Gene list
Applied filters:
COG category: General function prediction only
Organism: Dictyostelium lacteum
Number of genes found: 930
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 |
g10005 | DLA_11162 | GLQOFTK02JL55Q | CDS | 599710 | 489 | - | 0.345603 | |
g10012 | DLA_11170 | GLQOFTK02JL55Q | CDS | 610356 | 3012 | - | 0.324701 | |
g10022 | DLA_11184 | GLQOFTK02JL55Q | CDS | 639909 | 2118 | - | 0.315392 | |
g10037 | DLA_11200 | GLQOFTK02JL55Q | CDS | 670673 | 543 | - | 0.366482 | |
g10039 | DLA_11202 | GLQOFTK02JL55Q | CDS | 674498 | 2307 | - | 0.316862 | |
g10041 | DLA_11204 | GLQOFTK02JL55Q | CDS | 678449 | 2382 | - | 0.304366 | |
g10043 | DLA_11206 | GLQOFTK02JL55Q | CDS | 683801 | 1260 | - | 0.281746 | |
g10044 | DLA_11207 | GLQOFTK02JL55Q | CDS | 685183 | 1239 | - | 0.297014 | |
g10075 | DLA_11248 | GLQOFTK02JL55Q | CDS | 756239 | 1938 | + | 0.288958 | |
g10086 | DLA_11259 | GLQOFTK02JL55Q | CDS | 780755 | 444 | + | 0.31982 | |
g10088 | DLA_11261 | GLQOFTK02JL55Q | CDS | 782177 | 3021 | + | 0.3095 | |
g10092 | DLA_11265 | GLQOFTK02JL55Q | CDS | 793666 | 870 | + | 0.342529 | |
g10106 | DLA_11284 | GLQOFTK02JL55Q | CDS | 823910 | 2478 | + | 0.307103 | |
g10107 | DLA_11285 | GLQOFTK02JL55Q | CDS | 826825 | 1434 | - | 0.340307 | |
g1011 | DLA_01122 | F4PJNLW01A00V1 | CDS | 858219 | 1269 | - | 0.327029 | |
g10170 | DLA_11362 | GLQOFTK02JL55Q | CDS | 965973 | 9987 | + | 0.323521 | |
g10172 | DLA_11364 | GLQOFTK02JL55Q | CDS | 978154 | 1128 | + | 0.332447 | |
g10173 | DLA_11366 | GLQOFTK02JL55Q | CDS | 980702 | 4050 | + | 0.339012 | |
g10175 | DLA_11368 | GLQOFTK02JL55Q | CDS | 988280 | 2964 | + | 0.354251 | |
g10205 | DLA_11401 | newcontig00824_1.exp | CDS | 14727 | 1668 | - | 0.285372 | |
g10210 | DLA_11407 | newcontig00824_1.exp | CDS | 23809 | 1209 | + | 0.303557 | |
g10218 | DLA_11414 | newcontig00824_1.exp | CDS | 49521 | 582 | + | 0.268041 | |
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 |
g1035 | DLA_01146 | F4PJNLW01A00V1 | CDS | 896334 | 2064 | + | 0.35126 | |
g1041 | DLA_01151 | F4PJNLW01A00V1 | CDS | 908661 | 2589 | + | 0.3708 | |
g1058 | DLA_01168 | F4PJNLW01A00V1 | CDS | 950617 | 2925 | + | 0.367863 | |
g1065 | DLA_01173 | F4PJNLW01A00V1 | CDS | 962636 | 1800 | - | 0.364444 | |
g1067 | DLA_01175 | F4PJNLW01A00V1 | CDS | 966915 | 1383 | - | 0.339118 | |
g1069 | DLA_01177 | F4PJNLW01A00V1 | CDS | 970180 | 2199 | + | 0.313324 | |
g1097 | DLA_01213 | F4PJNLW01A00V1 | CDS | 1034101 | 2148 | - | 0.366853 | |
g1128 | DLA_01245 | F4PJNLW01A00V1 | CDS | 1127299 | 963 | - | 0.34891 | |
g113 | DLA_00132 | contig05409_1.exp | CDS | 268227 | 543 | - | 0.289134 | |
g1130 | DLA_01247 | F4PJNLW01A00V1 | CDS | 1130542 | 1641 | + | 0.393053 | |
g114 | DLA_00133 | contig05409_1.exp | CDS | 269373 | 2523 | + | 0.328181 | |
g1163 | DLA_01280 | F4PJNLW01A00V1 | CDS | 1218879 | 3033 | + | 0.352456 | |
g1167 | DLA_01284 | F4PJNLW01A00V1 | CDS | 1225330 | 4419 | - | 0.342838 | |
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 |
g119 | DLA_00140 | contig05409_1.exp | CDS | 284072 | 360 | - | 0.302778 | |
g1193 | DLA_01312 | F4PJNLW01A00V1 | CDS | 1285676 | 1476 | + | 0.347561 | |
g122 | DLA_00143 | contig05409_1.exp | CDS | 286540 | 1053 | - | 0.309592 | |
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 |
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 |
g1264 | DLA_01388 | F4PJNLW01A00V1 | CDS | 1456550 | 3531 | + | 0.34013 | |
g1273 | DLA_01397 | F4PJNLW01AQJ8S | CDS | 8325 | 624 | + | 0.338141 | |
g1282 | DLA_01406 | F4PJNLW01AQJ8S | CDS | 31744 | 1515 | - | 0.316172 | |
g129 | DLA_00150 | contig05409_1.exp | CDS | 297512 | 885 | + | 0.319774 | |
g13 | DLA_00015 | contig05409_1.exp | CDS | 39192 | 2106 | - | 0.353276 | |
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 |
g131 | DLA_00152 | contig05409_1.exp | CDS | 301614 | 885 | + | 0.302825 | |
g1313 | DLA_01437 | F4PJNLW01B0TO9 | CDS | 48608 | 2238 | + | 0.289991 | |
g1319 | DLA_01443 | F4PJNLW01B0TO9 | CDS | 60158 | 1917 | - | 0.337507 | |
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 |
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 |
g1366 | DLA_01498 | F4PJNLW01B0TO9 | CDS | 178526 | 729 | - | 0.323731 | |
g1369 | DLA_01501 | F4PJNLW01B0TO9 | CDS | 182304 | 753 | - | 0.310757 | |
g1379 | DLA_01512 | F4PJNLW01B0TO9 | CDS | 203975 | 489 | - | 0.310838 | |
g1387 | DLA_11481 | F4PJNLW01B0TO9 | CDS | 220295 | 465 | + | 0.378495 | |
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 |
g1405 | DLA_11482 | F4PJNLW01B0TO9 | CDS | 250482 | 1833 | - | 0.371522 | |
g141 | DLA_00164 | contig05409_1.exp | CDS | 330453 | 939 | - | 0.369542 | |
g1411 | DLA_01547 | F4PJNLW01B0TO9 | CDS | 266367 | 1086 | + | 0.279006 | |
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 |
g142 | DLA_00165 | contig05409_1.exp | CDS | 332861 | 1857 | + | 0.325256 | |
g1428 | DLA_01566 | F4PJNLW01B0TO9 | CDS | 306077 | 1953 | - | 0.296979 | |
g1434 | DLA_01575 | F4PJNLW01B0TO9 | CDS | 320553 | 1359 | + | 0.290655 | |
g144 | DLA_00167 | contig05409_1.exp | CDS | 337749 | 2379 | - | 0.349306 | |
g1441 | DLA_01583 | F4PJNLW01B0TO9 | CDS | 339799 | 954 | + | 0.353249 | |
g1456 | DLA_01599 | F4PJNLW01B0TO9 | CDS | 376074 | 1890 | - | 0.346561 | |
g146 | DLA_00170 | contig05409_1.exp | CDS | 344785 | 1284 | - | 0.281153 | |
g1482 | DLA_01625 | F4PJNLW01B0TO9 | CDS | 420914 | 1470 | + | 0.314286 | |
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 |
g1537 | DLA_01685 | F4PJNLW01B0TO9 | CDS | 545256 | 10653 | + | 0.344692 | |
g154 | DLA_00180 | contig05409_1.exp | CDS | 359511 | 285 | - | 0.410526 | |
g1549 | DLA_11488 | F4PJNLW01B0TO9 | CDS | 580805 | 2460 | + | 0.387398 | |
g1550 | DLA_01697 | F4PJNLW01B0TO9 | CDS | 583710 | 5862 | + | 0.360628 | |
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 |
g1573 | DLA_01726 | F4PJNLW01B0TO9 | CDS | 633140 | 1266 | - | 0.332543 | |
g1591 | DLA_01745 | F4PJNLW01B0TO9 | CDS | 668508 | 2676 | + | 0.351644 | |
g1606 | DLA_01758 | F4PJNLW01B0TO9 | CDS | 707303 | 1743 | - | 0.327022 | |
g162 | DLA_00188 | contig05409_1.exp | CDS | 376542 | 1929 | + | 0.369103 | |
g1624 | DLA_01779 | F4PJNLW01B0TO9 | CDS | 740189 | 1752 | - | 0.358447 | |
g1646 | DLA_11494 | F4PJNLW01B0TO9 | CDS | 789076 | 1209 | + | 0.304384 | |
g1653 | DLA_01810 | F4PJNLW01B0TO9 | CDS | 812101 | 3480 | - | 0.308333 | |
g1658 | DLA_01815 | F4PJNLW01B0TO9 | CDS | 824502 | 2334 | + | 0.325621 | |
g1668 | DLA_01824 | F4PJNLW01B0TO9 | CDS | 846981 | 2520 | + | 0.289286 | |
g1669 | DLA_01825 | F4PJNLW01B0TO9 | CDS | 849641 | 1386 | + | 0.34127 | |
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 |
g1697 | DLA_01857 | F4PJNLW01B0TO9 | CDS | 918129 | 1437 | - | 0.347251 | |
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 |
g1716 | DLA_01876 | F4PJNLW01B0TO9 | CDS | 959478 | 1047 | - | 0.319007 | |
g1728 | DLA_01892 | F4PJNLW01B0TO9 | CDS | 988245 | 3060 | + | 0.32451 | |
g1735 | DLA_01900 | F4PJNLW01B0TO9 | CDS | 1008318 | 1452 | - | 0.409091 | |
g1737 | DLA_01902 | F4PJNLW01B0TO9 | CDS | 1011607 | 1668 | + | 0.340528 | |
g1757 | DLA_11499 | F4PJNLW01BNQ9D | CDS | 5154 | 582 | + | 0.364261 | |
g177 | DLA_00204 | contig05409_1.exp | CDS | 413350 | 1287 | + | 0.370629 | |
g1778 | DLA_01942 | F4PJNLW01C9MXC | CDS | 28299 | 4908 | + | 0.282192 | |
g178 | DLA_00205 | contig05409_1.exp | CDS | 414878 | 573 | - | 0.321117 | |
g1794 | DLA_01957 | F4PJNLW01C9MXC | CDS | 67445 | 2940 | + | 0.339796 | |
g1795 | DLA_01958 | F4PJNLW01C9MXC | CDS | 70975 | 4878 | + | 0.356294 | |
g1801 | DLA_01964 | F4PJNLW01C9MXC | CDS | 86554 | 222 | - | 0.31982 | |
g1833 | DLA_01998 | F4PJNLW01C9MXC | CDS | 161915 | 1767 | + | 0.367855 | |
g185 | DLA_00210 | contig05409_1.exp | CDS | 425058 | 3720 | + | 0.335753 | |
g1858 | DLA_02027 | F4PJNLW01CH19P | CDS | 35595 | 846 | + | 0.258865 | |
g1870 | DLA_02041 | F4PJNLW01CH19P | CDS | 61010 | 759 | - | 0.345191 | |
g1889 | DLA_02061 | F4PJNLW01CH19P | CDS | 96374 | 2988 | - | 0.351406 | |
g1898 | DLA_11513 | F4PJNLW01DERRH | CDS | 15159 | 2400 | + | 0.26375 | |
g1909 | DLA_02083 | F4PJNLW01DERRH | CDS | 52075 | 2175 | - | 0.308506 | |
g1910 | DLA_02084 | F4PJNLW01DERRH | CDS | 55904 | 642 | - | 0.397196 | |
g1921 | DLA_02099 | F4PJNLW01DERRH | CDS | 87436 | 1557 | - | 0.337829 | |
g1935 | DLA_02117 | F4PJNLW01DERRH | CDS | 124838 | 2322 | - | 0.314384 | |
g1943 | DLA_02126 | F4PJNLW01DERRH | CDS | 148360 | 1062 | - | 0.295669 | |
g1992 | DLA_02188 | F4PJNLW01DERRH | CDS | 265721 | 1827 | - | 0.313082 | |
g1998 | DLA_02194 | F4PJNLW01DERRH | CDS | 279280 | 1236 | + | 0.307443 | |
g2015 | DLA_02214 | F4PJNLW01DERRH | CDS | 317437 | 816 | - | 0.308824 | |
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 |
g2037 | DLA_02238 | F4PJNLW01DERRH | CDS | 365219 | 2718 | + | 0.337748 | |
g2041 | DLA_02243 | F4PJNLW01DERRH | CDS | 375261 | 840 | - | 0.308333 | |
g2049 | DLA_02252 | F4PJNLW01DERRH | CDS | 385220 | 5760 | + | 0.336111 | |
g2073 | DLA_02279 | F4PJNLW01DERRH | CDS | 435245 | 2370 | + | 0.353165 | |
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 |
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 |
g2116 | DLA_02331 | F4PJNLW01DERRH | CDS | 531195 | 5007 | + | 0.317955 | |
g2121 | DLA_02336 | F4PJNLW01DERRH | CDS | 543900 | 4401 | - | 0.329016 | |
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 |
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 |
g2131 | DLA_02346 | F4PJNLW01DERRH | CDS | 568066 | 1404 | + | 0.318376 | |
g2140 | DLA_02355 | F4PJNLW01DERRH | CDS | 582450 | 618 | + | 0.338188 | |
g2151 | DLA_02366 | F4PJNLW01DERRH | CDS | 604902 | 573 | + | 0.356021 | |
g2152 | DLA_02367 | F4PJNLW01DERRH | CDS | 605747 | 2016 | - | 0.364087 | |
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 |
g2173 | DLA_02393 | F4PJNLW01DERRH | CDS | 660867 | 1635 | + | 0.310703 | |
g2176 | DLA_02396 | F4PJNLW01DERRH | CDS | 667623 | 1647 | + | 0.313904 | |
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 |
g2201 | DLA_02422 | F4PJNLW01DL4V0 | CDS | 8281 | 1506 | + | 0.282869 | |
g2206 | DLA_02429 | F4PJNLW01EE5MJ | CDS | 154 | 1812 | + | 0.312362 | |
g2233 | DLA_02465 | F4PJNLW01EE5MJ | CDS | 73342 | 2217 | + | 0.28507 | |
g2238 | DLA_02472 | F4PJNLW01EE5MJ | CDS | 86819 | 1212 | - | 0.306931 | |
g2247 | DLA_02484 | catalyzes the reaction alpha-D-mannose 1-phosphate D-mannose 6-phosphate | F4PJNLW01EE5MJ | CDS | 104560 | 741 | + | 0.306343 |
g2260 | DLA_02495 | F4PJNLW01EE5MJ | CDS | 138880 | 2247 | - | 0.365821 | |
g2264 | DLA_02500 | F4PJNLW01EE5MJ | CDS | 158741 | 1872 | - | 0.313034 | |
g2281 | DLA_02523 | F4PJNLW01EE5MJ | CDS | 195831 | 1731 | + | 0.302137 | |
g2300 | DLA_02543 | F4PJNLW01EE5MJ | CDS | 242888 | 2571 | + | 0.317775 | |
g2306 | DLA_02550 | F4PJNLW01EE5MJ | CDS | 260902 | 897 | - | 0.338907 | |
g2307 | DLA_11525 | F4PJNLW01EE5MJ | CDS | 262147 | 885 | - | 0.310734 | |
g2317 | DLA_02562 | F4PJNLW01EE5MJ | CDS | 278398 | 1965 | - | 0.354198 | |
g2336 | DLA_02584 | F4PJNLW01EE5MJ | CDS | 316180 | 1230 | - | 0.321138 | |
g2343 | DLA_11526 | F4PJNLW01EE5MJ | CDS | 329858 | 801 | - | 0.324594 | |
g2355 | DLA_02605 | F4PJNLW01EE5MJ | CDS | 349403 | 1944 | + | 0.297839 | |
g2368 | DLA_02619 | F4PJNLW01EE5MJ | CDS | 375408 | 1371 | - | 0.408461 | |
g241 | DLA_00268 | contig05409_1.exp | CDS | 550759 | 1434 | - | 0.324268 | |
g2434 | DLA_02699 | F4PJNLW01EE5MJ | CDS | 525262 | 972 | + | 0.337449 | |
g2448 | DLA_02718 | F4PJNLW01EE5MJ | CDS | 555757 | 1047 | - | 0.321872 | |
g2455 | DLA_02725 | F4PJNLW01EE5MJ | CDS | 579082 | 2658 | - | 0.322047 | |
g246 | DLA_00273 | contig05409_1.exp | CDS | 559447 | 2865 | + | 0.37103 | |
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 |
g2465 | DLA_02735 | F4PJNLW01EE5MJ | CDS | 610087 | 1056 | - | 0.356061 | |
g2495 | DLA_02767 | F4PJNLW01EE5MJ | CDS | 685824 | 1446 | + | 0.375519 | |
g2507 | DLA_02780 | F4PJNLW01EE5MJ | CDS | 704784 | 1113 | - | 0.322552 | |
g2514 | DLA_02788 | F4PJNLW01EE5MJ | CDS | 721035 | 2421 | + | 0.327551 | |
g2520 | DLA_02794 | F4PJNLW01EE5MJ | CDS | 732818 | 813 | - | 0.341943 | |
g2539 | DLA_02813 | F4PJNLW01EE5MJ | CDS | 774560 | 1326 | - | 0.273002 | |
g2542 | DLA_02816 | F4PJNLW01EE5MJ | CDS | 781075 | 2442 | + | 0.285831 | |
g2556 | DLA_02834 | F4PJNLW01EE5MJ | CDS | 820222 | 621 | + | 0.294686 | |
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 |
g2569 | DLA_02853 | F4PJNLW01EE5MJ | CDS | 847624 | 3453 | - | 0.32812 | |
g2578 | DLA_02861 | F4PJNLW01EE5MJ | CDS | 864104 | 2604 | - | 0.320276 | |
g26 | DLA_00031 | contig05409_1.exp | CDS | 70155 | 735 | - | 0.338776 | |
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 |
g2607 | DLA_02893 | F4PJNLW01EE5MJ | CDS | 946211 | 1323 | + | 0.357521 | |
g2620 | DLA_02908 | F4PJNLW01EE5MJ | CDS | 969208 | 3174 | - | 0.333018 | |
g2636 | DLA_02926 | F4PJNLW01EE5MJ | CDS | 1000811 | 2118 | - | 0.344193 | |
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 |
g2649 | DLA_02940 | F4PJNLW01EE5MJ | CDS | 1028129 | 6285 | + | 0.322832 | |
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 |
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 |
g267 | DLA_00295 | contig05409_1.exp | CDS | 618353 | 1266 | - | 0.28594 | |
g2672 | DLA_02965 | F4PJNLW01EE5MJ | CDS | 1078535 | 3300 | + | 0.35697 | |
g2673 | DLA_02966 | F4PJNLW01EE5MJ | CDS | 1082165 | 1071 | - | 0.3324 | |
g2684 | DLA_02980 | F4PJNLW01EE5MJ | CDS | 1104230 | 873 | + | 0.315006 | |
g2692 | DLA_02987 | F4PJNLW01EE5MJ | CDS | 1117694 | 1050 | + | 0.345714 | |
g270 | DLA_00300 | contig05409_1.exp | CDS | 625941 | 2418 | + | 0.35732 | |
g2701 | DLA_02995 | F4PJNLW01EE5MJ | CDS | 1132168 | 750 | - | 0.357333 | |
g2705 | DLA_02999 | F4PJNLW01EE5MJ | CDS | 1138608 | 2625 | - | 0.299429 | |
g2706 | DLA_03000 | F4PJNLW01EE5MJ | CDS | 1141772 | 873 | + | 0.317297 | |
g2712 | DLA_03008 | F4PJNLW01EE5MJ | CDS | 1150620 | 1479 | - | 0.338742 | |
g2720 | DLA_03016 | F4PJNLW01EE5MJ | CDS | 1170267 | 1944 | + | 0.314815 | |
g2730 | DLA_03025 | F4PJNLW01EE5MJ | CDS | 1196433 | 2709 | + | 0.287929 | |
g2738 | DLA_03034 | F4PJNLW01EE5MJ | CDS | 1212538 | 609 | - | 0.341544 | |
g2739 | DLA_03035 | F4PJNLW01EE5MJ | CDS | 1213710 | 1593 | + | 0.338983 | |
g2760 | DLA_03055 | F4PJNLW02GJ9ZB | CDS | 12747 | 3666 | - | 0.321877 | |
g2763 | DLA_03061 | F4PJNLW02GJ9ZB | CDS | 23701 | 594 | - | 0.338384 | |
g2771 | DLA_03069 | F4PJNLW02GJ9ZB | CDS | 38713 | 2556 | - | 0.353678 | |
g2774 | DLA_03071 | F4PJNLW02GJ9ZB | CDS | 45194 | 1554 | - | 0.331403 | |
g2786 | DLA_03085 | F4PJNLW02GJ9ZB | CDS | 67097 | 867 | + | 0.320646 | |
g279 | DLA_00309 | contig05409_1.exp | CDS | 642788 | 738 | + | 0.345528 | |
g2799 | DLA_03100 | F4PJNLW02GJ9ZB | CDS | 89678 | 1719 | - | 0.399069 | |
g2823 | DLA_03126 | F4PJNLW02GJ9ZB | CDS | 143581 | 2193 | - | 0.321021 | |
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 |
g2828 | DLA_03131 | F4PJNLW02GJ9ZB | CDS | 154793 | 1191 | + | 0.315701 | |
g2835 | DLA_03138 | F4PJNLW02GJ9ZB | CDS | 169414 | 1224 | - | 0.291667 | |
g2838 | DLA_03141 | F4PJNLW02GJ9ZB | CDS | 176752 | 1095 | + | 0.313242 | |
g2879 | DLA_03191 | F4PJNLW02HBBIY | CDS | 3696 | 846 | + | 0.329787 | |
g2881 | DLA_03193 | F4PJNLW02HBBIY | CDS | 6961 | 1041 | + | 0.361191 | |
g2882 | DLA_03194 | F4PJNLW02HBBIY | CDS | 8492 | 3045 | - | 0.336617 | |
g2888 | DLA_03202 | F4PJNLW02HBBIY | CDS | 26108 | 1389 | + | 0.314615 | |
g289 | DLA_00320 | contig05409_1.exp | CDS | 668785 | 627 | + | 0.317384 | |
g291 | DLA_00322 | contig05409_1.exp | CDS | 673007 | 2217 | - | 0.348218 | |
g2919 | DLA_03234 | F4PJNLW02HBBIY | CDS | 93924 | 1290 | - | 0.343411 | |
g2921 | DLA_03236 | F4PJNLW02HBBIY | CDS | 97770 | 1467 | - | 0.334015 | |
g2933 | DLA_03248 | F4PJNLW02HBBIY | CDS | 118459 | 1113 | + | 0.338724 | |
g2946 | DLA_03264 | F4PJNLW02HBBIY | CDS | 154894 | 1431 | - | 0.328442 | |
g2958 | DLA_03279 | F4PJNLW02HBBIY | CDS | 186711 | 555 | - | 0.313514 | |
g2964 | DLA_03285 | F4PJNLW02HBBIY | CDS | 197662 | 273 | - | 0.278388 | |
g2967 | DLA_03288 | F4PJNLW02HBBIY | CDS | 199659 | 1515 | + | 0.368977 | |
g2968 | DLA_03289 | F4PJNLW02HBBIY | CDS | 201439 | 1026 | - | 0.359649 | |
g2971 | DLA_03291 | F4PJNLW02HBBIY | CDS | 206822 | 2460 | + | 0.34878 | |
g2983 | DLA_03303 | F4PJNLW02HBBIY | CDS | 236901 | 2343 | - | 0.33248 | |
g2990 | DLA_03312 | F4PJNLW02HBBIY | CDS | 249623 | 546 | - | 0.31685 | |
g3008 | DLA_11548 | F4PJNLW02HBBIY | CDS | 285549 | 3285 | - | 0.333333 | |
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 |
g3019 | DLA_03345 | F4PJNLW02HBBIY | CDS | 318594 | 1884 | + | 0.333864 | |
g302 | DLA_00335 | contig05409_1.exp | CDS | 693895 | 2262 | + | 0.276304 | |
g303 | DLA_00336 | contig05409_1.exp | CDS | 696740 | 2211 | + | 0.289462 | |
g3035 | DLA_03362 | F4PJNLW02HBBIY | CDS | 361414 | 2673 | + | 0.34306 | |
g3037 | DLA_03363 | F4PJNLW02HBBIY | CDS | 366615 | 2451 | - | 0.339861 | |
g3051 | DLA_03376 | F4PJNLW02HBBIY | CDS | 394666 | 4044 | - | 0.3227 | |
g3061 | DLA_03388 | F4PJNLW02HBBIY | CDS | 422744 | 2760 | + | 0.350362 | |
g3063 | DLA_03390 | F4PJNLW02HBBIY | CDS | 426670 | 852 | - | 0.327465 | |
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 |
g3108 | DLA_03441 | F4PJNLW02HBBIY | CDS | 508940 | 1194 | + | 0.292295 | |
g3111 | DLA_03444 | F4PJNLW02HBBIY | CDS | 514355 | 1509 | + | 0.304838 | |
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 |
g3117 | DLA_03451 | F4PJNLW02HBBIY | CDS | 526519 | 1467 | + | 0.29516 | |
g3127 | DLA_03462 | F4PJNLW02HBBIY | CDS | 546113 | 1023 | + | 0.312805 | |
g3166 | DLA_03511 | GAOABQK02FRRQV | CDS | 65654 | 624 | - | 0.267628 | |
g3168 | DLA_03513 | GAOABQK02FRRQV | CDS | 68726 | 1254 | + | 0.338118 | |
g3172 | DLA_03517 | GAOABQK02FRRQV | CDS | 75694 | 1617 | + | 0.28757 | |
g3179 | DLA_03525 | GAOABQK02FRRQV | CDS | 89834 | 633 | - | 0.268562 | |
g3183 | DLA_03529 | GAOABQK02FRRQV | CDS | 94417 | 1041 | + | 0.338136 | |
g3201 | DLA_03548 | GAOABQK02FWKR3 | CDS | 9226 | 1002 | - | 0.419162 | |
g3209 | DLA_03557 | GAOABQK02FWKR3 | CDS | 20867 | 1314 | + | 0.266362 | |
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 |
g3224 | DLA_03572 | GAOABQK02FWKR3 | CDS | 52412 | 1107 | - | 0.34869 | |
g3226 | DLA_03575 | GAOABQK02G6SYV | CDS | 543 | 768 | - | 0.304688 | |
g325 | DLA_00363 | contig05409_1.exp | CDS | 749479 | 909 | - | 0.330033 | |
g326 | DLA_00364 | contig05409_1.exp | CDS | 750574 | 1857 | + | 0.351104 | |
g3276 | DLA_03625 | GAOABQK02G6SYV | CDS | 117700 | 2319 | + | 0.29323 | |
g329 | DLA_11441 | contig05409_1.exp | CDS | 758528 | 1401 | + | 0.306924 | |
g3298 | DLA_03649 | GAOABQK02G6SYV | CDS | 161683 | 453 | - | 0.337748 | |
g33 | DLA_00037 | contig05409_1.exp | CDS | 83093 | 4545 | - | 0.331133 | |
g3305 | DLA_03655 | GAOABQK02G6SYV | CDS | 171413 | 1791 | + | 0.400335 | |
g3317 | DLA_03668 | GAOABQK02G6SYV | CDS | 196045 | 3507 | + | 0.312803 | |
g3322 | DLA_03673 | GAOABQK02G6SYV | CDS | 207498 | 4548 | + | 0.348505 | |
g3348 | DLA_03703 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | GAOABQK02G6SYV | CDS | 259800 | 1452 | - | 0.403581 |
g3350 | DLA_03706 | GAOABQK02G6SYV | CDS | 264850 | 3468 | - | 0.364475 | |
g3354 | DLA_03710 | GAOABQK02G6SYV | CDS | 276246 | 1026 | - | 0.296296 | |
g3368 | DLA_03724 | GAOABQK02G6SYV | CDS | 302063 | 1557 | + | 0.398844 | |
g3374 | DLA_03731 | GAOABQK02G6SYV | CDS | 322155 | 2322 | + | 0.327304 | |
g3396 | DLA_03756 | GAOABQK02G6SYV | CDS | 364614 | 840 | - | 0.360714 | |
g341 | DLA_00383 | contig05409_1.exp | CDS | 782753 | 1023 | - | 0.333333 | |
g3412 | DLA_03775 | GAOABQK02G6SYV | CDS | 393352 | 3546 | + | 0.368302 | |
g3467 | DLA_03832 | GAOABQK02G6SYV | CDS | 518766 | 1185 | - | 0.298734 | |
g3492 | DLA_03868 | GAOABQK02G6SYV | CDS | 578793 | 1689 | - | 0.357608 | |
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 |
g3512 | DLA_03890 | GAOABQK02G6SYV | CDS | 631330 | 567 | - | 0.322751 | |
g3520 | DLA_03897 | GAOABQK02G6SYV | CDS | 647761 | 2139 | + | 0.306685 | |
g3533 | DLA_03912 | GAOABQK02G6SYV | CDS | 680633 | 1791 | + | 0.339475 | |
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 |
g3543 | DLA_03922 | GAOABQK02G6SYV | CDS | 697620 | 2601 | - | 0.323337 | |
g3549 | DLA_03930 | GAOABQK02G7M1S | CDS | 12808 | 2847 | + | 0.334387 | |
g3558 | DLA_03938 | GAOABQK02G7M1S | CDS | 31797 | 4113 | + | 0.292001 | |
g3573 | DLA_03957 | GAOABQK02G7M1S | CDS | 83998 | 852 | + | 0.255869 | |
g3585 | DLA_03972 | GAOABQK02G7M1S | CDS | 117205 | 999 | - | 0.314314 | |
g3588 | DLA_03975 | GAOABQK02G7M1S | CDS | 122669 | 888 | + | 0.292793 | |
g360 | DLA_00402 | contig05409_1.exp | CDS | 832845 | 675 | + | 0.355556 | |
g3613 | DLA_04004 | GAOABQK02G7M1S | CDS | 184890 | 462 | + | 0.28355 | |
g3616 | DLA_04007 | GAOABQK02G7M1S | CDS | 187236 | 1224 | + | 0.335784 | |
g3633 | DLA_04028 | GAOABQK02G7M1S | CDS | 224475 | 774 | + | 0.351421 | |
g3655 | DLA_11571 | GAOABQK02G7M1S | CDS | 280149 | 549 | + | 0.333333 | |
g3673 | DLA_04070 | GAOABQK02G7M1S | CDS | 329319 | 1029 | + | 0.347911 | |
g3679 | DLA_04077 | GAOABQK02G7M1S | CDS | 342331 | 696 | + | 0.326149 | |
g3685 | DLA_04082 | GAOABQK02G7M1S | CDS | 353676 | 741 | - | 0.34143 | |
g3689 | DLA_04086 | GAOABQK02G7M1S | CDS | 360092 | 6528 | + | 0.339614 | |
g3709 | DLA_04110 | GAOABQK02G7M1S | CDS | 406536 | 1113 | - | 0.327942 | |
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 |
g3723 | DLA_04126 | GAOABQK02G7M1S | CDS | 432623 | 1785 | + | 0.322129 | |
g3732 | DLA_04135 | GAOABQK02G7M1S | CDS | 453346 | 2685 | - | 0.347858 | |
g3741 | DLA_04144 | GAOABQK02G7M1S | CDS | 471893 | 2535 | - | 0.341223 | |
g3771 | DLA_04178 | GAOABQK02G7M1S | CDS | 530995 | 1695 | - | 0.359292 | |
g3772 | DLA_04179 | GAOABQK02G7M1S | CDS | 533102 | 561 | + | 0.322638 | |
g3784 | DLA_04196 | GAOABQK02G7M1S | CDS | 566511 | 1071 | + | 0.345472 | |
g3788 | DLA_04200 | GAOABQK02G7M1S | CDS | 577819 | 1269 | - | 0.319937 | |
g3799 | DLA_04213 | GAOABQK02G7M1S | CDS | 604665 | 1314 | + | 0.362253 | |
g3803 | DLA_04218 | GAOABQK02G7M1S | CDS | 612161 | 795 | + | 0.354717 | |
g3824 | DLA_04242 | GAOABQK02G7M1S | CDS | 671261 | 2346 | + | 0.331628 | |
g3830 | DLA_04248 | GAOABQK02G7M1S | CDS | 681315 | 441 | - | 0.321995 | |
g384 | DLA_00427 | contig05409_1.exp | CDS | 879047 | 2526 | + | 0.342043 | |
g3844 | DLA_04263 | GAOABQK02G7M1S | CDS | 710196 | 2940 | - | 0.337415 | |
g3850 | DLA_04270 | GAOABQK02G7M1S | CDS | 735441 | 1416 | - | 0.358757 | |
g3861 | DLA_04281 | GAOABQK02G7M1S | CDS | 756703 | 675 | + | 0.308148 | |
g3864 | DLA_04284 | GAOABQK02G7M1S | CDS | 761256 | 1530 | + | 0.336601 | |
g3869 | DLA_04291 | GAOABQK02GQAQJ | CDS | 2867 | 2811 | + | 0.282818 | |
g3871 | DLA_04293 | GAOABQK02GQAQJ | CDS | 7589 | 1095 | + | 0.315068 | |
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 |
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 |
g391 | DLA_00435 | contig05409_1.exp | CDS | 893058 | 660 | - | 0.290909 | |
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 |
g3926 | DLA_04353 | GAOABQK02GQAQJ | CDS | 136067 | 750 | + | 0.342667 | |
g3933 | DLA_04362 | GAOABQK02GQAQJ | CDS | 149257 | 885 | + | 0.352542 | |
g3934 | DLA_04363 | GAOABQK02GQAQJ | CDS | 151071 | 2484 | + | 0.355878 | |
g3959 | DLA_04388 | GAOABQK02GQAQJ | CDS | 198231 | 4212 | + | 0.315052 | |
g3962 | DLA_04391 | GAOABQK02GQAQJ | CDS | 209901 | 624 | - | 0.355769 | |
g398 | DLA_00442 | contig05409_1.exp | CDS | 911085 | 2340 | + | 0.334188 | |
g399 | DLA_00443 | contig05409_1.exp | CDS | 913600 | 978 | - | 0.299591 | |
g3991 | DLA_04426 | GAOABQK02GQAQJ | CDS | 279816 | 1689 | + | 0.352872 | |
g400 | DLA_00444 | contig05409_1.exp | CDS | 914889 | 855 | - | 0.336842 | |
g4002 | DLA_04437 | GAOABQK02GQAQJ | CDS | 306561 | 1497 | - | 0.309953 | |
g4011 | DLA_04450 | GAOABQK02GQAQJ | CDS | 329479 | 546 | + | 0.358974 | |
g4012 | DLA_04451 | GAOABQK02GQAQJ | CDS | 330396 | 939 | - | 0.342918 | |
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 |
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 |
g4039 | DLA_04480 | GAOABQK02GQAQJ | CDS | 392617 | 1245 | - | 0.360643 | |
g4040 | DLA_04481 | GAOABQK02GQAQJ | CDS | 394557 | 1035 | - | 0.342995 | |
g4045 | DLA_04487 | GAOABQK02GQAQJ | CDS | 400910 | 1077 | + | 0.336119 | |
g4050 | DLA_04492 | GAOABQK02GQAQJ | CDS | 411092 | 1170 | - | 0.351282 | |
g4060 | DLA_04503 | GAOABQK02GQAQJ | CDS | 435813 | 933 | + | 0.332262 | |
g4071 | DLA_04515 | GAOABQK02GQAQJ | CDS | 458487 | 3120 | + | 0.324038 | |
g4074 | DLA_04518 | similar to human TBC1D22B S. pombe gyp1 | GAOABQK02GQAQJ | CDS | 464498 | 1419 | + | 0.331924 |
g4082 | DLA_04525 | GAOABQK02GQAQJ | CDS | 482239 | 897 | - | 0.322185 | |
g4086 | DLA_04529 | GAOABQK02GQAQJ | CDS | 488304 | 657 | + | 0.340944 | |
g4088 | DLA_04531 | GAOABQK02GQAQJ | CDS | 490671 | 2940 | + | 0.337415 | |
g4098 | DLA_04542 | GAOABQK02GQAQJ | CDS | 514858 | 1209 | - | 0.321754 | |
g4108 | DLA_04554 | GAOABQK02GQAQJ | CDS | 534500 | 795 | + | 0.289308 | |
g4112 | DLA_04559 | GAOABQK02GQAQJ | CDS | 542937 | 870 | - | 0.312644 | |
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 |
g4134 | DLA_04583 | GAOABQK02GQAQJ | CDS | 577478 | 2601 | + | 0.315263 | |
g4135 | DLA_04584 | GAOABQK02GQAQJ | CDS | 580189 | 2076 | - | 0.310694 | |
g4148 | DLA_04596 | GAOABQK02GQAQJ | CDS | 608908 | 2157 | + | 0.265647 | |
g4149 | DLA_04597 | GAOABQK02GQAQJ | CDS | 611526 | 2625 | - | 0.32419 | |
g4158 | DLA_04605 | GAOABQK02GQAQJ | CDS | 630116 | 7644 | + | 0.354003 | |
g416 | DLA_00461 | contig05409_1.exp | CDS | 947446 | 1215 | + | 0.412346 | |
g4163 | DLA_04610 | GAOABQK02GQAQJ | CDS | 643235 | 2076 | - | 0.307803 | |
g4167 | DLA_04614 | GAOABQK02GQAQJ | CDS | 652471 | 2319 | - | 0.362656 | |
g417 | DLA_00462 | contig05409_1.exp | CDS | 949108 | 918 | + | 0.392157 | |
g4185 | DLA_04630 | GAOABQK02GQAQJ | CDS | 688201 | 1161 | - | 0.296296 | |
g419 | DLA_00464 | contig05409_1.exp | CDS | 951487 | 711 | + | 0.326301 | |
g4203 | DLA_04648 | GAOABQK02GQAQJ | CDS | 718818 | 1494 | + | 0.309906 | |
g4211 | DLA_04658 | GAOABQK02GQAQJ | CDS | 735323 | 2208 | + | 0.317482 | |
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 |
g422 | DLA_00468 | contig05409_1.exp | CDS | 956594 | 576 | + | 0.300347 | |
g4222 | DLA_04669 | GAOABQK02GQAQJ | CDS | 763149 | 1296 | + | 0.328704 | |
g4236 | DLA_04684 | GAOABQK02GQAQJ | CDS | 793404 | 1899 | + | 0.339126 | |
g4258 | DLA_04705 | GAOABQK02GQAQJ | CDS | 842046 | 2043 | - | 0.380813 | |
g4271 | DLA_04716 | GAOABQK02GQAQJ | CDS | 869762 | 8682 | - | 0.349804 | |
g4280 | DLA_04726 | GAOABQK02GQAQJ | CDS | 895678 | 2187 | + | 0.328304 | |
g4290 | DLA_04736 | GAOABQK02GQAQJ | CDS | 920116 | 1251 | - | 0.293365 | |
g4298 | DLA_04744 | GAOABQK02GQAQJ | CDS | 941546 | 1119 | - | 0.321716 | |
g4301 | DLA_04747 | GAOABQK02GQAQJ | CDS | 948296 | 1629 | + | 0.34868 | |
g4303 | DLA_04749 | GAOABQK02GQAQJ | CDS | 952334 | 1602 | + | 0.338951 | |
g4336 | DLA_04789 | GAOABQK02GQAQJ | CDS | 1046815 | 4053 | + | 0.339255 | |
g4338 | DLA_04792 | GAOABQK02GQAQJ | CDS | 1052595 | 2424 | + | 0.312706 | |
g4357 | DLA_04816 | GAOABQK02GRIAE | CDS | 4785 | 3231 | - | 0.316311 | |
g4362 | DLA_04821 | GAOABQK02GRIAE | CDS | 20539 | 2247 | - | 0.315532 | |
g4365 | DLA_04824 | GAOABQK02GRIAE | CDS | 30234 | 594 | - | 0.323232 | |
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 |
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 |
g4374 | DLA_04834 | GAOABQK02GRIAE | CDS | 53831 | 6273 | + | 0.326957 | |
g4379 | DLA_04840 | GAOABQK02GRIAE | CDS | 76672 | 567 | + | 0.266314 | |
g4384 | DLA_04846 | GAOABQK02GRIAE | CDS | 87383 | 1194 | + | 0.345059 | |
g4386 | DLA_04849 | GAOABQK02GRIAE | CDS | 89763 | 588 | + | 0.336735 | |
g4396 | DLA_04859 | GAOABQK02GRIAE | CDS | 112322 | 543 | - | 0.290976 | |
g44 | DLA_00053 | contig05409_1.exp | CDS | 113335 | 4518 | - | 0.340859 | |
g4400 | DLA_04862 | GAOABQK02GRIAE | CDS | 124812 | 489 | + | 0.300613 | |
g4401 | DLA_04863 | GAOABQK02GRIAE | CDS | 128848 | 537 | + | 0.292365 | |
g4412 | DLA_04878 | GAOABQK02GRIAE | CDS | 155358 | 4623 | + | 0.307376 | |
g4419 | DLA_04886 | GAOABQK02GRIAE | CDS | 172157 | 2103 | + | 0.292915 | |
g4425 | DLA_04892 | GAOABQK02GRIAE | CDS | 179861 | 516 | + | 0.294574 | |
g4427 | DLA_04894 | GAOABQK02GRIAE | CDS | 181916 | 1023 | + | 0.356794 | |
g4437 | DLA_04909 | GAOABQK02GRIAE | CDS | 211845 | 804 | + | 0.262438 | |
g4441 | DLA_04914 | GAOABQK02GRIAE | CDS | 216906 | 537 | + | 0.3054 | |
g445 | DLA_00492 | contig05409_1.exp | CDS | 1021410 | 618 | - | 0.322006 | |
g4456 | DLA_04935 | GAOABQK02H81I9 | CDS | 23754 | 2466 | - | 0.345904 | |
g447 | DLA_00495 | contig05409_1.exp | CDS | 1025554 | 1761 | + | 0.33674 | |
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 |
g4491 | DLA_04974 | GAOABQK02H81I9 | CDS | 110403 | 924 | + | 0.350649 | |
g4493 | DLA_04976 | GAOABQK02H81I9 | CDS | 112900 | 2298 | + | 0.289817 | |
g4520 | DLA_05010 | GAOABQK02H81I9 | CDS | 173524 | 972 | + | 0.341564 | |
g4526 | DLA_05016 | GAOABQK02H81I9 | CDS | 188618 | 3891 | + | 0.311488 | |
g4541 | DLA_05032 | GAOABQK02H81I9 | CDS | 237598 | 576 | - | 0.314236 | |
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 |
g4556 | DLA_05049 | GAOABQK02H81I9 | CDS | 264313 | 708 | + | 0.289548 | |
g4573 | DLA_05067 | GAOABQK02H81I9 | CDS | 302078 | 5169 | + | 0.336235 | |
g4579 | DLA_05074 | GAOABQK02H81I9 | CDS | 319505 | 474 | + | 0.280591 | |
g4592 | DLA_05087 | GAOABQK02H81I9 | CDS | 346046 | 441 | + | 0.324263 | |
g4600 | DLA_05095 | GAOABQK02H81I9 | CDS | 365480 | 840 | + | 0.294048 | |
g4604 | DLA_05099 | GAOABQK02H81I9 | CDS | 375330 | 2349 | + | 0.325671 | |
g4628 | DLA_05125 | GAOABQK02H81I9 | CDS | 434500 | 4944 | + | 0.344053 | |
g4629 | DLA_05126 | GAOABQK02H81I9 | CDS | 440362 | 2097 | - | 0.379113 | |
g4645 | DLA_05143 | GAOABQK02H81I9 | CDS | 472960 | 663 | - | 0.319759 | |
g4693 | DLA_05196 | GAOABQK02H81I9 | CDS | 588581 | 867 | - | 0.327566 | |
g4694 | DLA_05197 | GAOABQK02H81I9 | CDS | 589804 | 1263 | - | 0.360253 | |
g4715 | DLA_05222 | GAOABQK02H81I9 | CDS | 629973 | 1425 | + | 0.322807 | |
g4717 | DLA_05223 | GAOABQK02H81I9 | CDS | 632704 | 2310 | + | 0.321645 | |
g4718 | DLA_05224 | GAOABQK02H81I9 | CDS | 635593 | 2496 | + | 0.338141 | |
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 | |
g4731 | DLA_05238 | GAOABQK02H81I9 | CDS | 679874 | 2391 | - | 0.327896 | |
g4743 | DLA_05251 | GAOABQK02H81I9 | CDS | 707370 | 3147 | + | 0.328249 | |
g4774 | DLA_05283 | GAOABQK02H81I9 | CDS | 787377 | 876 | - | 0.317352 | |
g4784 | DLA_05295 | GAOABQK02H81I9 | CDS | 806986 | 5853 | - | 0.320178 | |
g4809 | DLA_05326 | GAOABQK02H81I9 | CDS | 861777 | 900 | + | 0.285556 | |
g4811 | DLA_05328 | GAOABQK02H81I9 | CDS | 864922 | 1761 | + | 0.284497 | |
g4816 | DLA_05332 | GAOABQK02H81I9 | CDS | 873335 | 2250 | - | 0.326667 | |
g4847 | DLA_05366 | GAOABQK02HUB3S | CDS | 47127 | 969 | - | 0.338493 | |
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 | |
g4865 | DLA_05387 | GAOABQK02HUB3S | CDS | 93561 | 675 | + | 0.322963 | |
g4868 | DLA_05390 | GAOABQK02HUB3S | CDS | 96467 | 561 | - | 0.301248 | |
g4877 | DLA_05401 | GAOABQK02HUB3S | CDS | 123004 | 7272 | + | 0.331958 | |
g4899 | DLA_05423 | GAOABQK02HUB3S | CDS | 176252 | 405 | + | 0.325926 | |
g4917 | DLA_05443 | GAOABQK02HUB3S | CDS | 218537 | 4035 | + | 0.294176 | |
g4926 | DLA_05454 | GAOABQK02HUB3S | CDS | 239569 | 1560 | + | 0.317949 | |
g4936 | DLA_05464 | GAOABQK02HUB3S | CDS | 261635 | 1611 | - | 0.290503 | |
g4944 | DLA_05473 | GAOABQK02HUB3S | CDS | 272308 | 903 | + | 0.315615 | |
g4968 | DLA_05498 | GAOABQK02HUB3S | CDS | 326938 | 1095 | - | 0.331507 | |
g497 | DLA_00550 | contig05409_1.exp | CDS | 1139170 | 624 | + | 0.339744 | |
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 |
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 |
g4991 | DLA_05525 | GAOABQK02HUB3S | CDS | 383190 | 1203 | - | 0.320033 | |
g5030 | DLA_05570 | GAOABQK02HUB3S | CDS | 460304 | 1029 | + | 0.367347 | |
g5043 | DLA_05585 | GAOABQK02HUB3S | CDS | 487469 | 603 | - | 0.3466 | |
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 |
g5073 | DLA_05618 | GAOABQK02HUB3S | CDS | 562805 | 2460 | - | 0.314634 | |
g5087 | DLA_05635 | GAOABQK02HUB3S | CDS | 593660 | 1707 | - | 0.313415 | |
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 |
g5098 | DLA_05646 | putative ortholog of S. cerevisiae BUB2 a mitotic checkpoint protein | GAOABQK02HUB3S | CDS | 629459 | 993 | + | 0.306143 |
g51 | DLA_00060 | contig05409_1.exp | CDS | 131668 | 1317 | - | 0.351557 | |
g5101 | DLA_05649 | GAOABQK02HUB3S | CDS | 632679 | 1317 | + | 0.355353 | |
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 |
g5108 | DLA_05657 | GAOABQK02HUB3S | CDS | 648858 | 2475 | - | 0.298586 | |
g5119 | DLA_05669 | GAOABQK02HUB3S | CDS | 674700 | 711 | + | 0.293952 | |
g5131 | DLA_05681 | GAOABQK02HUB3S | CDS | 698121 | 765 | + | 0.330719 | |
g5149 | DLA_05710 | GAOABQK02HUB3S | CDS | 752623 | 576 | - | 0.375 | |
g5166 | DLA_05731 | GAOABQK02HUB3S | CDS | 789142 | 501 | - | 0.337325 | |
g5177 | DLA_05743 | GAOABQK02HUB3S | CDS | 833073 | 2523 | + | 0.320254 | |
g5184 | DLA_05748 | GAOABQK02HUB3S | CDS | 875626 | 2385 | + | 0.398323 | |
g5206 | DLA_05778 | GAOABQK02HUB3S | CDS | 932143 | 1695 | - | 0.379941 | |
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 | |
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 |
g5261 | DLA_05838 | GAOABQK02HUB3S | CDS | 1050392 | 1218 | - | 0.293103 | |
g5270 | DLA_05848 | contains 2 GRAM domains one RabGAPTBC domain and one EF hand domain | GAOABQK02HUB3S | CDS | 1069188 | 3243 | - | 0.307431 |
g5303 | DLA_05892 | GAOABQK02HUB3S | CDS | 1162273 | 1578 | - | 0.287706 | |
g5310 | DLA_05900 | GAOABQK02HUB3S | CDS | 1179641 | 2886 | + | 0.288635 | |
g5319 | DLA_05913 | GAOABQK02HUB3S | CDS | 1205322 | 1737 | + | 0.28152 | |
g5323 | DLA_05918 | GAOABQK02HUB3S | CDS | 1211262 | 1065 | + | 0.288263 | |
g5324 | DLA_05919 | GAOABQK02HUB3S | CDS | 1212357 | 1665 | - | 0.306306 | |
g533 | DLA_00586 | contig05409_1.exp | CDS | 1220530 | 1668 | - | 0.361511 | |
g5336 | DLA_05934 | GAOABQK02HUB3S | CDS | 1241031 | 3873 | + | 0.32662 | |
g5344 | DLA_05945 | GAOABQK02HUB3S | CDS | 1261425 | 951 | + | 0.299685 | |
g5365 | DLA_05969 | GAOABQK02HUB3S | CDS | 1321176 | 2610 | - | 0.355172 | |
g5371 | DLA_05977 | GAOABQK02HUB3S | CDS | 1332472 | 1851 | - | 0.353323 | |
g5404 | DLA_06013 | GAOABQK02HUB3S | CDS | 1398433 | 1575 | + | 0.299683 | |
g5425 | DLA_06038 | GAOABQK02HUB3S | CDS | 1448988 | 582 | - | 0.314433 | |
g5428 | DLA_06042 | GAOABQK02HUB3S | CDS | 1453817 | 2178 | + | 0.305785 | |
g543 | DLA_00598 | contig05409_1.exp | CDS | 1240640 | 540 | + | 0.281481 | |
g5441 | DLA_06061 | GAOABQK02HUB3S | CDS | 1481957 | 1038 | + | 0.370906 | |
g5445 | DLA_06065 | GAOABQK02HUB3S | CDS | 1494646 | 993 | + | 0.316213 | |
g5448 | DLA_06068 | GAOABQK02HUB3S | CDS | 1502068 | 3438 | - | 0.331006 | |
g5453 | DLA_06073 | GAOABQK02HUB3S | CDS | 1515061 | 2583 | + | 0.351529 | |
g5464 | DLA_06088 | GAOABQK02HUB3S | CDS | 1537886 | 579 | + | 0.331606 | |
g5468 | DLA_06093 | GAOABQK02HUB3S | CDS | 1546733 | 414 | - | 0.330918 | |
g5476 | DLA_06103 | GAOABQK02HUB3S | CDS | 1561289 | 1536 | - | 0.321615 | |
g5492 | DLA_06121 | GAOABQK02HUB3S | CDS | 1591514 | 1812 | - | 0.381347 | |
g550 | DLA_00606 | contig05409_1.exp | CDS | 1260908 | 3054 | + | 0.332351 | |
g5502 | DLA_06133 | GAOABQK02HUB3S | CDS | 1616160 | 888 | + | 0.353604 | |
g5506 | DLA_06137 | GAOABQK02HUB3S | CDS | 1622539 | 1359 | + | 0.343635 | |
g5507 | DLA_06138 | GAOABQK02HUB3S | CDS | 1624230 | 3615 | + | 0.355463 | |
g5528 | DLA_06160 | GAOABQK02HUB3S | CDS | 1685610 | 1227 | - | 0.410758 | |
g5539 | DLA_06171 | GAOABQK02HUB3S | CDS | 1711237 | 777 | + | 0.337194 | |
g5544 | DLA_06176 | GAOABQK02HUB3S | CDS | 1719698 | 585 | + | 0.326496 | |
g556 | DLA_00612 | contig05409_1.exp | CDS | 1270367 | 2211 | + | 0.352782 | |
g5575 | DLA_06212 | GAOABQK02HUB3S | CDS | 1794723 | 999 | + | 0.324324 | |
g5583 | DLA_06223 | GAOABQK02HUB3S | CDS | 1812442 | 573 | + | 0.321117 | |
g5587 | DLA_06231 | GAOABQK02HUB3S | CDS | 1823015 | 1125 | - | 0.362667 | |
g561 | DLA_00617 | contig05409_1.exp | CDS | 1280986 | 912 | - | 0.358553 | |
g5612 | DLA_06257 | GAOABQK02IBA3P | CDS | 4134 | 1986 | + | 0.330312 | |
g5623 | DLA_06269 | GAOABQK02IBA3P | CDS | 27290 | 1902 | - | 0.302313 | |
g5635 | DLA_11648 | GAOABQK02IBA3P | CDS | 57940 | 519 | - | 0.310212 | |
g5647 | DLA_06294 | GAOABQK02IBA3P | CDS | 85170 | 930 | - | 0.291398 | |
g5654 | DLA_06300 | GAOABQK02IBA3P | CDS | 100124 | 4236 | - | 0.344901 | |
g5656 | DLA_06302 | GAOABQK02IBA3P | CDS | 108795 | 564 | + | 0.296099 | |
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 |
g5692 | DLA_06342 | GAOABQK02IBA3P | CDS | 191924 | 846 | - | 0.320331 | |
g5700 | DLA_06353 | GAOABQK02IBA3P | CDS | 213493 | 846 | + | 0.323877 | |
g5706 | DLA_06359 | GAOABQK02IBA3P | CDS | 227474 | 1104 | - | 0.289855 | |
g5723 | DLA_06381 | GAOABQK02IBA3P | CDS | 288304 | 660 | - | 0.365152 | |
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 |
g5736 | DLA_06398 | GAOABQK02IBA3P | CDS | 322686 | 810 | - | 0.376543 | |
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 |
g5777 | DLA_06443 | GAOABQK02IBA3P | CDS | 418948 | 1335 | - | 0.323595 | |
g579 | DLA_00640 | contig05409_1.exp | CDS | 1318963 | 909 | - | 0.326733 | |
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 |
g5816 | DLA_06488 | GAOABQK02IBA3P | CDS | 502384 | 864 | + | 0.30787 | |
g5827 | DLA_11654 | GAOABQK02IBA3P | CDS | 523356 | 699 | + | 0.314735 | |
g5842 | DLA_06516 | GAOABQK02IBA3P | CDS | 553910 | 3255 | - | 0.349309 | |
g585 | DLA_00646 | contig05409_1.exp | CDS | 1331666 | 3348 | - | 0.344086 | |
g5852 | DLA_06527 | GAOABQK02IBA3P | CDS | 573481 | 759 | - | 0.328063 | |
g5864 | DLA_06538 | GAOABQK02IBA3P | CDS | 591603 | 657 | + | 0.30137 | |
g5872 | DLA_06546 | GAOABQK02IBA3P | CDS | 607739 | 1356 | + | 0.312684 | |
g5887 | DLA_06559 | GAOABQK02IBA3P | CDS | 652072 | 1149 | + | 0.311575 | |
g5888 | DLA_06560 | GAOABQK02IBA3P | CDS | 654139 | 1140 | + | 0.317544 | |
g5898 | DLA_06571 | GAOABQK02IBA3P | CDS | 678603 | 771 | + | 0.32166 | |
g59 | DLA_00069 | contig05409_1.exp | CDS | 150114 | 1017 | + | 0.304818 | |
g5914 | DLA_06590 | GAOABQK02IBA3P | CDS | 731425 | 1725 | + | 0.327536 | |
g5924 | DLA_06601 | GAOABQK02IBA3P | CDS | 762982 | 1317 | - | 0.279423 | |
g5927 | DLA_06604 | GAOABQK02IBA3P | CDS | 769846 | 4020 | + | 0.340547 | |
g5932 | DLA_06609 | GAOABQK02IBA3P | CDS | 784027 | 2964 | + | 0.324899 | |
g5949 | DLA_06628 | GAOABQK02IBA3P | CDS | 821083 | 732 | - | 0.319672 | |
g5959 | DLA_11661 | GAOABQK02IBA3P | CDS | 839364 | 762 | - | 0.368766 | |
g5960 | DLA_06638 | GAOABQK02IBA3P | CDS | 840559 | 1410 | - | 0.308511 | |
g5966 | DLA_06644 | GAOABQK02IBA3P | CDS | 847549 | 1014 | + | 0.342209 | |
g6002 | DLA_06684 | GAOABQK02IBA3P | CDS | 951201 | 2358 | - | 0.337574 | |
g6005 | DLA_11664 | GAOABQK02IBA3P | CDS | 957917 | 2136 | - | 0.326779 | |
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 |
g6027 | DLA_06714 | GAOABQK02IBA3P | CDS | 1012536 | 2217 | - | 0.352278 | |
g6033 | DLA_06720 | GAOABQK02IBA3P | CDS | 1022975 | 1392 | + | 0.3125 | |
g6043 | DLA_06730 | GAOABQK02IBA3P | CDS | 1043040 | 615 | - | 0.331707 | |
g6051 | DLA_06739 | GAOABQK02IBA3P | CDS | 1060888 | 1035 | - | 0.342995 | |
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 |
g6083 | DLA_06771 | GAOABQK02INHKB | CDS | 9919 | 3717 | - | 0.313963 | |
g6086 | DLA_06774 | GAOABQK02INHKB | CDS | 19513 | 852 | + | 0.338028 | |
g6104 | DLA_06797 | GAOABQK02IO52T | CDS | 34493 | 996 | - | 0.365462 | |
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 |
g6116 | DLA_06811 | GAOABQK02IO52T | CDS | 56795 | 1080 | + | 0.383333 | |
g6119 | DLA_06814 | GAOABQK02IO52T | CDS | 60772 | 1845 | + | 0.299729 | |
g6122 | DLA_06817 | GAOABQK02IO52T | CDS | 66465 | 2757 | - | 0.328255 | |
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 |
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 |
g614 | DLA_00678 | contig05409_1.exp | CDS | 1397455 | 1068 | - | 0.328652 | |
g6149 | DLA_06849 | GAOABQK02IO52T | CDS | 138582 | 3204 | + | 0.334582 | |
g6164 | DLA_06867 | GAOABQK02IO52T | CDS | 169190 | 2802 | + | 0.275161 | |
g6169 | DLA_11669 | GAOABQK02IO52T | CDS | 175395 | 651 | - | 0.347158 | |
g6183 | DLA_06893 | GAOABQK02IO52T | CDS | 203312 | 987 | + | 0.300912 | |
g6195 | DLA_06906 | GAOABQK02IO52T | CDS | 243026 | 1500 | + | 0.308 | |
g6198 | DLA_06909 | GAOABQK02IO52T | CDS | 247376 | 1623 | + | 0.32101 | |
g6206 | DLA_11671 | GAOABQK02IO52T | CDS | 263677 | 567 | + | 0.310406 | |
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 |
g622 | DLA_00688 | DDLF0038h09.f4 | CDS | 7986 | 1059 | - | 0.355996 | |
g6238 | DLA_06951 | GAOABQK02IO52T | CDS | 326148 | 726 | + | 0.319559 | |
g6260 | DLA_06974 | GAOABQK02IO52T | CDS | 373105 | 1275 | + | 0.294902 | |
g6261 | DLA_06975 | GAOABQK02IO52T | CDS | 374940 | 633 | + | 0.301738 | |
g6291 | DLA_07006 | GAOABQK02IO52T | CDS | 442754 | 867 | - | 0.348328 | |
g6301 | DLA_07015 | GAOABQK02IO52T | CDS | 461803 | 660 | - | 0.343939 | |
g6304 | DLA_07018 | GAOABQK02IO52T | CDS | 465283 | 2589 | - | 0.312476 | |
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 | |
g6330 | DLA_11678 | GAOABQK02IO52T | CDS | 530240 | 618 | - | 0.331715 | |
g6334 | DLA_07053 | GAOABQK02IO52T | CDS | 534110 | 3546 | + | 0.319515 | |
g634 | DLA_00702 | F4PJNLW01A00V1 | CDS | 4965 | 2502 | + | 0.278577 | |
g6341 | DLA_07060 | GAOABQK02IO52T | CDS | 545602 | 2247 | + | 0.336894 | |
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 |
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 |
g637 | DLA_00705 | F4PJNLW01A00V1 | CDS | 11526 | 2700 | + | 0.33 | |
g6373 | DLA_07093 | GAOABQK02IO52T | CDS | 617780 | 627 | - | 0.370016 | |
g639 | DLA_00707 | F4PJNLW01A00V1 | CDS | 17774 | 2130 | + | 0.349296 | |
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 | |
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 |
g6409 | DLA_07133 | GAOABQK02IO52T | CDS | 690319 | 3717 | - | 0.379338 | |
g6421 | DLA_11680 | GAOABQK02JBK0O | CDS | 20921 | 588 | - | 0.340136 | |
g6422 | DLA_07145 | GAOABQK02JBK0O | CDS | 22326 | 543 | - | 0.279926 | |
g643 | DLA_00711 | F4PJNLW01A00V1 | CDS | 22496 | 918 | - | 0.302832 | |
g6438 | DLA_07164 | GAOABQK02JBK0O | CDS | 60708 | 1098 | + | 0.273224 | |
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 |
g6497 | DLA_07234 | GAOABQK02JEBFV | CDS | 45755 | 2196 | - | 0.331056 | |
g6498 | DLA_07235 | GAOABQK02JEBFV | CDS | 48636 | 2055 | - | 0.331873 | |
g652 | DLA_00721 | F4PJNLW01A00V1 | CDS | 38734 | 642 | - | 0.32866 | |
g6522 | DLA_07264 | GAOABQK02JOCCH | CDS | 44662 | 1047 | - | 0.334288 | |
g6524 | DLA_07265 | GAOABQK02JOCCH | CDS | 48097 | 3072 | + | 0.277995 | |
g6529 | DLA_07270 | GAOABQK02JOCCH | CDS | 58644 | 1905 | - | 0.290814 | |
g6530 | DLA_07272 | GAOABQK02JOCCH | CDS | 61204 | 2685 | + | 0.297952 | |
g6540 | DLA_07283 | GAOABQK02JOCCH | CDS | 86736 | 2736 | - | 0.339547 | |
g6549 | DLA_07294 | GAOABQK02JOCCH | CDS | 103562 | 1458 | + | 0.397119 | |
g6550 | DLA_07295 | GAOABQK02JOCCH | CDS | 105545 | 579 | - | 0.340242 | |
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 |
g6575 | DLA_07326 | GAOABQK02JOCCH | CDS | 168295 | 1659 | + | 0.335744 | |
g6610 | DLA_07361 | GAOABQK02JOCCH | CDS | 258156 | 1071 | + | 0.294118 | |
g6615 | DLA_07366 | GAOABQK02JOCCH | CDS | 271307 | 2067 | + | 0.351717 | |
g6620 | DLA_07373 | GAOABQK02JOCCH | CDS | 290458 | 534 | + | 0.284644 | |
g6635 | DLA_07389 | GAOABQK02JOCCH | CDS | 318164 | 1002 | + | 0.357285 | |
g6644 | DLA_07400 | GAOABQK02JOCCH | CDS | 337771 | 756 | - | 0.37963 | |
g6667 | DLA_07428 | GAOABQK02JOCCH | CDS | 383578 | 390 | - | 0.34359 | |
g6674 | DLA_07435 | GAOABQK02JOCCH | CDS | 403183 | 3987 | + | 0.346627 | |
g6679 | DLA_07439 | GAOABQK02JOCCH | CDS | 414241 | 1386 | - | 0.368687 | |
g6689 | DLA_07449 | GAOABQK02JOCCH | CDS | 434842 | 1197 | - | 0.314954 | |
g670 | DLA_00740 | F4PJNLW01A00V1 | CDS | 74728 | 1353 | + | 0.350333 | |
g6706 | DLA_07468 | GAOABQK02JOCCH | CDS | 462640 | 657 | - | 0.342466 | |
g6712 | DLA_07475 | GAOABQK02JOCCH | CDS | 478671 | 2856 | + | 0.290966 | |
g6716 | DLA_07481 | GAOABQK02JOCCH | CDS | 487529 | 2154 | - | 0.327298 | |
g6731 | DLA_07497 | GAOABQK02JOCCH | CDS | 527724 | 1686 | - | 0.281139 | |
g6735 | DLA_07501 | GAOABQK02JOCCH | CDS | 534441 | 861 | - | 0.341463 | |
g6741 | DLA_07507 | GAOABQK02JOCCH | CDS | 546798 | 1653 | - | 0.30732 | |
g6748 | DLA_07514 | GAOABQK02JOCCH | CDS | 560934 | 2172 | - | 0.351289 | |
g6759 | DLA_07528 | GAOABQK02JOCCH | CDS | 597731 | 2229 | - | 0.368775 | |
g6767 | DLA_07539 | GAOABQK02JOCCH | CDS | 612594 | 942 | - | 0.323779 | |
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 |
g6789 | DLA_07565 | GAOABQK02JOCCH | CDS | 652815 | 3417 | - | 0.347381 | |
g679 | DLA_00749 | F4PJNLW01A00V1 | CDS | 98677 | 858 | + | 0.342657 | |
g6791 | DLA_07569 | GAOABQK02JOCCH | CDS | 660363 | 1011 | + | 0.297725 | |
g6805 | DLA_07584 | GAOABQK02JOCCH | CDS | 703635 | 1395 | - | 0.314695 | |
g6812 | DLA_07592 | GAOABQK02JOCCH | CDS | 719832 | 4098 | - | 0.363836 | |
g6827 | DLA_07606 | GAOABQK02JOCCH | CDS | 750878 | 1497 | - | 0.342685 | |
g6843 | DLA_07626 | GAOABQK02JOCCH | CDS | 788486 | 1056 | - | 0.327652 | |
g6844 | DLA_07628 | GAOABQK02JOCCH | CDS | 790410 | 2037 | - | 0.305842 | |
g6857 | DLA_07643 | GAOABQK02JOCCH | CDS | 812714 | 6405 | - | 0.340515 | |
g6858 | DLA_07645 | GAOABQK02JOCCH | CDS | 820122 | 2751 | + | 0.338059 | |
g6883 | DLA_07677 | GAOABQK02JOCCH | CDS | 880767 | 1194 | + | 0.326633 | |
g6891 | DLA_07687 | GLQOFTK02FH5TG | CDS | 13232 | 609 | - | 0.316913 | |
g6893 | DLA_07689 | GLQOFTK02FH5TG | CDS | 15683 | 1479 | - | 0.284652 | |
g6897 | DLA_07692 | GLQOFTK02FH5TG | CDS | 24610 | 693 | - | 0.326118 | |
g6909 | DLA_07705 | GLQOFTK02FH5TG | CDS | 51342 | 663 | - | 0.26546 | |
g6914 | DLA_07710 | GLQOFTK02FH5TG | CDS | 59516 | 2574 | - | 0.289044 | |
g6929 | DLA_11693 | GLQOFTK02FH5TG | CDS | 95960 | 2934 | + | 0.316633 | |
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 |
g6950 | DLA_07748 | GLQOFTK02FH5TG | CDS | 134949 | 351 | - | 0.299145 | |
g6963 | DLA_07761 | GLQOFTK02FH5TG | CDS | 162248 | 3084 | - | 0.308366 | |
g6974 | DLA_07774 | GLQOFTK02FH5TG | CDS | 192719 | 681 | + | 0.33627 | |
g7 | DLA_00008 | contig05409_1.exp | CDS | 13806 | 10869 | - | 0.308584 | |
g7006 | DLA_07809 | GLQOFTK02FH5TG | CDS | 256365 | 1926 | - | 0.34839 | |
g7011 | DLA_07814 | GLQOFTK02FH5TG | CDS | 269937 | 6186 | + | 0.35257 | |
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 | |
g7018 | DLA_07822 | GLQOFTK02FH5TG | CDS | 297080 | 3927 | + | 0.330278 | |
g7059 | DLA_07875 | GLQOFTK02FH5TG | CDS | 400463 | 828 | + | 0.293478 | |
g7062 | DLA_07878 | GLQOFTK02FH5TG | CDS | 407406 | 591 | - | 0.314721 | |
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 |
g7071 | DLA_07891 | GLQOFTK02FH5TG | CDS | 433993 | 429 | - | 0.314685 | |
g7079 | DLA_07898 | GLQOFTK02FH5TG | CDS | 449014 | 7215 | - | 0.360776 | |
g7103 | DLA_07930 | GLQOFTK02FH5TG | CDS | 496861 | 1425 | + | 0.320702 | |
g7117 | DLA_07945 | GLQOFTK02FH5TG | CDS | 526254 | 1326 | - | 0.294872 | |
g713 | DLA_00785 | F4PJNLW01A00V1 | CDS | 167363 | 1281 | + | 0.323966 | |
g7130 | DLA_07959 | GLQOFTK02FH5TG | CDS | 553267 | 1290 | + | 0.322481 | |
g7136 | DLA_07966 | GLQOFTK02FH5TG | CDS | 567020 | 600 | - | 0.34 | |
g7145 | DLA_07975 | GLQOFTK02FH5TG | CDS | 582475 | 1227 | + | 0.320293 | |
g7146 | DLA_07976 | GLQOFTK02FH5TG | CDS | 583863 | 1821 | - | 0.298737 | |
g7166 | DLA_07997 | GLQOFTK02FH5TG | CDS | 636543 | 4971 | - | 0.356468 | |
g7167 | DLA_07998 | GLQOFTK02FH5TG | CDS | 642697 | 237 | + | 0.379747 | |
g7169 | DLA_08000 | GLQOFTK02FH5TG | CDS | 644830 | 6462 | - | 0.33844 | |
g719 | DLA_00791 | F4PJNLW01A00V1 | CDS | 178857 | 1383 | - | 0.336226 | |
g72 | DLA_00083 | contig05409_1.exp | CDS | 171875 | 1356 | - | 0.338496 | |
g7206 | DLA_08040 | GLQOFTK02FH5TG | CDS | 722028 | 927 | + | 0.326861 | |
g7212 | DLA_08048 | GLQOFTK02FH5TG | CDS | 731330 | 741 | - | 0.390013 | |
g7217 | DLA_08053 | GLQOFTK02FH5TG | CDS | 742825 | 5442 | - | 0.34932 | |
g7224 | DLA_08064 | GLQOFTK02FH5TG | CDS | 762109 | 2898 | + | 0.359213 | |
g7247 | DLA_08085 | GLQOFTK02FH5TG | CDS | 811394 | 1674 | - | 0.350657 | |
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 |
g7280 | DLA_08130 | GLQOFTK02FH5TG | CDS | 889945 | 807 | + | 0.298637 | |
g7283 | DLA_08133 | GLQOFTK02FH5TG | CDS | 894541 | 1524 | + | 0.324803 | |
g7288 | DLA_08141 | GLQOFTK02FH5TG | CDS | 904404 | 1536 | + | 0.32487 | |
g729 | DLA_00802 | F4PJNLW01A00V1 | CDS | 212215 | 1983 | + | 0.348462 | |
g7307 | DLA_08163 | GLQOFTK02FH5TG | CDS | 945122 | 2166 | + | 0.388735 | |
g7308 | DLA_08164 | GLQOFTK02FH5TG | CDS | 947412 | 822 | - | 0.298054 | |
g732 | DLA_00804 | F4PJNLW01A00V1 | CDS | 216545 | 2196 | + | 0.338798 | |
g7335 | DLA_08196 | GLQOFTK02FH5TG | CDS | 1020217 | 1299 | + | 0.341032 | |
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 |
g7368 | DLA_08235 | GLQOFTK02FH5TG | CDS | 1089007 | 984 | + | 0.362805 | |
g7391 | DLA_08264 | GLQOFTK02FH5TG | CDS | 1143655 | 2562 | + | 0.325527 | |
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 |
g7402 | DLA_08275 | GLQOFTK02FH5TG | CDS | 1173475 | 3729 | - | 0.320729 | |
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 |
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 | |
g7452 | DLA_08335 | GLQOFTK02FH5TG | CDS | 1293598 | 1518 | + | 0.296443 | |
g7456 | DLA_08340 | GLQOFTK02FH5TG | CDS | 1301682 | 3168 | - | 0.308081 | |
g7469 | DLA_08356 | GLQOFTK02FH5TG | CDS | 1335202 | 1944 | - | 0.308128 | |
g7499 | DLA_08390 | GLQOFTK02FH5TG | CDS | 1404152 | 11397 | + | 0.347899 | |
g7504 | DLA_08396 | similar to S. cerevisiae Lgs1 a putative GTPase involved in 60S ribosomal subunit biogenesis | GLQOFTK02FH5TG | CDS | 1424073 | 2001 | + | 0.337331 |
g7509 | DLA_08403 | GLQOFTK02FH5TG | CDS | 1436204 | 3498 | - | 0.333905 | |
g7515 | DLA_08410 | GLQOFTK02FH5TG | CDS | 1451510 | 642 | + | 0.32866 | |
g7516 | DLA_08411 | GLQOFTK02FH5TG | CDS | 1453541 | 675 | + | 0.29037 | |
g7559 | DLA_08454 | GLQOFTK02FH5TG | CDS | 1529803 | 975 | + | 0.267692 | |
g7560 | DLA_08455 | GLQOFTK02FH5TG | CDS | 1530851 | 4974 | - | 0.271009 | |
g7591 | DLA_08493 | GLQOFTK02G2F2O | CDS | 63296 | 1386 | + | 0.37013 | |
g76 | DLA_00088 | contig05409_1.exp | CDS | 179466 | 888 | + | 0.334459 | |
g7602 | DLA_08506 | GLQOFTK02G2F2O | CDS | 89225 | 2895 | + | 0.334715 | |
g7658 | DLA_08561 | GLQOFTK02G2F2O | CDS | 215043 | 1401 | + | 0.359743 | |
g7660 | DLA_08564 | GLQOFTK02G2F2O | CDS | 218083 | 2028 | - | 0.336292 | |
g7666 | DLA_08571 | GLQOFTK02G2F2O | CDS | 229400 | 3729 | + | 0.335747 | |
g7741 | DLA_08656 | GLQOFTK02G2F2O | CDS | 425482 | 1005 | + | 0.337313 | |
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 |
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 | |
g7793 | DLA_08711 | GLQOFTK02G2F2O | CDS | 538241 | 2769 | - | 0.340195 | |
g7808 | DLA_08728 | GLQOFTK02G2F2O | CDS | 571786 | 318 | + | 0.308176 | |
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 |
g7875 | DLA_08807 | GLQOFTK02G2F2O | CDS | 710380 | 1500 | - | 0.32 | |
g7877 | DLA_08810 | GLQOFTK02G2F2O | CDS | 713075 | 1005 | - | 0.304478 | |
g7884 | DLA_08817 | GLQOFTK02G2F2O | CDS | 730782 | 2313 | - | 0.348033 | |
g7887 | DLA_08820 | GLQOFTK02G2F2O | CDS | 737416 | 6120 | - | 0.315523 | |
g7892 | DLA_08825 | GLQOFTK02G2F2O | CDS | 749498 | 1536 | + | 0.326172 | |
g7909 | DLA_08843 | GLQOFTK02G2F2O | CDS | 779995 | 1656 | + | 0.300121 | |
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 |
g7923 | DLA_08857 | GLQOFTK02G2F2O | CDS | 804563 | 1752 | + | 0.304224 | |
g7924 | DLA_08859 | GLQOFTK02G2F2O | CDS | 807298 | 1602 | + | 0.320225 | |
g7953 | DLA_08888 | GLQOFTK02G2F2O | CDS | 886835 | 1737 | + | 0.35118 | |
g7963 | DLA_08898 | GLQOFTK02G2F2O | CDS | 906086 | 780 | + | 0.355128 | |
g7987 | DLA_08923 | GLQOFTK02G2F2O | CDS | 954719 | 609 | + | 0.320197 | |
g8032 | DLA_08979 | GLQOFTK02G2F2O | CDS | 1052648 | 3534 | - | 0.344086 | |
g8049 | DLA_08998 | GLQOFTK02G2F2O | CDS | 1100752 | 609 | + | 0.334975 | |
g8051 | DLA_09000 | GLQOFTK02G2F2O | CDS | 1103132 | 576 | - | 0.34375 | |
g8061 | DLA_09010 | GLQOFTK02G2F2O | CDS | 1128020 | 939 | - | 0.297125 | |
g807 | DLA_00887 | F4PJNLW01A00V1 | CDS | 364301 | 1164 | + | 0.361684 | |
g8076 | DLA_09027 | GLQOFTK02G2F2O | CDS | 1167491 | 3087 | + | 0.295432 | |
g8077 | DLA_09028 | GLQOFTK02G2F2O | CDS | 1171541 | 1416 | + | 0.336158 | |
g8085 | DLA_09036 | GLQOFTK02G2F2O | CDS | 1191341 | 969 | - | 0.273478 | |
g8099 | DLA_09052 | GLQOFTK02G2F2O | CDS | 1220399 | 549 | + | 0.264117 | |
g810 | DLA_00890 | similar to mammalian NIT1 there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 369236 | 939 | + | 0.339723 |
g8121 | DLA_09076 | GLQOFTK02G2F2O | CDS | 1288437 | 813 | + | 0.314883 | |
g8123 | DLA_09078 | GLQOFTK02G2F2O | CDS | 1290791 | 1539 | + | 0.345679 | |
g8160 | DLA_09118 | GLQOFTK02G2F2O | CDS | 1379715 | 2157 | + | 0.351414 | |
g8165 | DLA_09124 | GLQOFTK02G2F2O | CDS | 1390924 | 984 | - | 0.355691 | |
g8198 | DLA_09155 | GLQOFTK02G2F2O | CDS | 1456584 | 1122 | + | 0.356506 | |
g82 | DLA_00094 | contig05409_1.exp | CDS | 186440 | 2235 | - | 0.365101 | |
g8204 | DLA_09161 | GLQOFTK02G2F2O | CDS | 1464176 | 636 | - | 0.272013 | |
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 |
g8215 | DLA_09172 | GLQOFTK02G2F2O | CDS | 1482132 | 1758 | - | 0.289534 | |
g8218 | DLA_09175 | GLQOFTK02G2F2O | CDS | 1490003 | 1221 | - | 0.329238 | |
g8226 | DLA_09184 | GLQOFTK02G2F2O | CDS | 1504448 | 561 | - | 0.342246 | |
g8229 | DLA_09187 | GLQOFTK02G2F2O | CDS | 1510146 | 3015 | + | 0.330348 | |
g8238 | DLA_09199 | GLQOFTK02G2F2O | CDS | 1547185 | 1107 | + | 0.399277 | |
g8244 | DLA_09206 | GLQOFTK02G2F2O | CDS | 1560139 | 615 | + | 0.347967 | |
g8248 | DLA_09210 | GLQOFTK02G2F2O | CDS | 1566643 | 300 | + | 0.303333 | |
g8250 | DLA_09212 | GLQOFTK02G2F2O | CDS | 1568149 | 1248 | + | 0.334135 | |
g8261 | DLA_09221 | GLQOFTK02G2F2O | CDS | 1591695 | 1860 | + | 0.374731 | |
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 |
g83 | DLA_00095 | contig05409_1.exp | CDS | 189619 | 3597 | + | 0.350014 | |
g8301 | DLA_09263 | GLQOFTK02G2F2O | CDS | 1681686 | 522 | - | 0.295019 | |
g8315 | DLA_09280 | GLQOFTK02G2F2O | CDS | 1706839 | 684 | - | 0.321637 | |
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 |
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 | |
g8342 | DLA_09310 | GLQOFTK02G2F2O | CDS | 1759887 | 2610 | - | 0.318391 | |
g8349 | DLA_09317 | GLQOFTK02G2F2O | CDS | 1775471 | 933 | + | 0.327974 | |
g835 | DLA_00916 | F4PJNLW01A00V1 | CDS | 428746 | 1794 | - | 0.375697 | |
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 |
g8357 | DLA_09324 | GLQOFTK02G2F2O | CDS | 1787804 | 918 | - | 0.330065 | |
g8368 | DLA_09334 | GLQOFTK02G2F2O | CDS | 1804605 | 483 | + | 0.337474 | |
g8405 | DLA_09374 | GLQOFTK02G2F2O | CDS | 1867535 | 615 | - | 0.302439 | |
g8411 | DLA_09380 | GLQOFTK02G2F2O | CDS | 1876839 | 2823 | - | 0.307474 | |
g8416 | DLA_09385 | GLQOFTK02G2F2O | CDS | 1890456 | 453 | + | 0.335541 | |
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 |
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 |
g8438 | DLA_09409 | GLQOFTK02G2F2O | CDS | 1936897 | 486 | + | 0.27572 | |
g8462 | DLA_09433 | GLQOFTK02G2F2O | CDS | 1993768 | 675 | - | 0.340741 | |
g8474 | DLA_09447 | GLQOFTK02G2F2O | CDS | 2023625 | 2490 | + | 0.317671 | |
g8478 | DLA_09451 | homolog of human Sphk1 phosphorylates sphinganine to sphinganine 1-phosphate | GLQOFTK02G2F2O | CDS | 2029787 | 1752 | + | 0.31621 |
g85 | DLA_11431 | contig05409_1.exp | CDS | 195949 | 1239 | - | 0.329298 | |
g8501 | DLA_09478 | GLQOFTK02GHM7A | CDS | 27802 | 1296 | + | 0.334877 | |
g8509 | DLA_09485 | GLQOFTK02GHM7A | CDS | 40990 | 7914 | + | 0.321203 | |
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 | |
g8549 | DLA_09533 | GLQOFTK02GHM7A | CDS | 142400 | 813 | - | 0.305043 | |
g8556 | DLA_09540 | GLQOFTK02GHM7A | CDS | 152126 | 555 | - | 0.338739 | |
g8581 | DLA_09565 | GLQOFTK02GHM7A | CDS | 205126 | 1794 | + | 0.348383 | |
g8594 | DLA_09586 | GLQOFTK02GHM7A | CDS | 251508 | 717 | + | 0.313808 | |
g8597 | DLA_09589 | GLQOFTK02GHM7A | CDS | 256496 | 2496 | - | 0.306891 | |
g8612 | DLA_09605 | GLQOFTK02GHM7A | CDS | 289302 | 549 | - | 0.313297 | |
g8635 | DLA_09628 | GLQOFTK02GHM7A | CDS | 354334 | 981 | - | 0.367992 | |
g8652 | DLA_09647 | GLQOFTK02GHM7A | CDS | 389024 | 693 | - | 0.300144 | |
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 |
g8675 | DLA_09672 | GLQOFTK02GHM7A | CDS | 440164 | 2031 | - | 0.36583 | |
g8683 | DLA_09679 | GLQOFTK02GHM7A | CDS | 455956 | 2016 | + | 0.288194 | |
g8695 | DLA_09691 | GLQOFTK02GHM7A | CDS | 481830 | 1944 | - | 0.360082 | |
g87 | DLA_00099 | contig05409_1.exp | CDS | 199998 | 1878 | - | 0.309372 | |
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 |
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 | |
g8750 | DLA_09746 | GLQOFTK02GHM7A | CDS | 602081 | 4905 | - | 0.312946 | |
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 |
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 |
g8770 | DLA_09768 | GLQOFTK02GHM7A | CDS | 645448 | 873 | + | 0.32646 | |
g8782 | DLA_09781 | GLQOFTK02GHM7A | CDS | 666017 | 873 | - | 0.321879 | |
g8785 | DLA_09786 | GLQOFTK02GHM7A | CDS | 673423 | 864 | + | 0.325231 | |
g8786 | DLA_09787 | GLQOFTK02GHM7A | CDS | 674780 | 3354 | + | 0.335122 | |
g8796 | DLA_09798 | GLQOFTK02GHM7A | CDS | 698755 | 1263 | + | 0.391132 | |
g8806 | DLA_09811 | GLQOFTK02GHM7A | CDS | 729001 | 2019 | - | 0.414562 | |
g8818 | DLA_11791 | GLQOFTK02GHM7A | CDS | 769360 | 4740 | - | 0.316245 | |
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 |
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 |
g886 | DLA_00977 | F4PJNLW01A00V1 | CDS | 562847 | 1089 | - | 0.311295 | |
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 |
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 |
g8900 | DLA_09918 | GLQOFTK02GQ36N | CDS | 86387 | 2031 | - | 0.293451 | |
g8906 | DLA_09925 | GLQOFTK02GQ36N | CDS | 97926 | 1716 | - | 0.327506 | |
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 |
g8925 | DLA_09945 | GLQOFTK02GQ36N | CDS | 149946 | 1824 | - | 0.320724 | |
g8941 | DLA_09960 | GLQOFTK02GQ36N | CDS | 186083 | 1941 | - | 0.325605 | |
g8948 | DLA_09967 | GLQOFTK02GQ36N | CDS | 199825 | 330 | + | 0.321212 | |
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 |
g8972 | DLA_09994 | GLQOFTK02GQ36N | CDS | 253220 | 861 | + | 0.307782 | |
g8973 | DLA_09995 | GLQOFTK02GQ36N | CDS | 254501 | 858 | + | 0.317016 | |
g8976 | DLA_09998 | GLQOFTK02GQ36N | CDS | 260339 | 3603 | + | 0.360533 | |
g8977 | DLA_10000 | GLQOFTK02GQ36N | CDS | 264677 | 615 | + | 0.336585 | |
g8998 | DLA_10021 | GLQOFTK02GQ36N | CDS | 309236 | 1692 | + | 0.339244 | |
g90 | DLA_00106 | contig05409_1.exp | CDS | 210207 | 1308 | - | 0.340214 | |
g9020 | DLA_10041 | GLQOFTK02GQ36N | CDS | 349782 | 984 | + | 0.279472 | |
g9022 | DLA_10043 | GLQOFTK02GQ36N | CDS | 352081 | 636 | - | 0.325472 | |
g9034 | DLA_10055 | GLQOFTK02GQ36N | CDS | 375331 | 1425 | + | 0.350175 | |
g9035 | DLA_10056 | GLQOFTK02GQ36N | CDS | 377200 | 1983 | + | 0.33535 | |
g9038 | DLA_10059 | GLQOFTK02GQ36N | CDS | 383424 | 1023 | - | 0.318671 | |
g9056 | DLA_10077 | GLQOFTK02GQ36N | CDS | 417938 | 447 | - | 0.288591 | |
g9060 | DLA_10082 | GLQOFTK02GQ36N | CDS | 423257 | 6573 | - | 0.314012 | |
g9076 | DLA_10100 | GLQOFTK02GQ36N | CDS | 470773 | 537 | - | 0.299814 | |
g9100 | DLA_10131 | GLQOFTK02GQ36N | CDS | 547114 | 3396 | + | 0.326855 | |
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 |
g9120 | DLA_10154 | GLQOFTK02GQ36N | CDS | 597098 | 552 | - | 0.298913 | |
g9122 | DLA_10157 | GLQOFTK02GQ36N | CDS | 599686 | 3750 | - | 0.333067 | |
g9137 | DLA_10173 | GLQOFTK02GQ36N | CDS | 627095 | 1566 | + | 0.346105 | |
g9149 | DLA_10189 | GLQOFTK02GQ36N | CDS | 655472 | 837 | - | 0.354839 | |
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 |
g9211 | DLA_10262 | GLQOFTK02GUKFG | CDS | 134644 | 849 | + | 0.319199 | |
g9246 | DLA_10301 | GLQOFTK02GUKFG | CDS | 212252 | 948 | + | 0.338608 | |
g9250 | DLA_10305 | GLQOFTK02GUKFG | CDS | 219627 | 555 | - | 0.295496 | |
g9264 | DLA_10322 | GLQOFTK02GUKFG | CDS | 262470 | 1731 | + | 0.317735 | |
g9276 | DLA_10335 | GLQOFTK02GUKFG | CDS | 303006 | 2415 | + | 0.370186 | |
g928 | DLA_01027 | F4PJNLW01A00V1 | CDS | 656534 | 405 | + | 0.306173 | |
g9304 | DLA_10371 | GLQOFTK02GUKFG | CDS | 369405 | 732 | - | 0.327869 | |
g9309 | DLA_10377 | catalyzes the reaction: ATP L-fucose ADP beta-L-fucose 1-phosphate | GLQOFTK02GUKFG | CDS | 376640 | 3456 | + | 0.338542 |
g932 | DLA_01032 | F4PJNLW01A00V1 | CDS | 665942 | 846 | + | 0.336879 | |
g933 | DLA_01033 | F4PJNLW01A00V1 | CDS | 667032 | 873 | + | 0.342497 | |
g9337 | DLA_10410 | GLQOFTK02GUKFG | CDS | 433150 | 678 | + | 0.320059 | |
g9346 | DLA_11809 | actin binding protein regulating actin nucleation involved in cytokinesis and cell motility | GLQOFTK02GUKFG | CDS | 448979 | 1359 | + | 0.38337 |
g9359 | DLA_10430 | GLQOFTK02GUKFG | CDS | 477421 | 723 | - | 0.344398 | |
g9360 | DLA_10431 | GLQOFTK02GUKFG | CDS | 478564 | 858 | + | 0.29021 | |
g9366 | DLA_10437 | GLQOFTK02GUKFG | CDS | 488096 | 2061 | + | 0.312955 | |
g9373 | DLA_10444 | GLQOFTK02GUKFG | CDS | 502462 | 690 | + | 0.276812 | |
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 |
g9383 | DLA_10454 | GLQOFTK02GUKFG | CDS | 519874 | 1305 | + | 0.306513 | |
g939 | DLA_01038 | F4PJNLW01A00V1 | CDS | 675097 | 1035 | - | 0.256039 | |
g9427 | DLA_10503 | GLQOFTK02IIOHN | CDS | 42864 | 1668 | + | 0.344724 | |
g9435 | DLA_10512 | GLQOFTK02IIOHN | CDS | 61093 | 897 | + | 0.327759 | |
g9438 | DLA_10515 | GLQOFTK02IIOHN | CDS | 66408 | 798 | + | 0.274436 | |
g9466 | DLA_10549 | GLQOFTK02IIOHN | CDS | 133276 | 1392 | - | 0.369971 | |
g947 | DLA_01046 | F4PJNLW01A00V1 | CDS | 696119 | 843 | - | 0.329775 | |
g9470 | DLA_10554 | GLQOFTK02IIOHN | CDS | 143002 | 2214 | + | 0.325655 | |
g9483 | DLA_10570 | GLQOFTK02IJPNF | CDS | 4491 | 1311 | - | 0.280702 | |
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 |
g949 | DLA_01048 | F4PJNLW01A00V1 | CDS | 701075 | 1980 | + | 0.283333 | |
g9496 | DLA_10585 | GLQOFTK02IJPNF | CDS | 31255 | 825 | - | 0.307879 | |
g95 | DLA_00110 | contig05409_1.exp | CDS | 221480 | 1122 | + | 0.335116 | |
g9527 | DLA_10619 | GLQOFTK02IJPNF | CDS | 111897 | 849 | + | 0.342756 | |
g9532 | DLA_10624 | GLQOFTK02IJPNF | CDS | 122365 | 414 | + | 0.338164 | |
g9577 | DLA_10676 | GLQOFTK02IJPNF | CDS | 217738 | 495 | - | 0.333333 | |
g9582 | DLA_10683 | GLQOFTK02IJPNF | CDS | 228054 | 1320 | - | 0.393182 | |
g9588 | DLA_10690 | GLQOFTK02IJPNF | CDS | 237690 | 5268 | - | 0.351557 | |
g9592 | DLA_10694 | GLQOFTK02IJPNF | CDS | 253538 | 2442 | + | 0.330467 | |
g9594 | DLA_10696 | GLQOFTK02IJPNF | CDS | 257585 | 3006 | + | 0.357285 | |
g9599 | DLA_10703 | GLQOFTK02IJPNF | CDS | 270793 | 4284 | + | 0.2507 | |
g960 | DLA_01063 | F4PJNLW01A00V1 | CDS | 727967 | 435 | + | 0.312644 | |
g9602 | DLA_10710 | GLQOFTK02IRMR1 | CDS | 2800 | 642 | - | 0.334891 | |
g9604 | DLA_10712 | GLQOFTK02IRMR1 | CDS | 5471 | 990 | - | 0.276768 | |
g9606 | DLA_10714 | GLQOFTK02IRMR1 | CDS | 8405 | 2478 | - | 0.322841 | |
g961 | DLA_01064 | F4PJNLW01A00V1 | CDS | 729224 | 540 | - | 0.298148 | |
g9617 | DLA_10723 | GLQOFTK02IRMR1 | CDS | 31401 | 4668 | - | 0.336118 | |
g9634 | DLA_10741 | GLQOFTK02IRMR1 | CDS | 78600 | 876 | + | 0.294521 | |
g9636 | DLA_10743 | GLQOFTK02IRMR1 | CDS | 81280 | 1392 | - | 0.333333 | |
g9642 | DLA_10750 | GLQOFTK02IRMR1 | CDS | 94956 | 5625 | - | 0.323022 | |
g9648 | DLA_10760 | GLQOFTK02IRMR1 | CDS | 111344 | 1833 | - | 0.346972 | |
g9649 | DLA_10761 | GLQOFTK02IRMR1 | CDS | 113543 | 921 | - | 0.343105 | |
g9650 | DLA_10762 | GLQOFTK02IRMR1 | CDS | 114914 | 897 | + | 0.311037 | |
g9651 | DLA_10763 | GLQOFTK02IRMR1 | CDS | 116295 | 897 | + | 0.322185 | |
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 | |
g9667 | DLA_10782 | GLQOFTK02IRMR1 | CDS | 155904 | 621 | - | 0.288245 | |
g9675 | DLA_10792 | GLQOFTK02IRMR1 | CDS | 175074 | 570 | + | 0.247368 | |
g9677 | DLA_10794 | GLQOFTK02IRMR1 | CDS | 177572 | 651 | - | 0.321045 | |
g968 | DLA_01076 | F4PJNLW01A00V1 | CDS | 755516 | 921 | - | 0.30836 | |
g9683 | DLA_10802 | GLQOFTK02IRMR1 | CDS | 189497 | 582 | - | 0.285223 | |
g9697 | DLA_10821 | GLQOFTK02JCFFB | CDS | 17599 | 2241 | - | 0.361446 | |
g9698 | DLA_10822 | GLQOFTK02JCFFB | CDS | 20581 | 3990 | - | 0.335338 | |
g971 | DLA_01080 | F4PJNLW01A00V1 | CDS | 761769 | 591 | + | 0.324873 | |
g9711 | DLA_10837 | plays a role in the regulation of cleavage furrow formation similar to S. pombe cdc7 | GLQOFTK02JCFFB | CDS | 55659 | 3321 | + | 0.350196 |
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 | |
g9730 | DLA_10862 | GLQOFTK02JCFFB | CDS | 106430 | 2298 | - | 0.295909 | |
g9757 | DLA_10892 | GLQOFTK02JL55Q | CDS | 50940 | 1017 | + | 0.292035 | |
g9761 | DLA_10896 | GLQOFTK02JL55Q | CDS | 59863 | 855 | - | 0.308772 | |
g9763 | DLA_10898 | GLQOFTK02JL55Q | CDS | 66060 | 1236 | + | 0.307443 | |
g9764 | DLA_10899 | GLQOFTK02JL55Q | CDS | 67729 | 2514 | + | 0.334527 | |
g9785 | DLA_10918 | GLQOFTK02JL55Q | CDS | 114371 | 1506 | - | 0.326029 | |
g9799 | DLA_10939 | GLQOFTK02JL55Q | CDS | 152479 | 1332 | + | 0.339339 | |
g9800 | DLA_10940 | GLQOFTK02JL55Q | CDS | 153859 | 897 | - | 0.283166 | |
g9828 | DLA_10968 | GLQOFTK02JL55Q | CDS | 211592 | 1659 | + | 0.380952 | |
g9829 | DLA_10969 | GLQOFTK02JL55Q | CDS | 213688 | 1734 | + | 0.375433 | |
g9859 | DLA_11004 | GLQOFTK02JL55Q | CDS | 280021 | 1545 | - | 0.374757 | |
g9860 | DLA_11005 | GLQOFTK02JL55Q | CDS | 282149 | 861 | - | 0.369338 | |
g9866 | DLA_11011 | GLQOFTK02JL55Q | CDS | 300619 | 1866 | - | 0.341908 | |
g9870 | DLA_11015 | GLQOFTK02JL55Q | CDS | 307354 | 3702 | + | 0.337655 | |
g9874 | DLA_11022 | GLQOFTK02JL55Q | CDS | 321065 | 1380 | + | 0.294928 | |
g9877 | DLA_11025 | GLQOFTK02JL55Q | CDS | 327533 | 1737 | + | 0.352332 | |
g9903 | DLA_11052 | GLQOFTK02JL55Q | CDS | 378327 | 1635 | - | 0.322324 | |
g9924 | DLA_11071 | GLQOFTK02JL55Q | CDS | 428140 | 684 | + | 0.314327 | |
g9952 | DLA_11101 | GLQOFTK02JL55Q | CDS | 501663 | 1545 | + | 0.331392 | |
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 |
g9968 | DLA_11118 | GLQOFTK02JL55Q | CDS | 534853 | 912 | + | 0.380482 | |
g9980 | DLA_11133 | GLQOFTK02JL55Q | CDS | 555380 | 903 | - | 0.284607 | |
g9985 | DLA_11138 | GLQOFTK02JL55Q | CDS | 561405 | 1842 | + | 0.325733 | |
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 |