiens TATA element modulatory factor (TMF1) which binds the HIV-1 TATA element and inhibits transcriptional activation by the TATA-binding protein TBP | GLQOFTK02GHM7A | CDS | 533331 | 2712 | - | 0.31674 |
g8717 | DLA_09713 | contains three EF hands similar to mammalian neuron specific calcium-binding protein hippocalcin belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | GLQOFTK02GHM7A | CDS | 536286 | 837 | - | 0.287933 |
g8718 | DLA_09714 | catalyzes the reaction 2Hsub2subOsub2sub catalase 2Hsub2subO Osub2sub expressed throughout development expression restricted to prestalk cells during post-aggregationbr bNomenclature conflict:b Do not confuse the acrA gene encoding the late development adenylate cyclase ACR with the genetic locus acrA corresponding to the catA catalase that confers resistance to acriflavin ( | GLQOFTK02GHM7A | CDS | 537522 | 1482 | - | 0.409582 |
g8719 | DLA_09715 | GLQOFTK02GHM7A | CDS | 540819 | 747 | + | 0.319946 | |
g872 | DLA_00956 | F4PJNLW01A00V1 | CDS | 532952 | 3276 | + | 0.330891 | |
g8720 | DLA_09716 | GLQOFTK02GHM7A | CDS | 541933 | 1368 | - | 0.301901 | |
g8721 | DLA_09717 | GLQOFTK02GHM7A | CDS | 544611 | 516 | + | 0.327519 | |
g8722 | DLA_09718 | GLQOFTK02GHM7A | CDS | 545520 | 3552 | + | 0.334459 | |
g8723 | DLA_09720 | GLQOFTK02GHM7A | CDS | 549835 | 1032 | + | 0.390504 | |
g8724 | DLA_09721 | GLQOFTK02GHM7A | CDS | 552287 | 891 | + | 0.297419 | |
g8725 | DLA_09722 | GLQOFTK02GHM7A | CDS | 553497 | 735 | + | 0.359184 | |
g8726 | DLA_09723 | GLQOFTK02GHM7A | CDS | 554712 | 1785 | + | 0.372549 | |
g8727 | DLA_09724 | GLQOFTK02GHM7A | CDS | 557399 | 255 | + | 0.352941 | |
g8728 | DLA_09725 | GLQOFTK02GHM7A | CDS | 557825 | 1521 | + | 0.380013 | |
g8729 | DLA_09727 | GLQOFTK02GHM7A | CDS | 561060 | 294 | + | 0.367347 | |
g873 | DLA_00957 | ortholog of MYH which removes misincorporated adenine residues opposite template 8-oxoguanine during DNA replication | F4PJNLW01A00V1 | CDS | 536344 | 1554 | - | 0.301158 |
g8730 | DLA_11784 | GLQOFTK02GHM7A | CDS | 561492 | 957 | - | 0.376176 | |
g8731 | DLA_11785 | GLQOFTK02GHM7A | CDS | 563102 | 981 | - | 0.376147 | |
g8732 | DLA_09728 | GLQOFTK02GHM7A | CDS | 564558 | 1026 | - | 0.390838 | |
g8733 | DLA_09729 | GLQOFTK02GHM7A | CDS | 566355 | 3732 | + | 0.30493 | |
g8734 | DLA_09730 | GLQOFTK02GHM7A | CDS | 570376 | 5259 | - | 0.289218 | |
g8735 | DLA_09732 | component of the U5 sRNP complex may act in the tri-snRNP complex as a bridging factor between U5 and U4U6 snRNPs | GLQOFTK02GHM7A | CDS | 576587 | 2844 | + | 0.37166 |
g8736 | DLA_09733 | GLQOFTK02GHM7A | CDS | 579679 | 654 | - | 0.313456 | |
g8737 | DLA_09734 | GLQOFTK02GHM7A | CDS | 580512 | 726 | + | 0.294766 | |
g8738 | DLA_09735 | GLQOFTK02GHM7A | CDS | 581573 | 2085 | + | 0.269544 | |
g8739 | DLA_09736 | GLQOFTK02GHM7A | CDS | 583909 | 483 | + | 0.310559 | |
g874 | DLA_00958 | F4PJNLW01A00V1 | CDS | 538081 | 1455 | - | 0.386942 | |
g8740 | DLA_09737 | GLQOFTK02GHM7A | CDS | 584480 | 675 | - | 0.305185 | |
g8741 | DLA_09738 | GLQOFTK02GHM7A | CDS | 585312 | 1593 | - | 0.300063 | |
g8742 | DLA_09739 | GLQOFTK02GHM7A | CDS | 587191 | 927 | - | 0.295577 | |
g8743 | DLA_09740 | GLQOFTK02GHM7A | CDS | 588567 | 843 | + | 0.336892 | |
g8744 | DLA_09741 | GLQOFTK02GHM7A | CDS | 590452 | 1473 | + | 0.356415 | |
g8745 | DLA_09742 | GLQOFTK02GHM7A | CDS | 592611 | 1947 | + | 0.329224 | |
g8746 | DLA_09743 | GLQOFTK02GHM7A | CDS | 595087 | 2847 | + | 0.346329 | |
g8747 | DLA_09744 | GLQOFTK02GHM7A | CDS | 597960 | 1692 | - | 0.277778 | |
g8748 | DLA_11786 | GLQOFTK02GHM7A | CDS | 599878 | 1221 | - | 0.273546 | |
g8749 | DLA_09745 | GLQOFTK02GHM7A | CDS | 601385 | 399 | + | 0.285714 | |
g875 | DLA_00959 | F4PJNLW01A00V1 | CDS | 539707 | 5337 | - | 0.34214 | |
g8750 | DLA_09746 | GLQOFTK02GHM7A | CDS | 602081 | 4905 | - | 0.312946 | |
g8751 | DLA_11787 | GLQOFTK02GHM7A | CDS | 607254 | 2847 | - | 0.324903 | |
g8752 | DLA_09747 | GLQOFTK02GHM7A | CDS | 610444 | 1233 | - | 0.339822 | |
g8753 | DLA_09748 | GLQOFTK02GHM7A | CDS | 612429 | 1968 | + | 0.297256 | |
g8754 | DLA_09749 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | GLQOFTK02GHM7A | CDS | 614852 | 1455 | - | 0.364948 |
g8755 | DLA_09751 | GLQOFTK02GHM7A | CDS | 616873 | 1812 | - | 0.336093 | |
g8756 | DLA_09752 | GLQOFTK02GHM7A | CDS | 619563 | 1119 | - | 0.339589 | |
g8757 | DLA_09753 | GLQOFTK02GHM7A | CDS | 621454 | 1257 | - | 0.324582 | |
g8758 | DLA_09754 | members of the NAD-dependent epimerasedehydratase family use nucleotide-sugar substrates for a variety of chemical reactions | GLQOFTK02GHM7A | CDS | 623170 | 1011 | + | 0.339268 |
g8759 | DLA_09755 | GLQOFTK02GHM7A | CDS | 624241 | 1302 | - | 0.277266 | |
g876 | DLA_00960 | F4PJNLW01A00V1 | CDS | 545252 | 1101 | + | 0.347866 | |
g8760 | DLA_09756 | AGC group AKT family protein serinethreonine kinase similar to other metazoan AktPKB including an N-terminal PH domain homologous kinase and C-terminal regulatory domains and phosphorylation sites required for AktPKB activation | GLQOFTK02GHM7A | CDS | 625916 | 2046 | - | 0.351417 |
g8761 | DLA_11788 | GLQOFTK02GHM7A | CDS | 628385 | 732 | - | 0.280055 | |
g8762 | DLA_09757 | GLQOFTK02GHM7A | CDS | 629690 | 306 | - | 0.330065 | |
g8763 | DLA_09758 | GLQOFTK02GHM7A | CDS | 630584 | 249 | - | 0.481928 | |
g8764 | DLA_09759 | GLQOFTK02GHM7A | CDS | 631054 | 1386 | - | 0.321789 | |
g8765 | DLA_09760 | GLQOFTK02GHM7A | CDS | 633213 | 1644 | - | 0.290754 | |
g8766 | DLA_09762 | GLQOFTK02GHM7A | CDS | 635603 | 2544 | - | 0.314858 | |
g8767 | DLA_09764 | Ca(2)-dependent phospholipid-binding protein contains two C2 domains and a VWFA domain. | GLQOFTK02GHM7A | CDS | 638795 | 2274 | - | 0.319701 |
g8768 | DLA_09766 | GLQOFTK02GHM7A | CDS | 641742 | 1161 | + | 0.332472 | |
g8769 | DLA_09767 | GLQOFTK02GHM7A | CDS | 643096 | 1899 | - | 0.339652 | |
g877 | DLA_00961 | F4PJNLW01A00V1 | CDS | 546414 | 765 | - | 0.351634 | |
g8770 | DLA_09768 | GLQOFTK02GHM7A | CDS | 645448 | 873 | + | 0.32646 | |
g8771 | DLA_09769 | GLQOFTK02GHM7A | CDS | 648180 | 312 | + | 0.262821 | |
g8772 | DLA_09770 | GLQOFTK02GHM7A | CDS | 648872 | 1158 | - | 0.364421 | |
g8773 | DLA_09771 | GLQOFTK02GHM7A | CDS | 650361 | 2175 | + | 0.322299 | |
g8774 | DLA_09772 | GLQOFTK02GHM7A | CDS | 652668 | 639 | - | 0.333333 | |
g8775 | DLA_09773 | GLQOFTK02GHM7A | CDS | 653896 | 1479 | + | 0.329277 | |
g8776 | DLA_09774 | GLQOFTK02GHM7A | CDS | 655437 | 1593 | - | 0.296924 | |
g8777 | DLA_09775 | GLQOFTK02GHM7A | CDS | 657671 | 687 | + | 0.426492 | |
g8778 | DLA_09776 | GLQOFTK02GHM7A | CDS | 658485 | 1215 | + | 0.302058 | |
g8779 | DLA_09777 | GLQOFTK02GHM7A | CDS | 660006 | 933 | + | 0.394427 | |
g878 | DLA_00962 | F4PJNLW01A00V1 | CDS | 547571 | 732 | + | 0.289617 | |
g8780 | DLA_09778 | GLQOFTK02GHM7A | CDS | 660980 | 1743 | - | 0.278256 | |
g8781 | DLA_09780 | GLQOFTK02GHM7A | CDS | 664361 | 1377 | - | 0.329702 | |
g8782 | DLA_09781 | GLQOFTK02GHM7A | CDS | 666017 | 873 | - | 0.321879 | |
g8783 | DLA_09782 | GLQOFTK02GHM7A | CDS | 667313 | 3525 | + | 0.283121 | |
g8784 | DLA_09784 | GLQOFTK02GHM7A | CDS | 671036 | 1572 | - | 0.363232 | |
g8785 | DLA_09786 | GLQOFTK02GHM7A | CDS | 673423 | 864 | + | 0.325231 | |
g8786 | DLA_09787 | GLQOFTK02GHM7A | CDS | 674780 | 3354 | + | 0.335122 | |
g8787 | DLA_09788 | GLQOFTK02GHM7A | CDS | 678408 | 690 | - | 0.336232 | |
g8788 | DLA_09789 | GLQOFTK02GHM7A | CDS | 679382 | 1746 | + | 0.297824 | |
g8789 | DLA_09790 | GLQOFTK02GHM7A | CDS | 681282 | 2670 | - | 0.300749 | |
g879 | DLA_00963 | F4PJNLW01A00V1 | CDS | 548403 | 1671 | - | 0.348294 | |
g8790 | DLA_09791 | GLQOFTK02GHM7A | CDS | 685158 | 1509 | + | 0.31279 | |
g8791 | DLA_09792 | GLQOFTK02GHM7A | CDS | 686833 | 1758 | - | 0.306598 | |
g8792 | DLA_09793 | GLQOFTK02GHM7A | CDS | 689057 | 1203 | - | 0.315046 | |
g8793 | DLA_09795 | GLQOFTK02GHM7A | CDS | 691123 | 1554 | - | 0.301158 | |
g8794 | DLA_09796 | GLQOFTK02GHM7A | CDS | 694705 | 1320 | - | 0.303788 | |
g8795 | DLA_09797 | GLQOFTK02GHM7A | CDS | 696259 | 1446 | - | 0.32296 | |
g8796 | DLA_09798 | GLQOFTK02GHM7A | CDS | 698755 | 1263 | + | 0.391132 | |
g8797 | DLA_09801 | GLQOFTK02GHM7A | CDS | 702072 | 3678 | + | 0.329799 | |
g8798 | DLA_09803 | GLQOFTK02GHM7A | CDS | 706458 | 7053 | + | 0.309514 | |
g8799 | DLA_09804 | GLQOFTK02GHM7A | CDS | 714552 | 1941 | + | 0.341061 | |
g88 | DLA_00103 | contig05409_1.exp | CDS | 204243 | 645 | - | 0.286822 | |
g880 | DLA_00964 | F4PJNLW01A00V1 | CDS | 550332 | 1758 | - | 0.344141 | |
g8800 | DLA_09805 | GLQOFTK02GHM7A | CDS | 716619 | 2418 | - | 0.311001 | |
g8801 | DLA_09806 | GLQOFTK02GHM7A | CDS | 719199 | 1218 | + | 0.270936 | |
g8802 | DLA_09807 | contains an actin-binding WH2 (Wiskott Aldrich syndrome homology region 2) domain near its N-terminus and a C-terminal SH3 (src Homology-3) domain predicted to have an N-terminal signal peptide | GLQOFTK02GHM7A | CDS | 721172 | 1098 | + | 0.423497 |
g8803 | DLA_09808 | GLQOFTK02GHM7A | CDS | 722907 | 1860 | - | 0.350538 | |
g8804 | DLA_09809 | GLQOFTK02GHM7A | CDS | 725493 | 903 | + | 0.358804 | |
g8805 | DLA_09810 | GLQOFTK02GHM7A | CDS | 726834 | 1869 | + | 0.316212 | |
g8806 | DLA_09811 | GLQOFTK02GHM7A | CDS | 729001 | 2019 | - | 0.414562 | |
g8807 | DLA_09812 | GLQOFTK02GHM7A | CDS | 731715 | 1755 | - | 0.337892 | |
g8808 | DLA_09813 | GLQOFTK02GHM7A | CDS | 733952 | 807 | + | 0.408922 | |
g8809 | DLA_09814 | GLQOFTK02GHM7A | CDS | 735423 | 7614 | + | 0.329262 | |
g881 | DLA_00965 | similar to H. sapiens SWISNF subunit SMARCC1 and the yeast subunit SWI3 of the chromatin remodeling complex | F4PJNLW01A00V1 | CDS | 552489 | 3174 | + | 0.331758 |
g8810 | DLA_09815 | GLQOFTK02GHM7A | CDS | 743144 | 3093 | - | 0.295506 | |
g8811 | DLA_09816 | GLQOFTK02GHM7A | CDS | 746456 | 4923 | - | 0.347552 | |
g8812 | DLA_09817 | GLQOFTK02GHM7A | CDS | 752042 | 438 | + | 0.30137 | |
g8813 | DLA_09818 | GLQOFTK02GHM7A | CDS | 753314 | 2151 | + | 0.296141 | |
g8814 | DLA_11789 | GLQOFTK02GHM7A | CDS | 756885 | 1809 | + | 0.349917 | |
g8815 | DLA_09819 | GLQOFTK02GHM7A | CDS | 759334 | 3354 | + | 0.376565 | |
g8816 | DLA_09820 | GLQOFTK02GHM7A | CDS | 763353 | 624 | + | 0.315705 | |
g8817 | DLA_11790 | GLQOFTK02GHM7A | CDS | 764032 | 5049 | - | 0.298079 | |
g8818 | DLA_11791 | GLQOFTK02GHM7A | CDS | 769360 | 4740 | - | 0.316245 | |
g8819 | DLA_09821 | GLQOFTK02GHM7A | CDS | 774623 | 1158 | - | 0.310881 | |
g882 | DLA_00969 | F4PJNLW01A00V1 | CDS | 557087 | 288 | + | 0.28125 | |
g8820 | DLA_09823 | GLQOFTK02GHM7A | CDS | 776526 | 963 | + | 0.326064 | |
g8821 | DLA_09824 | GLQOFTK02GHM7A | CDS | 777619 | 408 | - | 0.318627 | |
g8822 | DLA_09825 | GLQOFTK02GHM7A | CDS | 778495 | 2256 | - | 0.308067 | |
g8823 | DLA_09826 | GLQOFTK02GHM7A | CDS | 780898 | 738 | - | 0.308943 | |
g8824 | DLA_09827 | GLQOFTK02GHM7A | CDS | 781985 | 1257 | - | 0.324582 | |
g8825 | DLA_09828 | GLQOFTK02GHM7A | CDS | 783361 | 543 | - | 0.294659 | |
g8826 | DLA_09829 | GLQOFTK02GHM7A | CDS | 784323 | 3144 | + | 0.284987 | |
g8827 | DLA_09830 | GLQOFTK02GHM7A | CDS | 787659 | 6021 | + | 0.282013 | |
g8828 | DLA_09832 | GLQOFTK02GHM7A | CDS | 794189 | 3807 | - | 0.324402 | |
g8829 | DLA_09833 | GLQOFTK02GHM7A | CDS | 798932 | 1485 | + | 0.301684 | |
g883 | DLA_00972 | belongs to the costars family similar to the C terminal region of mammalian striated muscle activator of Rho signaling | F4PJNLW01A00V1 | CDS | 558983 | 252 | + | 0.281746 |
g8830 | DLA_11792 | GLQOFTK02GHM7A | CDS | 800687 | 3699 | + | 0.319546 | |
g8831 | DLA_09834 | GLQOFTK02GHM7A | CDS | 804812 | 4203 | + | 0.353081 | |
g8832 | DLA_09835 | GLQOFTK02GHM7A | CDS | 809734 | 2730 | - | 0.289377 | |
g8833 | DLA_09836 | GLQOFTK02GHM7A | CDS | 812631 | 3195 | - | 0.293584 | |
g8834 | DLA_09837 | GLQOFTK02GHM7A | CDS | 815985 | 1809 | + | 0.291321 | |
g8835 | DLA_09838 | GLQOFTK02GHM7A | CDS | 818207 | 726 | - | 0.269972 | |
g8836 | DLA_09839 | GLQOFTK02GHM7A | CDS | 819605 | 3366 | + | 0.333928 | |
g8837 | DLA_11793 | GLQOFTK02GHM7A | CDS | 823565 | 3309 | + | 0.309459 | |
g8838 | DLA_09840 | GLQOFTK02GHM7A | CDS | 827167 | 3333 | + | 0.314731 | |
g8839 | DLA_09841 | GLQOFTK02GHM7A | CDS | 831002 | 3390 | + | 0.325664 | |
g884 | DLA_00974 | contains two selenocysteine residues at positions 20 and 88 conserved in the green algae such as Chlamydomonas Ostreococcus and Volvox contains 4 transmembrane domains | F4PJNLW01A00V1 | CDS | 559580 | 660 | + | 0.371212 |
g8840 | DLA_09842 | GLQOFTK02GHM7A | CDS | 834595 | 3273 | + | 0.309502 | |
g8841 | DLA_09843 | GLQOFTK02GHM7A | CDS | 837974 | 2934 | - | 0.325835 | |
g8842 | DLA_09844 | GLQOFTK02GHM7A | CDS | 841718 | 1458 | + | 0.281207 | |
g8843 | DLA_09845 | GLQOFTK02GHM7A | CDS | 843423 | 963 | + | 0.369678 | |
g8844 | DLA_09846 | GLQOFTK02GHM7A | CDS | 844455 | 393 | - | 0.21883 | |
g8845 | DLA_09847 | GLQOFTK02GHM7A | CDS | 845045 | 3372 | + | 0.320878 | |
g8846 | DLA_09848 | GLQOFTK02GHM7A | CDS | 848909 | 684 | - | 0.368421 | |
g8847 | DLA_09849 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis not a human Nek3 homolog | GLQOFTK02GHM7A | CDS | 851623 | 2403 | + | 0.293383 |
g8848 | DLA_09851 | contains one RING-type zinc finger and one IBR (In Between Ring fingers) domain similar to S. cerevisiae RING finger protein YKR017C | GLQOFTK02GHM7A | CDS | 854254 | 1662 | - | 0.347172 |
g8849 | DLA_09852 | GLQOFTK02GHM7A | CDS | 856436 | 654 | - | 0.269113 | |
g885 | DLA_00976 | F4PJNLW01A00V1 | CDS | 561707 | 996 | + | 0.35743 | |
g8850 | DLA_09853 | similar to S. cerevisiae AKR1 (palmitoyltransferase AKR1) contains 5 ankyrin repeats and 1 zinc finger DHHC domain contains 6 putative transmembrane domains | GLQOFTK02GHM7A | CDS | 857274 | 1740 | + | 0.286207 |
g8851 | DLA_09854 | GLQOFTK02GHM7A | CDS | 859222 | 810 | - | 0.308642 | |
g8852 | DLA_09855 | GLQOFTK02GHM7A | CDS | 860965 | 2049 | + | 0.308931 | |
g8853 | DLA_09857 | GLQOFTK02GHM7A | CDS | 863369 | 2757 | - | 0.299238 | |
g8854 | DLA_11794 | GLQOFTK02GHM7A | CDS | 866535 | 1302 | - | 0.288018 | |
g8855 | DLA_09859 | GLQOFTK02GHM7A | CDS | 868255 | 576 | - | 0.267361 | |
g8856 | DLA_09860 | GLQOFTK02GHM7A | CDS | 870621 | 1491 | + | 0.348089 | |
g8857 | DLA_09861 | GLQOFTK02GHM7A | CDS | 872304 | 1011 | - | 0.302671 | |
g8858 | DLA_09862 | GLQOFTK02GHM7A | CDS | 873448 | 2925 | + | 0.304274 | |
g8859 | DLA_09863 | GLQOFTK02GHM7A | CDS | 876530 | 2010 | + | 0.274627 | |
g886 | DLA_00977 | F4PJNLW01A00V1 | CDS | 562847 | 1089 | - | 0.311295 | |
g8860 | DLA_09865 | GLQOFTK02GK2WV | CDS | 787 | 1341 | - | 0.272185 | |
g8861 | DLA_09872 | GLQOFTK02GQ36N | CDS | 4189 | 597 | - | 0.380235 | |
g8862 | DLA_09873 | GLQOFTK02GQ36N | CDS | 5043 | 504 | + | 0.253968 | |
g8863 | DLA_09875 | GLQOFTK02GQ36N | CDS | 6044 | 441 | - | 0.346939 | |
g8864 | DLA_09876 | GLQOFTK02GQ36N | CDS | 7761 | 5028 | - | 0.309666 | |
g8865 | DLA_09877 | GLQOFTK02GQ36N | CDS | 13249 | 546 | + | 0.283883 | |
g8866 | DLA_09878 | GLQOFTK02GQ36N | CDS | 14099 | 231 | - | 0.350649 | |
g8867 | DLA_09881 | regulatory subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase contains an EF-hand calcium binding motif | GLQOFTK02GQ36N | CDS | 15916 | 540 | + | 0.274074 |
g8868 | DLA_09882 | GLQOFTK02GQ36N | CDS | 16889 | 783 | + | 0.312899 | |
g8869 | DLA_09883 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases belongs to the PAKL subfamilystress-responsive kinase there is a second copy of this gene | GLQOFTK02GQ36N | CDS | 17991 | 1569 | - | 0.297642 |
g887 | DLA_00979 | F4PJNLW01A00V1 | CDS | 564254 | 1008 | + | 0.28373 | |
g8870 | DLA_09885 | GLQOFTK02GQ36N | CDS | 20614 | 3354 | - | 0.281455 | |
g8871 | DLA_11795 | GLQOFTK02GQ36N | CDS | 25629 | 672 | - | 0.270833 | |
g8872 | DLA_09886 | GLQOFTK02GQ36N | CDS | 26595 | 408 | + | 0.252451 | |
g8873 | DLA_09888 | GLQOFTK02GQ36N | CDS | 27402 | 336 | + | 0.244048 | |
g8874 | DLA_09889 | GLQOFTK02GQ36N | CDS | 28057 | 1536 | - | 0.340495 | |
g8875 | DLA_09890 | GLQOFTK02GQ36N | CDS | 30164 | 1221 | - | 0.298116 | |
g8876 | DLA_09891 | GLQOFTK02GQ36N | CDS | 32246 | 507 | - | 0.289941 | |
g8877 | DLA_09892 | GLQOFTK02GQ36N | CDS | 33353 | 351 | + | 0.316239 | |
g8878 | DLA_09893 | GLQOFTK02GQ36N | CDS | 34005 | 594 | - | 0.383838 | |
g8879 | DLA_09894 | GLQOFTK02GQ36N | CDS | 35483 | 1599 | - | 0.270169 | |
g888 | DLA_11458 | F4PJNLW01A00V1 | CDS | 565346 | 681 | + | 0.331865 | |
g8880 | DLA_09895 | GLQOFTK02GQ36N | CDS | 37449 | 2145 | + | 0.327273 | |
g8881 | DLA_09896 | GLQOFTK02GQ36N | CDS | 40006 | 1131 | + | 0.396994 | |
g8882 | DLA_11796 | GLQOFTK02GQ36N | CDS | 41397 | 225 | + | 0.253333 | |
g8883 | DLA_09897 | GLQOFTK02GQ36N | CDS | 42045 | 939 | + | 0.332268 | |
g8884 | DLA_09898 | GLQOFTK02GQ36N | CDS | 43185 | 900 | + | 0.333333 | |
g8885 | DLA_09899 | GLQOFTK02GQ36N | CDS | 44251 | 708 | + | 0.323446 | |
g8886 | DLA_09901 | GLQOFTK02GQ36N | CDS | 45614 | 7734 | + | 0.351952 | |
g8887 | DLA_09902 | GLQOFTK02GQ36N | CDS | 53723 | 924 | + | 0.310606 | |
g8888 | DLA_09903 | GLQOFTK02GQ36N | CDS | 54848 | 1197 | + | 0.319131 | |
g8889 | DLA_09904 | there is an identical copy of this gene on chromosome 5 | GLQOFTK02GQ36N | CDS | 56341 | 1740 | + | 0.331034 |
g889 | DLA_00980 | F4PJNLW01A00V1 | CDS | 566096 | 345 | + | 0.33913 | |
g8890 | DLA_09905 | GLQOFTK02GQ36N | CDS | 58683 | 2037 | - | 0.312224 | |
g8891 | DLA_09907 | GLQOFTK02GQ36N | CDS | 61314 | 372 | - | 0.344086 | |
g8892 | DLA_09908 | GLQOFTK02GQ36N | CDS | 61851 | 3879 | + | 0.321217 | |
g8893 | DLA_09909 | GLQOFTK02GQ36N | CDS | 66450 | 7359 | + | 0.318522 | |
g8894 | DLA_09912 | GLQOFTK02GQ36N | CDS | 75224 | 3864 | + | 0.311594 | |
g8895 | DLA_09913 | GLQOFTK02GQ36N | CDS | 79294 | 375 | - | 0.293333 | |
g8896 | DLA_09914 | GLQOFTK02GQ36N | CDS | 80933 | 2232 | - | 0.336022 | |
g8897 | DLA_09915 | GLQOFTK02GQ36N | CDS | 83747 | 1104 | - | 0.371377 | |
g8898 | DLA_09916 | GLQOFTK02GQ36N | CDS | 85058 | 489 | + | 0.288344 | |
g8899 | DLA_09917 | GLQOFTK02GQ36N | CDS | 85787 | 330 | + | 0.266667 | |
g89 | DLA_00104 | contig05409_1.exp | CDS | 205615 | 3432 | + | 0.337121 | |
g890 | DLA_00982 | F4PJNLW01A00V1 | CDS | 566858 | 1032 | - | 0.312016 | |
g8900 | DLA_09918 | GLQOFTK02GQ36N | CDS | 86387 | 2031 | - | 0.293451 | |
g8901 | DLA_09920 | GLQOFTK02GQ36N | CDS | 89739 | 2292 | - | 0.297993 | |
g8902 | DLA_09921 | GLQOFTK02GQ36N | CDS | 92458 | 543 | + | 0.267035 | |
g8903 | DLA_09922 | GLQOFTK02GQ36N | CDS | 93131 | 2757 | - | 0.309032 | |
g8904 | DLA_09923 | GLQOFTK02GQ36N | CDS | 96353 | 597 | + | 0.276382 | |
g8905 | DLA_09924 | GLQOFTK02GQ36N | CDS | 97368 | 315 | - | 0.333333 | |
g8906 | DLA_09925 | GLQOFTK02GQ36N | CDS | 97926 | 1716 | - | 0.327506 | |
g8907 | DLA_09926 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | GLQOFTK02GQ36N | CDS | 100032 | 2586 | - | 0.310905 |
g8908 | DLA_09927 | GLQOFTK02GQ36N | CDS | 103566 | 1089 | + | 0.28742 | |
g8909 | DLA_09928 | GLQOFTK02GQ36N | CDS | 105093 | 2010 | - | 0.30995 | |
g891 | DLA_00983 | F4PJNLW01A00V1 | CDS | 569380 | 1380 | - | 0.301449 | |
g8910 | DLA_09929 | GLQOFTK02GQ36N | CDS | 107710 | 1641 | - | 0.307739 | |
g8911 | DLA_09930 | GLQOFTK02GQ36N | CDS | 109550 | 822 | - | 0.30292 | |
g8912 | DLA_09931 | GLQOFTK02GQ36N | CDS | 110544 | 1551 | + | 0.31528 | |
g8913 | DLA_09932 | GLQOFTK02GQ36N | CDS | 112219 | 882 | - | 0.289116 | |
g8914 | DLA_09933 | GLQOFTK02GQ36N | CDS | 113500 | 1767 | + | 0.325976 | |
g8915 | DLA_09934 | GLQOFTK02GQ36N | CDS | 119279 | 1308 | + | 0.35474 | |
g8916 | DLA_09935 | GLQOFTK02GQ36N | CDS | 120955 | 1737 | - | 0.295337 | |
g8917 | DLA_09936 | GLQOFTK02GQ36N | CDS | 122863 | 1386 | - | 0.305916 | |
g8918 | DLA_09937 | full transporter consisting of two ABC domains and two transmembrane domains | GLQOFTK02GQ36N | CDS | 125115 | 4932 | + | 0.336375 |
g8919 | DLA_09938 | GLQOFTK02GQ36N | CDS | 132556 | 7536 | + | 0.348726 | |
g892 | DLA_00985 | putative ortholog of H. sapiens POMP similar to S. cerevisiae UMP1 involved in maturation of the 20S proteasome | F4PJNLW01A00V1 | CDS | 571149 | 375 | - | 0.288 |
g8920 | DLA_09940 | GLQOFTK02GQ36N | CDS | 141002 | 1515 | + | 0.315512 | |
g8921 | DLA_09941 | ortholog of human coronin-7 (CORO7) long protein corresponding to two coronin equivalents regulates F-actin depolymerization and is thus involved in substrate adhesion phagocytosis and cell motility | GLQOFTK02GQ36N | CDS | 142713 | 2751 | - | 0.371501 |
g8922 | DLA_09942 | GLQOFTK02GQ36N | CDS | 145796 | 1659 | - | 0.330922 | |
g8923 | DLA_09943 | GLQOFTK02GQ36N | CDS | 147898 | 870 | + | 0.273563 | |
g8924 | DLA_09944 | GLQOFTK02GQ36N | CDS | 149197 | 498 | + | 0.301205 | |
g8925 | DLA_09945 | GLQOFTK02GQ36N | CDS | 149946 | 1824 | - | 0.320724 | |
g8926 | DLA_09946 | GLQOFTK02GQ36N | CDS | 152018 | 1947 | - | 0.302517 | |
g8927 | DLA_09947 | GLQOFTK02GQ36N | CDS | 154341 | 636 | - | 0.33805 | |
g8928 | DLA_09948 | GLQOFTK02GQ36N | CDS | 155095 | 903 | - | 0.33887 | |
g8929 | DLA_09949 | mitochondrial enzyme catalyzes the oxidation of D-2-hydroxyglutarate to alpha-ketoglutarate ortholog of the H. sapiens D2HGDH which when defect causes D-2-hydroxyglutaric aciduria a rare recessive neurometabolic disorder | GLQOFTK02GQ36N | CDS | 156335 | 1482 | - | 0.338057 |
g893 | DLA_00986 | F4PJNLW01A00V1 | CDS | 572060 | 1311 | + | 0.293669 | |
g8930 | DLA_09950 | GLQOFTK02GQ36N | CDS | 160484 | 1854 | + | 0.303128 | |
g8931 | DLA_09951 | GLQOFTK02GQ36N | CDS | 162602 | 438 | - | 0.294521 | |
g8932 | DLA_09952 | GLQOFTK02GQ36N | CDS | 163422 | 2862 | - | 0.300839 | |
g8933 | DLA_11797 | catalyzes the degradation of GABA :4-aminobutanoate 2-oxoglutarate succinate semialdehyde L-glutamate null mutant has a very mild developmental delay | GLQOFTK02GQ36N | CDS | 167369 | 1491 | - | 0.366197 |
g8934 | DLA_09953 | ortholog of human and S. pombe nucleolar protein 58 members of this family are involved in a variety of functions during pre-mRNA splicing | GLQOFTK02GQ36N | CDS | 169506 | 1965 | - | 0.33028 |
g8935 | DLA_09954 | GLQOFTK02GQ36N | CDS | 171883 | 2679 | - | 0.380366 | |
g8936 | DLA_11798 | GLQOFTK02GQ36N | CDS | 174915 | 618 | - | 0.304207 | |
g8937 | DLA_09955 | GLQOFTK02GQ36N | CDS | 175543 | 3084 | - | 0.321336 | |
g8938 | DLA_09956 | catalyzes the reaction ATP L-asparagine tRNAAsn AMP diphosphate L-asparaginyl-tRNAAsn similar to bacterial Asn-tRNA-ligases | GLQOFTK02GQ36N | CDS | 178818 | 1461 | + | 0.362765 |
g8939 | DLA_09957 | GLQOFTK02GQ36N | CDS | 180401 | 1821 | + | 0.32235 | |
g894 | DLA_00987 | F4PJNLW01A00V1 | CDS | 573450 | 2103 | - | 0.320495 | |
g8940 | DLA_09959 | GLQOFTK02GQ36N | CDS | 182914 | 2091 | - | 0.361071 | |
g8941 | DLA_09960 | GLQOFTK02GQ36N | CDS | 186083 | 1941 | - | 0.325605 | |
g8942 | DLA_09962 | GLQOFTK02GQ36N | CDS | 188932 | 795 | + | 0.344654 | |
g8943 | DLA_11799 | GLQOFTK02GQ36N | CDS | 190262 | 798 | + | 0.338346 | |
g8944 | DLA_09963 | GLQOFTK02GQ36N | CDS | 191376 | 1266 | + | 0.339652 | |
g8945 | DLA_09964 | GLQOFTK02GQ36N | CDS | 192760 | 1866 | - | 0.329582 | |
g8946 | DLA_09965 | GLQOFTK02GQ36N | CDS | 194888 | 3636 | - | 0.278053 | |
g8947 | DLA_09966 | GLQOFTK02GQ36N | CDS | 198666 | 789 | - | 0.287706 | |
g8948 | DLA_09967 | GLQOFTK02GQ36N | CDS | 199825 | 330 | + | 0.321212 | |
g8949 | DLA_09968 | GLQOFTK02GQ36N | CDS | 200327 | 2259 | - | 0.367419 | |
g895 | DLA_00988 | F4PJNLW01A00V1 | CDS | 575860 | 2082 | - | 0.303554 | |
g8950 | DLA_09969 | GLQOFTK02GQ36N | CDS | 202877 | 246 | - | 0.272358 | |
g8951 | DLA_09970 | GLQOFTK02GQ36N | CDS | 203562 | 2256 | - | 0.310727 | |
g8952 | DLA_09971 | GLQOFTK02GQ36N | CDS | 206764 | 1143 | - | 0.293088 | |
g8953 | DLA_09972 | GLQOFTK02GQ36N | CDS | 208589 | 1623 | - | 0.279113 | |
g8954 | DLA_09973 | GLQOFTK02GQ36N | CDS | 210318 | 732 | - | 0.35929 | |
g8955 | DLA_09974 | GLQOFTK02GQ36N | CDS | 212241 | 2091 | - | 0.295552 | |
g8956 | DLA_09975 | GLQOFTK02GQ36N | CDS | 214548 | 1446 | + | 0.280775 | |
g8957 | DLA_09976 | GLQOFTK02GQ36N | CDS | 216238 | 1842 | + | 0.32899 | |
g8958 | DLA_09977 | GLQOFTK02GQ36N | CDS | 218203 | 1653 | + | 0.320024 | |
g8959 | DLA_09978 | GLQOFTK02GQ36N | CDS | 220110 | 1962 | - | 0.333333 | |
g896 | DLA_00989 | F4PJNLW01A00V1 | CDS | 578251 | 2115 | - | 0.334279 | |
g8960 | DLA_09979 | catalyzes the reaction aldehyde NAD Hsub2subO an acid NADH H | GLQOFTK02GQ36N | CDS | 222979 | 1491 | - | 0.34943 |
g8961 | DLA_09982 | ortholog of the yeast IRE1 serinethreonine kinaseendoribonuclease a transmembrane protein involved in the unfolded protein response contains a ribonuclease 2-5A domain and 3 pyrrolo-quinoline quinone (PQQ) domains | GLQOFTK02GQ36N | CDS | 225395 | 3168 | - | 0.322285 |
g8962 | DLA_11800 | GLQOFTK02GQ36N | CDS | 228881 | 903 | - | 0.320044 | |
g8963 | DLA_09983 | GLQOFTK02GQ36N | CDS | 230092 | 1185 | + | 0.383122 | |
g8964 | DLA_09984 | GLQOFTK02GQ36N | CDS | 231808 | 2487 | + | 0.327704 | |
g8965 | DLA_09985 | GLQOFTK02GQ36N | CDS | 234926 | 1770 | + | 0.280791 | |
g8966 | DLA_09986 | GLQOFTK02GQ36N | CDS | 236814 | 5184 | - | 0.337191 | |
g8967 | DLA_09988 | GLQOFTK02GQ36N | CDS | 242614 | 4104 | - | 0.323099 | |
g8968 | DLA_09989 | GLQOFTK02GQ36N | CDS | 247665 | 1032 | + | 0.292636 | |
g8969 | DLA_09990 | GLQOFTK02GQ36N | CDS | 248917 | 750 | - | 0.322667 | |
g897 | DLA_00990 | F4PJNLW01A00V1 | CDS | 580658 | 1035 | - | 0.264734 | |
g8970 | DLA_09992 | GLQOFTK02GQ36N | CDS | 250327 | 1662 | + | 0.306258 | |
g8971 | DLA_09993 | GLQOFTK02GQ36N | CDS | 252069 | 840 | + | 0.34881 | |
g8972 | DLA_09994 | GLQOFTK02GQ36N | CDS | 253220 | 861 | + | 0.307782 | |
g8973 | DLA_09995 | GLQOFTK02GQ36N | CDS | 254501 | 858 | + | 0.317016 | |
g8974 | DLA_09996 | GLQOFTK02GQ36N | CDS | 255511 | 1887 | + | 0.329094 | |
g8975 | DLA_09997 | GLQOFTK02GQ36N | CDS | 257526 | 2103 | - | 0.314788 | |
g8976 | DLA_09998 | GLQOFTK02GQ36N | CDS | 260339 | 3603 | + | 0.360533 | |
g8977 | DLA_10000 | GLQOFTK02GQ36N | CDS | 264677 | 615 | + | 0.336585 | |
g8978 | DLA_10001 | GLQOFTK02GQ36N | CDS | 265383 | 3807 | - | 0.321513 | |
g8979 | DLA_10002 | GLQOFTK02GQ36N | CDS | 269504 | 678 | - | 0.272861 | |
g898 | DLA_00991 | conserved protein alpha-galactosidase (melibiase) catalyses the hydrolysis of melibiose into galactose and glucose | F4PJNLW01A00V1 | CDS | 582053 | 1026 | - | 0.395712 |
g8980 | DLA_10003 | GLQOFTK02GQ36N | CDS | 270268 | 1119 | + | 0.302949 | |
g8981 | DLA_10004 | catalyzes the reaction nicotinate D-ribonucleotide diphosphate COsub2sub pyridine-23-dicarboxylate 5-phospho-alpha-D-ribose 1-diphosphate | GLQOFTK02GQ36N | CDS | 271421 | 873 | - | 0.335624 |
g8982 | DLA_10005 | GLQOFTK02GQ36N | CDS | 272420 | 555 | - | 0.264865 | |
g8983 | DLA_10006 | GLQOFTK02GQ36N | CDS | 273128 | 441 | - | 0.396825 | |
g8984 | DLA_10008 | GLQOFTK02GQ36N | CDS | 275832 | 465 | + | 0.311828 | |
g8985 | DLA_10009 | GLQOFTK02GQ36N | CDS | 276878 | 1524 | + | 0.292651 | |
g8986 | DLA_10010 | GLQOFTK02GQ36N | CDS | 278602 | 1359 | - | 0.292127 | |
g8987 | DLA_10011 | GLQOFTK02GQ36N | CDS | 280110 | 5451 | + | 0.303431 | |
g8988 | DLA_10012 | GLQOFTK02GQ36N | CDS | 287833 | 2991 | + | 0.30224 | |
g8989 | DLA_10013 | GLQOFTK02GQ36N | CDS | 291555 | 2976 | + | 0.295027 | |
g899 | DLA_00992 | F4PJNLW01A00V1 | CDS | 583527 | 1824 | - | 0.305921 | |
g8990 | DLA_11801 | GLQOFTK02GQ36N | CDS | 295397 | 828 | - | 0.35628 | |
g8991 | DLA_10014 | GLQOFTK02GQ36N | CDS | 296639 | 1890 | - | 0.348148 | |
g8992 | DLA_10015 | GLQOFTK02GQ36N | CDS | 299037 | 1047 | - | 0.283668 | |
g8993 | DLA_10016 | GLQOFTK02GQ36N | CDS | 300271 | 894 | + | 0.316555 | |
g8994 | DLA_10017 | GLQOFTK02GQ36N | CDS | 301585 | 636 | + | 0.366352 | |
g8995 | DLA_10018 | GLQOFTK02GQ36N | CDS | 302622 | 807 | + | 0.354399 | |
g8996 | DLA_10019 | GLQOFTK02GQ36N | CDS | 303634 | 2121 | - | 0.313531 | |
g8997 | DLA_10020 | GLQOFTK02GQ36N | CDS | 306260 | 2289 | - | 0.311927 | |
g8998 | DLA_10021 | GLQOFTK02GQ36N | CDS | 309236 | 1692 | + | 0.339244 | |
g8999 | DLA_10022 | GLQOFTK02GQ36N | CDS | 311053 | 237 | - | 0.333333 | |
g9 | DLA_00010 | contig05409_1.exp | CDS | 29991 | 561 | - | 0.386809 | |
g90 | DLA_00106 | contig05409_1.exp | CDS | 210207 | 1308 | - | 0.340214 | |
g900 | DLA_00994 | F4PJNLW01A00V1 | CDS | 585872 | 1056 | - | 0.354167 | |
g9000 | DLA_10023 | GLQOFTK02GQ36N | CDS | 311593 | 1686 | + | 0.358837 | |
g9001 | DLA_10024 | GLQOFTK02GQ36N | CDS | 313487 | 1713 | + | 0.279043 | |
g9002 | DLA_10025 | GLQOFTK02GQ36N | CDS | 315308 | 3954 | - | 0.321194 | |
g9003 | DLA_10026 | protein component of the large (60S) ribosomal subunitthere is a second copy of this gene | GLQOFTK02GQ36N | CDS | 319836 | 615 | + | 0.42439 |
g9004 | DLA_10027 | GLQOFTK02GQ36N | CDS | 321008 | 777 | + | 0.323037 | |
g9005 | DLA_10028 | GLQOFTK02GQ36N | CDS | 321999 | 1242 | - | 0.338969 | |
g9006 | DLA_11802 | CAZy family GT22 catalyzes N-linked mannosylation | GLQOFTK02GQ36N | CDS | 323917 | 1560 | - | 0.319872 |
g9007 | DLA_10029 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | GLQOFTK02GQ36N | CDS | 325674 | 2499 | - | 0.339336 |
g9008 | DLA_10030 | GLQOFTK02GQ36N | CDS | 328584 | 2367 | - | 0.324884 | |
g9009 | DLA_10031 | GLQOFTK02GQ36N | CDS | 331767 | 2796 | + | 0.325107 | |
g901 | DLA_00995 | F4PJNLW01A00V1 | CDS | 587482 | 636 | + | 0.356918 | |
g9010 | DLA_10032 | catalyzes the oxidation of neutral and basic D-amino acids into their corresponding keto acids there is a second copy of this gene | GLQOFTK02GQ36N | CDS | 334864 | 1017 | + | 0.346116 |
g9011 | DLA_10033 | GLQOFTK02GQ36N | CDS | 335978 | 363 | - | 0.358127 | |
g9012 | DLA_10034 | ortholog of Saccharomyces cerevisiae Mbf1 protein expressed at high level in vegetative celly and decreases sharply in early development induced by cycloheximide there is a second copy of this gene | GLQOFTK02GQ36N | CDS | 336994 | 312 | - | 0.317308 |
g9013 | DLA_11803 | GLQOFTK02GQ36N | CDS | 337469 | 1128 | + | 0.301418 | |
g9014 | DLA_10035 | GLQOFTK02GQ36N | CDS | 339238 | 1092 | + | 0.32326 | |
g9015 | DLA_10036 | GLQOFTK02GQ36N | CDS | 340531 | 2205 | - | 0.356916 | |
g9016 | DLA_10037 | GLQOFTK02GQ36N | CDS | 343332 | 963 | + | 0.292835 | |
g9017 | DLA_10038 | GLQOFTK02GQ36N | CDS | 344526 | 1584 | - | 0.278409 | |
g9018 | DLA_10039 | conserved protein containing a Suneukaryotic nucleolar NOL1Nop2p domain | GLQOFTK02GQ36N | CDS | 346398 | 1962 | + | 0.284913 |
g9019 | DLA_10040 | GLQOFTK02GQ36N | CDS | 348802 | 546 | + | 0.326007 | |
g902 | DLA_00996 | F4PJNLW01A00V1 | CDS | 588650 | 1767 | - | 0.259196 | |
g9020 | DLA_10041 | GLQOFTK02GQ36N | CDS | 349782 | 984 | + | 0.279472 | |
g9021 | DLA_10042 | GLQOFTK02GQ36N | CDS | 351021 | 867 | - | 0.267589 | |
g9022 | DLA_10043 | GLQOFTK02GQ36N | CDS | 352081 | 636 | - | 0.325472 | |
g9023 | DLA_10044 | catalyzes the reaction ATP Hsub2subO Nasupsupn Ksupsupout ADP phosphate Nasupsupout Ksupsupn br contains 10 transmembrane domains | GLQOFTK02GQ36N | CDS | 353185 | 3483 | - | 0.347402 |
g9024 | DLA_10045 | GLQOFTK02GQ36N | CDS | 357677 | 2121 | - | 0.323904 | |
g9025 | DLA_10046 | GLQOFTK02GQ36N | CDS | 360023 | 1707 | - | 0.342707 | |
g9026 | DLA_10047 | GLQOFTK02GQ36N | CDS | 361979 | 2910 | + | 0.32646 | |
g9027 | DLA_11804 | GLQOFTK02GQ36N | CDS | 365392 | 1146 | + | 0.333333 | |
g9028 | DLA_10048 | GLQOFTK02GQ36N | CDS | 366630 | 585 | - | 0.278632 | |
g9029 | DLA_10049 | GLQOFTK02GQ36N | CDS | 367559 | 939 | - | 0.337593 | |
g903 | DLA_00997 | F4PJNLW01A00V1 | CDS | 590940 | 2199 | - | 0.35789 | |
g9030 | DLA_10050 | GLQOFTK02GQ36N | CDS | 369685 | 615 | + | 0.336585 | |
g9031 | DLA_10051 | GLQOFTK02GQ36N | CDS | 370753 | 606 | - | 0.363036 | |
g9032 | DLA_10052 | similar to the mammalian NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13 (NDUFA13) contains one predicted transmembrane domain | GLQOFTK02GQ36N | CDS | 371911 | 357 | + | 0.310924 |
g9033 | DLA_10053 | GLQOFTK02GQ36N | CDS | 372624 | 2058 | - | 0.329932 | |
g9034 | DLA_10055 | GLQOFTK02GQ36N | CDS | 375331 | 1425 | + | 0.350175 | |
g9035 | DLA_10056 | GLQOFTK02GQ36N | CDS | 377200 | 1983 | + | 0.33535 | |
g9036 | DLA_10057 | GLQOFTK02GQ36N | CDS | 379443 | 2373 | - | 0.387695 | |
g9037 | DLA_10058 | GLQOFTK02GQ36N | CDS | 382682 | 402 | - | 0.355721 | |
g9038 | DLA_10059 | GLQOFTK02GQ36N | CDS | 383424 | 1023 | - | 0.318671 | |
g9039 | DLA_10060 | GLQOFTK02GQ36N | CDS | 384751 | 1266 | - | 0.308847 | |
g904 | DLA_00998 | F4PJNLW01A00V1 | CDS | 594349 | 1296 | + | 0.323302 | |
g9040 | DLA_10061 | GLQOFTK02GQ36N | CDS | 386362 | 582 | - | 0.309278 | |
g9041 | DLA_10062 | GLQOFTK02GQ36N | CDS | 387355 | 1842 | + | 0.290988 | |
g9042 | DLA_10063 | GLQOFTK02GQ36N | CDS | 389660 | 1692 | - | 0.279551 | |
g9043 | DLA_10064 | GLQOFTK02GQ36N | CDS | 391466 | 2832 | - | 0.33863 | |
g9044 | DLA_10065 | GLQOFTK02GQ36N | CDS | 394709 | 2781 | - | 0.329018 | |
g9045 | DLA_11805 | GLQOFTK02GQ36N | CDS | 397918 | 615 | - | 0.328455 | |
g9046 | DLA_10066 | GLQOFTK02GQ36N | CDS | 399207 | 1962 | + | 0.372069 | |
g9047 | DLA_10067 | GLQOFTK02GQ36N | CDS | 401738 | 207 | + | 0.333333 | |
g9048 | DLA_10068 | GLQOFTK02GQ36N | CDS | 402496 | 612 | - | 0.308824 | |
g9049 | DLA_10069 | GLQOFTK02GQ36N | CDS | 403373 | 1791 | + | 0.326633 | |
g905 | DLA_00999 | F4PJNLW01A00V1 | CDS | 595915 | 1293 | + | 0.302398 | |
g9050 | DLA_10070 | GLQOFTK02GQ36N | CDS | 405624 | 510 | - | 0.337255 | |
g9051 | DLA_10071 | GLQOFTK02GQ36N | CDS | 407203 | 1869 | + | 0.329588 | |
g9052 | DLA_10073 | GLQOFTK02GQ36N | CDS | 410028 | 282 | + | 0.361702 | |
g9053 | DLA_10074 | GLQOFTK02GQ36N | CDS | 410926 | 1320 | - | 0.319697 | |
g9054 | DLA_10075 | GLQOFTK02GQ36N | CDS | 412715 | 1989 | + | 0.291604 | |
g9055 | DLA_10076 | GLQOFTK02GQ36N | CDS | 414797 | 2277 | - | 0.379886 | |
g9056 | DLA_10077 | GLQOFTK02GQ36N | CDS | 417938 | 447 | - | 0.288591 | |
g9057 | DLA_10078 | GLQOFTK02GQ36N | CDS | 418677 | 1122 | + | 0.300357 | |
g9058 | DLA_10080 | GLQOFTK02GQ36N | CDS | 419939 | 1536 | - | 0.299479 | |
g9059 | DLA_10081 | GLQOFTK02GQ36N | CDS | 421767 | 1410 | + | 0.353191 | |
g906 | DLA_01000 | F4PJNLW01A00V1 | CDS | 597281 | 2322 | - | 0.270026 | |
g9060 | DLA_10082 | GLQOFTK02GQ36N | CDS | 423257 | 6573 | - | 0.314012 | |
g9061 | DLA_10085 | GLQOFTK02GQ36N | CDS | 430741 | 1239 | + | 0.322034 | |
g9062 | DLA_10086 | GLQOFTK02GQ36N | CDS | 432012 | 2025 | - | 0.364444 | |
g9063 | DLA_10087 | GLQOFTK02GQ36N | CDS | 435152 | 1416 | + | 0.344633 | |
g9064 | DLA_10088 | GLQOFTK02GQ36N | CDS | 436677 | 1806 | - | 0.287929 | |
g9065 | DLA_10089 | GLQOFTK02GQ36N | CDS | 439195 | 636 | + | 0.314465 | |
g9066 | DLA_10090 | GLQOFTK02GQ36N | CDS | 440335 | 1194 | - | 0.332496 | |
g9067 | DLA_10091 | GLQOFTK02GQ36N | CDS | 442620 | 1395 | - | 0.32043 | |
g9068 | DLA_10092 | GLQOFTK02GQ36N | CDS | 445274 | 1551 | + | 0.319149 | |
g9069 | DLA_10093 | GLQOFTK02GQ36N | CDS | 447502 | 816 | - | 0.301471 | |
g907 | DLA_01002 | F4PJNLW01A00V1 | CDS | 600317 | 3663 | + | 0.340977 | |
g9070 | DLA_10094 | GLQOFTK02GQ36N | CDS | 449836 | 4854 | + | 0.323445 | |
g9071 | DLA_10095 | GLQOFTK02GQ36N | CDS | 454904 | 3888 | - | 0.315844 | |
g9072 | DLA_10096 | GLQOFTK02GQ36N | CDS | 459748 | 1770 | + | 0.365537 | |
g9073 | DLA_10097 | GLQOFTK02GQ36N | CDS | 462850 | 3201 | + | 0.321774 | |
g9074 | DLA_10098 | GLQOFTK02GQ36N | CDS | 466504 | 2472 | - | 0.263754 | |
g9075 | DLA_10099 | GLQOFTK02GQ36N | CDS | 469272 | 1191 | - | 0.275399 | |
g9076 | DLA_10100 | GLQOFTK02GQ36N | CDS | 470773 | 537 | - | 0.299814 | |
g9077 | DLA_10101 | GLQOFTK02GQ36N | CDS | 471545 | 3288 | - | 0.326338 | |
g9078 | DLA_10102 | GLQOFTK02GQ36N | CDS | 475751 | 975 | - | 0.32 | |
g9079 | DLA_10104 | GLQOFTK02GQ36N | CDS | 476945 | 2109 | + | 0.316738 | |
g908 | DLA_01003 | F4PJNLW01A00V1 | CDS | 604634 | 726 | + | 0.272727 | |
g9080 | DLA_10105 | GLQOFTK02GQ36N | CDS | 479729 | 3126 | - | 0.298464 | |
g9081 | DLA_10107 | similar to S. cerevisiae BUD7 (bud site selection protein 7) which is required for the export of specialised cargo from the Golgi. belongs to the CHAPS (Chs5p-Arf1p-binding proteins) family | GLQOFTK02GQ36N | CDS | 483645 | 2574 | + | 0.350816 |
g9082 | DLA_10110 | GLQOFTK02GQ36N | CDS | 487029 | 1656 | - | 0.347826 | |
g9083 | DLA_10111 | GLQOFTK02GQ36N | CDS | 490464 | 1086 | - | 0.314917 | |
g9084 | DLA_10112 | GLQOFTK02GQ36N | CDS | 491863 | 1269 | + | 0.368794 | |
g9085 | DLA_10113 | GLQOFTK02GQ36N | CDS | 493345 | 351 | + | 0.378917 | |
g9086 | DLA_10114 | GLQOFTK02GQ36N | CDS | 494843 | 1473 | + | 0.314324 | |
g9087 | DLA_10115 | GLQOFTK02GQ36N | CDS | 497102 | 2718 | - | 0.330758 | |
g9088 | DLA_10116 | GLQOFTK02GQ36N | CDS | 501736 | 2718 | + | 0.337012 | |
g9089 | DLA_10117 | GLQOFTK02GQ36N | CDS | 504795 | 1788 | + | 0.290828 | |
g909 | DLA_01004 | F4PJNLW01A00V1 | CDS | 605631 | 1041 | + | 0.254563 | |
g9090 | DLA_10118 | GLQOFTK02GQ36N | CDS | 506626 | 363 | - | 0.319559 | |
g9091 | DLA_10119 | GLQOFTK02GQ36N | CDS | 507744 | 8031 | + | 0.300087 | |
g9092 | DLA_10120 | GLQOFTK02GQ36N | CDS | 516384 | 8022 | + | 0.298429 | |
g9093 | DLA_10121 | GLQOFTK02GQ36N | CDS | 524743 | 7599 | + | 0.29925 | |
g9094 | DLA_10123 | GLQOFTK02GQ36N | CDS | 532976 | 1185 | - | 0.345992 | |
g9095 | DLA_10124 | GLQOFTK02GQ36N | CDS | 534708 | 522 | + | 0.335249 | |
g9096 | DLA_10125 | GLQOFTK02GQ36N | CDS | 535410 | 375 | - | 0.362667 | |
g9097 | DLA_10128 | GLQOFTK02GQ36N | CDS | 536720 | 1248 | + | 0.282051 | |
g9098 | DLA_10129 | putative PI3K that phosphorylates phosphoinositides on the 3-hydroxyl group of the inositol ring has the capacity to bind and be activated by the GTP-bound small GTPase ras | GLQOFTK02GQ36N | CDS | 538065 | 4770 | - | 0.341719 |
g9099 | DLA_10130 | GLQOFTK02GQ36N | CDS | 543431 | 3165 | - | 0.366193 | |
g91 | DLA_00107 | contig05409_1.exp | CDS | 212041 | 1722 | + | 0.29849 | |
g910 | DLA_01005 | F4PJNLW01A00V1 | CDS | 606787 | 522 | - | 0.316092 | |
g9100 | DLA_10131 | GLQOFTK02GQ36N | CDS | 547114 | 3396 | + | 0.326855 | |
g9101 | DLA_10132 | GLQOFTK02GQ36N | CDS | 550825 | 1503 | - | 0.312708 | |
g9102 | DLA_10133 | GLQOFTK02GQ36N | CDS | 552999 | 1683 | - | 0.367796 | |
g9103 | DLA_10134 | structural similarity to Zn-dependent peptidases contains a a predicted signal anchor sequence and 4 putative transmembrane domains | GLQOFTK02GQ36N | CDS | 554979 | 1998 | - | 0.309309 |
g9104 | DLA_11806 | GLQOFTK02GQ36N | CDS | 557330 | 1353 | - | 0.317073 | |
g9105 | DLA_10135 | GLQOFTK02GQ36N | CDS | 559750 | 1464 | - | 0.303962 | |
g9106 | DLA_10136 | GLQOFTK02GQ36N | CDS | 562430 | 1845 | + | 0.310027 | |
g9107 | DLA_10137 | GLQOFTK02GQ36N | CDS | 564809 | 2343 | + | 0.334614 | |
g9108 | DLA_10139 | GLQOFTK02GQ36N | CDS | 567791 | 1260 | - | 0.294444 | |
g9109 | DLA_10140 | GLQOFTK02GQ36N | CDS | 569324 | 1617 | - | 0.30303 | |
g911 | DLA_01006 | F4PJNLW01A00V1 | CDS | 607514 | 3234 | + | 0.325603 | |
g9110 | DLA_10141 | GLQOFTK02GQ36N | CDS | 571144 | 1098 | - | 0.346995 | |
g9111 | DLA_10143 | belongs to the Atypical Alpha protein kinases and contains a von Willebrand factor type A (VWFA) domain does not phosphorylate myosin heavy chain | GLQOFTK02GQ36N | CDS | 573382 | 1701 | - | 0.342152 |
g9112 | DLA_10144 | GLQOFTK02GQ36N | CDS | 575543 | 1305 | - | 0.28659 | |
g9113 | DLA_10146 | GLQOFTK02GQ36N | CDS | 577105 | 1857 | - | 0.344103 | |
g9114 | DLA_10147 | GLQOFTK02GQ36N | CDS | 580073 | 1521 | - | 0.321499 | |
g9115 | DLA_10149 | GLQOFTK02GQ36N | CDS | 584173 | 336 | + | 0.357143 | |
g9116 | DLA_10150 | GLQOFTK02GQ36N | CDS | 585302 | 933 | - | 0.315113 | |
g9117 | DLA_10151 | GLQOFTK02GQ36N | CDS | 586709 | 1158 | + | 0.35924 | |
g9118 | DLA_10152 | GLQOFTK02GQ36N | CDS | 588104 | 6948 | + | 0.312464 | |
g9119 | DLA_10153 | GLQOFTK02GQ36N | CDS | 595265 | 1629 | + | 0.311234 | |
g912 | DLA_01008 | F4PJNLW01A00V1 | CDS | 611271 | 201 | + | 0.328358 | |
g9120 | DLA_10154 | GLQOFTK02GQ36N | CDS | 597098 | 552 | - | 0.298913 | |
g9121 | DLA_10155 | GLQOFTK02GQ36N | CDS | 598035 | 573 | - | 0.321117 | |
g9122 | DLA_10157 | GLQOFTK02GQ36N | CDS | 599686 | 3750 | - | 0.333067 | |
g9123 | DLA_10158 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | GLQOFTK02GQ36N | CDS | 604252 | 1302 | + | 0.31874 |
g9124 | DLA_10159 | GLQOFTK02GQ36N | CDS | 605743 | 219 | - | 0.356164 | |
g9125 | DLA_10160 | GLQOFTK02GQ36N | CDS | 606178 | 2772 | + | 0.318182 | |
g9126 | DLA_10161 | GLQOFTK02GQ36N | CDS | 609180 | 198 | - | 0.378788 | |
g9127 | DLA_10162 | GLQOFTK02GQ36N | CDS | 610127 | 198 | + | 0.368687 | |
g9128 | DLA_10163 | GLQOFTK02GQ36N | CDS | 610539 | 1287 | - | 0.310023 | |
g9129 | DLA_10164 | GLQOFTK02GQ36N | CDS | 612338 | 675 | + | 0.294815 | |
g913 | DLA_01009 | F4PJNLW01A00V1 | CDS | 611778 | 2223 | + | 0.332434 | |
g9130 | DLA_10165 | similar to S. cerevisiae LCB1 dimerizes with SptB to catalyze the conversion of palmitoyl-CoA L-serine into CoA 3-dehydro-D-sphinganine COsub2sub | GLQOFTK02GQ36N | CDS | 613224 | 1428 | + | 0.359244 |
g9131 | DLA_10166 | GLQOFTK02GQ36N | CDS | 614694 | 2004 | - | 0.353293 | |
g9132 | DLA_10167 | GLQOFTK02GQ36N | CDS | 617004 | 198 | - | 0.373737 | |
g9133 | DLA_10168 | GLQOFTK02GQ36N | CDS | 618003 | 2250 | + | 0.283111 | |
g9134 | DLA_10169 | GLQOFTK02GQ36N | CDS | 620614 | 1866 | - | 0.266881 | |
g9135 | DLA_10170 | GLQOFTK02GQ36N | CDS | 623858 | 1821 | - | 0.265788 | |
g9136 | DLA_10172 | GLQOFTK02GQ36N | CDS | 626229 | 624 | - | 0.315705 | |
g9137 | DLA_10173 | GLQOFTK02GQ36N | CDS | 627095 | 1566 | + | 0.346105 | |
g9138 | DLA_10174 | GLQOFTK02GQ36N | CDS | 629271 | 6159 | + | 0.327326 | |
g9139 | DLA_10175 | GLQOFTK02GQ36N | CDS | 635712 | 1185 | + | 0.262447 | |
g914 | DLA_01010 | F4PJNLW01A00V1 | CDS | 614964 | 1410 | + | 0.236879 | |
g9140 | DLA_10176 | GLQOFTK02GQ36N | CDS | 636982 | 1134 | - | 0.402116 | |
g9141 | DLA_10177 | GLQOFTK02GQ36N | CDS | 638783 | 621 | - | 0.307568 | |
g9142 | DLA_10178 | GLQOFTK02GQ36N | CDS | 639852 | 651 | + | 0.328725 | |
g9143 | DLA_10179 | GLQOFTK02GQ36N | CDS | 640781 | 1809 | + | 0.257601 | |
g9144 | DLA_10181 | GLQOFTK02GQ36N | CDS | 644077 | 1791 | + | 0.249581 | |
g9145 | DLA_10183 | GLQOFTK02GQ36N | CDS | 647415 | 315 | + | 0.247619 | |
g9146 | DLA_10184 | GLQOFTK02GQ36N | CDS | 649109 | 1830 | - | 0.304918 | |
g9147 | DLA_10186 | GLQOFTK02GQ36N | CDS | 651982 | 1116 | + | 0.298387 | |
g9148 | DLA_10188 | GLQOFTK02GQ36N | CDS | 654084 | 1131 | + | 0.349248 | |
g9149 | DLA_10189 | GLQOFTK02GQ36N | CDS | 655472 | 837 | - | 0.354839 | |
g915 | DLA_01011 | F4PJNLW01A00V1 | CDS | 616468 | 4905 | - | 0.355759 | |
g9150 | DLA_10191 | ortholog of S. pombe ctu2 (cytosolic thiouridylase subunit 2) with ctu1 required for thiolation of the uridine at the wobble position of Lys(UUU) and Glu(UUC) tRNAs | GLQOFTK02GQ36N | CDS | 658082 | 1362 | + | 0.278267 |
g9151 | DLA_10192 | GLQOFTK02GQ36N | CDS | 659638 | 819 | + | 0.300366 | |
g9152 | DLA_10193 | protein serinethreonine kinase CK1 family similar to human CK1 and yeast YCK may play a role in DNA repair there is a second copy of this gene | GLQOFTK02GQ36N | CDS | 660860 | 1158 | - | 0.325561 |
g9153 | DLA_10194 | GLQOFTK02GUKFG | CDS | 2 | 5000 | - | 0.3594 | |
g9154 | DLA_10195 | GLQOFTK02GUKFG | CDS | 5453 | 2940 | + | 0.365646 | |
g9155 | DLA_10196 | GLQOFTK02GUKFG | CDS | 8513 | 783 | + | 0.353768 | |
g9156 | DLA_10197 | GLQOFTK02GUKFG | CDS | 9605 | 369 | + | 0.363144 | |
g9157 | DLA_10198 | GLQOFTK02GUKFG | CDS | 10139 | 837 | + | 0.292712 | |
g9158 | DLA_10199 | GLQOFTK02GUKFG | CDS | 11171 | 471 | - | 0.314225 | |
g9159 | DLA_10200 | GLQOFTK02GUKFG | CDS | 12408 | 1377 | + | 0.37618 | |
g916 | DLA_01012 | F4PJNLW01A00V1 | CDS | 621709 | 1854 | - | 0.330636 | |
g9160 | DLA_10202 | GLQOFTK02GUKFG | CDS | 14461 | 1215 | - | 0.296296 | |
g9161 | DLA_10203 | GLQOFTK02GUKFG | CDS | 16557 | 789 | - | 0.328264 | |
g9162 | DLA_10205 | GLQOFTK02GUKFG | CDS | 18112 | 5655 | - | 0.347303 | |
g9163 | DLA_10206 | GLQOFTK02GUKFG | CDS | 24804 | 315 | + | 0.31746 | |
g9164 | DLA_10207 | GLQOFTK02GUKFG | CDS | 25304 | 603 | - | 0.333333 | |
g9165 | DLA_10208 | GLQOFTK02GUKFG | CDS | 26113 | 852 | - | 0.346244 | |
g9166 | DLA_10209 | GLQOFTK02GUKFG | CDS | 27469 | 1284 | + | 0.378505 | |
g9167 | DLA_10210 | GLQOFTK02GUKFG | CDS | 28850 | 4482 | + | 0.329317 | |
g9168 | DLA_10211 | GLQOFTK02GUKFG | CDS | 33414 | 1893 | - | 0.293714 | |
g9169 | DLA_10212 | GLQOFTK02GUKFG | CDS | 35661 | 4281 | + | 0.305303 | |
g917 | DLA_01013 | F4PJNLW01A00V1 | CDS | 623958 | 3978 | + | 0.302162 | |
g9170 | DLA_10213 | GLQOFTK02GUKFG | CDS | 40171 | 3036 | - | 0.319829 | |
g9171 | DLA_10214 | GLQOFTK02GUKFG | CDS | 43488 | 3852 | - | 0.330997 | |
g9172 | DLA_10215 | GLQOFTK02GUKFG | CDS | 48194 | 735 | + | 0.368707 | |
g9173 | DLA_10216 | GLQOFTK02GUKFG | CDS | 50183 | 1506 | - | 0.334661 | |
g9174 | DLA_10217 | GLQOFTK02GUKFG | CDS | 52006 | 1224 | + | 0.331699 | |
g9175 | DLA_10218 | GLQOFTK02GUKFG | CDS | 53340 | 630 | - | 0.27619 | |
g9176 | DLA_10219 | GLQOFTK02GUKFG | CDS | 54133 | 1401 | - | 0.311206 | |
g9177 | DLA_10220 | GLQOFTK02GUKFG | CDS | 55910 | 2511 | - | 0.342493 | |
g9178 | DLA_10221 | GLQOFTK02GUKFG | CDS | 58559 | 1656 | + | 0.335145 | |
g9179 | DLA_10224 | GLQOFTK02GUKFG | CDS | 60674 | 2235 | - | 0.285459 | |
g918 | DLA_01014 | F4PJNLW01A00V1 | CDS | 628231 | 690 | + | 0.294203 | |
g9180 | DLA_10225 | GLQOFTK02GUKFG | CDS | 63770 | 834 | + | 0.275779 | |
g9181 | DLA_10226 | GLQOFTK02GUKFG | CDS | 65635 | 2250 | - | 0.290667 | |
g9182 | DLA_10227 | GLQOFTK02GUKFG | CDS | 68462 | 1551 | + | 0.286912 | |
g9183 | DLA_10230 | GLQOFTK02GUKFG | CDS | 72533 | 1542 | + | 0.276265 | |
g9184 | DLA_10231 | GLQOFTK02GUKFG | CDS | 74126 | 1401 | + | 0.295503 | |
g9185 | DLA_10232 | GLQOFTK02GUKFG | CDS | 75826 | 1572 | + | 0.340967 | |
g9186 | DLA_10233 | GLQOFTK02GUKFG | CDS | 77532 | 1506 | + | 0.295485 | |
g9187 | DLA_10234 | GLQOFTK02GUKFG | CDS | 79376 | 1509 | + | 0.290921 | |
g9188 | DLA_10235 | GLQOFTK02GUKFG | CDS | 80987 | 5043 | - | 0.340274 | |
g9189 | DLA_10237 | GLQOFTK02GUKFG | CDS | 86588 | 2523 | - | 0.370194 | |
g919 | DLA_01016 | F4PJNLW01A00V1 | CDS | 630388 | 348 | - | 0.29023 | |
g9190 | DLA_10238 | GLQOFTK02GUKFG | CDS | 89759 | 2550 | + | 0.372549 | |
g9191 | DLA_10239 | GLQOFTK02GUKFG | CDS | 92507 | 966 | + | 0.324017 | |
g9192 | DLA_10240 | GLQOFTK02GUKFG | CDS | 93628 | 900 | - | 0.381111 | |
g9193 | DLA_10241 | GLQOFTK02GUKFG | CDS | 94924 | 366 | - | 0.333333 | |
g9194 | DLA_10242 | GLQOFTK02GUKFG | CDS | 95640 | 222 | - | 0.288288 | |
g9195 | DLA_10243 | GLQOFTK02GUKFG | CDS | 96073 | 966 | + | 0.334369 | |
g9196 | DLA_10244 | GLQOFTK02GUKFG | CDS | 97091 | 624 | - | 0.331731 | |
g9197 | DLA_10245 | GLQOFTK02GUKFG | CDS | 98100 | 2916 | + | 0.33299 | |
g9198 | DLA_10247 | GLQOFTK02GUKFG | CDS | 101956 | 1779 | - | 0.291737 | |
g9199 | DLA_10248 | GLQOFTK02GUKFG | CDS | 103926 | 1632 | + | 0.301471 | |
g92 | DLA_00108 | contig05409_1.exp | CDS | 214181 | 438 | + | 0.273973 | |
g920 | DLA_01018 | F4PJNLW01A00V1 | CDS | 632223 | 8535 | + | 0.320211 | |
g9200 | DLA_10249 | GLQOFTK02GUKFG | CDS | 105613 | 1257 | - | 0.32856 | |
g9201 | DLA_10250 | GLQOFTK02GUKFG | CDS | 107087 | 2232 | - | 0.289875 | |
g9202 | DLA_10252 | GLQOFTK02GUKFG | CDS | 110321 | 2769 | + | 0.323944 | |
g9203 | DLA_10253 | GLQOFTK02GUKFG | CDS | 113533 | 1467 | - | 0.301977 | |
g9204 | DLA_10254 | GLQOFTK02GUKFG | CDS | 115868 | 2256 | + | 0.375 | |
g9205 | DLA_10256 | GLQOFTK02GUKFG | CDS | 119492 | 1467 | + | 0.321063 | |
g9206 | DLA_10257 | contains a predicted signal peptide there is a second copy of this gene | GLQOFTK02GUKFG | CDS | 121297 | 1023 | - | 0.332356 |
g9207 | DLA_10258 | GLQOFTK02GUKFG | CDS | 122687 | 2775 | + | 0.366847 | |
g9208 | DLA_10259 | GLQOFTK02GUKFG | CDS | 125880 | 657 | + | 0.295282 | |
g9209 | DLA_10260 | GLQOFTK02GUKFG | CDS | 126587 | 2445 | - | 0.334151 | |
g921 | DLA_01019 | F4PJNLW01A00V1 | CDS | 641138 | 1953 | + | 0.293907 | |
g9210 | DLA_10261 | GLQOFTK02GUKFG | CDS | 129499 | 4644 | + | 0.343239 | |
g9211 | DLA_10262 | GLQOFTK02GUKFG | CDS | 134644 | 849 | + | 0.319199 | |
g9212 | DLA_10263 | GLQOFTK02GUKFG | CDS | 136301 | 891 | + | 0.353535 | |
g9213 | DLA_10264 | GLQOFTK02GUKFG | CDS | 137261 | 1503 | - | 0.314039 | |
g9214 | DLA_10265 | GLQOFTK02GUKFG | CDS | 139015 | 558 | + | 0.304659 | |
g9215 | DLA_10266 | GLQOFTK02GUKFG | CDS | 142415 | 3375 | + | 0.26637 | |
g9216 | DLA_10267 | GLQOFTK02GUKFG | CDS | 147007 | 1656 | + | 0.336353 | |
g9217 | DLA_10268 | GLQOFTK02GUKFG | CDS | 149316 | 663 | + | 0.355958 | |
g9218 | DLA_10269 | GLQOFTK02GUKFG | CDS | 150190 | 1467 | + | 0.331288 | |
g9219 | DLA_10270 | GLQOFTK02GUKFG | CDS | 151795 | 723 | + | 0.266943 | |
g922 | DLA_01020 | F4PJNLW01A00V1 | CDS | 643466 | 2934 | + | 0.308453 | |
g9220 | DLA_10271 | GLQOFTK02GUKFG | CDS | 152828 | 2082 | - | 0.353506 | |
g9221 | DLA_10272 | GLQOFTK02GUKFG | CDS | 155331 | 3063 | - | 0.3095 | |
g9222 | DLA_10273 | GLQOFTK02GUKFG | CDS | 158477 | 1419 | + | 0.309373 | |
g9223 | DLA_10274 | GLQOFTK02GUKFG | CDS | 160293 | 2016 | + | 0.373512 | |
g9224 | DLA_10275 | GLQOFTK02GUKFG | CDS | 162441 | 2637 | - | 0.308305 | |
g9225 | DLA_10277 | GLQOFTK02GUKFG | CDS | 165651 | 3759 | - | 0.329609 | |
g9226 | DLA_10279 | GLQOFTK02GUKFG | CDS | 170124 | 672 | + | 0.385417 | |
g9227 | DLA_10280 | GLQOFTK02GUKFG | CDS | 171124 | 1059 | - | 0.352219 | |
g9228 | DLA_10281 | GLQOFTK02GUKFG | CDS | 172480 | 714 | + | 0.323529 | |
g9229 | DLA_10282 | GLQOFTK02GUKFG | CDS | 173297 | 687 | + | 0.372635 | |
g923 | DLA_01021 | F4PJNLW01A00V1 | CDS | 646744 | 1170 | - | 0.331624 | |
g9230 | DLA_10283 | GLQOFTK02GUKFG | CDS | 174399 | 2559 | - | 0.407581 | |
g9231 | DLA_10284 | GLQOFTK02GUKFG | CDS | 178114 | 501 | - | 0.353293 | |
g9232 | DLA_10285 | GLQOFTK02GUKFG | CDS | 179058 | 4950 | + | 0.360808 | |
g9233 | DLA_10286 | GLQOFTK02GUKFG | CDS | 184201 | 1617 | - | 0.325294 | |
g9234 | DLA_10287 | GLQOFTK02GUKFG | CDS | 186185 | 1749 | + | 0.288736 | |
g9235 | DLA_10288 | GLQOFTK02GUKFG | CDS | 188252 | 387 | - | 0.276486 | |
g9236 | DLA_10289 | GLQOFTK02GUKFG | CDS | 189555 | 1299 | + | 0.326405 | |
g9237 | DLA_10291 | GLQOFTK02GUKFG | CDS | 191473 | 1047 | - | 0.387775 | |
g9238 | DLA_10292 | GLQOFTK02GUKFG | CDS | 192959 | 2199 | - | 0.336062 | |
g9239 | DLA_10293 | GLQOFTK02GUKFG | CDS | 195572 | 2127 | + | 0.342736 | |
g924 | DLA_01023 | F4PJNLW01A00V1 | CDS | 649237 | 2628 | + | 0.285008 | |
g9240 | DLA_10294 | GLQOFTK02GUKFG | CDS | 198640 | 1005 | + | 0.321393 | |
g9241 | DLA_10296 | GLQOFTK02GUKFG | CDS | 200123 | 756 | + | 0.357143 | |
g9242 | DLA_10297 | GLQOFTK02GUKFG | CDS | 200924 | 4278 | - | 0.312997 | |
g9243 | DLA_10298 | GLQOFTK02GUKFG | CDS | 205635 | 4011 | + | 0.388432 | |
g9244 | DLA_10299 | GLQOFTK02GUKFG | CDS | 209917 | 1197 | + | 0.328321 | |
g9245 | DLA_10300 | GLQOFTK02GUKFG | CDS | 211363 | 336 | - | 0.270833 | |
g9246 | DLA_10301 | GLQOFTK02GUKFG | CDS | 212252 | 948 | + | 0.338608 | |
g9247 | DLA_10302 | GLQOFTK02GUKFG | CDS | 213515 | 765 | + | 0.282353 | |
g9248 | DLA_10303 | GLQOFTK02GUKFG | CDS | 214545 | 2424 | + | 0.328383 | |
g9249 | DLA_10304 | GLQOFTK02GUKFG | CDS | 217251 | 2070 | + | 0.329469 | |
g925 | DLA_01024 | F4PJNLW01A00V1 | CDS | 652057 | 360 | - | 0.333333 | |
g9250 | DLA_10305 | GLQOFTK02GUKFG | CDS | 219627 | 555 | - | 0.295496 | |
g9251 | DLA_10306 | GLQOFTK02GUKFG | CDS | 220756 | 1092 | - | 0.354396 | |
g9252 | DLA_10307 | ortholog of prokaryotic penicillin-binding protein 4 (PBP4) inhibited by penicillin G | GLQOFTK02GUKFG | CDS | 223518 | 1488 | - | 0.388441 |
g9253 | DLA_10308 | subunit of the splicing factor SF3A required for spliceosome assembly contains PRP9 domain characteristic of splicing factor 3A subunit 3 expressed in pstO cells | GLQOFTK02GUKFG | CDS | 225464 | 1443 | - | 0.306306 |
g9254 | DLA_10309 | GLQOFTK02GUKFG | CDS | 227316 | 495 | + | 0.29899 | |
g9255 | DLA_10310 | GLQOFTK02GUKFG | CDS | 227868 | 4461 | - | 0.362026 | |
g9256 | DLA_10312 | GLQOFTK02GUKFG | CDS | 232772 | 1032 | - | 0.32655 | |
g9257 | DLA_10313 | GLQOFTK02GUKFG | CDS | 233946 | 2742 | + | 0.28264 | |
g9258 | DLA_10314 | GLQOFTK02GUKFG | CDS | 237299 | 2760 | + | 0.284058 | |
g9259 | DLA_10316 | GLQOFTK02GUKFG | CDS | 240693 | 10326 | + | 0.328879 | |
g926 | DLA_01025 | F4PJNLW01A00V1 | CDS | 652828 | 2121 | + | 0.311645 | |
g9260 | DLA_10317 | GLQOFTK02GUKFG | CDS | 251453 | 4065 | + | 0.301599 | |
g9261 | DLA_10318 | GLQOFTK02GUKFG | CDS | 255758 | 231 | - | 0.463203 | |
g9262 | DLA_10320 | GLQOFTK02GUKFG | CDS | 258563 | 918 | - | 0.262527 | |
g9263 | DLA_10321 | GLQOFTK02GUKFG | CDS | 259914 | 2292 | + | 0.356021 | |
g9264 | DLA_10322 | GLQOFTK02GUKFG | CDS | 262470 | 1731 | + | 0.317735 | |
g9265 | DLA_10323 | GLQOFTK02GUKFG | CDS | 264345 | 471 | - | 0.259023 | |
g9266 | DLA_10324 | GLQOFTK02GUKFG | CDS | 265535 | 5454 | + | 0.351485 | |
g9267 | DLA_10325 | GLQOFTK02GUKFG | CDS | 271238 | 16044 | - | 0.3501 | |
g9268 | DLA_10326 | GLQOFTK02GUKFG | CDS | 287774 | 3000 | + | 0.333 | |
g9269 | DLA_10327 | GLQOFTK02GUKFG | CDS | 290934 | 1272 | - | 0.310535 | |
g927 | DLA_01026 | F4PJNLW01A00V1 | CDS | 655383 | 900 | - | 0.258889 | |
g9270 | DLA_10328 | GLQOFTK02GUKFG | CDS | 292343 | 2208 | - | 0.347373 | |
g9271 | DLA_10329 | GLQOFTK02GUKFG | CDS | 295564 | 237 | + | 0.400844 | |
g9272 | DLA_10330 | GLQOFTK02GUKFG | CDS | 296870 | 468 | - | 0.388889 | |
g9273 | DLA_10332 | GLQOFTK02GUKFG | CDS | 299129 | 897 | + | 0.376812 | |
g9274 | DLA_10333 | GLQOFTK02GUKFG | CDS | 300050 | 1563 | - | 0.264875 | |
g9275 | DLA_10334 | GLQOFTK02GUKFG | CDS | 301730 | 1086 | + | 0.357274 | |
g9276 | DLA_10335 | GLQOFTK02GUKFG | CDS | 303006 | 2415 | + | 0.370186 | |
g9277 | DLA_10336 | GLQOFTK02GUKFG | CDS | 305924 | 426 | + | 0.399061 | |
g9278 | DLA_10337 | GLQOFTK02GUKFG | CDS | 306711 | 906 | + | 0.37638 | |
g9279 | DLA_10338 | GLQOFTK02GUKFG | CDS | 307641 | 1560 | - | 0.291667 | |
g928 | DLA_01027 | F4PJNLW01A00V1 | CDS | 656534 | 405 | + | 0.306173 | |
g9280 | DLA_10339 | GLQOFTK02GUKFG | CDS | 309518 | 1362 | + | 0.376652 | |
g9281 | DLA_10340 | GLQOFTK02GUKFG | CDS | 311211 | 3189 | - | 0.388209 | |
g9282 | DLA_10341 | GLQOFTK02GUKFG | CDS | 315277 | 1017 | + | 0.365782 | |
g9283 | DLA_10342 | GLQOFTK02GUKFG | CDS | 316595 | 606 | - | 0.326733 | |
g9284 | DLA_10343 | GLQOFTK02GUKFG | CDS | 317480 | 1251 | - | 0.408473 | |
g9285 | DLA_10344 | GLQOFTK02GUKFG | CDS | 319572 | 2232 | + | 0.33871 | |
g9286 | DLA_10345 | GLQOFTK02GUKFG | CDS | 322079 | 3249 | + | 0.392428 | |
g9287 | DLA_10349 | GLQOFTK02GUKFG | CDS | 327950 | 753 | - | 0.374502 | |
g9288 | DLA_10350 | GLQOFTK02GUKFG | CDS | 329379 | 3333 | + | 0.339634 | |
g9289 | DLA_10351 | GLQOFTK02GUKFG | CDS | 333008 | 1674 | - | 0.274791 | |
g929 | DLA_01028 | F4PJNLW01A00V1 | CDS | 657204 | 945 | + | 0.307937 | |
g9290 | DLA_10352 | GLQOFTK02GUKFG | CDS | 335128 | 1494 | + | 0.324632 | |
g9291 | DLA_10354 | GLQOFTK02GUKFG | CDS | 337651 | 675 | - | 0.299259 | |
g9292 | DLA_10356 | GLQOFTK02GUKFG | CDS | 339755 | 3516 | + | 0.321957 | |
g9293 | DLA_10359 | GLQOFTK02GUKFG | CDS | 345165 | 1008 | + | 0.301587 | |
g9294 | DLA_10361 | GLQOFTK02GUKFG | CDS | 347562 | 771 | - | 0.29572 | |
g9295 | DLA_10362 | GLQOFTK02GUKFG | CDS | 349071 | 987 | + | 0.298886 | |
g9296 | DLA_10363 | belongs to the NADP_Rossman superfamily similar to human NMRAL1 A. nidulans nmrA is a transcriptional regulator involved in nitrogen metabolite repression | GLQOFTK02GUKFG | CDS | 350129 | 897 | - | 0.365663 |
g9297 | DLA_10364 | GLQOFTK02GUKFG | CDS | 352336 | 1656 | + | 0.363527 | |
g9298 | DLA_10365 | GLQOFTK02GUKFG | CDS | 354524 | 3387 | + | 0.331267 | |
g9299 | DLA_10366 | catalyzes the reaction NADPH NAD NADP NADH | GLQOFTK02GUKFG | CDS | 358484 | 3477 | - | 0.381363 |
g93 | DLA_00109 | contig05409_1.exp | CDS | 215743 | 3420 | + | 0.338889 | |
g930 | DLA_01029 | F4PJNLW01A00V1 | CDS | 658432 | 2052 | - | 0.298733 | |
g9300 | DLA_10367 | GLQOFTK02GUKFG | CDS | 362660 | 213 | + | 0.305164 | |
g9301 | DLA_10368 | GLQOFTK02GUKFG | CDS | 363163 | 1305 | - | 0.314943 | |
g9302 | DLA_10369 | GLQOFTK02GUKFG | CDS | 364725 | 2112 | - | 0.38447 | |
g9303 | DLA_10370 | GLQOFTK02GUKFG | CDS | 367168 | 1077 | - | 0.322191 | |
g9304 | DLA_10371 | GLQOFTK02GUKFG | CDS | 369405 | 732 | - | 0.327869 | |
g9305 | DLA_10372 | GLQOFTK02GUKFG | CDS | 370431 | 816 | + | 0.292892 | |
g9306 | DLA_10373 | GLQOFTK02GUKFG | CDS | 371338 | 861 | - | 0.361208 | |
g9307 | DLA_10375 | GLQOFTK02GUKFG | CDS | 373057 | 1695 | + | 0.375221 | |
g9308 | DLA_10376 | GLQOFTK02GUKFG | CDS | 375001 | 1371 | + | 0.384391 | |
g9309 | DLA_10377 | catalyzes the reaction: ATP L-fucose ADP beta-L-fucose 1-phosphate | GLQOFTK02GUKFG | CDS | 376640 | 3456 | + | 0.338542 |
g931 | DLA_01031 | F4PJNLW01A00V1 | CDS | 661501 | 4101 | + | 0.333821 | |
g9310 | DLA_11807 | GLQOFTK02GUKFG | CDS | 380335 | 828 | - | 0.270531 | |
g9311 | DLA_10378 | similar to FKBP-type peptidyl-prolyl isomerase which functions as a receptor for immunosuppressants in vertebrates | GLQOFTK02GUKFG | CDS | 381321 | 543 | - | 0.314917 |
g9312 | DLA_10379 | GLQOFTK02GUKFG | CDS | 381941 | 1743 | + | 0.325875 | |
g9313 | DLA_10380 | GLQOFTK02GUKFG | CDS | 383812 | 1698 | + | 0.282686 | |
g9314 | DLA_10381 | ortholog of the H. sapiens lysosomal alpha-glucosidase which is essential for the degradation of glygogen to glucose in lysosomes defects in GAA are the cause of glycogen storage disease II a recessive disorder which results in a massive accumulation of glycogen in muscle heart and liver leading to a life expectancy of less than two years | GLQOFTK02GUKFG | CDS | 385590 | 2730 | - | 0.348718 |
g9315 | DLA_10382 | GLQOFTK02GUKFG | CDS | 388619 | 750 | - | 0.305333 | |
g9316 | DLA_10383 | GLQOFTK02GUKFG | CDS | 389670 | 975 | - | 0.30359 | |
g9317 | DLA_10384 | catalyzes the transfer of a farnesyl group or a geranylgeranyl group via a thioether linkage (-C-S-C-) to a cysteine at or near the carboxyl terminus of the protein forms a heterodimer with the | GLQOFTK02GUKFG | CDS | 390893 | 1323 | - | 0.312169 |
g9318 | DLA_10385 | catalyzes the first of three steps required to remove two C-4 methyl groups from an intermediate in ergosterol biosynthesis almost identical to the neighboring gene | GLQOFTK02GUKFG | CDS | 392617 | 792 | - | 0.344697 |
g9319 | DLA_10387 | GLQOFTK02GUKFG | CDS | 393942 | 573 | - | 0.34904 | |
g932 | DLA_01032 | F4PJNLW01A00V1 | CDS | 665942 | 846 | + | 0.336879 | |
g9320 | DLA_10388 | GLQOFTK02GUKFG | CDS | 394874 | 2424 | - | 0.32302 | |
g9321 | DLA_10390 | GLQOFTK02GUKFG | CDS | 397920 | 1440 | + | 0.329167 | |
g9322 | DLA_10391 | GLQOFTK02GUKFG | CDS | 399458 | 501 | - | 0.305389 | |
g9323 | DLA_11808 | GLQOFTK02GUKFG | CDS | 400622 | 450 | - | 0.275556 | |
g9324 | DLA_10392 | GLQOFTK02GUKFG | CDS | 401174 | 390 | + | 0.271795 | |
g9325 | DLA_10393 | GLQOFTK02GUKFG | CDS | 401655 | 1722 | + | 0.283391 | |
g9326 | DLA_10394 | GLQOFTK02GUKFG | CDS | 403426 | 1143 | - | 0.299213 | |
g9327 | DLA_10395 | GLQOFTK02GUKFG | CDS | 404946 | 1500 | - | 0.340667 | |
g9328 | DLA_10397 | GLQOFTK02GUKFG | CDS | 407337 | 1068 | - | 0.324906 | |
g9329 | DLA_10398 | GLQOFTK02GUKFG | CDS | 408631 | 2688 | - | 0.292783 | |
g933 | DLA_01033 | F4PJNLW01A00V1 | CDS | 667032 | 873 | + | 0.342497 | |
g9330 | DLA_10401 | GLQOFTK02GUKFG | CDS | 413012 | 1170 | + | 0.340171 | |
g9331 | DLA_10402 | GLQOFTK02GUKFG | CDS | 414480 | 5160 | - | 0.312403 | |
g9332 | DLA_10403 | GLQOFTK02GUKFG | CDS | 420454 | 4110 | + | 0.3382 | |
g9333 | DLA_10405 | GLQOFTK02GUKFG | CDS | 424713 | 669 | - | 0.29148 | |
g9334 | DLA_10407 | GLQOFTK02GUKFG | CDS | 426570 | 1731 | - | 0.346043 | |
g9335 | DLA_10408 | GLQOFTK02GUKFG | CDS | 428539 | 1335 | + | 0.310861 | |
g9336 | DLA_10409 | GLQOFTK02GUKFG | CDS | 430370 | 1767 | + | 0.327108 | |
g9337 | DLA_10410 | GLQOFTK02GUKFG | CDS | 433150 | 678 | + | 0.320059 | |
g9338 | DLA_10411 | GLQOFTK02GUKFG | CDS | 434616 | 312 | - | 0.365385 | |
g9339 | DLA_10412 | GLQOFTK02GUKFG | CDS | 436075 | 3642 | + | 0.354201 | |
g934 | DLA_01034 | F4PJNLW01A00V1 | CDS | 668187 | 690 | - | 0.347826 | |
g9340 | DLA_10413 | GLQOFTK02GUKFG | CDS | 439988 | 1347 | - | 0.30735 | |
g9341 | DLA_10414 | GLQOFTK02GUKFG | CDS | 441544 | 1935 | + | 0.312145 | |
g9342 | DLA_10415 | the Maf protein is a putative inhibitor of septum formation found in eukaryotes bacteria and archaea | GLQOFTK02GUKFG | CDS | 443608 | 648 | - | 0.279321 |
g9343 | DLA_10416 | GLQOFTK02GUKFG | CDS | 444432 | 381 | - | 0.265092 | |
g9344 | DLA_10417 | GLQOFTK02GUKFG | CDS | 444987 | 276 | + | 0.347826 | |
g9345 | DLA_10418 | GLQOFTK02GUKFG | CDS | 445559 | 2502 | - | 0.329337 | |
g9346 | DLA_11809 | actin binding protein regulating actin nucleation involved in cytokinesis and cell motility | GLQOFTK02GUKFG | CDS | 448979 | 1359 | + | 0.38337 |
g9347 | DLA_10419 | GLQOFTK02GUKFG | CDS | 450664 | 3126 | + | 0.318618 | |
g9348 | DLA_10420 | GLQOFTK02GUKFG | CDS | 454202 | 2037 | + | 0.302896 | |
g9349 | DLA_10421 | GLQOFTK02GUKFG | CDS | 456574 | 1878 | - | 0.317891 | |
g935 | DLA_11459 | F4PJNLW01A00V1 | CDS | 669504 | 240 | - | 0.279167 | |
g9350 | DLA_11810 | GLQOFTK02GUKFG | CDS | 458657 | 987 | - | 0.315096 | |
g9351 | DLA_10422 | similar to plant expansins which modify the cell wall to allow expansion during cell growth contains a predicted signal peptide | GLQOFTK02GUKFG | CDS | 459864 | 1008 | - | 0.355159 |
g9352 | DLA_10423 | GLQOFTK02GUKFG | CDS | 462092 | 1788 | + | 0.310962 | |
g9353 | DLA_10424 | GLQOFTK02GUKFG | CDS | 464528 | 774 | - | 0.270026 | |
g9354 | DLA_10425 | GLQOFTK02GUKFG | CDS | 465659 | 2880 | - | 0.319444 | |
g9355 | DLA_10426 | GLQOFTK02GUKFG | CDS | 469346 | 4071 | + | 0.316875 | |
g9356 | DLA_10427 | GLQOFTK02GUKFG | CDS | 473618 | 888 | + | 0.280405 | |
g9357 | DLA_10428 | highly similar to plant and bacterial O-methyltransferases expressed in pstA cells | GLQOFTK02GUKFG | CDS | 474714 | 1029 | - | 0.295432 |
g9358 | DLA_10429 | GLQOFTK02GUKFG | CDS | 476181 | 975 | - | 0.310769 | |
g9359 | DLA_10430 | GLQOFTK02GUKFG | CDS | 477421 | 723 | - | 0.344398 | |
g936 | DLA_01035 | F4PJNLW01A00V1 | CDS | 670163 | 411 | + | 0.304136 | |
g9360 | DLA_10431 | GLQOFTK02GUKFG | CDS | 478564 | 858 | + | 0.29021 | |
g9361 | DLA_10432 | GLQOFTK02GUKFG | CDS | 479709 | 351 | - | 0.404558 | |
g9362 | DLA_10433 | GLQOFTK02GUKFG | CDS | 480877 | 1527 | + | 0.293386 | |
g9363 | DLA_10434 | GLQOFTK02GUKFG | CDS | 482800 | 1047 | + | 0.266476 | |
g9364 | DLA_10435 | GLQOFTK02GUKFG | CDS | 484222 | 453 | - | 0.406181 | |
g9365 | DLA_10436 | conserved protein in S.cerevisiae required for 60S pre-ribosomal subunits export to the cytoplasm | GLQOFTK02GUKFG | CDS | 485428 | 2280 | + | 0.319298 |
g9366 | DLA_10437 | GLQOFTK02GUKFG | CDS | 488096 | 2061 | + | 0.312955 | |
g9367 | DLA_10438 | GLQOFTK02GUKFG | CDS | 490499 | 1197 | - | 0.319131 | |
g9368 | DLA_10439 | GLQOFTK02GUKFG | CDS | 491811 | 900 | - | 0.313333 | |
g9369 | DLA_10440 | component of the RNA polymerase III complex ortholog of S. cerevisiae RPO31 | GLQOFTK02GUKFG | CDS | 492905 | 4203 | - | 0.343088 |
g937 | DLA_01036 | F4PJNLW01A00V1 | CDS | 670824 | 549 | - | 0.391621 | |
g9370 | DLA_10441 | belongs to the RAS-like GTPase superfamily ortholog of human OLA1 | GLQOFTK02GUKFG | CDS | 497556 | 1182 | + | 0.36802 |
g9371 | DLA_10442 | GLQOFTK02GUKFG | CDS | 498948 | 1455 | - | 0.315464 | |
g9372 | DLA_10443 | GLQOFTK02GUKFG | CDS | 500564 | 1152 | - | 0.296875 | |
g9373 | DLA_10444 | GLQOFTK02GUKFG | CDS | 502462 | 690 | + | 0.276812 | |
g9374 | DLA_10445 | GLQOFTK02GUKFG | CDS | 503492 | 468 | - | 0.297009 | |
g9375 | DLA_10446 | GLQOFTK02GUKFG | CDS | 503991 | 1782 | - | 0.277217 | |
g9376 | DLA_10447 | GLQOFTK02GUKFG | CDS | 506113 | 3342 | - | 0.289348 | |
g9377 | DLA_10448 | CAMK group RAD53 family protein kinase similar to mammalian cell cycle checkpoint kinases chk2 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteinsbrbr bCommunity annotation:b The five fhk-X genes differ substantially in their response to the disruption of the retinoblastoma-like gene rblA. FhkA is substantially and highly signficantly upregulated in the ko strain while none of the other genes show major changes. Consistent with its regulation the fhkA promoter contains a putative E2F-type binding site (TTTGCGCCTTTT). Virtually all genes associated with replication fork progression are upregulated in the rblA disruptant these include cdc45 all mcm genes all gins genes all rfc genes four polA subunits three polD subunits two putatitive polE subunits PCNA the single-strand binding protein rfa1 the flap endonuclease repG as well as DNA ligase-1 and topoisomerase-2. All these genes show overexpression factors ranging from 4 to 15 | GLQOFTK02GUKFG | CDS | 509525 | 1584 | - | 0.297348 |
g9378 | DLA_10449 | GLQOFTK02GUKFG | CDS | 511230 | 1665 | - | 0.263664 | |
g9379 | DLA_10450 | GLQOFTK02GUKFG | CDS | 513116 | 483 | + | 0.271222 | |
g938 | DLA_01037 | F4PJNLW01A00V1 | CDS | 673562 | 1203 | - | 0.412303 | |
g9380 | DLA_10451 | GLQOFTK02GUKFG | CDS | 513746 | 1341 | - | 0.319911 | |
g9381 | DLA_10452 | GLQOFTK02GUKFG | CDS | 515519 | 2829 | - | 0.339343 | |
g9382 | DLA_10453 | GLQOFTK02GUKFG | CDS | 518994 | 381 | - | 0.272966 | |
g9383 | DLA_10454 | GLQOFTK02GUKFG | CDS | 519874 | 1305 | + | 0.306513 | |
g9384 | DLA_10456 | GLQOFTK02GUKFG | CDS | 522389 | 2139 | - | 0.283777 | |
g9385 | DLA_10457 | GLQOFTK02GUKFG | CDS | 525926 | 312 | + | 0.394231 | |
g9386 | DLA_10458 | GLQOFTK02GUKFG | CDS | 526366 | 714 | + | 0.415966 | |
g9387 | DLA_10461 | GLQOFTK02GUKFG | CDS | 528731 | 1254 | - | 0.308612 | |
g9388 | DLA_10462 | GLQOFTK02GUKFG | CDS | 530965 | 522 | - | 0.222222 | |
g9389 | DLA_10464 | GLQOFTK02GUKFG | CDS | 532103 | 1818 | - | 0.286029 | |
g939 | DLA_01038 | F4PJNLW01A00V1 | CDS | 675097 | 1035 | - | 0.256039 | |
g9390 | DLA_10467 | GLQOFTK02GUKFG | CDS | 535246 | 531 | + | 0.303201 | |
g9391 | DLA_10468 | GLQOFTK02GUKFG | CDS | 535973 | 1701 | + | 0.270429 | |
g9392 | DLA_10469 | GLQOFTK02GUKFG | CDS | 538240 | 1641 | + | 0.269957 | |
g9393 | DLA_10470 | GLQOFTK02GUKFG | CDS | 539916 | 858 | - | 0.269231 | |
g9394 | DLA_10471 | GLQOFTK02I2I9N | CDS | 3 | 3461 | + | 0.424733 | |
g9395 | DLA_10473 | GLQOFTK02I8QA1 | CDS | 1930 | 687 | - | 0.302766 | |
g9396 | DLA_10474 | GLQOFTK02IIIWT | CDS | 278 | 360 | + | 0.283333 | |
g9397 | DLA_10476 | GLQOFTK02IIIWT | CDS | 1809 | 201 | + | 0.283582 | |
g9398 | DLA_10477 | catalyzes the reactoin L-tryptophan Osub2sub L-formylkynurenine | GLQOFTK02IIIWT | CDS | 2230 | 1197 | - | 0.288221 |
g9399 | DLA_10478 | GLQOFTK02IIOHN | CDS | 408 | 1821 | - | 0.315761 | |
g94 | DLA_11432 | involved in protein transport into the nucleus known to bind Ran in yeast and Arabidopsis | contig05409_1.exp | CDS | 220302 | 357 | + | 0.316527 |
g940 | DLA_01039 | F4PJNLW01A00V1 | CDS | 676275 | 627 | - | 0.266348 | |
g9400 | DLA_10479 | GLQOFTK02IIOHN | CDS | 2547 | 537 | + | 0.340782 | |
g9401 | DLA_10480 | GLQOFTK02IIOHN | CDS | 3280 | 846 | - | 0.34279 | |
g9402 | DLA_10482 | GLQOFTK02IIOHN | CDS | 4894 | 3600 | + | 0.303889 | |
g9403 | DLA_11811 | GLQOFTK02IIOHN | CDS | 8991 | 477 | - | 0.295597 | |
g9404 | DLA_10483 | GLQOFTK02IIOHN | CDS | 10531 | 2001 | - | 0.310845 | |
g9405 | DLA_11812 | GLQOFTK02IIOHN | CDS | 14106 | 360 | + | 0.283333 | |
g9406 | DLA_11813 | GLQOFTK02IIOHN | CDS | 15091 | 717 | + | 0.320781 | |
g9407 | DLA_11814 | GLQOFTK02IIOHN | CDS | 16363 | 1308 | + | 0.357798 | |
g9408 | DLA_10484 | GLQOFTK02IIOHN | CDS | 17847 | 1482 | + | 0.350202 | |
g9409 | DLA_10485 | GLQOFTK02IIOHN | CDS | 19471 | 390 | + | 0.315385 | |
g941 | DLA_01040 | F4PJNLW01A00V1 | CDS | 677007 | 867 | - | 0.342561 | |
g9410 | DLA_10488 | GLQOFTK02IIOHN | CDS | 20766 | 216 | + | 0.328704 | |
g9411 | DLA_10489 | GLQOFTK02IIOHN | CDS | 21131 | 1317 | - | 0.320425 | |
g9412 | DLA_10490 | GLQOFTK02IIOHN | CDS | 22468 | 1185 | - | 0.334177 | |
g9413 | DLA_11815 | GLQOFTK02IIOHN | CDS | 23853 | 330 | + | 0.30303 | |
g9414 | DLA_10491 | GLQOFTK02IIOHN | CDS | 24834 | 1428 | + | 0.337535 | |
g9415 | DLA_11816 | GLQOFTK02IIOHN | CDS | 26373 | 399 | + | 0.305764 | |
g9416 | DLA_10492 | GLQOFTK02IIOHN | CDS | 26795 | 849 | + | 0.300353 | |
g9417 | DLA_10493 | GLQOFTK02IIOHN | CDS | 27676 | 417 | + | 0.402878 | |
g9418 | DLA_10494 | GLQOFTK02IIOHN | CDS | 28526 | 1533 | + | 0.331376 | |
g9419 | DLA_10495 | GLQOFTK02IIOHN | CDS | 31295 | 264 | - | 0.30303 | |
g942 | DLA_01041 | F4PJNLW01A00V1 | CDS | 678385 | 510 | - | 0.288235 | |
g9420 | DLA_10496 | GLQOFTK02IIOHN | CDS | 32070 | 582 | - | 0.331615 | |
g9421 | DLA_10497 | GLQOFTK02IIOHN | CDS | 33132 | 1974 | - | 0.288247 | |
g9422 | DLA_10498 | GLQOFTK02IIOHN | CDS | 35498 | 1224 | - | 0.289216 | |
g9423 | DLA_10499 | GLQOFTK02IIOHN | CDS | 36831 | 654 | - | 0.319572 | |
g9424 | DLA_10500 | GLQOFTK02IIOHN | CDS | 37703 | 2343 | - | 0.364063 | |
g9425 | DLA_10501 | GLQOFTK02IIOHN | CDS | 40443 | 1530 | + | 0.345098 | |
g9426 | DLA_10502 | GLQOFTK02IIOHN | CDS | 42281 | 291 | - | 0.28866 | |
g9427 | DLA_10503 | GLQOFTK02IIOHN | CDS | 42864 | 1668 | + | 0.344724 | |
g9428 | DLA_10504 | GLQOFTK02IIOHN | CDS | 44679 | 3150 | + | 0.326349 | |
g9429 | DLA_10505 | GLQOFTK02IIOHN | CDS | 48075 | 1011 | - | 0.310584 | |
g943 | DLA_01042 | F4PJNLW01A00V1 | CDS | 678951 | 1272 | - | 0.275157 | |
g9430 | DLA_10507 | GLQOFTK02IIOHN | CDS | 50069 | 675 | - | 0.284444 | |
g9431 | DLA_10508 | GLQOFTK02IIOHN | CDS | 51158 | 861 | - | 0.40302 | |
g9432 | DLA_10509 | GLQOFTK02IIOHN | CDS | 52960 | 3138 | + | 0.299235 | |
g9433 | DLA_10510 | GLQOFTK02IIOHN | CDS | 56360 | 1986 | - | 0.353978 | |
g9434 | DLA_10511 | GLQOFTK02IIOHN | CDS | 59304 | 1284 | + | 0.380841 | |
g9435 | DLA_10512 | GLQOFTK02IIOHN | CDS | 61093 | 897 | + | 0.327759 | |
g9436 | DLA_10513 | GLQOFTK02IIOHN | CDS | 62481 | 1218 | - | 0.288998 | |
g9437 | DLA_10514 | GLQOFTK02IIOHN | CDS | 65384 | 732 | + | 0.346995 | |
g9438 | DLA_10515 | GLQOFTK02IIOHN | CDS | 66408 | 798 | + | 0.274436 | |
g9439 | DLA_10516 | GLQOFTK02IIOHN | CDS | 67356 | 4107 | - | 0.32822 | |
g944 | DLA_01043 | fatty acid synthases catalyze the formation of long-chain fatty acids from acetyl-CoA malonyl-CoA and NADPH multifunctional protein with several catalytic activities and an acyl carrier protein enriched in gametes | F4PJNLW01A00V1 | CDS | 681151 | 7635 | + | 0.339358 |
g9440 | DLA_10518 | GLQOFTK02IIOHN | CDS | 74115 | 4074 | + | 0.368189 | |
g9441 | DLA_10519 | GLQOFTK02IIOHN | CDS | 78504 | 1665 | - | 0.276276 | |
g9442 | DLA_10520 | GLQOFTK02IIOHN | CDS | 80606 | 1563 | - | 0.325016 | |
g9443 | DLA_10521 | GLQOFTK02IIOHN | CDS | 83068 | 621 | + | 0.259259 | |
g9444 | DLA_10522 | GLQOFTK02IIOHN | CDS | 83987 | 1074 | - | 0.292365 | |
g9445 | DLA_10523 | GLQOFTK02IIOHN | CDS | 85920 | 4386 | + | 0.332421 | |
g9446 | DLA_10524 | GLQOFTK02IIOHN | CDS | 90478 | 507 | - | 0.236686 | |
g9447 | DLA_10525 | GLQOFTK02IIOHN | CDS | 91510 | 2901 | + | 0.268183 | |
g9448 | DLA_10526 | GLQOFTK02IIOHN | CDS | 94605 | 228 | - | 0.280702 | |
g9449 | DLA_10528 | GLQOFTK02IIOHN | CDS | 96517 | 2610 | + | 0.310728 | |
g945 | DLA_01044 | F4PJNLW01A00V1 | CDS | 689006 | 3144 | - | 0.310433 | |
g9450 | DLA_10529 | GLQOFTK02IIOHN | CDS | 99402 | 2697 | + | 0.313682 | |
g9451 | DLA_10531 | GLQOFTK02IIOHN | CDS | 102553 | 1290 | - | 0.272093 | |
g9452 | DLA_10533 | GLQOFTK02IIOHN | CDS | 104597 | 558 | - | 0.249104 | |
g9453 | DLA_10534 | GLQOFTK02IIOHN | CDS | 105273 | 1467 | + | 0.225631 | |
g9454 | DLA_10537 | GLQOFTK02IIOHN | CDS | 108618 | 1056 | - | 0.331439 | |
g9455 | DLA_10539 | GLQOFTK02IIOHN | CDS | 111271 | 483 | - | 0.308489 | |
g9456 | DLA_10540 | GLQOFTK02IIOHN | CDS | 111927 | 1881 | - | 0.267943 | |
g9457 | DLA_10541 | GLQOFTK02IIOHN | CDS | 114315 | 2391 | - | 0.28189 | |
g9458 | DLA_10542 | GLQOFTK02IIOHN | CDS | 117147 | 471 | - | 0.284501 | |
g9459 | DLA_10543 | GLQOFTK02IIOHN | CDS | 118203 | 1749 | - | 0.277301 | |
g946 | DLA_01045 | F4PJNLW01A00V1 | CDS | 692544 | 3042 | - | 0.323143 | |
g9460 | DLA_10544 | GLQOFTK02IIOHN | CDS | 120101 | 987 | - | 0.258359 | |
g9461 | DLA_10545 | GLQOFTK02IIOHN | CDS | 121629 | 1893 | + | 0.300581 | |
g9462 | DLA_10546 | GLQOFTK02IIOHN | CDS | 124160 | 1593 | + | 0.259887 | |
g9463 | DLA_10547 | GLQOFTK02IIOHN | CDS | 125810 | 2967 | - | 0.290529 | |
g9464 | DLA_11817 | GLQOFTK02IIOHN | CDS | 129006 | 2769 | - | 0.346334 | |
g9465 | DLA_10548 | GLQOFTK02IIOHN | CDS | 132135 | 963 | + | 0.288681 | |
g9466 | DLA_10549 | GLQOFTK02IIOHN | CDS | 133276 | 1392 | - | 0.369971 | |
g9467 | DLA_10550 | GLQOFTK02IIOHN | CDS | 135570 | 1791 | - | 0.299274 | |
g9468 | DLA_10551 | GLQOFTK02IIOHN | CDS | 137545 | 1716 | - | 0.321096 | |
g9469 | DLA_10552 | GLQOFTK02IIOHN | CDS | 139697 | 2595 | - | 0.301349 | |
g947 | DLA_01046 | F4PJNLW01A00V1 | CDS | 696119 | 843 | - | 0.329775 | |
g9470 | DLA_10554 | GLQOFTK02IIOHN | CDS | 143002 | 2214 | + | 0.325655 | |
g9471 | DLA_10556 | GLQOFTK02IIOHN | CDS | 147330 | 2253 | + | 0.317798 | |
g9472 | DLA_10558 | GLQOFTK02IIOHN | CDS | 150894 | 963 | + | 0.271028 | |
g9473 | DLA_10559 | GLQOFTK02IIOHN | CDS | 152030 | 861 | - | 0.288037 | |
g9474 | DLA_10560 | GLQOFTK02IIOHN | CDS | 153321 | 312 | + | 0.317308 | |
g9475 | DLA_10561 | GLQOFTK02IIOHN | CDS | 154011 | 3360 | - | 0.273512 | |
g9476 | DLA_10563 | GLQOFTK02IIOHN | CDS | 160638 | 1140 | - | 0.335088 | |
g9477 | DLA_11818 | GLQOFTK02IIOHN | CDS | 162418 | 321 | - | 0.258567 | |
g9478 | DLA_10564 | GLQOFTK02IIOHN | CDS | 163137 | 2754 | + | 0.316993 | |
g9479 | DLA_10566 | GLQOFTK02IIOHN | CDS | 166749 | 364 | + | 0.142857 | |
g9480 | DLA_10567 | GLQOFTK02IJPNF | CDS | 2 | 2065 | - | 0.232446 | |
g9481 | DLA_10568 | GLQOFTK02IJPNF | CDS | 2411 | 786 | + | 0.296438 | |
g9482 | DLA_10569 | GLQOFTK02IJPNF | CDS | 3493 | 501 | - | 0.289421 | |
g9483 | DLA_10570 | GLQOFTK02IJPNF | CDS | 4491 | 1311 | - | 0.280702 | |
g9484 | DLA_10571 | GLQOFTK02IJPNF | CDS | 6637 | 1104 | - | 0.322464 | |
g9485 | DLA_10572 | GLQOFTK02IJPNF | CDS | 8032 | 1290 | + | 0.285271 | |
g9486 | DLA_10573 | ortholog of yeast HIR1 a transcriptional corepressor involved in the cell cycle-regulated transcription of histone H2A H2B H3 and H4 genes | GLQOFTK02IJPNF | CDS | 9488 | 2976 | - | 0.310484 |
g9487 | DLA_10574 | GLQOFTK02IJPNF | CDS | 12820 | 2427 | + | 0.263288 | |
g9488 | DLA_11819 | GLQOFTK02IJPNF | CDS | 15417 | 306 | - | 0.24183 | |
g9489 | DLA_10575 | GLQOFTK02IJPNF | CDS | 15892 | 1671 | + | 0.225613 | |
g949 | DLA_01048 | F4PJNLW01A00V1 | CDS | 701075 | 1980 | + | 0.283333 | |
g9490 | DLA_10576 | GLQOFTK02IJPNF | CDS | 17802 | 2613 | - | 0.258706 | |
g9491 | DLA_10579 | GLQOFTK02IJPNF | CDS | 21239 | 453 | + | 0.286976 | |
g9492 | DLA_10580 | GLQOFTK02IJPNF | CDS | 23114 | 237 | + | 0.324895 | |
g9493 | DLA_10582 | GLQOFTK02IJPNF | CDS | 25801 | 645 | + | 0.28062 | |
g9494 | DLA_10583 | GLQOFTK02IJPNF | CDS | 26753 | 2523 | - | 0.315497 | |
g9495 | DLA_10584 | GLQOFTK02IJPNF | CDS | 30408 | 738 | + | 0.337398 | |
g9496 | DLA_10585 | GLQOFTK02IJPNF | CDS | 31255 | 825 | - | 0.307879 | |
g9497 | DLA_10586 | GLQOFTK02IJPNF | CDS | 32208 | 753 | + | 0.284197 | |
g9498 | DLA_10587 | GLQOFTK02IJPNF | CDS | 33190 | 1704 | - | 0.287559 | |
g9499 | DLA_10589 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention in D. discoideum involved in early development and tip formation | GLQOFTK02IJPNF | CDS | 37254 | 10056 | - | 0.289081 |
g95 | DLA_00110 | contig05409_1.exp | CDS | 221480 | 1122 | + | 0.335116 | |
g950 | DLA_01049 | F4PJNLW01A00V1 | CDS | 703367 | 771 | - | 0.302205 | |
g9500 | DLA_10590 | GLQOFTK02IJPNF | CDS | 47682 | 1065 | + | 0.353052 | |
g9501 | DLA_10591 | GLQOFTK02IJPNF | CDS | 49092 | 777 | - | 0.301158 | |
g9502 | DLA_10592 | GLQOFTK02IJPNF | CDS | 50018 | 1581 | + | 0.320683 | |
g9503 | DLA_10593 | GLQOFTK02IJPNF | CDS | 52101 | 615 | + | 0.304065 | |
g9504 | DLA_10594 | GLQOFTK02IJPNF | CDS | 54736 | 2634 | + | 0.316249 | |
g9505 | DLA_10595 | GLQOFTK02IJPNF | CDS | 57841 | 495 | + | 0.30101 | |
g9506 | DLA_10596 | single D. discoideum ortholog of the highly conserved yippee protein family | GLQOFTK02IJPNF | CDS | 58836 | 330 | - | 0.293939 |
g9507 | DLA_10597 | GLQOFTK02IJPNF | CDS | 59829 | 780 | - | 0.346154 | |
g9508 | DLA_11820 | GLQOFTK02IJPNF | CDS | 64180 | 543 | - | 0.366482 | |
g9509 | DLA_10599 | GLQOFTK02IJPNF | CDS | 65645 | 1266 | - | 0.309637 | |
g951 | DLA_01050 | F4PJNLW01A00V1 | CDS | 704291 | 1440 | + | 0.311111 | |
g9510 | DLA_10600 | GLQOFTK02IJPNF | CDS | 67191 | 783 | - | 0.254151 | |
g9511 | DLA_10601 | GLQOFTK02IJPNF | CDS | 68158 | 744 | - | 0.336022 | |
g9512 | DLA_10602 | GLQOFTK02IJPNF | CDS | 69653 | 3168 | + | 0.313763 | |
g9513 | DLA_10603 | GLQOFTK02IJPNF | CDS | 73209 | 1731 | + | 0.290006 | |
g9514 | DLA_10604 | GLQOFTK02IJPNF | CDS | 75252 | 1143 | + | 0.337708 | |
g9515 | DLA_10605 | GLQOFTK02IJPNF | CDS | 76485 | 993 | - | 0.336354 | |
g9516 | DLA_10607 | GLQOFTK02IJPNF | CDS | 78464 | 4281 | + | 0.301331 | |
g9517 | DLA_10609 | ortholog of the yeast ODC2 and mammalian SLCA2521 which transport C5-C7 oxodicarboxylates across the mitochondrial membrane belongs to the mitochondrial substrate carrier family brbr bCommunity annotation:b Overview of the | GLQOFTK02IJPNF | CDS | 83866 | 879 | - | 0.359499 |
g9518 | DLA_10610 | GLQOFTK02IJPNF | CDS | 85022 | 2883 | + | 0.302463 | |
g9519 | DLA_10611 | GLQOFTK02IJPNF | CDS | 88262 | 3198 | - | 0.334271 | |
g952 | DLA_01051 | F4PJNLW01A00V1 | CDS | 706016 | 1749 | + | 0.317324 | |
g9520 | DLA_10612 | GLQOFTK02IJPNF | CDS | 91656 | 2298 | - | 0.336815 | |
g9521 | DLA_10613 | GLQOFTK02IJPNF | CDS | 94205 | 2922 | - | 0.348049 | |
g9522 | DLA_10614 | GLQOFTK02IJPNF | CDS | 97366 | 2982 | - | 0.32495 | |
g9523 | DLA_10615 | GLQOFTK02IJPNF | CDS | 100587 | 2991 | - | 0.323972 | |
g9524 | DLA_10616 | GLQOFTK02IJPNF | CDS | 103825 | 1968 | - | 0.329268 | |
g9525 | DLA_10617 | GLQOFTK02IJPNF | CDS | 107405 | 2001 | + | 0.318341 | |
g9526 | DLA_10618 | GLQOFTK02IJPNF | CDS | 110291 | 1242 | - | 0.318035 | |
g9527 | DLA_10619 | GLQOFTK02IJPNF | CDS | 111897 | 849 | + | 0.342756 | |
g9528 | DLA_10620 | GLQOFTK02IJPNF | CDS | 112779 | 1242 | - | 0.381643 | |
g9529 | DLA_10621 | similar to eukaryotic initiation factor 4A isoform 3 | GLQOFTK02IJPNF | CDS | 114540 | 1242 | + | 0.36715 |
g953 | DLA_01052 | F4PJNLW01A00V1 | CDS | 707902 | 3888 | - | 0.273663 | |
g9530 | DLA_10622 | GLQOFTK02IJPNF | CDS | 117466 | 1098 | + | 0.335155 | |
g9531 | DLA_10623 | GLQOFTK02IJPNF | CDS | 119215 | 2970 | + | 0.341751 | |
g9532 | DLA_10624 | GLQOFTK02IJPNF | CDS | 122365 | 414 | + | 0.338164 | |
g9533 | DLA_10625 | GLQOFTK02IJPNF | CDS | 123216 | 1623 | + | 0.315465 | |
g9534 | DLA_10626 | GLQOFTK02IJPNF | CDS | 124911 | 1101 | - | 0.364214 | |
g9535 | DLA_10628 | GLQOFTK02IJPNF | CDS | 126629 | 1635 | + | 0.33578 | |
g9536 | DLA_10629 | GLQOFTK02IJPNF | CDS | 128602 | 1698 | + | 0.295642 | |
g9537 | DLA_10630 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane has similarity to the calcium-dependent mitochondrial aspartate and glutamate carriers aralar1 and 2 (slc25A12 and 13) but does not contain a EF-hand calcium-binding domain such as | GLQOFTK02IJPNF | CDS | 130411 | 897 | + | 0.32553 |
g9538 | DLA_10631 | GLQOFTK02IJPNF | CDS | 131487 | 1545 | - | 0.32233 | |
g9539 | DLA_10633 | GLQOFTK02IJPNF | CDS | 133679 | 1458 | - | 0.288066 | |
g954 | DLA_01057 | F4PJNLW01A00V1 | CDS | 715689 | 1680 | - | 0.289881 | |
g9540 | DLA_10634 | GLQOFTK02IJPNF | CDS | 135427 | 1278 | + | 0.330986 | |
g9541 | DLA_11821 | GLQOFTK02IJPNF | CDS | 136790 | 531 | + | 0.344633 | |
g9542 | DLA_10636 | GLQOFTK02IJPNF | CDS | 138096 | 1788 | + | 0.322148 | |
g9543 | DLA_10638 | GLQOFTK02IJPNF | CDS | 140295 | 1518 | - | 0.235837 | |
g9544 | DLA_10639 | GLQOFTK02IJPNF | CDS | 141893 | 1461 | - | 0.325804 | |
g9545 | DLA_10640 | GLQOFTK02IJPNF | CDS | 144255 | 516 | + | 0.242248 | |
g9546 | DLA_10641 | GLQOFTK02IJPNF | CDS | 145183 | 819 | + | 0.31746 | |
g9547 | DLA_10642 | GLQOFTK02IJPNF | CDS | 147775 | 2226 | - | 0.329739 | |
g9548 | DLA_10643 | GLQOFTK02IJPNF | CDS | 150947 | 948 | - | 0.293249 | |
g9549 | DLA_10644 | GLQOFTK02IJPNF | CDS | 152115 | 1227 | + | 0.310513 | |
g955 | DLA_01058 | F4PJNLW01A00V1 | CDS | 717747 | 477 | + | 0.377358 | |
g9550 | DLA_10645 | GLQOFTK02IJPNF | CDS | 154510 | 2538 | + | 0.351458 | |
g9551 | DLA_10646 | GLQOFTK02IJPNF | CDS | 157194 | 1092 | + | 0.337912 | |
g9552 | DLA_10647 | GLQOFTK02IJPNF | CDS | 159064 | 615 | - | 0.334959 | |
g9553 | DLA_10648 | GLQOFTK02IJPNF | CDS | 160389 | 657 | + | 0.283105 | |
g9554 | DLA_10649 | GLQOFTK02IJPNF | CDS | 161974 | 1392 | + | 0.382902 | |
g9555 | DLA_10650 | GLQOFTK02IJPNF | CDS | 163581 | 4230 | - | 0.3026 | |
g9556 | DLA_10652 | GLQOFTK02IJPNF | CDS | 168131 | 3003 | + | 0.302031 | |
g9557 | DLA_10653 | GLQOFTK02IJPNF | CDS | 171219 | 5517 | - | 0.341671 | |
g9558 | DLA_10654 | GLQOFTK02IJPNF | CDS | 177103 | 3243 | - | 0.304965 | |
g9559 | DLA_10655 | GLQOFTK02IJPNF | CDS | 180695 | 1656 | + | 0.28744 | |
g956 | DLA_01059 | F4PJNLW01A00V1 | CDS | 718550 | 678 | + | 0.353982 | |
g9560 | DLA_10656 | GLQOFTK02IJPNF | CDS | 182537 | 393 | + | 0.256997 | |
g9561 | DLA_10658 | GLQOFTK02IJPNF | CDS | 183164 | 4869 | + | 0.332923 | |
g9562 | DLA_10659 | GLQOFTK02IJPNF | CDS | 188308 | 1272 | + | 0.324686 | |
g9563 | DLA_10660 | GLQOFTK02IJPNF | CDS | 190140 | 1746 | + | 0.322451 | |
g9564 | DLA_10661 | GLQOFTK02IJPNF | CDS | 192062 | 1197 | - | 0.342523 | |
g9565 | DLA_10662 | GLQOFTK02IJPNF | CDS | 193949 | 972 | - | 0.300412 | |
g9566 | DLA_10663 | GLQOFTK02IJPNF | CDS | 196086 | 1866 | + | 0.293676 | |
g9567 | DLA_10664 | GLQOFTK02IJPNF | CDS | 198604 | 471 | + | 0.301486 | |
g9568 | DLA_10665 | GLQOFTK02IJPNF | CDS | 199472 | 1593 | - | 0.328939 | |
g9569 | DLA_10666 | GLQOFTK02IJPNF | CDS | 201687 | 1137 | + | 0.348285 | |
g957 | DLA_01060 | F4PJNLW01A00V1 | CDS | 720039 | 5316 | + | 0.357976 | |
g9570 | DLA_10667 | GLQOFTK02IJPNF | CDS | 203506 | 1143 | + | 0.317585 | |
g9571 | DLA_10668 | GLQOFTK02IJPNF | CDS | 204952 | 1149 | + | 0.32376 | |
g9572 | DLA_10670 | GLQOFTK02IJPNF | CDS | 208011 | 3246 | + | 0.227357 | |
g9573 | DLA_10671 | GLQOFTK02IJPNF | CDS | 211818 | 1749 | - | 0.326472 | |
g9574 | DLA_10673 | GLQOFTK02IJPNF | CDS | 214365 | 1524 | + | 0.228346 | |
g9575 | DLA_10674 | GLQOFTK02IJPNF | CDS | 215981 | 204 | - | 0.220588 | |
g9576 | DLA_10675 | GLQOFTK02IJPNF | CDS | 216499 | 1107 | + | 0.268293 | |
g9577 | DLA_10676 | GLQOFTK02IJPNF | CDS | 217738 | 495 | - | 0.333333 | |
g9578 | DLA_10677 | GLQOFTK02IJPNF | CDS | 219303 | 1491 | - | 0.317237 | |
g9579 | DLA_10678 | GLQOFTK02IJPNF | CDS | 221847 | 1344 | + | 0.310268 | |
g958 | DLA_01061 | F4PJNLW01A00V1 | CDS | 726071 | 399 | - | 0.278196 | |
g9580 | DLA_10681 | GLQOFTK02IJPNF | CDS | 225672 | 912 | + | 0.384868 | |
g9581 | DLA_10682 | GLQOFTK02IJPNF | CDS | 226692 | 1065 | - | 0.279812 | |
g9582 | DLA_10683 | GLQOFTK02IJPNF | CDS | 228054 | 1320 | - | 0.393182 | |
g9583 | DLA_10684 | GLQOFTK02IJPNF | CDS | 229554 | 705 | - | 0.333333 | |
g9584 | DLA_11822 | GLQOFTK02IJPNF | CDS | 231526 | 216 | + | 0.273148 | |
g9585 | DLA_10685 | GLQOFTK02IJPNF | CDS | 231821 | 1119 | - | 0.286863 | |
g9586 | DLA_10686 | GLQOFTK02IJPNF | CDS | 233238 | 3378 | + | 0.293961 | |
g9587 | DLA_10689 | GLQOFTK02IJPNF | CDS | 236964 | 531 | + | 0.299435 | |
g9588 | DLA_10690 | GLQOFTK02IJPNF | CDS | 237690 | 5268 | - | 0.351557 | |
g9589 | DLA_10691 | GLQOFTK02IJPNF | CDS | 243465 | 4671 | - | 0.357311 | |
g959 | DLA_01062 | F4PJNLW01A00V1 | CDS | 726650 | 957 | + | 0.289446 | |
g9590 | DLA_10692 | GLQOFTK02IJPNF | CDS | 248642 | 2847 | + | 0.328416 | |
g9591 | DLA_10693 | GLQOFTK02IJPNF | CDS | 251966 | 645 | - | 0.251163 | |
g9592 | DLA_10694 | GLQOFTK02IJPNF | CDS | 253538 | 2442 | + | 0.330467 | |
g9593 | DLA_10695 | GLQOFTK02IJPNF | CDS | 256147 | 768 | - | 0.286458 | |
g9594 | DLA_10696 | GLQOFTK02IJPNF | CDS | 257585 | 3006 | + | 0.357285 | |
g9595 | DLA_10698 | GLQOFTK02IJPNF | CDS | 261718 | 1779 | - | 0.287802 | |
g9596 | DLA_10699 | GLQOFTK02IJPNF | CDS | 264019 | 1329 | + | 0.332581 | |
g9597 | DLA_10700 | GLQOFTK02IJPNF | CDS | 265664 | 1596 | + | 0.335213 | |
g9598 | DLA_10702 | GLQOFTK02IJPNF | CDS | 268302 | 2259 | + | 0.291722 | |
g9599 | DLA_10703 | GLQOFTK02IJPNF | CDS | 270793 | 4284 | + | 0.2507 | |
g96 | DLA_00111 | contig05409_1.exp | CDS | 223650 | 1884 | + | 0.355096 | |
g960 | DLA_01063 | F4PJNLW01A00V1 | CDS | 727967 | 435 | + | 0.312644 | |
g9600 | DLA_10706 | GLQOFTK02IJPNF | CDS | 276176 | 1242 | - | 0.214976 | |
g9601 | DLA_10709 | GLQOFTK02IRMR1 | CDS | 1633 | 624 | - | 0.293269 | |
g9602 | DLA_10710 | GLQOFTK02IRMR1 | CDS | 2800 | 642 | - | 0.334891 | |
g9603 | DLA_10711 | GLQOFTK02IRMR1 | CDS | 4854 | 534 | + | 0.340824 | |
g9604 | DLA_10712 | GLQOFTK02IRMR1 | CDS | 5471 | 990 | - | 0.276768 | |
g9605 | DLA_10713 | GLQOFTK02IRMR1 | CDS | 6595 | 1380 | - | 0.286232 | |
g9606 | DLA_10714 | GLQOFTK02IRMR1 | CDS | 8405 | 2478 | - | 0.322841 | |
g9607 | DLA_10715 | GLQOFTK02IRMR1 | CDS | 11197 | 1326 | - | 0.319759 | |
g9608 | DLA_10716 | ubiquitin carboxyl-terminal hydrolase shown to deubiquinate mkkA putative ortholog of H. sapiens USP10 | GLQOFTK02IRMR1 | CDS | 12831 | 3240 | - | 0.292284 |
g9609 | DLA_10717 | GLQOFTK02IRMR1 | CDS | 16666 | 1035 | - | 0.279227 | |
g961 | DLA_01064 | F4PJNLW01A00V1 | CDS | 729224 | 540 | - | 0.298148 | |
g9610 | DLA_11823 | GLQOFTK02IRMR1 | CDS | 17951 | 420 | - | 0.304762 | |
g9611 | DLA_10718 | GLQOFTK02IRMR1 | CDS | 18538 | 1791 | + | 0.281407 | |
g9612 | DLA_10719 | GLQOFTK02IRMR1 | CDS | 21311 | 1110 | - | 0.315315 | |
g9613 | DLA_11824 | GLQOFTK02IRMR1 | CDS | 22433 | 1455 | - | 0.294845 | |
g9614 | DLA_10720 | GLQOFTK02IRMR1 | CDS | 24809 | 675 | - | 0.285926 | |
g9615 | DLA_10721 | GLQOFTK02IRMR1 | CDS | 27178 | 2865 | - | 0.342408 | |
g9616 | DLA_10722 | GLQOFTK02IRMR1 | CDS | 30769 | 435 | + | 0.308046 | |
g9617 | DLA_10723 | GLQOFTK02IRMR1 | CDS | 31401 | 4668 | - | 0.336118 | |
g9618 | DLA_11825 | GLQOFTK02IRMR1 | CDS | 38641 | 1596 | - | 0.346491 | |
g9619 | DLA_10724 | GLQOFTK02IRMR1 | CDS | 40948 | 1125 | + | 0.347556 | |
g962 | DLA_01065 | F4PJNLW01A00V1 | CDS | 733365 | 2331 | - | 0.324324 | |
g9620 | DLA_11826 | GLQOFTK02IRMR1 | CDS | 42155 | 696 | + | 0.281609 | |
g9621 | DLA_10725 | GLQOFTK02IRMR1 | CDS | 43505 | 1566 | + | 0.35696 | |
g9622 | DLA_10726 | GLQOFTK02IRMR1 | CDS | 45746 | 3639 | + | 0.307777 | |
g9623 | DLA_10727 | GLQOFTK02IRMR1 | CDS | 50166 | 2634 | + | 0.323842 | |
g9624 | DLA_10729 | GLQOFTK02IRMR1 | CDS | 53933 | 4098 | + | 0.340898 | |
g9625 | DLA_10730 | ortholog of S. cerevisiae ESF1 a nucleolar protein involved in pre-rRNA processing | GLQOFTK02IRMR1 | CDS | 58323 | 2313 | + | 0.310419 |
g9626 | DLA_10731 | GLQOFTK02IRMR1 | CDS | 60754 | 987 | - | 0.270517 | |
g9627 | DLA_10732 | GLQOFTK02IRMR1 | CDS | 61875 | 945 | - | 0.287831 | |
g9628 | DLA_10733 | GLQOFTK02IRMR1 | CDS | 63184 | 1983 | - | 0.299042 | |
g9629 | DLA_10735 | GLQOFTK02IRMR1 | CDS | 66509 | 1560 | - | 0.275 | |
g963 | DLA_01066 | F4PJNLW01A00V1 | CDS | 736130 | 7947 | - | 0.317227 | |
g9630 | DLA_10736 | GLQOFTK02IRMR1 | CDS | 68288 | 2472 | - | 0.304612 | |
g9631 | DLA_10737 | GLQOFTK02IRMR1 | CDS | 70950 | 3321 | - | 0.298404 | |
g9632 | DLA_10739 | GLQOFTK02IRMR1 | CDS | 74589 | 1431 | - | 0.291405 | |
g9633 | DLA_10740 | GLQOFTK02IRMR1 | CDS | 76300 | 1401 | - | 0.30621 | |
g9634 | DLA_10741 | GLQOFTK02IRMR1 | CDS | 78600 | 876 | + | 0.294521 | |
g9635 | DLA_10742 | GLQOFTK02IRMR1 | CDS | 79981 | 822 | + | 0.312652 | |
g9636 | DLA_10743 | GLQOFTK02IRMR1 | CDS | 81280 | 1392 | - | 0.333333 | |
g9637 | DLA_10744 | GLQOFTK02IRMR1 | CDS | 83409 | 1119 | - | 0.306524 | |
g9638 | DLA_10745 | GLQOFTK02IRMR1 | CDS | 84697 | 975 | - | 0.325128 | |
g9639 | DLA_10746 | GLQOFTK02IRMR1 | CDS | 85950 | 1179 | + | 0.294317 | |
g964 | DLA_01067 | F4PJNLW01A00V1 | CDS | 746101 | 276 | + | 0.358696 | |
g9640 | DLA_10747 | GLQOFTK02IRMR1 | CDS | 87594 | 4137 | + | 0.32729 | |
g9641 | DLA_10749 | GLQOFTK02IRMR1 | CDS | 92290 | 2538 | + | 0.305753 | |
g9642 | DLA_10750 | GLQOFTK02IRMR1 | CDS | 94956 | 5625 | - | 0.323022 | |
g9643 | DLA_10753 | GLQOFTK02IRMR1 | CDS | 101282 | 1185 | + | 0.310549 | |
g9644 | DLA_10754 | GLQOFTK02IRMR1 | CDS | 102795 | 3597 | - | 0.293578 | |
g9645 | DLA_10755 | GLQOFTK02IRMR1 | CDS | 107957 | 471 | + | 0.33121 | |
g9646 | DLA_10757 | GLQOFTK02IRMR1 | CDS | 108946 | 207 | + | 0.323671 | |
g9647 | DLA_10759 | GLQOFTK02IRMR1 | CDS | 110059 | 624 | + | 0.379808 | |
g9648 | DLA_10760 | GLQOFTK02IRMR1 | CDS | 111344 | 1833 | - | 0.346972 | |
g9649 | DLA_10761 | GLQOFTK02IRMR1 | CDS | 113543 | 921 | - | 0.343105 | |
g965 | DLA_01070 | F4PJNLW01A00V1 | CDS | 747836 | 2991 | - | 0.348378 | |
g9650 | DLA_10762 | GLQOFTK02IRMR1 | CDS | 114914 | 897 | + | 0.311037 | |
g9651 | DLA_10763 | GLQOFTK02IRMR1 | CDS | 116295 | 897 | + | 0.322185 | |
g9652 | DLA_10764 | GLQOFTK02IRMR1 | CDS | 117319 | 5427 | + | 0.296112 | |
g9653 | DLA_10765 | GLQOFTK02IRMR1 | CDS | 122918 | 480 | - | 0.333333 | |
g9654 | DLA_10766 | GLQOFTK02IRMR1 | CDS | 123810 | 3429 | + | 0.314669 | |
g9655 | DLA_10767 | GLQOFTK02IRMR1 | CDS | 127549 | 768 | - | 0.33724 | |
g9656 | DLA_10768 | GLQOFTK02IRMR1 | CDS | 129035 | 243 | - | 0.26749 | |
g9657 | DLA_10770 | GLQOFTK02IRMR1 | CDS | 131584 | 1497 | + | 0.334001 | |
g9658 | DLA_10771 | GLQOFTK02IRMR1 | CDS | 133790 | 9963 | + | 0.329118 | |
g9659 | DLA_10772 | GLQOFTK02IRMR1 | CDS | 144218 | 393 | - | 0.379135 | |
g966 | DLA_01072 | 40S ribosomal protein SA (p40) homolog belongs to the ribosomal protein S2P family contains ribosomal protein S2 domain | F4PJNLW01A00V1 | CDS | 751133 | 1494 | - | 0.349398 |
g9660 | DLA_10773 | peptidase M20 family zinc metallopeptidases which are glutamate carboxypeptidases contains peptidase dimerization domain | GLQOFTK02IRMR1 | CDS | 145134 | 1428 | - | 0.37465 |
g9661 | DLA_10775 | GLQOFTK02IRMR1 | CDS | 148650 | 687 | - | 0.262009 | |
g9662 | DLA_10776 | GLQOFTK02IRMR1 | CDS | 149841 | 1716 | + | 0.350233 | |
g9663 | DLA_10777 | GLQOFTK02IRMR1 | CDS | 151630 | 633 | - | 0.255924 | |
g9664 | DLA_10778 | GLQOFTK02IRMR1 | CDS | 152372 | 585 | - | 0.288889 | |
g9665 | DLA_10779 | GLQOFTK02IRMR1 | CDS | 153065 | 1191 | - | 0.29555 | |
g9666 | DLA_10781 | GLQOFTK02IRMR1 | CDS | 154803 | 759 | - | 0.343874 | |
g9667 | DLA_10782 | GLQOFTK02IRMR1 | CDS | 155904 | 621 | - | 0.288245 | |
g9668 | DLA_10783 | GLQOFTK02IRMR1 | CDS | 157202 | 699 | + | 0.309013 | |
g9669 | DLA_10784 | GLQOFTK02IRMR1 | CDS | 157951 | 768 | + | 0.313802 | |
g967 | DLA_01073 | F4PJNLW01A00V1 | CDS | 753088 | 2076 | - | 0.315029 | |
g9670 | DLA_10786 | GLQOFTK02IRMR1 | CDS | 159676 | 3780 | + | 0.28836 | |
g9671 | DLA_10787 | GLQOFTK02IRMR1 | CDS | 163913 | 3831 | + | 0.290786 | |
g9672 | DLA_10788 | GLQOFTK02IRMR1 | CDS | 168273 | 3537 | + | 0.294317 | |
g9673 | DLA_10790 | GLQOFTK02IRMR1 | CDS | 172452 | 591 | - | 0.299492 | |
g9674 | DLA_10791 | ortholog of the human DPYS defects in DPYS cause cause of DHP (dihydropyrimidinase) deficiency second enzyme in the reductive pyrimidine degradation pathway (EC 3.5.2.2) catalyzes the reaction: 56-dihydrouracil Hsub2subO 3-ureidopropanoate | GLQOFTK02IRMR1 | CDS | 173273 | 1485 | + | 0.358923 |
g9675 | DLA_10792 | GLQOFTK02IRMR1 | CDS | 175074 | 570 | + | 0.247368 | |
g9676 | DLA_10793 | GLQOFTK02IRMR1 | CDS | 175845 | 744 | - | 0.306452 | |
g9677 | DLA_10794 | GLQOFTK02IRMR1 | CDS | 177572 | 651 | - | 0.321045 | |
g9678 | DLA_10795 | GLQOFTK02IRMR1 | CDS | 178605 | 936 | - | 0.305556 | |
g9679 | DLA_10796 | GLQOFTK02IRMR1 | CDS | 179689 | 276 | + | 0.264493 | |
g968 | DLA_01076 | F4PJNLW01A00V1 | CDS | 755516 | 921 | - | 0.30836 | |
g9680 | DLA_10797 | GLQOFTK02IRMR1 | CDS | 180196 | 1116 | - | 0.336918 | |
g9681 | DLA_10800 | GLQOFTK02IRMR1 | CDS | 183288 | 3780 | - | 0.319577 | |
g9682 | DLA_10801 | GLQOFTK02IRMR1 | CDS | 187757 | 1581 | - | 0.292853 | |
g9683 | DLA_10802 | GLQOFTK02IRMR1 | CDS | 189497 | 582 | - | 0.285223 | |
g9684 | DLA_10803 | GLQOFTK02IRMR1 | CDS | 190509 | 834 | + | 0.269784 | |
g9685 | DLA_10804 | GLQOFTK02IRMR1 | CDS | 192316 | 2004 | + | 0.308383 | |
g9686 | DLA_10806 | GLQOFTK02IRMR1 | CDS | 197386 | 237 | + | 0.320675 | |
g9687 | DLA_10808 | GLQOFTK02IRMR1 | CDS | 198882 | 2685 | - | 0.230912 | |
g9688 | DLA_10810 | GLQOFTK02IRMR1 | CDS | 202491 | 621 | - | 0.31401 | |
g9689 | DLA_10813 | GLQOFTK02JCFFB | CDS | 1937 | 1194 | - | 0.309045 | |
g969 | DLA_01078 | F4PJNLW01A00V1 | CDS | 758688 | 597 | - | 0.370184 | |
g9690 | DLA_10814 | GLQOFTK02JCFFB | CDS | 3414 | 2112 | + | 0.297822 | |
g9691 | DLA_10815 | GLQOFTK02JCFFB | CDS | 5703 | 1158 | + | 0.346287 | |
g9692 | DLA_10817 | GLQOFTK02JCFFB | CDS | 8011 | 1368 | + | 0.266813 | |
g9693 | DLA_10818 | GLQOFTK02JCFFB | CDS | 9811 | 1545 | + | 0.275728 | |
g9694 | DLA_11827 | GLQOFTK02JCFFB | CDS | 12071 | 1485 | + | 0.30101 | |
g9695 | DLA_10819 | homolog of S. cerevisiae CDC50 (cell division control protein 50) which is required for polarized cell growth contains two putative transmembrane domains | GLQOFTK02JCFFB | CDS | 13761 | 924 | - | 0.32684 |
g9696 | DLA_10820 | GLQOFTK02JCFFB | CDS | 15576 | 1908 | + | 0.29717 | |
g9697 | DLA_10821 | GLQOFTK02JCFFB | CDS | 17599 | 2241 | - | 0.361446 | |
g9698 | DLA_10822 | GLQOFTK02JCFFB | CDS | 20581 | 3990 | - | 0.335338 | |
g9699 | DLA_10823 | GLQOFTK02JCFFB | CDS | 25966 | 732 | - | 0.29235 | |
g97 | DLA_00112 | contig05409_1.exp | CDS | 225840 | 918 | + | 0.299564 | |
g970 | DLA_01079 | F4PJNLW01A00V1 | CDS | 759689 | 1269 | + | 0.332545 | |
g9700 | DLA_10825 | GLQOFTK02JCFFB | CDS | 28249 | 4023 | + | 0.306736 | |
g9701 | DLA_10826 | GLQOFTK02JCFFB | CDS | 32641 | 2970 | - | 0.295623 | |
g9702 | DLA_11828 | GLQOFTK02JCFFB | CDS | 39259 | 492 | - | 0.343496 | |
g9703 | DLA_10827 | GLQOFTK02JCFFB | CDS | 40244 | 1062 | - | 0.345574 | |
g9704 | DLA_10829 | GLQOFTK02JCFFB | CDS | 41837 | 228 | - | 0.307018 | |
g9705 | DLA_10831 | GLQOFTK02JCFFB | CDS | 43236 | 879 | - | 0.339022 | |
g9706 | DLA_10832 | GLQOFTK02JCFFB | CDS | 45177 | 2976 | - | 0.297715 | |
g9707 | DLA_10833 | GLQOFTK02JCFFB | CDS | 49381 | 1329 | - | 0.367193 | |
g9708 | DLA_10834 | GLQOFTK02JCFFB | CDS | 51967 | 1026 | - | 0.285575 | |
g9709 | DLA_10835 | related to glutaredoxin which functions as an electron carrier in the glutathione-dependent synthesis of deoxyribonucleotides | GLQOFTK02JCFFB | CDS | 53625 | 456 | + | 0.302632 |
g971 | DLA_01080 | F4PJNLW01A00V1 | CDS | 761769 | 591 | + | 0.324873 | |
g9710 | DLA_10836 | GLQOFTK02JCFFB | CDS | 54347 | 1029 | + | 0.361516 | |
g9711 | DLA_10837 | plays a role in the regulation of cleavage furrow formation similar to S. pombe cdc7 | GLQOFTK02JCFFB | CDS | 55659 | 3321 | + | 0.350196 |
g9712 | DLA_10838 | GLQOFTK02JCFFB | CDS | 59577 | 249 | - | 0.301205 | |
g9713 | DLA_10840 | putative U3 snoRNP protein ortholog of H. sapiens WDR36 and S. cerevisiae UTP21 WDR36 has been implicated in open angle glaucoma 1 type G (GLC1G) | GLQOFTK02JCFFB | CDS | 62219 | 2973 | + | 0.322233 |
g9714 | DLA_10841 | GLQOFTK02JCFFB | CDS | 65398 | 1035 | - | 0.300483 | |
g9715 | DLA_10842 | GLQOFTK02JCFFB | CDS | 66833 | 2652 | - | 0.337858 | |
g9716 | DLA_10843 | GLQOFTK02JCFFB | CDS | 70179 | 1023 | - | 0.301075 | |
g9717 | DLA_10845 | GLQOFTK02JCFFB | CDS | 71988 | 6054 | - | 0.279319 | |
g9718 | DLA_10847 | GLQOFTK02JCFFB | CDS | 80281 | 1215 | + | 0.279835 | |
g9719 | DLA_10849 | GLQOFTK02JCFFB | CDS | 82398 | 3561 | + | 0.262005 | |
g972 | DLA_01081 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains one predicted transmembrane domain | F4PJNLW01A00V1 | CDS | 762954 | 1002 | + | 0.352295 |
g9720 | DLA_10851 | GLQOFTK02JCFFB | CDS | 88551 | 2454 | - | 0.320701 | |
g9721 | DLA_10852 | GLQOFTK02JCFFB | CDS | 91645 | 2967 | + | 0.345804 | |
g9722 | DLA_10853 | GLQOFTK02JCFFB | CDS | 95007 | 798 | - | 0.298246 | |
g9723 | DLA_10854 | GLQOFTK02JCFFB | CDS | 96576 | 1644 | + | 0.350365 | |
g9724 | DLA_10856 | GLQOFTK02JCFFB | CDS | 98932 | 1053 | - | 0.305793 | |
g9725 | DLA_10857 | ortholog of the 62 kDa nucleoporin an essential component of the nuclear pore complex | GLQOFTK02JCFFB | CDS | 100197 | 2154 | + | 0.381151 |
g9726 | DLA_10858 | GLQOFTK02JCFFB | CDS | 102404 | 834 | - | 0.288969 | |
g9727 | DLA_10859 | GLQOFTK02JCFFB | CDS | 103652 | 807 | + | 0.282528 | |
g9728 | DLA_10860 | GLQOFTK02JCFFB | CDS | 104620 | 963 | - | 0.339564 | |
g9729 | DLA_10861 | GLQOFTK02JCFFB | CDS | 105805 | 279 | + | 0.261649 | |
g973 | DLA_01082 | full transporter consisting of two ABC domains and two transmembrane domains | F4PJNLW01A00V1 | CDS | 764221 | 4836 | - | 0.341605 |
g9730 | DLA_10862 | GLQOFTK02JCFFB | CDS | 106430 | 2298 | - | 0.295909 | |
g9731 | DLA_10863 | GLQOFTK02JCFFB | CDS | 109436 | 1845 | - | 0.280759 | |
g9732 | DLA_10864 | GLQOFTK02JCFFB | CDS | 111849 | 3135 | + | 0.290909 | |
g9733 | DLA_10866 | GLQOFTK02JCFFB | CDS | 116470 | 240 | - | 0.316667 | |
g9734 | DLA_10867 | GLQOFTK02JCFFB | CDS | 116729 | 210 | - | 0.32381 | |
g9735 | DLA_10868 | GLQOFTK02JF4TJ | CDS | 52 | 2541 | + | 0.32625 | |
g9736 | DLA_10869 | GLQOFTK02JL55Q | CDS | 554 | 1218 | + | 0.252874 | |
g9737 | DLA_10870 | GLQOFTK02JL55Q | CDS | 2057 | 1113 | + | 0.299191 | |
g9738 | DLA_10871 | GLQOFTK02JL55Q | CDS | 3263 | 1593 | - | 0.323917 | |
g9739 | DLA_10872 | GLQOFTK02JL55Q | CDS | 6333 | 3564 | + | 0.307239 | |
g974 | DLA_01083 | F4PJNLW01A00V1 | CDS | 770184 | 1392 | + | 0.280172 | |
g9740 | DLA_10873 | GLQOFTK02JL55Q | CDS | 10237 | 3756 | + | 0.273429 | |
g9741 | DLA_10874 | GLQOFTK02JL55Q | CDS | 14256 | 312 | + | 0.336538 | |
g9742 | DLA_11829 | GLQOFTK02JL55Q | CDS | 14710 | 936 | + | 0.369658 | |
g9743 | DLA_10875 | GLQOFTK02JL55Q | CDS | 15675 | 519 | + | 0.327553 | |
g9744 | DLA_10878 | GLQOFTK02JL55Q | CDS | 18609 | 327 | - | 0.33945 | |
g9745 | DLA_10880 | GLQOFTK02JL55Q | CDS | 19590 | 3366 | - | 0.361854 | |
g9746 | DLA_10881 | GLQOFTK02JL55Q | CDS | 25693 | 465 | + | 0.251613 | |
g9747 | DLA_10882 | GLQOFTK02JL55Q | CDS | 26748 | 2031 | + | 0.265387 | |
g9748 | DLA_10883 | GLQOFTK02JL55Q | CDS | 28870 | 2109 | + | 0.297771 | |
g9749 | DLA_10884 | GLQOFTK02JL55Q | CDS | 31163 | 915 | - | 0.310383 | |
g975 | DLA_01084 | F4PJNLW01A00V1 | CDS | 771802 | 2058 | - | 0.322157 | |
g9750 | DLA_10885 | GLQOFTK02JL55Q | CDS | 32776 | 4392 | + | 0.307605 | |
g9751 | DLA_10886 | GLQOFTK02JL55Q | CDS | 37305 | 1005 | - | 0.294527 | |
g9752 | DLA_10887 | GLQOFTK02JL55Q | CDS | 38349 | 870 | + | 0.257471 | |
g9753 | DLA_10888 | GLQOFTK02JL55Q | CDS | 39721 | 3369 | - | 0.322648 | |
g9754 | DLA_10889 | GLQOFTK02JL55Q | CDS | 43907 | 2400 | - | 0.28625 | |
g9755 | DLA_10890 | GLQOFTK02JL55Q | CDS | 46977 | 957 | + | 0.327064 | |
g9756 | DLA_10891 | GLQOFTK02JL55Q | CDS | 49780 | 693 | + | 0.300144 | |
g9757 | DLA_10892 | GLQOFTK02JL55Q | CDS | 50940 | 1017 | + | 0.292035 | |
g9758 | DLA_10893 | GLQOFTK02JL55Q | CDS | 52154 | 2799 | + | 0.335834 | |
g9759 | DLA_10894 | GLQOFTK02JL55Q | CDS | 55164 | 3003 | - | 0.290043 | |
g976 | DLA_01085 | F4PJNLW01A00V1 | CDS | 774402 | 1425 | + | 0.29614 | |
g9760 | DLA_10895 | GLQOFTK02JL55Q | CDS | 58557 | 1233 | + | 0.321979 | |
g9761 | DLA_10896 | GLQOFTK02JL55Q | CDS | 59863 | 855 | - | 0.308772 | |
g9762 | DLA_10897 | GLQOFTK02JL55Q | CDS | 63590 | 1998 | + | 0.307808 | |
g9763 | DLA_10898 | GLQOFTK02JL55Q | CDS | 66060 | 1236 | + | 0.307443 | |
g9764 | DLA_10899 | GLQOFTK02JL55Q | CDS | 67729 | 2514 | + | 0.334527 | |
g9765 | DLA_11830 | GLQOFTK02JL55Q | CDS | 70794 | 612 | - | 0.330065 | |
g9766 | DLA_10900 | GLQOFTK02JL55Q | CDS | 71824 | 864 | - | 0.304398 | |
g9767 | DLA_11831 | GLQOFTK02JL55Q | CDS | 72935 | 570 | - | 0.305263 | |
g9768 | DLA_10901 | GLQOFTK02JL55Q | CDS | 74205 | 1005 | - | 0.319403 | |
g9769 | DLA_10902 | GLQOFTK02JL55Q | CDS | 76087 | 1863 | + | 0.281267 | |
g977 | DLA_01087 | F4PJNLW01A00V1 | CDS | 776180 | 2457 | - | 0.293447 | |
g9770 | DLA_10903 | GLQOFTK02JL55Q | CDS | 78176 | 4608 | + | 0.298177 | |
g9771 | DLA_10904 | GLQOFTK02JL55Q | CDS | 83421 | 915 | - | 0.308197 | |
g9772 | DLA_10906 | GLQOFTK02JL55Q | CDS | 87239 | 1032 | + | 0.293605 | |
g9773 | DLA_10907 | GLQOFTK02JL55Q | CDS | 88899 | 249 | + | 0.305221 | |
g9774 | DLA_10908 | GLQOFTK02JL55Q | CDS | 89227 | 3039 | - | 0.367884 | |
g9775 | DLA_11832 | GLQOFTK02JL55Q | CDS | 92516 | 291 | - | 0.347079 | |
g9776 | DLA_10909 | GLQOFTK02JL55Q | CDS | 93508 | 807 | - | 0.307311 | |
g9777 | DLA_10911 | GLQOFTK02JL55Q | CDS | 94586 | 4047 | + | 0.308129 | |
g9778 | DLA_10912 | GLQOFTK02JL55Q | CDS | 99171 | 1221 | + | 0.283374 | |
g9779 | DLA_10913 | GLQOFTK02JL55Q | CDS | 100615 | 1128 | - | 0.35461 | |
g978 | DLA_01088 | F4PJNLW01A00V1 | CDS | 779353 | 1389 | + | 0.264939 | |
g9780 | DLA_10914 | GLQOFTK02JL55Q | CDS | 102400 | 2127 | - | 0.339445 | |
g9781 | DLA_11833 | GLQOFTK02JL55Q | CDS | 104982 | 399 | + | 0.275689 | |
g9782 | DLA_10915 | GLQOFTK02JL55Q | CDS | 106018 | 3444 | + | 0.299942 | |
g9783 | DLA_10916 | GLQOFTK02JL55Q | CDS | 109669 | 846 | + | 0.306147 | |
g9784 | DLA_10917 | GLQOFTK02JL55Q | CDS | 110602 | 3375 | - | 0.285926 | |
g9785 | DLA_10918 | GLQOFTK02JL55Q | CDS | 114371 | 1506 | - | 0.326029 | |
g9786 | DLA_10920 | GLQOFTK02JL55Q | CDS | 116759 | 981 | - | 0.244648 | |
g9787 | DLA_10921 | GLQOFTK02JL55Q | CDS | 117940 | 1812 | - | 0.339404 | |
g9788 | DLA_10922 | GLQOFTK02JL55Q | CDS | 120316 | 3048 | - | 0.331693 | |
g9789 | DLA_10923 | GLQOFTK02JL55Q | CDS | 123855 | 309 | + | 0.2589 | |
g979 | DLA_01089 | ortholog of mammalian ubxn7 (UBX domain-containing protein 7) contains a UBX domain found in ubiquitin-regulatory proteins | F4PJNLW01A00V1 | CDS | 781092 | 1422 | - | 0.291139 |
g9790 | DLA_10924 | GLQOFTK02JL55Q | CDS | 124410 | 3543 | + | 0.338978 | |
g9791 | DLA_10925 | GLQOFTK02JL55Q | CDS | 128102 | 7848 | - | 0.334225 | |
g9792 | DLA_10926 | GLQOFTK02JL55Q | CDS | 136760 | 2091 | - | 0.360593 | |
g9793 | DLA_10930 | GLQOFTK02JL55Q | CDS | 141638 | 1140 | + | 0.282456 | |
g9794 | DLA_10931 | GLQOFTK02JL55Q | CDS | 142970 | 522 | - | 0.318008 | |
g9795 | DLA_10933 | GLQOFTK02JL55Q | CDS | 145056 | 2145 | - | 0.324009 | |
g9796 | DLA_10934 | GLQOFTK02JL55Q | CDS | 148212 | 882 | - | 0.324263 | |
g9797 | DLA_10937 | GLQOFTK02JL55Q | CDS | 150107 | 822 | + | 0.344282 | |
g9798 | DLA_10938 | GLQOFTK02JL55Q | CDS | 151132 | 1005 | - | 0.349254 | |
g9799 | DLA_10939 | GLQOFTK02JL55Q | CDS | 152479 | 1332 | + | 0.339339 | |
g98 | DLA_00113 | contig05409_1.exp | CDS | 227338 | 1422 | - | 0.359353 | |
g980 | DLA_01090 | F4PJNLW01A00V1 | CDS | 782778 | 2493 | - | 0.347774 | |
g9800 | DLA_10940 | GLQOFTK02JL55Q | CDS | 153859 | 897 | - | 0.283166 | |
g9801 | DLA_10942 | GLQOFTK02JL55Q | CDS | 155102 | 4476 | + | 0.317471 | |
g9802 | DLA_10943 | GLQOFTK02JL55Q | CDS | 160201 | 1782 | + | 0.323232 | |
g9803 | DLA_10944 | GLQOFTK02JL55Q | CDS | 162014 | 801 | - | 0.333333 | |
g9804 | DLA_10945 | GLQOFTK02JL55Q | CDS | 163033 | 1044 | + | 0.26341 | |
g9805 | DLA_11834 | GLQOFTK02JL55Q | CDS | 164243 | 648 | + | 0.246914 | |
g9806 | DLA_10946 | GLQOFTK02JL55Q | CDS | 164996 | 1188 | - | 0.315657 | |
g9807 | DLA_10948 | GLQOFTK02JL55Q | CDS | 167180 | 7812 | - | 0.34959 | |
g9808 | DLA_10949 | GLQOFTK02JL55Q | CDS | 175992 | 2862 | + | 0.368623 | |
g9809 | DLA_11835 | GLQOFTK02JL55Q | CDS | 179244 | 1476 | + | 0.28523 | |
g981 | DLA_01091 | F4PJNLW01A00V1 | CDS | 785704 | 2373 | + | 0.337969 | |
g9810 | DLA_10950 | GLQOFTK02JL55Q | CDS | 180772 | 792 | - | 0.27904 | |
g9811 | DLA_10953 | GLQOFTK02JL55Q | CDS | 182880 | 912 | - | 0.384868 | |
g9812 | DLA_11836 | GLQOFTK02JL55Q | CDS | 184802 | 294 | - | 0.258503 | |
g9813 | DLA_10954 | catalyzes the reaction ATP L-glutamate tRNAGlu AMP diphosphate L-glutamyl-tRNAGlu | GLQOFTK02JL55Q | CDS | 185237 | 1698 | - | 0.309776 |
g9814 | DLA_10955 | GLQOFTK02JL55Q | CDS | 187288 | 1419 | + | 0.334743 | |
g9815 | DLA_10956 | GLQOFTK02JL55Q | CDS | 188863 | 972 | - | 0.333333 | |
g9816 | DLA_10957 | GLQOFTK02JL55Q | CDS | 190429 | 1911 | + | 0.300366 | |
g9817 | DLA_10958 | GLQOFTK02JL55Q | CDS | 192885 | 444 | + | 0.31982 | |
g9818 | DLA_10959 | GLQOFTK02JL55Q | CDS | 194676 | 324 | - | 0.265432 | |
g9819 | DLA_10960 | GLQOFTK02JL55Q | CDS | 195158 | 1359 | + | 0.309051 | |
g982 | DLA_01092 | F4PJNLW01A00V1 | CDS | 788419 | 816 | + | 0.300245 | |
g9820 | DLA_10961 | GLQOFTK02JL55Q | CDS | 197335 | 471 | + | 0.312102 | |
g9821 | DLA_11837 | GLQOFTK02JL55Q | CDS | 197894 | 216 | + | 0.287037 | |
g9822 | DLA_10962 | GLQOFTK02JL55Q | CDS | 198296 | 678 | - | 0.284661 | |
g9823 | DLA_10963 | GLQOFTK02JL55Q | CDS | 199771 | 906 | + | 0.333333 | |
g9824 | DLA_10964 | GLQOFTK02JL55Q | CDS | 200934 | 5226 | + | 0.326445 | |
g9825 | DLA_10965 | GLQOFTK02JL55Q | CDS | 206420 | 1035 | - | 0.312077 | |
g9826 | DLA_10966 | GLQOFTK02JL55Q | CDS | 207745 | 2394 | + | 0.326232 | |
g9827 | DLA_10967 | GLQOFTK02JL55Q | CDS | 210284 | 876 | + | 0.297945 | |
g9828 | DLA_10968 | GLQOFTK02JL55Q | CDS | 211592 | 1659 | + | 0.380952 | |
g9829 | DLA_10969 | GLQOFTK02JL55Q | CDS | 213688 | 1734 | + | 0.375433 | |
g983 | DLA_01093 | F4PJNLW01A00V1 | CDS | 790191 | 747 | + | 0.368139 | |
g9830 | DLA_10970 | GLQOFTK02JL55Q | CDS | 215652 | 2241 | + | 0.289603 | |
g9831 | DLA_10971 | GLQOFTK02JL55Q | CDS | 218229 | 2355 | + | 0.325265 | |
g9832 | DLA_10972 | GLQOFTK02JL55Q | CDS | 220824 | 417 | - | 0.342926 | |
g9833 | DLA_10973 | GLQOFTK02JL55Q | CDS | 221712 | 990 | - | 0.378788 | |
g9834 | DLA_10974 | GLQOFTK02JL55Q | CDS | 223375 | 3783 | + | 0.317209 | |
g9835 | DLA_10976 | GLQOFTK02JL55Q | CDS | 227285 | 1164 | - | 0.274914 | |
g9836 | DLA_10977 | GLQOFTK02JL55Q | CDS | 228806 | 1806 | + | 0.347176 | |
g9837 | DLA_10978 | GLQOFTK02JL55Q | CDS | 231106 | 378 | - | 0.277778 | |
g9838 | DLA_10980 | GLQOFTK02JL55Q | CDS | 231734 | 777 | + | 0.341055 | |
g9839 | DLA_10981 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane has similarity to the calcium-dependent mitochondrial aspartate and glutamate carriers aralar1 and 2 (slc25A12 and 13) but does not contain a EF-hand calcium-binding domain such as | GLQOFTK02JL55Q | CDS | 232961 | 2193 | + | 0.367533 |
g984 | DLA_01094 | F4PJNLW01A00V1 | CDS | 792035 | 897 | + | 0.294314 | |
g9840 | DLA_10982 | GLQOFTK02JL55Q | CDS | 235595 | 1380 | + | 0.392754 | |
g9841 | DLA_10984 | GLQOFTK02JL55Q | CDS | 237648 | 519 | - | 0.354528 | |
g9842 | DLA_10986 | GLQOFTK02JL55Q | CDS | 239839 | 6612 | + | 0.296733 | |
g9843 | DLA_10987 | GLQOFTK02JL55Q | CDS | 246652 | 1692 | + | 0.258274 | |
g9844 | DLA_10988 | elongation factor 1 alpha one of two genes coding for the same protein binds and bundles F-actin | GLQOFTK02JL55Q | CDS | 248441 | 1365 | - | 0.378755 |
g9845 | DLA_10989 | GLQOFTK02JL55Q | CDS | 250366 | 1527 | + | 0.316306 | |
g9846 | DLA_10990 | GLQOFTK02JL55Q | CDS | 252028 | 1686 | + | 0.306643 | |
g9847 | DLA_10991 | GLQOFTK02JL55Q | CDS | 253846 | 7749 | - | 0.300039 | |
g9848 | DLA_10992 | GLQOFTK02JL55Q | CDS | 262484 | 300 | + | 0.296667 | |
g9849 | DLA_10993 | GLQOFTK02JL55Q | CDS | 262907 | 1407 | - | 0.32978 | |
g985 | DLA_01095 | F4PJNLW01A00V1 | CDS | 793082 | 369 | + | 0.311653 | |
g9850 | DLA_10994 | GLQOFTK02JL55Q | CDS | 264475 | 1245 | + | 0.320482 | |
g9851 | DLA_10995 | GLQOFTK02JL55Q | CDS | 266307 | 1428 | - | 0.29972 | |
g9852 | DLA_10996 | GLQOFTK02JL55Q | CDS | 267819 | 1119 | + | 0.276139 | |
g9853 | DLA_10997 | protein serinethreonine phosphatase required for chemotaxis and development suppresses the | GLQOFTK02JL55Q | CDS | 269264 | 924 | - | 0.338745 |
g9854 | DLA_10998 | GLQOFTK02JL55Q | CDS | 270723 | 1974 | + | 0.369301 | |
g9855 | DLA_10999 | GLQOFTK02JL55Q | CDS | 273237 | 996 | + | 0.303213 | |
g9856 | DLA_11000 | GLQOFTK02JL55Q | CDS | 274467 | 2949 | + | 0.302475 | |
g9857 | DLA_11002 | GLQOFTK02JL55Q | CDS | 277439 | 1440 | - | 0.271528 | |
g9858 | DLA_11003 | GLQOFTK02JL55Q | CDS | 279254 | 222 | - | 0.238739 | |
g9859 | DLA_11004 | GLQOFTK02JL55Q | CDS | 280021 | 1545 | - | 0.374757 | |
g986 | DLA_01096 | F4PJNLW01A00V1 | CDS | 794819 | 3531 | + | 0.353724 | |
g9860 | DLA_11005 | GLQOFTK02JL55Q | CDS | 282149 | 861 | - | 0.369338 | |
g9861 | DLA_11006 | GLQOFTK02JL55Q | CDS | 283411 | 981 | + | 0.352701 | |
g9862 | DLA_11007 | GLQOFTK02JL55Q | CDS | 285054 | 6018 | - | 0.295115 | |
g9863 | DLA_11008 | GLQOFTK02JL55Q | CDS | 291397 | 2823 | - | 0.33971 | |
g9864 | DLA_11009 | GLQOFTK02JL55Q | CDS | 295117 | 2361 | - | 0.350275 | |
g9865 | DLA_11010 | GLQOFTK02JL55Q | CDS | 297959 | 1536 | - | 0.311198 | |
g9866 | DLA_11011 | GLQOFTK02JL55Q | CDS | 300619 | 1866 | - | 0.341908 | |
g9867 | DLA_11012 | GLQOFTK02JL55Q | CDS | 303415 | 648 | + | 0.341049 | |
g9868 | DLA_11013 | GLQOFTK02JL55Q | CDS | 304566 | 594 | + | 0.329966 | |
g9869 | DLA_11014 | GLQOFTK02JL55Q | CDS | 305354 | 1491 | - | 0.299128 | |
g987 | DLA_11460 | F4PJNLW01A00V1 | CDS | 798527 | 3270 | + | 0.355352 | |
g9870 | DLA_11015 | GLQOFTK02JL55Q | CDS | 307354 | 3702 | + | 0.337655 | |
g9871 | DLA_11016 | GLQOFTK02JL55Q | CDS | 311209 | 948 | - | 0.266878 | |
g9872 | DLA_11019 | GLQOFTK02JL55Q | CDS | 314302 | 1431 | + | 0.32914 | |
g9873 | DLA_11020 | GLQOFTK02JL55Q | CDS | 315820 | 4698 | - | 0.346105 | |
g9874 | DLA_11022 | GLQOFTK02JL55Q | CDS | 321065 | 1380 | + | 0.294928 | |
g9875 | DLA_11023 | GLQOFTK02JL55Q | CDS | 322954 | 2853 | - | 0.340694 | |
g9876 | DLA_11024 | catalyzes the reaction L-asparagine Hsub2subO L-aspartate NHsub3sub | GLQOFTK02JL55Q | CDS | 326188 | 1128 | + | 0.35195 |
g9877 | DLA_11025 | GLQOFTK02JL55Q | CDS | 327533 | 1737 | + | 0.352332 | |
g9878 | DLA_11026 | GLQOFTK02JL55Q | CDS | 329729 | 1578 | + | 0.271863 | |
g9879 | DLA_11838 | GLQOFTK02JL55Q | CDS | 331618 | 480 | - | 0.389583 | |
g988 | DLA_01097 | F4PJNLW01A00V1 | CDS | 802039 | 576 | - | 0.369792 | |
g9880 | DLA_11027 | GLQOFTK02JL55Q | CDS | 332870 | 549 | - | 0.335155 | |
g9881 | DLA_11028 | GLQOFTK02JL55Q | CDS | 334040 | 3078 | + | 0.393762 | |
g9882 | DLA_11029 | GLQOFTK02JL55Q | CDS | 337473 | 615 | + | 0.245528 | |
g9883 | DLA_11030 | GLQOFTK02JL55Q | CDS | 338848 | 1359 | + | 0.289919 | |
g9884 | DLA_11031 | GLQOFTK02JL55Q | CDS | 340309 | 936 | + | 0.311966 | |
g9885 | DLA_11032 | GLQOFTK02JL55Q | CDS | 341336 | 444 | + | 0.304054 | |
g9886 | DLA_11033 | GLQOFTK02JL55Q | CDS | 341901 | 513 | - | 0.300195 | |
g9887 | DLA_11034 | GLQOFTK02JL55Q | CDS | 342663 | 873 | + | 0.303551 | |
g9888 | DLA_11035 | GLQOFTK02JL55Q | CDS | 344527 | 1569 | + | 0.342256 | |
g9889 | DLA_11037 | GLQOFTK02JL55Q | CDS | 347985 | 3282 | + | 0.343388 | |
g989 | DLA_01098 | F4PJNLW01A00V1 | CDS | 803485 | 516 | - | 0.286822 | |
g9890 | DLA_11038 | GLQOFTK02JL55Q | CDS | 351729 | 2700 | + | 0.317778 | |
g9891 | DLA_11039 | GLQOFTK02JL55Q | CDS | 354517 | 1455 | - | 0.318213 | |
g9892 | DLA_11040 | GLQOFTK02JL55Q | CDS | 356281 | 3630 | + | 0.320661 | |
g9893 | DLA_11041 | GLQOFTK02JL55Q | CDS | 360080 | 2334 | - | 0.342759 | |
g9894 | DLA_11042 | GLQOFTK02JL55Q | CDS | 362714 | 1011 | + | 0.29179 | |
g9895 | DLA_11043 | GLQOFTK02JL55Q | CDS | 363874 | 1050 | + | 0.300952 | |
g9896 | DLA_11044 | GLQOFTK02JL55Q | CDS | 365203 | 417 | + | 0.318945 | |
g9897 | DLA_11046 | GLQOFTK02JL55Q | CDS | 366394 | 2460 | - | 0.367886 | |
g9898 | DLA_11047 | GLQOFTK02JL55Q | CDS | 370035 | 2007 | + | 0.305431 | |
g9899 | DLA_11048 | GLQOFTK02JL55Q | CDS | 372268 | 2136 | + | 0.361423 | |
g99 | DLA_00114 | contig05409_1.exp | CDS | 232890 | 1314 | + | 0.31583 | |
g990 | DLA_01099 | F4PJNLW01A00V1 | CDS | 804435 | 1251 | - | 0.311751 | |
g9900 | DLA_11049 | GLQOFTK02JL55Q | CDS | 374658 | 1362 | + | 0.314244 | |
g9901 | DLA_11050 | GLQOFTK02JL55Q | CDS | 376118 | 957 | - | 0.322884 | |
g9902 | DLA_11051 | GLQOFTK02JL55Q | CDS | 377635 | 501 | - | 0.299401 | |
g9903 | DLA_11052 | GLQOFTK02JL55Q | CDS | 378327 | 1635 | - | 0.322324 | |
g9904 | DLA_11053 | GLQOFTK02JL55Q | CDS | 381222 | 3312 | + | 0.348128 | |
g9905 | DLA_11054 | GLQOFTK02JL55Q | CDS | 384841 | 2220 | - | 0.293694 | |
g9906 | DLA_11055 | GLQOFTK02JL55Q | CDS | 387500 | 4497 | - | 0.308428 | |
g9907 | DLA_11056 | GLQOFTK02JL55Q | CDS | 392228 | 837 | + | 0.32497 | |
g9908 | DLA_11057 | GLQOFTK02JL55Q | CDS | 393344 | 1809 | + | 0.301824 | |
g9909 | DLA_11058 | GLQOFTK02JL55Q | CDS | 395316 | 990 | - | 0.390909 | |
g991 | DLA_01100 | F4PJNLW01A00V1 | CDS | 805807 | 1434 | - | 0.35007 | |
g9910 | DLA_11839 | GLQOFTK02JL55Q | CDS | 396356 | 237 | - | 0.295359 | |
g9911 | DLA_11059 | GLQOFTK02JL55Q | CDS | 397671 | 1128 | + | 0.350177 | |
g9912 | DLA_11060 | subunit of TFIID and SAGA complexes involved in RNA polymerase II transcription initiation and in chromatin modification | GLQOFTK02JL55Q | CDS | 398897 | 951 | - | 0.360673 |
g9913 | DLA_11840 | weakly similar to hssA2C7E family protein N terminal exon is 10 nt rather than 13 as the other genes of that family | GLQOFTK02JL55Q | CDS | 400531 | 210 | + | 0.380952 |
g9914 | DLA_11061 | GLQOFTK02JL55Q | CDS | 401435 | 5616 | + | 0.371973 | |
g9915 | DLA_11062 | GLQOFTK02JL55Q | CDS | 407305 | 1269 | - | 0.291568 | |
g9916 | DLA_11063 | GLQOFTK02JL55Q | CDS | 409678 | 3450 | + | 0.31913 | |
g9917 | DLA_11064 | GLQOFTK02JL55Q | CDS | 413573 | 351 | + | 0.333333 | |
g9918 | DLA_11065 | GLQOFTK02JL55Q | CDS | 414444 | 1878 | + | 0.280085 | |
g9919 | DLA_11066 | GLQOFTK02JL55Q | CDS | 416819 | 1689 | + | 0.288928 | |
g992 | DLA_01101 | F4PJNLW01A00V1 | CDS | 807902 | 7191 | + | 0.329996 | |
g9920 | DLA_11067 | GLQOFTK02JL55Q | CDS | 418933 | 1692 | + | 0.287234 | |
g9921 | DLA_11068 | GLQOFTK02JL55Q | CDS | 420714 | 1692 | + | 0.29078 | |
g9922 | DLA_11069 | GLQOFTK02JL55Q | CDS | 422552 | 738 | - | 0.340108 | |
g9923 | DLA_11070 | GLQOFTK02JL55Q | CDS | 424161 | 3399 | + | 0.340394 | |
g9924 | DLA_11071 | GLQOFTK02JL55Q | CDS | 428140 | 684 | + | 0.314327 | |
g9925 | DLA_11072 | GLQOFTK02JL55Q | CDS | 429091 | 369 | - | 0.273713 | |
g9926 | DLA_11073 | GLQOFTK02JL55Q | CDS | 430094 | 1266 | - | 0.337283 | |
g9927 | DLA_11074 | GLQOFTK02JL55Q | CDS | 431503 | 573 | + | 0.284468 | |
g9928 | DLA_11075 | GLQOFTK02JL55Q | CDS | 432211 | 1164 | - | 0.358247 | |
g9929 | DLA_11076 | GLQOFTK02JL55Q | CDS | 433901 | 11370 | + | 0.340106 | |
g993 | DLA_01103 | similar to UPF0451 family proteins contains 3 predicted transmembrane domains there is an almost identical gene | F4PJNLW01A00V1 | CDS | 816787 | 357 | - | 0.358543 |
g9930 | DLA_11077 | GLQOFTK02JL55Q | CDS | 445386 | 1203 | - | 0.323358 | |
g9931 | DLA_11078 | GLQOFTK02JL55Q | CDS | 446870 | 1413 | - | 0.314225 | |
g9932 | DLA_11079 | GLQOFTK02JL55Q | CDS | 449060 | 2265 | + | 0.335099 | |
g9933 | DLA_11080 | involved in vesicle trafficking in yeast and mammals expressed in endosome | GLQOFTK02JL55Q | CDS | 451780 | 636 | + | 0.339623 |
g9934 | DLA_11081 | GLQOFTK02JL55Q | CDS | 452769 | 1713 | - | 0.308815 | |
g9935 | DLA_11082 | GLQOFTK02JL55Q | CDS | 454717 | 4041 | + | 0.330859 | |
g9936 | DLA_11083 | GLQOFTK02JL55Q | CDS | 459392 | 993 | + | 0.32427 | |
g9937 | DLA_11084 | GLQOFTK02JL55Q | CDS | 460990 | 558 | + | 0.25448 | |
g9938 | DLA_11841 | GLQOFTK02JL55Q | CDS | 461619 | 1854 | - | 0.325243 | |
g9939 | DLA_11085 | GLQOFTK02JL55Q | CDS | 463697 | 3456 | - | 0.311343 | |
g994 | DLA_01104 | F4PJNLW01A00V1 | CDS | 817343 | 3006 | - | 0.311045 | |
g9940 | DLA_11086 | GLQOFTK02JL55Q | CDS | 467667 | 1395 | - | 0.355556 | |
g9941 | DLA_11087 | GLQOFTK02JL55Q | CDS | 469288 | 1413 | - | 0.332626 | |
g9942 | DLA_11089 | GLQOFTK02JL55Q | CDS | 471702 | 1158 | + | 0.303109 | |
g9943 | DLA_11090 | GLQOFTK02JL55Q | CDS | 472932 | 606 | - | 0.331683 | |
g9944 | DLA_11091 | GLQOFTK02JL55Q | CDS | 473787 | 621 | - | 0.31401 | |
g9945 | DLA_11092 | GLQOFTK02JL55Q | CDS | 474597 | 2394 | + | 0.327485 | |
g9946 | DLA_11093 | GLQOFTK02JL55Q | CDS | 477370 | 1752 | - | 0.292237 | |
g9947 | DLA_11094 | GLQOFTK02JL55Q | CDS | 479457 | 5568 | - | 0.349497 | |
g9948 | DLA_11095 | GLQOFTK02JL55Q | CDS | 485869 | 6384 | + | 0.344142 | |
g9949 | DLA_11096 | putative ortholog of the poorly conserved mediator of RNA polymerase II transcription subunit 27 (metazoa) or 3 (fungi) the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | GLQOFTK02JL55Q | CDS | 492467 | 1281 | + | 0.326308 |
g995 | DLA_01105 | F4PJNLW01A00V1 | CDS | 820466 | 2223 | + | 0.332883 | |
g9950 | DLA_11097 | GLQOFTK02JL55Q | CDS | 494116 | 2682 | - | 0.316182 | |
g9951 | DLA_11098 | GLQOFTK02JL55Q | CDS | 497059 | 1659 | - | 0.271851 | |
g9952 | DLA_11101 | GLQOFTK02JL55Q | CDS | 501663 | 1545 | + | 0.331392 | |
g9953 | DLA_11102 | catalyzes the reaction ATP a long-chain carboxylic acid CoA AMP diphosphate an acyl-CoA mediates the retrieval of fatty acids from endosomes to the cytoplasm | GLQOFTK02JL55Q | CDS | 503773 | 1995 | + | 0.381955 |
g9954 | DLA_11104 | GLQOFTK02JL55Q | CDS | 507261 | 888 | + | 0.313063 | |
g9955 | DLA_11105 | GLQOFTK02JL55Q | CDS | 508193 | 1704 | - | 0.31162 | |
g9956 | DLA_11106 | GLQOFTK02JL55Q | CDS | 510499 | 4143 | - | 0.34685 | |
g9957 | DLA_11107 | GLQOFTK02JL55Q | CDS | 515358 | 1275 | - | 0.381176 | |
g9958 | DLA_11842 | GLQOFTK02JL55Q | CDS | 516748 | 2367 | - | 0.368399 | |
g9959 | DLA_11108 | GLQOFTK02JL55Q | CDS | 519959 | 1137 | - | 0.333333 | |
g996 | DLA_01106 | F4PJNLW01A00V1 | CDS | 823363 | 1206 | + | 0.35738 | |
g9960 | DLA_11110 | GLQOFTK02JL55Q | CDS | 521788 | 3342 | - | 0.361759 | |
g9961 | DLA_11111 | GLQOFTK02JL55Q | CDS | 525328 | 519 | - | 0.300578 | |
g9962 | DLA_11112 | GLQOFTK02JL55Q | CDS | 526182 | 1782 | + | 0.292929 | |
g9963 | DLA_11113 | GLQOFTK02JL55Q | CDS | 528033 | 660 | + | 0.313636 | |
g9964 | DLA_11114 | GLQOFTK02JL55Q | CDS | 528893 | 810 | + | 0.322222 | |
g9965 | DLA_11115 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis | GLQOFTK02JL55Q | CDS | 530149 | 2103 | + | 0.32525 |
g9966 | DLA_11116 | GLQOFTK02JL55Q | CDS | 532766 | 414 | + | 0.316425 | |
g9967 | DLA_11117 | GLQOFTK02JL55Q | CDS | 533625 | 825 | - | 0.37697 | |
g9968 | DLA_11118 | GLQOFTK02JL55Q | CDS | 534853 | 912 | + | 0.380482 | |
g9969 | DLA_11119 | GLQOFTK02JL55Q | CDS | 535778 | 1548 | - | 0.288114 | |
g997 | DLA_01108 | F4PJNLW01A00V1 | CDS | 825611 | 1149 | + | 0.302872 | |
g9970 | DLA_11121 | GLQOFTK02JL55Q | CDS | 537609 | 1725 | + | 0.302609 | |
g9971 | DLA_11122 | GLQOFTK02JL55Q | CDS | 539362 | 1269 | - | 0.34673 | |
g9972 | DLA_11125 | GLQOFTK02JL55Q | CDS | 541515 | 867 | + | 0.322953 | |
g9973 | DLA_11127 | GLQOFTK02JL55Q | CDS | 542490 | 1047 | - | 0.280802 | |
g9974 | DLA_11128 | GLQOFTK02JL55Q | CDS | 543681 | 2217 | - | 0.299955 | |
g9975 | DLA_11129 | GLQOFTK02JL55Q | CDS | 546141 | 2235 | - | 0.298881 | |
g9976 | DLA_11843 | GLQOFTK02JL55Q | CDS | 548489 | 378 | + | 0.248677 | |
g9977 | DLA_11130 | GLQOFTK02JL55Q | CDS | 549197 | 2079 | + | 0.339105 | |
g9978 | DLA_11131 | GLQOFTK02JL55Q | CDS | 551557 | 3174 | + | 0.334594 | |
g9979 | DLA_11132 | GLQOFTK02JL55Q | CDS | 554960 | 303 | + | 0.280528 | |
g998 | DLA_11461 | F4PJNLW01A00V1 | CDS | 826790 | 339 | - | 0.230089 | |
g9980 | DLA_11133 | GLQOFTK02JL55Q | CDS | 555380 | 903 | - | 0.284607 | |
g9981 | DLA_11134 | GLQOFTK02JL55Q | CDS | 556346 | 198 | - | 0.338384 | |
g9982 | DLA_11135 | GLQOFTK02JL55Q | CDS | 557193 | 588 | + | 0.294218 | |
g9983 | DLA_11136 | similar to syntaxin 16 a subfamily of the SNARE family (Soluble NSF Attachment Protein REceptor) involved in vesicle fusion | GLQOFTK02JL55Q | CDS | 557966 | 924 | - | 0.311688 |
g9984 | DLA_11137 | GLQOFTK02JL55Q | CDS | 559331 | 1464 | + | 0.359973 | |
g9985 | DLA_11138 | GLQOFTK02JL55Q | CDS | 561405 | 1842 | + | 0.325733 | |
g9986 | DLA_11139 | GLQOFTK02JL55Q | CDS | 563602 | 1473 | + | 0.319756 | |
g9987 | DLA_11140 | GLQOFTK02JL55Q | CDS | 565294 | 384 | - | 0.320312 | |
g9988 | DLA_11141 | GLQOFTK02JL55Q | CDS | 565699 | 345 | - | 0.292754 | |
g9989 | DLA_11143 | GLQOFTK02JL55Q | CDS | 566515 | 252 | + | 0.384921 | |
g999 | DLA_01109 | F4PJNLW01A00V1 | CDS | 827257 | 1368 | - | 0.33845 | |
g9990 | DLA_11144 | GLQOFTK02JL55Q | CDS | 568126 | 1911 | - | 0.349032 | |
g9991 | DLA_11145 | GLQOFTK02JL55Q | CDS | 570985 | 1212 | + | 0.320957 | |
g9992 | DLA_11146 | GLQOFTK02JL55Q | CDS | 572480 | 1254 | - | 0.371611 | |
g9993 | DLA_11147 | similar to S. cerevisiae SHQ1 which is required for box HACA small nucleolar ribonucleoprotein particle biogenesis contains one CS domain | GLQOFTK02JL55Q | CDS | 576182 | 1689 | - | 0.292481 |
g9994 | DLA_11148 | GLQOFTK02JL55Q | CDS | 578157 | 810 | + | 0.290123 | |
g9995 | DLA_11149 | GLQOFTK02JL55Q | CDS | 579099 | 1845 | - | 0.302439 | |
g9996 | DLA_11151 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family contains RasGEF nucleotide exchange factor domain | GLQOFTK02JL55Q | CDS | 582167 | 2604 | + | 0.355607 |
g9997 | DLA_11154 | introduces a double bond at the delta position of fatty acids during the biosynthesis of monounsaturated fatty acids there is a second copy of this gene | GLQOFTK02JL55Q | CDS | 586002 | 2256 | + | 0.370567 |
g9998 | DLA_11155 | GLQOFTK02JL55Q | CDS | 588614 | 1824 | - | 0.356908 | |
g9999 | DLA_11844 | belongs to the drugmetabolite transporter superfamily similar to human SLC35D1 (UDP-glucuronic acidUDP-N-acetylgalactosamine transporter) and S. cerevisiae VRG4 (GDP-mannose transporter 1) contains 8 putative transmembrane domains | GLQOFTK02JL55Q | CDS | 591072 | 942 | - | 0.321656 |