Gene list
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COG category: Replication, recombination and repair
Organism: Dictyostelium lacteum
Number of genes found: 421
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 |
g10022 | DLA_11184 | GLQOFTK02JL55Q | CDS | 639909 | 2118 | - | 0.315392 | |
g10043 | DLA_11206 | GLQOFTK02JL55Q | CDS | 683801 | 1260 | - | 0.281746 | |
g10044 | DLA_11207 | GLQOFTK02JL55Q | CDS | 685183 | 1239 | - | 0.297014 | |
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 |
g1007 | DLA_01117 | F4PJNLW01A00V1 | CDS | 843560 | 7092 | + | 0.326424 | |
g10075 | DLA_11248 | GLQOFTK02JL55Q | CDS | 756239 | 1938 | + | 0.288958 | |
g10106 | DLA_11284 | GLQOFTK02JL55Q | CDS | 823910 | 2478 | + | 0.307103 | |
g10109 | DLA_11287 | GLQOFTK02JL55Q | CDS | 829023 | 804 | - | 0.298507 | |
g10113 | DLA_11293 | hydrolyses alkylated adenine residues on DNA releasing 3-methyladenine | GLQOFTK02JL55Q | CDS | 836557 | 678 | + | 0.306785 |
g10123 | DLA_11305 | GLQOFTK02JL55Q | CDS | 865248 | 873 | + | 0.353952 | |
g10139 | DLA_11326 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | GLQOFTK02JL55Q | CDS | 904155 | 1899 | + | 0.319115 |
g10154 | DLA_11344 | GLQOFTK02JL55Q | CDS | 936163 | 1962 | + | 0.284913 | |
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 |
g1097 | DLA_01213 | F4PJNLW01A00V1 | CDS | 1034101 | 2148 | - | 0.366853 | |
g1137 | DLA_01255 | F4PJNLW01A00V1 | CDS | 1143780 | 1638 | + | 0.310745 | |
g1144 | DLA_01262 | F4PJNLW01A00V1 | CDS | 1157028 | 3807 | - | 0.353297 | |
g1167 | DLA_01284 | F4PJNLW01A00V1 | CDS | 1225330 | 4419 | - | 0.342838 | |
g1215 | DLA_01337 | F4PJNLW01A00V1 | CDS | 1341753 | 5667 | - | 0.341803 | |
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 |
g1258 | DLA_01381 | F4PJNLW01A00V1 | CDS | 1444033 | 1494 | + | 0.281125 | |
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 |
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 |
g1326 | DLA_01452 | F4PJNLW01B0TO9 | CDS | 76843 | 4308 | + | 0.333798 | |
g1332 | DLA_01462 | F4PJNLW01B0TO9 | CDS | 92167 | 1032 | + | 0.300388 | |
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 |
g1354 | DLA_01484 | F4PJNLW01B0TO9 | CDS | 149734 | 3606 | - | 0.344981 | |
g136 | DLA_00157 | contig05409_1.exp | CDS | 313401 | 3300 | + | 0.308182 | |
g1387 | DLA_11481 | F4PJNLW01B0TO9 | CDS | 220295 | 465 | + | 0.378495 | |
g140 | DLA_00163 | contig05409_1.exp | CDS | 327309 | 2994 | + | 0.327321 | |
g1409 | DLA_01545 | F4PJNLW01B0TO9 | CDS | 262242 | 1941 | + | 0.327666 | |
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 | |
g144 | DLA_00167 | contig05409_1.exp | CDS | 337749 | 2379 | - | 0.349306 | |
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 |
g1548 | DLA_01696 | F4PJNLW01B0TO9 | CDS | 576002 | 3606 | - | 0.311425 | |
g1549 | DLA_11488 | F4PJNLW01B0TO9 | CDS | 580805 | 2460 | + | 0.387398 | |
g1550 | DLA_01697 | F4PJNLW01B0TO9 | CDS | 583710 | 5862 | + | 0.360628 | |
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 |
g1606 | DLA_01758 | F4PJNLW01B0TO9 | CDS | 707303 | 1743 | - | 0.327022 | |
g1618 | DLA_01772 | F4PJNLW01B0TO9 | CDS | 729828 | 1833 | - | 0.333879 | |
g162 | DLA_00188 | contig05409_1.exp | CDS | 376542 | 1929 | + | 0.369103 | |
g1668 | DLA_01824 | F4PJNLW01B0TO9 | CDS | 846981 | 2520 | + | 0.289286 | |
g1691 | DLA_01851 | F4PJNLW01B0TO9 | CDS | 905167 | 3105 | - | 0.335266 | |
g1697 | DLA_01857 | F4PJNLW01B0TO9 | CDS | 918129 | 1437 | - | 0.347251 | |
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 |
g1728 | DLA_01892 | F4PJNLW01B0TO9 | CDS | 988245 | 3060 | + | 0.32451 | |
g1751 | DLA_01915 | belongs to a superfamily of metalloenzymes induced by Legionella pneumophila infection | F4PJNLW01B3KKL | CDS | 5796 | 1023 | + | 0.297165 |
g1794 | DLA_01957 | F4PJNLW01C9MXC | CDS | 67445 | 2940 | + | 0.339796 | |
g1833 | DLA_01998 | F4PJNLW01C9MXC | CDS | 161915 | 1767 | + | 0.367855 | |
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 | |
g1935 | DLA_02117 | F4PJNLW01DERRH | CDS | 124838 | 2322 | - | 0.314384 | |
g1976 | DLA_02166 | F4PJNLW01DERRH | CDS | 222365 | 723 | - | 0.305671 | |
g1978 | DLA_02169 | F4PJNLW01DERRH | CDS | 225983 | 1635 | - | 0.329664 | |
g1985 | DLA_02178 | putative RNA helicase contains an RWD domain (RING finger and WD repeat) | F4PJNLW01DERRH | CDS | 241601 | 4122 | - | 0.318535 |
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 |
g2035 | DLA_02237 | F4PJNLW01DERRH | CDS | 361545 | 1866 | + | 0.369775 | |
g2049 | DLA_02252 | F4PJNLW01DERRH | CDS | 385220 | 5760 | + | 0.336111 | |
g2055 | DLA_02260 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | F4PJNLW01DERRH | CDS | 399702 | 2160 | + | 0.346296 |
g2071 | DLA_02277 | F4PJNLW01DERRH | CDS | 430969 | 1344 | + | 0.3125 | |
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 |
g2105 | DLA_02319 | F4PJNLW01DERRH | CDS | 497752 | 2889 | + | 0.283143 | |
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 |
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 | |
g2174 | DLA_02394 | F4PJNLW01DERRH | CDS | 662630 | 2847 | - | 0.336495 | |
g2175 | DLA_02395 | F4PJNLW01DERRH | CDS | 665801 | 1602 | + | 0.303371 | |
g2181 | DLA_02401 | F4PJNLW01DERRH | CDS | 675835 | 1575 | + | 0.290159 | |
g2206 | DLA_02429 | F4PJNLW01EE5MJ | CDS | 154 | 1812 | + | 0.312362 | |
g2236 | DLA_02470 | F4PJNLW01EE5MJ | CDS | 81014 | 1212 | + | 0.285479 | |
g2260 | DLA_02495 | F4PJNLW01EE5MJ | CDS | 138880 | 2247 | - | 0.365821 | |
g2282 | DLA_02524 | F4PJNLW01EE5MJ | CDS | 198242 | 2193 | - | 0.336981 | |
g2306 | DLA_02550 | F4PJNLW01EE5MJ | CDS | 260902 | 897 | - | 0.338907 | |
g2364 | DLA_02614 | F4PJNLW01EE5MJ | CDS | 365601 | 5229 | - | 0.347676 | |
g2426 | DLA_02687 | F4PJNLW01EE5MJ | CDS | 499115 | 4104 | + | 0.34308 | |
g2428 | DLA_02691 | F4PJNLW01EE5MJ | CDS | 508852 | 2733 | + | 0.320161 | |
g2455 | DLA_02725 | F4PJNLW01EE5MJ | CDS | 579082 | 2658 | - | 0.322047 | |
g2464 | DLA_02733 | F4PJNLW01EE5MJ | CDS | 603644 | 5577 | - | 0.337637 | |
g2473 | DLA_02744 | F4PJNLW01EE5MJ | CDS | 624351 | 3513 | + | 0.317108 | |
g2488 | DLA_02759 | F4PJNLW01EE5MJ | CDS | 667342 | 6816 | + | 0.359008 | |
g2514 | DLA_02788 | F4PJNLW01EE5MJ | CDS | 721035 | 2421 | + | 0.327551 | |
g2520 | DLA_02794 | F4PJNLW01EE5MJ | CDS | 732818 | 813 | - | 0.341943 | |
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 |
g2542 | DLA_02816 | F4PJNLW01EE5MJ | CDS | 781075 | 2442 | + | 0.285831 | |
g2578 | DLA_02861 | F4PJNLW01EE5MJ | CDS | 864104 | 2604 | - | 0.320276 | |
g2586 | DLA_02869 | F4PJNLW01EE5MJ | CDS | 880997 | 1695 | + | 0.315634 | |
g2620 | DLA_02908 | F4PJNLW01EE5MJ | CDS | 969208 | 3174 | - | 0.333018 | |
g2636 | DLA_02926 | F4PJNLW01EE5MJ | CDS | 1000811 | 2118 | - | 0.344193 | |
g270 | DLA_00300 | contig05409_1.exp | CDS | 625941 | 2418 | + | 0.35732 | |
g2705 | DLA_02999 | F4PJNLW01EE5MJ | CDS | 1138608 | 2625 | - | 0.299429 | |
g2720 | DLA_03016 | F4PJNLW01EE5MJ | CDS | 1170267 | 1944 | + | 0.314815 | |
g2739 | DLA_03035 | F4PJNLW01EE5MJ | CDS | 1213710 | 1593 | + | 0.338983 | |
g2797 | DLA_03097 | F4PJNLW02GJ9ZB | CDS | 85137 | 2370 | - | 0.337975 | |
g2816 | DLA_03116 | similar to eukaryotic translation initiation factor 4A isoform 2 | F4PJNLW02GJ9ZB | CDS | 129122 | 1155 | + | 0.386147 |
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 |
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 |
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 |
g284 | DLA_00314 | contig05409_1.exp | CDS | 652127 | 3645 | + | 0.322908 | |
g2857 | DLA_11542 | similar to eukaryotic initiation factor 4A isoform 3 | F4PJNLW02GJ9ZB | CDS | 228496 | 1212 | + | 0.319307 |
g2874 | DLA_03185 | F4PJNLW02GJ9ZB | CDS | 270085 | 927 | - | 0.316073 | |
g2880 | DLA_03192 | F4PJNLW02HBBIY | CDS | 4701 | 1035 | - | 0.27343 | |
g292 | DLA_00324 | contig05409_1.exp | CDS | 676113 | 1521 | + | 0.293886 | |
g2921 | DLA_03236 | F4PJNLW02HBBIY | CDS | 97770 | 1467 | - | 0.334015 | |
g2922 | DLA_03237 | F4PJNLW02HBBIY | CDS | 100288 | 2214 | + | 0.337398 | |
g2942 | DLA_03260 | F4PJNLW02HBBIY | CDS | 138381 | 11952 | + | 0.347808 | |
g3037 | DLA_03363 | F4PJNLW02HBBIY | CDS | 366615 | 2451 | - | 0.339861 | |
g3060 | DLA_03387 | F4PJNLW02HBBIY | CDS | 418335 | 3711 | - | 0.306656 | |
g3061 | DLA_03388 | F4PJNLW02HBBIY | CDS | 422744 | 2760 | + | 0.350362 | |
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 |
g3211 | DLA_03560 | GAOABQK02FWKR3 | CDS | 24327 | 2148 | + | 0.293762 | |
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 |
g3267 | DLA_03616 | GAOABQK02G6SYV | CDS | 97173 | 2745 | - | 0.289982 | |
g3277 | DLA_03627 | GAOABQK02G6SYV | CDS | 120541 | 1149 | - | 0.314186 | |
g3322 | DLA_03673 | GAOABQK02G6SYV | CDS | 207498 | 4548 | + | 0.348505 | |
g3350 | DLA_03706 | GAOABQK02G6SYV | CDS | 264850 | 3468 | - | 0.364475 | |
g3401 | DLA_03761 | GAOABQK02G6SYV | CDS | 373601 | 1809 | + | 0.342731 | |
g3412 | DLA_03775 | GAOABQK02G6SYV | CDS | 393352 | 3546 | + | 0.368302 | |
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 |
g3477 | DLA_03851 | GAOABQK02G6SYV | CDS | 543912 | 2457 | + | 0.307692 | |
g3479 | DLA_03854 | GAOABQK02G6SYV | CDS | 548414 | 2544 | - | 0.307783 | |
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 |
g3499 | DLA_03877 | GAOABQK02G6SYV | CDS | 599757 | 1542 | - | 0.328794 | |
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 |
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 |
g3549 | DLA_03930 | GAOABQK02G7M1S | CDS | 12808 | 2847 | + | 0.334387 | |
g3558 | DLA_03938 | GAOABQK02G7M1S | CDS | 31797 | 4113 | + | 0.292001 | |
g3567 | DLA_03951 | GAOABQK02G7M1S | CDS | 67898 | 3429 | + | 0.345582 | |
g36 | DLA_00041 | contig05409_1.exp | CDS | 91681 | 2490 | - | 0.377108 | |
g3635 | DLA_04031 | GAOABQK02G7M1S | CDS | 227137 | 1110 | + | 0.362162 | |
g3647 | DLA_04044 | GAOABQK02G7M1S | CDS | 257955 | 1452 | - | 0.304408 | |
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 |
g3725 | DLA_04128 | GAOABQK02G7M1S | CDS | 436959 | 2169 | - | 0.323651 | |
g3741 | DLA_04144 | GAOABQK02G7M1S | CDS | 471893 | 2535 | - | 0.341223 | |
g3784 | DLA_04196 | GAOABQK02G7M1S | CDS | 566511 | 1071 | + | 0.345472 | |
g3799 | DLA_04213 | GAOABQK02G7M1S | CDS | 604665 | 1314 | + | 0.362253 | |
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 |
g3821 | DLA_04239 | GAOABQK02G7M1S | CDS | 664421 | 2448 | - | 0.319853 | |
g3836 | DLA_04254 | GAOABQK02G7M1S | CDS | 693478 | 3450 | - | 0.325507 | |
g3864 | DLA_04284 | GAOABQK02G7M1S | CDS | 761256 | 1530 | + | 0.336601 | |
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 |
g3918 | DLA_04343 | GAOABQK02GQAQJ | CDS | 111354 | 2523 | - | 0.317876 | |
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 | |
g3934 | DLA_04363 | GAOABQK02GQAQJ | CDS | 151071 | 2484 | + | 0.355878 | |
g3960 | DLA_04389 | GAOABQK02GQAQJ | CDS | 202770 | 3390 | - | 0.314454 | |
g3962 | DLA_04391 | GAOABQK02GQAQJ | CDS | 209901 | 624 | - | 0.355769 | |
g3974 | DLA_04404 | GAOABQK02GQAQJ | CDS | 230653 | 6513 | + | 0.340243 | |
g398 | DLA_00442 | contig05409_1.exp | CDS | 911085 | 2340 | + | 0.334188 | |
g4011 | DLA_04450 | GAOABQK02GQAQJ | CDS | 329479 | 546 | + | 0.358974 | |
g4012 | DLA_04451 | GAOABQK02GQAQJ | CDS | 330396 | 939 | - | 0.342918 | |
g403 | DLA_00447 | contig05409_1.exp | CDS | 920565 | 2895 | - | 0.331606 | |
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 |
g4062 | DLA_04505 | GAOABQK02GQAQJ | CDS | 438051 | 5988 | - | 0.305945 | |
g4083 | DLA_04526 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | GAOABQK02GQAQJ | CDS | 483386 | 2190 | - | 0.336073 |
g4149 | DLA_04597 | GAOABQK02GQAQJ | CDS | 611526 | 2625 | - | 0.32419 | |
g4153 | DLA_04601 | GAOABQK02GQAQJ | CDS | 620307 | 2193 | + | 0.367533 | |
g4158 | DLA_04605 | GAOABQK02GQAQJ | CDS | 630116 | 7644 | + | 0.354003 | |
g4163 | DLA_04610 | GAOABQK02GQAQJ | CDS | 643235 | 2076 | - | 0.307803 | |
g4190 | DLA_04635 | GAOABQK02GQAQJ | CDS | 698291 | 2691 | - | 0.302861 | |
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 |
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 |
g4250 | DLA_04697 | ortholog of TOP3 a nuclear topoisomerase responsible for relaxing single-stranded negatively-supercoiled DNA | GAOABQK02GQAQJ | CDS | 825795 | 2313 | - | 0.342412 |
g4257 | DLA_04703 | GAOABQK02GQAQJ | CDS | 838889 | 2607 | - | 0.322593 | |
g4271 | DLA_04716 | GAOABQK02GQAQJ | CDS | 869762 | 8682 | - | 0.349804 | |
g430 | DLA_00477 | contig05409_1.exp | CDS | 974153 | 4065 | + | 0.327429 | |
g4303 | DLA_04749 | GAOABQK02GQAQJ | CDS | 952334 | 1602 | + | 0.338951 | |
g4324 | DLA_04772 | GAOABQK02GQAQJ | CDS | 1004164 | 999 | - | 0.332332 | |
g4336 | DLA_04789 | GAOABQK02GQAQJ | CDS | 1046815 | 4053 | + | 0.339255 | |
g4349 | DLA_04805 | GAOABQK02GQAQJ | CDS | 1078207 | 1833 | + | 0.26132 | |
g4362 | DLA_04821 | GAOABQK02GRIAE | CDS | 20539 | 2247 | - | 0.315532 | |
g4412 | DLA_04878 | GAOABQK02GRIAE | CDS | 155358 | 4623 | + | 0.307376 | |
g4457 | DLA_04936 | GAOABQK02H81I9 | CDS | 26587 | 2580 | - | 0.312403 | |
g4458 | DLA_04937 | GAOABQK02H81I9 | CDS | 29274 | 1683 | + | 0.322044 | |
g4489 | DLA_04970 | GAOABQK02H81I9 | CDS | 97703 | 8262 | + | 0.26398 | |
g4538 | DLA_05029 | GAOABQK02H81I9 | CDS | 228244 | 4599 | - | 0.346815 | |
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 |
g4577 | DLA_05072 | GAOABQK02H81I9 | CDS | 314015 | 1854 | - | 0.326321 | |
g4604 | DLA_05099 | GAOABQK02H81I9 | CDS | 375330 | 2349 | + | 0.325671 | |
g4615 | DLA_05112 | GAOABQK02H81I9 | CDS | 404366 | 2184 | - | 0.322344 | |
g4619 | DLA_05116 | GAOABQK02H81I9 | CDS | 415520 | 3084 | + | 0.32393 | |
g4628 | DLA_05125 | GAOABQK02H81I9 | CDS | 434500 | 4944 | + | 0.344053 | |
g4629 | DLA_05126 | GAOABQK02H81I9 | CDS | 440362 | 2097 | - | 0.379113 | |
g4681 | DLA_05182 | GAOABQK02H81I9 | CDS | 554984 | 3123 | + | 0.32789 | |
g4683 | DLA_05184 | GAOABQK02H81I9 | CDS | 559866 | 1626 | - | 0.346248 | |
g4689 | DLA_05192 | GAOABQK02H81I9 | CDS | 578951 | 4812 | + | 0.341854 | |
g4784 | DLA_05295 | GAOABQK02H81I9 | CDS | 806986 | 5853 | - | 0.320178 | |
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 |
g4811 | DLA_05328 | GAOABQK02H81I9 | CDS | 864922 | 1761 | + | 0.284497 | |
g4816 | DLA_05332 | GAOABQK02H81I9 | CDS | 873335 | 2250 | - | 0.326667 | |
g4863 | DLA_05385 | GAOABQK02HUB3S | CDS | 82935 | 5202 | + | 0.328143 | |
g49 | DLA_00058 | contig05409_1.exp | CDS | 128252 | 1062 | - | 0.322034 | |
g4930 | DLA_11628 | GAOABQK02HUB3S | CDS | 246344 | 969 | + | 0.268318 | |
g4991 | DLA_05525 | GAOABQK02HUB3S | CDS | 383190 | 1203 | - | 0.320033 | |
g4993 | DLA_05527 | GAOABQK02HUB3S | CDS | 385563 | 792 | + | 0.305556 | |
g5031 | DLA_05571 | GAOABQK02HUB3S | CDS | 461404 | 2952 | - | 0.32893 | |
g5032 | DLA_05572 | GAOABQK02HUB3S | CDS | 464705 | 1032 | + | 0.319767 | |
g5070 | DLA_05615 | GAOABQK02HUB3S | CDS | 553749 | 6030 | - | 0.315091 | |
g5073 | DLA_05618 | GAOABQK02HUB3S | CDS | 562805 | 2460 | - | 0.314634 | |
g5074 | DLA_05619 | GAOABQK02HUB3S | CDS | 566617 | 2586 | - | 0.317479 | |
g5087 | DLA_05635 | GAOABQK02HUB3S | CDS | 593660 | 1707 | - | 0.313415 | |
g5104 | DLA_05653 | GAOABQK02HUB3S | CDS | 640198 | 1047 | + | 0.295129 | |
g5108 | DLA_05657 | GAOABQK02HUB3S | CDS | 648858 | 2475 | - | 0.298586 | |
g5135 | DLA_05687 | GAOABQK02HUB3S | CDS | 709936 | 2475 | + | 0.30101 | |
g5141 | DLA_05701 | GAOABQK02HUB3S | CDS | 728826 | 4296 | + | 0.30703 | |
g5144 | DLA_05704 | GAOABQK02HUB3S | CDS | 739651 | 3900 | + | 0.332564 | |
g5146 | DLA_05706 | GAOABQK02HUB3S | CDS | 745347 | 4065 | + | 0.342927 | |
g5285 | DLA_05866 | GAOABQK02HUB3S | CDS | 1120661 | 2448 | - | 0.330474 | |
g5310 | DLA_05900 | GAOABQK02HUB3S | CDS | 1179641 | 2886 | + | 0.288635 | |
g5324 | DLA_05919 | GAOABQK02HUB3S | CDS | 1212357 | 1665 | - | 0.306306 | |
g5336 | DLA_05934 | GAOABQK02HUB3S | CDS | 1241031 | 3873 | + | 0.32662 | |
g5344 | DLA_05945 | GAOABQK02HUB3S | CDS | 1261425 | 951 | + | 0.299685 | |
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 |
g5418 | DLA_06031 | GAOABQK02HUB3S | CDS | 1431770 | 2691 | - | 0.353772 | |
g5428 | DLA_06042 | GAOABQK02HUB3S | CDS | 1453817 | 2178 | + | 0.305785 | |
g5445 | DLA_06065 | GAOABQK02HUB3S | CDS | 1494646 | 993 | + | 0.316213 | |
g5448 | DLA_06068 | GAOABQK02HUB3S | CDS | 1502068 | 3438 | - | 0.331006 | |
g5479 | DLA_06106 | GAOABQK02HUB3S | CDS | 1564607 | 1050 | - | 0.340952 | |
g5480 | DLA_06107 | GAOABQK02HUB3S | CDS | 1565814 | 2001 | + | 0.34083 | |
g5538 | DLA_06170 | GAOABQK02HUB3S | CDS | 1707826 | 2439 | + | 0.345223 | |
g56 | DLA_00066 | contig05409_1.exp | CDS | 143247 | 2988 | - | 0.319946 | |
g561 | DLA_00617 | contig05409_1.exp | CDS | 1280986 | 912 | - | 0.358553 | |
g5647 | DLA_06294 | GAOABQK02IBA3P | CDS | 85170 | 930 | - | 0.291398 | |
g565 | DLA_00622 | contig05409_1.exp | CDS | 1291713 | 2670 | - | 0.320225 | |
g5654 | DLA_06300 | GAOABQK02IBA3P | CDS | 100124 | 4236 | - | 0.344901 | |
g5659 | DLA_06305 | GAOABQK02IBA3P | CDS | 119528 | 4551 | + | 0.307185 | |
g5675 | DLA_06322 | GAOABQK02IBA3P | CDS | 154496 | 3345 | + | 0.339611 | |
g5712 | DLA_06367 | GAOABQK02IBA3P | CDS | 238671 | 2769 | + | 0.313109 | |
g5729 | DLA_06391 | GAOABQK02IBA3P | CDS | 305679 | 2820 | - | 0.324823 | |
g5743 | DLA_06406 | GAOABQK02IBA3P | CDS | 334439 | 2538 | + | 0.326241 | |
g5751 | DLA_06414 | GAOABQK02IBA3P | CDS | 360993 | 1308 | + | 0.29052 | |
g5758 | DLA_06422 | GAOABQK02IBA3P | CDS | 377139 | 4905 | - | 0.332518 | |
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 |
g5785 | DLA_06452 | GAOABQK02IBA3P | CDS | 440360 | 4989 | + | 0.338144 | |
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 |
g5833 | DLA_06505 | GAOABQK02IBA3P | CDS | 533689 | 4170 | - | 0.356115 | |
g5842 | DLA_06516 | GAOABQK02IBA3P | CDS | 553910 | 3255 | - | 0.349309 | |
g5889 | DLA_06561 | GAOABQK02IBA3P | CDS | 655419 | 3693 | - | 0.355808 | |
g5922 | DLA_06599 | GAOABQK02IBA3P | CDS | 753807 | 4353 | + | 0.316334 | |
g5959 | DLA_11661 | GAOABQK02IBA3P | CDS | 839364 | 762 | - | 0.368766 | |
g5988 | DLA_06668 | GAOABQK02IBA3P | CDS | 902080 | 2700 | + | 0.346296 | |
g5991 | DLA_06672 | GAOABQK02IBA3P | CDS | 909843 | 3057 | + | 0.298659 | |
g6002 | DLA_06684 | GAOABQK02IBA3P | CDS | 951201 | 2358 | - | 0.337574 | |
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 |
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 |
g6070 | DLA_06756 | contains one 5'-3' exonuclease domain and one 3'-5' exonuclease domain | GAOABQK02IBA3P | CDS | 1094275 | 6369 | - | 0.302245 |
g6083 | DLA_06771 | GAOABQK02INHKB | CDS | 9919 | 3717 | - | 0.313963 | |
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 |
g6149 | DLA_06849 | GAOABQK02IO52T | CDS | 138582 | 3204 | + | 0.334582 | |
g6260 | DLA_06974 | GAOABQK02IO52T | CDS | 373105 | 1275 | + | 0.294902 | |
g6279 | DLA_06993 | GAOABQK02IO52T | CDS | 413957 | 3456 | - | 0.303241 | |
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 |
g6318 | DLA_07037 | GAOABQK02IO52T | CDS | 497222 | 2205 | - | 0.317914 | |
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 |
g6377 | DLA_07097 | GAOABQK02IO52T | CDS | 627094 | 2634 | - | 0.314351 | |
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 |
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 |
g6426 | DLA_07149 | GAOABQK02JBK0O | CDS | 31261 | 1320 | + | 0.27197 | |
g6433 | DLA_07159 | GAOABQK02JBK0O | CDS | 45121 | 2970 | - | 0.306734 | |
g6445 | DLA_07172 | GAOABQK02JBK0O | CDS | 78619 | 2445 | - | 0.310429 | |
g6446 | DLA_07173 | GAOABQK02JBK0O | CDS | 81330 | 1440 | + | 0.301389 | |
g6469 | DLA_07198 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | GAOABQK02JBK0O | CDS | 135234 | 3006 | - | 0.294744 |
g6497 | DLA_07234 | GAOABQK02JEBFV | CDS | 45755 | 2196 | - | 0.331056 | |
g6524 | DLA_07265 | GAOABQK02JOCCH | CDS | 48097 | 3072 | + | 0.277995 | |
g6529 | DLA_07270 | GAOABQK02JOCCH | CDS | 58644 | 1905 | - | 0.290814 | |
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 |
g6607 | DLA_07358 | GAOABQK02JOCCH | CDS | 240004 | 12681 | - | 0.328365 | |
g6674 | DLA_07435 | GAOABQK02JOCCH | CDS | 403183 | 3987 | + | 0.346627 | |
g6679 | DLA_07439 | GAOABQK02JOCCH | CDS | 414241 | 1386 | - | 0.368687 | |
g6685 | DLA_07445 | GAOABQK02JOCCH | CDS | 426048 | 2004 | - | 0.313872 | |
g6686 | DLA_07446 | GAOABQK02JOCCH | CDS | 428514 | 2859 | - | 0.317943 | |
g6711 | DLA_07474 | GAOABQK02JOCCH | CDS | 471109 | 7059 | - | 0.374982 | |
g6712 | DLA_07475 | GAOABQK02JOCCH | CDS | 478671 | 2856 | + | 0.290966 | |
g6737 | DLA_07503 | GAOABQK02JOCCH | CDS | 537620 | 3087 | - | 0.308066 | |
g680 | DLA_00750 | F4PJNLW01A00V1 | CDS | 99661 | 993 | - | 0.352467 | |
g6839 | DLA_07621 | GAOABQK02JOCCH | CDS | 775507 | 6165 | + | 0.323114 | |
g6857 | DLA_07643 | GAOABQK02JOCCH | CDS | 812714 | 6405 | - | 0.340515 | |
g6883 | DLA_07677 | GAOABQK02JOCCH | CDS | 880767 | 1194 | + | 0.326633 | |
g6889 | DLA_07685 | GLQOFTK02FH5TG | CDS | 8846 | 2778 | - | 0.302736 | |
g6929 | DLA_11693 | GLQOFTK02FH5TG | CDS | 95960 | 2934 | + | 0.316633 | |
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 |
g6993 | DLA_07795 | GLQOFTK02FH5TG | CDS | 226617 | 3459 | + | 0.33449 | |
g6997 | DLA_07799 | GLQOFTK02FH5TG | CDS | 238572 | 1332 | - | 0.292793 | |
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 | |
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 |
g7120 | DLA_07948 | GLQOFTK02FH5TG | CDS | 536331 | 3279 | + | 0.351632 | |
g713 | DLA_00785 | F4PJNLW01A00V1 | CDS | 167363 | 1281 | + | 0.323966 | |
g7143 | DLA_07973 | GLQOFTK02FH5TG | CDS | 580542 | 771 | + | 0.325551 | |
g7217 | DLA_08053 | GLQOFTK02FH5TG | CDS | 742825 | 5442 | - | 0.34932 | |
g723 | DLA_00796 | F4PJNLW01A00V1 | CDS | 190893 | 4350 | + | 0.355632 | |
g7231 | DLA_08070 | GLQOFTK02FH5TG | CDS | 776119 | 1698 | + | 0.30742 | |
g726 | DLA_00799 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | F4PJNLW01A00V1 | CDS | 204635 | 3465 | - | 0.361039 |
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 |
g7283 | DLA_08133 | GLQOFTK02FH5TG | CDS | 894541 | 1524 | + | 0.324803 | |
g7311 | DLA_08167 | GLQOFTK02FH5TG | CDS | 950417 | 6909 | - | 0.345202 | |
g7334 | DLA_08195 | GLQOFTK02FH5TG | CDS | 1018729 | 1275 | - | 0.337255 | |
g7342 | DLA_08206 | GLQOFTK02FH5TG | CDS | 1036092 | 1260 | + | 0.292064 | |
g7344 | DLA_08208 | GLQOFTK02FH5TG | CDS | 1039642 | 2334 | - | 0.334619 | |
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 |
g7376 | DLA_08247 | GLQOFTK02FH5TG | CDS | 1107166 | 4839 | + | 0.356892 | |
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 |
g7419 | DLA_08295 | GLQOFTK02FH5TG | CDS | 1229535 | 1950 | - | 0.351795 | |
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 | |
g7469 | DLA_08356 | GLQOFTK02FH5TG | CDS | 1335202 | 1944 | - | 0.308128 | |
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 |
g7512 | DLA_08407 | GLQOFTK02FH5TG | CDS | 1442202 | 1704 | + | 0.33216 | |
g7550 | DLA_08444 | GLQOFTK02FH5TG | CDS | 1515984 | 2223 | + | 0.253261 | |
g7661 | DLA_08565 | GLQOFTK02G2F2O | CDS | 220668 | 1914 | - | 0.367816 | |
g7666 | DLA_08571 | GLQOFTK02G2F2O | CDS | 229400 | 3729 | + | 0.335747 | |
g769 | DLA_00847 | F4PJNLW01A00V1 | CDS | 288983 | 5649 | + | 0.355815 | |
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 |
g7724 | DLA_08642 | GLQOFTK02G2F2O | CDS | 383694 | 4512 | - | 0.359043 | |
g7744 | DLA_08659 | GLQOFTK02G2F2O | CDS | 430417 | 1089 | - | 0.337006 | |
g7760 | DLA_08678 | chromatin remodeling complex subunit R (CHR) protein SWI2SNF2 homolog | GLQOFTK02G2F2O | CDS | 466621 | 3690 | - | 0.304336 |
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 |
g7774 | DLA_08691 | GLQOFTK02G2F2O | CDS | 496310 | 2664 | - | 0.311937 | |
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 |
g7798 | DLA_08718 | GLQOFTK02G2F2O | CDS | 553106 | 5211 | - | 0.333525 | |
g7839 | DLA_08763 | SNF2 family protein similar to human SMARCA4 putative regulator of chromatin | GLQOFTK02G2F2O | CDS | 635822 | 6768 | + | 0.346927 |
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 |
g7923 | DLA_08857 | GLQOFTK02G2F2O | CDS | 804563 | 1752 | + | 0.304224 | |
g7953 | DLA_08888 | GLQOFTK02G2F2O | CDS | 886835 | 1737 | + | 0.35118 | |
g7959 | DLA_08894 | similar to metazoan cyclin H predicted to interact with cyclin-dependent kinase | GLQOFTK02G2F2O | CDS | 898007 | 1032 | + | 0.297481 |
g8026 | DLA_08974 | similar to metazoan cyclin C predicted to interact with cyclin-dependent kinase | GLQOFTK02G2F2O | CDS | 1043323 | 768 | + | 0.303385 |
g8047 | DLA_08996 | GLQOFTK02G2F2O | CDS | 1097062 | 1173 | + | 0.337596 | |
g8060 | DLA_09009 | GLQOFTK02G2F2O | CDS | 1125492 | 2442 | + | 0.320639 | |
g8072 | DLA_09022 | GLQOFTK02G2F2O | CDS | 1157651 | 3978 | + | 0.302916 | |
g8077 | DLA_09028 | GLQOFTK02G2F2O | CDS | 1171541 | 1416 | + | 0.336158 | |
g8100 | DLA_09053 | GLQOFTK02G2F2O | CDS | 1221193 | 1047 | - | 0.282713 | |
g8111 | DLA_09065 | GLQOFTK02G2F2O | CDS | 1252809 | 5997 | + | 0.31399 | |
g8123 | DLA_09078 | GLQOFTK02G2F2O | CDS | 1290791 | 1539 | + | 0.345679 | |
g82 | DLA_00094 | contig05409_1.exp | CDS | 186440 | 2235 | - | 0.365101 | |
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 |
g8218 | DLA_09175 | GLQOFTK02G2F2O | CDS | 1490003 | 1221 | - | 0.329238 | |
g8250 | DLA_09212 | GLQOFTK02G2F2O | CDS | 1568149 | 1248 | + | 0.334135 | |
g8258 | DLA_09218 | GLQOFTK02G2F2O | CDS | 1580676 | 4380 | - | 0.324886 | |
g8261 | DLA_09221 | GLQOFTK02G2F2O | CDS | 1591695 | 1860 | + | 0.374731 | |
g8273 | DLA_09234 | GLQOFTK02G2F2O | CDS | 1617316 | 1968 | + | 0.303862 | |
g8277 | DLA_11766 | GLQOFTK02G2F2O | CDS | 1623178 | 1323 | - | 0.284958 | |
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 |
g829 | DLA_00909 | F4PJNLW01A00V1 | CDS | 409957 | 3246 | + | 0.379544 | |
g8296 | DLA_09257 | GLQOFTK02G2F2O | CDS | 1667785 | 3975 | + | 0.318239 | |
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 |
g835 | DLA_00916 | F4PJNLW01A00V1 | CDS | 428746 | 1794 | - | 0.375697 | |
g8370 | DLA_09336 | GLQOFTK02G2F2O | CDS | 1806183 | 2058 | + | 0.31827 | |
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 |
g8442 | DLA_09414 | GLQOFTK02G2F2O | CDS | 1944715 | 3000 | - | 0.352333 | |
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 |
g8509 | DLA_09485 | GLQOFTK02GHM7A | CDS | 40990 | 7914 | + | 0.321203 | |
g8519 | DLA_09495 | GLQOFTK02GHM7A | CDS | 67461 | 948 | + | 0.291139 | |
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 |
g855 | DLA_00935 | F4PJNLW01A00V1 | CDS | 483602 | 570 | + | 0.308772 | |
g8564 | DLA_09547 | GLQOFTK02GHM7A | CDS | 162001 | 3615 | + | 0.333333 | |
g857 | DLA_00937 | F4PJNLW01A00V1 | CDS | 487333 | 2793 | + | 0.368779 | |
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 |
g8593 | DLA_09585 | GLQOFTK02GHM7A | CDS | 246755 | 4185 | + | 0.314934 | |
g8597 | DLA_09589 | GLQOFTK02GHM7A | CDS | 256496 | 2496 | - | 0.306891 | |
g8633 | DLA_09626 | GLQOFTK02GHM7A | CDS | 349150 | 3288 | - | 0.327251 | |
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 |
g8695 | DLA_09691 | GLQOFTK02GHM7A | CDS | 481830 | 1944 | - | 0.360082 | |
g873 | DLA_00957 | ortholog of MYH which removes misincorporated adenine residues opposite template 8-oxoguanine during DNA replication | F4PJNLW01A00V1 | CDS | 536344 | 1554 | - | 0.301158 |
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 |
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 |
g8857 | DLA_09861 | GLQOFTK02GHM7A | CDS | 872304 | 1011 | - | 0.302671 | |
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 |
g8880 | DLA_09895 | GLQOFTK02GQ36N | CDS | 37449 | 2145 | + | 0.327273 | |
g8900 | DLA_09918 | GLQOFTK02GQ36N | CDS | 86387 | 2031 | - | 0.293451 | |
g8906 | DLA_09925 | GLQOFTK02GQ36N | CDS | 97926 | 1716 | - | 0.327506 | |
g8919 | DLA_09938 | GLQOFTK02GQ36N | CDS | 132556 | 7536 | + | 0.348726 | |
g8941 | DLA_09960 | GLQOFTK02GQ36N | CDS | 186083 | 1941 | - | 0.325605 | |
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 |
g8978 | DLA_10001 | GLQOFTK02GQ36N | CDS | 265383 | 3807 | - | 0.321513 | |
g8980 | DLA_10003 | GLQOFTK02GQ36N | CDS | 270268 | 1119 | + | 0.302949 | |
g9002 | DLA_10025 | GLQOFTK02GQ36N | CDS | 315308 | 3954 | - | 0.321194 | |
g9035 | DLA_10056 | GLQOFTK02GQ36N | CDS | 377200 | 1983 | + | 0.33535 | |
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 |
g9105 | DLA_10135 | GLQOFTK02GQ36N | CDS | 559750 | 1464 | - | 0.303962 | |
g9122 | DLA_10157 | GLQOFTK02GQ36N | CDS | 599686 | 3750 | - | 0.333067 | |
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 |
g9210 | DLA_10261 | GLQOFTK02GUKFG | CDS | 129499 | 4644 | + | 0.343239 | |
g922 | DLA_01020 | F4PJNLW01A00V1 | CDS | 643466 | 2934 | + | 0.308453 | |
g9266 | DLA_10324 | GLQOFTK02GUKFG | CDS | 265535 | 5454 | + | 0.351485 | |
g9282 | DLA_10341 | GLQOFTK02GUKFG | CDS | 315277 | 1017 | + | 0.365782 | |
g931 | DLA_01031 | F4PJNLW01A00V1 | CDS | 661501 | 4101 | + | 0.333821 | |
g9331 | DLA_10402 | GLQOFTK02GUKFG | CDS | 414480 | 5160 | - | 0.312403 | |
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 |
g9430 | DLA_10507 | GLQOFTK02IIOHN | CDS | 50069 | 675 | - | 0.284444 | |
g9445 | DLA_10523 | GLQOFTK02IIOHN | CDS | 85920 | 4386 | + | 0.332421 | |
g9459 | DLA_10543 | GLQOFTK02IIOHN | CDS | 118203 | 1749 | - | 0.277301 | |
g9463 | DLA_10547 | GLQOFTK02IIOHN | CDS | 125810 | 2967 | - | 0.290529 | |
g9485 | DLA_10572 | GLQOFTK02IJPNF | CDS | 8032 | 1290 | + | 0.285271 | |
g9529 | DLA_10621 | similar to eukaryotic initiation factor 4A isoform 3 | GLQOFTK02IJPNF | CDS | 114540 | 1242 | + | 0.36715 |
g959 | DLA_01062 | F4PJNLW01A00V1 | CDS | 726650 | 957 | + | 0.289446 | |
g9617 | DLA_10723 | GLQOFTK02IRMR1 | CDS | 31401 | 4668 | - | 0.336118 | |
g963 | DLA_01066 | F4PJNLW01A00V1 | CDS | 736130 | 7947 | - | 0.317227 | |
g9636 | DLA_10743 | GLQOFTK02IRMR1 | CDS | 81280 | 1392 | - | 0.333333 | |
g9648 | DLA_10760 | GLQOFTK02IRMR1 | CDS | 111344 | 1833 | - | 0.346972 | |
g9654 | DLA_10766 | GLQOFTK02IRMR1 | CDS | 123810 | 3429 | + | 0.314669 | |
g9690 | DLA_10814 | GLQOFTK02JCFFB | CDS | 3414 | 2112 | + | 0.297822 | |
g9711 | DLA_10837 | plays a role in the regulation of cleavage furrow formation similar to S. pombe cdc7 | GLQOFTK02JCFFB | CDS | 55659 | 3321 | + | 0.350196 |
g9730 | DLA_10862 | GLQOFTK02JCFFB | CDS | 106430 | 2298 | - | 0.295909 | |
g9754 | DLA_10889 | GLQOFTK02JL55Q | CDS | 43907 | 2400 | - | 0.28625 | |
g977 | DLA_01087 | F4PJNLW01A00V1 | CDS | 776180 | 2457 | - | 0.293447 | |
g9859 | DLA_11004 | GLQOFTK02JL55Q | CDS | 280021 | 1545 | - | 0.374757 | |
g9870 | DLA_11015 | GLQOFTK02JL55Q | CDS | 307354 | 3702 | + | 0.337655 | |
g9891 | DLA_11039 | GLQOFTK02JL55Q | CDS | 354517 | 1455 | - | 0.318213 | |
g990 | DLA_01099 | F4PJNLW01A00V1 | CDS | 804435 | 1251 | - | 0.311751 | |
g9911 | DLA_11059 | GLQOFTK02JL55Q | CDS | 397671 | 1128 | + | 0.350177 | |
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 |
g9972 | DLA_11125 | GLQOFTK02JL55Q | CDS | 541515 | 867 | + | 0.322953 | |
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 |