Gene list
Applied filters:
COG category: Signal transduction mechanisms
Organism: Dictyostelium lacteum
Number of genes found: 357
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 | |
g10075 | DLA_11248 | GLQOFTK02JL55Q | CDS | 756239 | 1938 | + | 0.288958 | |
g10078 | DLA_11251 | GLQOFTK02JL55Q | CDS | 762875 | 3936 | + | 0.306657 | |
g10086 | DLA_11259 | GLQOFTK02JL55Q | CDS | 780755 | 444 | + | 0.31982 | |
g10100 | DLA_11276 | localizes to the cell cortex binds myosin II and regulates microtubule length the cortical cytoskeleton and cytokinesis functions in the same pathway as racE to regulate these processes | GLQOFTK02JL55Q | CDS | 811197 | 741 | - | 0.368421 |
g10106 | DLA_11284 | GLQOFTK02JL55Q | CDS | 823910 | 2478 | + | 0.307103 | |
g10127 | DLA_11309 | GLQOFTK02JL55Q | CDS | 869532 | 4638 | + | 0.335058 | |
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 |
g1040 | DLA_01150 | F4PJNLW01A00V1 | CDS | 904204 | 1107 | - | 0.31617 | |
g1067 | DLA_01175 | F4PJNLW01A00V1 | CDS | 966915 | 1383 | - | 0.339118 | |
g1097 | DLA_01213 | F4PJNLW01A00V1 | CDS | 1034101 | 2148 | - | 0.366853 | |
g1115 | DLA_01232 | F4PJNLW01A00V1 | CDS | 1092890 | 2142 | + | 0.332866 | |
g1167 | DLA_01284 | F4PJNLW01A00V1 | CDS | 1225330 | 4419 | - | 0.342838 | |
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 |
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 |
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 |
g1373 | DLA_01505 | F4PJNLW01B0TO9 | CDS | 188605 | 4566 | - | 0.318003 | |
g1387 | DLA_11481 | F4PJNLW01B0TO9 | CDS | 220295 | 465 | + | 0.378495 | |
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 | |
g1549 | DLA_11488 | F4PJNLW01B0TO9 | CDS | 580805 | 2460 | + | 0.387398 | |
g1550 | DLA_01697 | F4PJNLW01B0TO9 | CDS | 583710 | 5862 | + | 0.360628 | |
g1606 | DLA_01758 | F4PJNLW01B0TO9 | CDS | 707303 | 1743 | - | 0.327022 | |
g162 | DLA_00188 | contig05409_1.exp | CDS | 376542 | 1929 | + | 0.369103 | |
g1635 | DLA_01790 | F4PJNLW01B0TO9 | CDS | 765011 | 3840 | - | 0.359635 | |
g1664 | DLA_01820 | F4PJNLW01B0TO9 | CDS | 835697 | 6819 | + | 0.307816 | |
g1665 | DLA_01821 | F4PJNLW01B0TO9 | CDS | 842624 | 606 | - | 0.293729 | |
g1668 | DLA_01824 | F4PJNLW01B0TO9 | CDS | 846981 | 2520 | + | 0.289286 | |
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 |
g1728 | DLA_01892 | F4PJNLW01B0TO9 | CDS | 988245 | 3060 | + | 0.32451 | |
g1734 | DLA_01899 | F4PJNLW01B0TO9 | CDS | 1004895 | 2139 | - | 0.322113 | |
g1790 | DLA_01953 | F4PJNLW01C9MXC | CDS | 59749 | 2139 | - | 0.320243 | |
g1794 | DLA_01957 | F4PJNLW01C9MXC | CDS | 67445 | 2940 | + | 0.339796 | |
g1801 | DLA_01964 | F4PJNLW01C9MXC | CDS | 86554 | 222 | - | 0.31982 | |
g1819 | DLA_01984 | F4PJNLW01C9MXC | CDS | 134212 | 2448 | + | 0.33415 | |
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 | |
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 |
g2049 | DLA_02252 | F4PJNLW01DERRH | CDS | 385220 | 5760 | + | 0.336111 | |
g2067 | DLA_02273 | protein serinethreonine phosphatase required for chemotaxis and development suppresses the | F4PJNLW01DERRH | CDS | 424814 | 915 | - | 0.339891 |
g210 | DLA_00235 | contig05409_1.exp | CDS | 490745 | 477 | - | 0.278826 | |
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 |
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 |
g2142 | DLA_02357 | F4PJNLW01DERRH | CDS | 587571 | 909 | - | 0.354235 | |
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 | |
g219 | DLA_00243 | conserved low molecular weight phosphotyrosine protein phosphatase acts on tyrosine phosphorylated proteins low-MW aryl phosphates and natural and synthetic acyl phosphates | contig05409_1.exp | CDS | 504881 | 534 | + | 0.299625 |
g2206 | DLA_02429 | F4PJNLW01EE5MJ | CDS | 154 | 1812 | + | 0.312362 | |
g2239 | DLA_02473 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | F4PJNLW01EE5MJ | CDS | 89204 | 498 | + | 0.359438 |
g2260 | DLA_02495 | F4PJNLW01EE5MJ | CDS | 138880 | 2247 | - | 0.365821 | |
g2269 | DLA_02508 | F4PJNLW01EE5MJ | CDS | 174693 | 1038 | + | 0.266859 | |
g2276 | DLA_02517 | F4PJNLW01EE5MJ | CDS | 187796 | 369 | + | 0.289973 | |
g2305 | DLA_02548 | F4PJNLW01EE5MJ | CDS | 256752 | 3549 | - | 0.31051 | |
g2306 | DLA_02550 | F4PJNLW01EE5MJ | CDS | 260902 | 897 | - | 0.338907 | |
g2359 | DLA_02609 | F4PJNLW01EE5MJ | CDS | 357944 | 339 | - | 0.312684 | |
g237 | DLA_00264 | contig05409_1.exp | CDS | 540310 | 1800 | - | 0.360556 | |
g2381 | DLA_02636 | F4PJNLW01EE5MJ | CDS | 406795 | 3672 | + | 0.353214 | |
g2385 | DLA_02640 | catalytic subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase | F4PJNLW01EE5MJ | CDS | 416797 | 1710 | + | 0.330994 |
g24 | DLA_00028 | contig05409_1.exp | CDS | 61377 | 3906 | - | 0.323605 | |
g2432 | DLA_02697 | F4PJNLW01EE5MJ | CDS | 519322 | 3981 | + | 0.373524 | |
g245 | DLA_00272 | contig05409_1.exp | CDS | 557093 | 1836 | - | 0.283769 | |
g2455 | DLA_02725 | F4PJNLW01EE5MJ | CDS | 579082 | 2658 | - | 0.322047 | |
g2467 | DLA_02737 | F4PJNLW01EE5MJ | CDS | 614224 | 2649 | + | 0.348056 | |
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 | |
g2542 | DLA_02816 | F4PJNLW01EE5MJ | CDS | 781075 | 2442 | + | 0.285831 | |
g2578 | DLA_02861 | F4PJNLW01EE5MJ | CDS | 864104 | 2604 | - | 0.320276 | |
g2594 | DLA_02877 | F4PJNLW01EE5MJ | CDS | 918769 | 3492 | + | 0.340779 | |
g2620 | DLA_02908 | F4PJNLW01EE5MJ | CDS | 969208 | 3174 | - | 0.333018 | |
g2636 | DLA_02926 | F4PJNLW01EE5MJ | CDS | 1000811 | 2118 | - | 0.344193 | |
g2653 | DLA_02945 | F4PJNLW01EE5MJ | CDS | 1040175 | 618 | - | 0.326861 | |
g2657 | DLA_02949 | F4PJNLW01EE5MJ | CDS | 1044784 | 1410 | - | 0.338298 | |
g270 | DLA_00300 | contig05409_1.exp | CDS | 625941 | 2418 | + | 0.35732 | |
g2705 | DLA_02999 | F4PJNLW01EE5MJ | CDS | 1138608 | 2625 | - | 0.299429 | |
g2711 | DLA_03007 | F4PJNLW01EE5MJ | CDS | 1148480 | 1926 | + | 0.286085 | |
g2720 | DLA_03016 | F4PJNLW01EE5MJ | CDS | 1170267 | 1944 | + | 0.314815 | |
g2728 | DLA_03023 | F4PJNLW01EE5MJ | CDS | 1186112 | 7353 | - | 0.300286 | |
g2739 | DLA_03035 | F4PJNLW01EE5MJ | CDS | 1213710 | 1593 | + | 0.338983 | |
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 |
g2845 | DLA_03151 | F4PJNLW02GJ9ZB | CDS | 197599 | 3150 | + | 0.292064 | |
g2921 | DLA_03236 | F4PJNLW02HBBIY | CDS | 97770 | 1467 | - | 0.334015 | |
g2924 | DLA_03239 | F4PJNLW02HBBIY | CDS | 103863 | 957 | - | 0.345873 | |
g2927 | DLA_03242 | F4PJNLW02HBBIY | CDS | 108985 | 1764 | - | 0.3322 | |
g2942 | DLA_03260 | F4PJNLW02HBBIY | CDS | 138381 | 11952 | + | 0.347808 | |
g2958 | DLA_03279 | F4PJNLW02HBBIY | CDS | 186711 | 555 | - | 0.313514 | |
g3035 | DLA_03362 | F4PJNLW02HBBIY | CDS | 361414 | 2673 | + | 0.34306 | |
g3037 | DLA_03363 | F4PJNLW02HBBIY | CDS | 366615 | 2451 | - | 0.339861 | |
g3043 | DLA_03369 | F4PJNLW02HBBIY | CDS | 378053 | 4266 | - | 0.339897 | |
g3045 | DLA_03370 | F4PJNLW02HBBIY | CDS | 384208 | 672 | - | 0.33631 | |
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 |
g315 | DLA_00350 | contig05409_1.exp | CDS | 728057 | 2577 | - | 0.327901 | |
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 |
g3232 | DLA_03581 | GAOABQK02G6SYV | CDS | 10896 | 894 | - | 0.394855 | |
g3298 | DLA_03649 | GAOABQK02G6SYV | CDS | 161683 | 453 | - | 0.337748 | |
g3322 | DLA_03673 | GAOABQK02G6SYV | CDS | 207498 | 4548 | + | 0.348505 | |
g3350 | DLA_03706 | GAOABQK02G6SYV | CDS | 264850 | 3468 | - | 0.364475 | |
g3405 | DLA_03766 | GAOABQK02G6SYV | CDS | 380671 | 1143 | + | 0.32021 | |
g3412 | DLA_03775 | GAOABQK02G6SYV | CDS | 393352 | 3546 | + | 0.368302 | |
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 |
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 | |
g3557 | DLA_03937 | GAOABQK02G7M1S | CDS | 30188 | 774 | + | 0.352713 | |
g3558 | DLA_03938 | GAOABQK02G7M1S | CDS | 31797 | 4113 | + | 0.292001 | |
g3568 | DLA_03952 | GAOABQK02G7M1S | CDS | 71620 | 3717 | + | 0.312618 | |
g3587 | DLA_03974 | GAOABQK02G7M1S | CDS | 120773 | 726 | - | 0.318182 | |
g3644 | DLA_04041 | GAOABQK02G7M1S | CDS | 250249 | 3735 | - | 0.326104 | |
g3664 | DLA_04060 | GAOABQK02G7M1S | CDS | 303809 | 1908 | + | 0.343816 | |
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 |
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 |
g3830 | DLA_04248 | GAOABQK02G7M1S | CDS | 681315 | 441 | - | 0.321995 | |
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 |
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 | |
g3962 | DLA_04391 | GAOABQK02GQAQJ | CDS | 209901 | 624 | - | 0.355769 | |
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 | |
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 |
g4037 | DLA_04478 | GAOABQK02GQAQJ | CDS | 388513 | 2502 | + | 0.328137 | |
g4065 | DLA_04509 | GAOABQK02GQAQJ | CDS | 450958 | 357 | + | 0.333333 | |
g4145 | DLA_04594 | ortholog of the human PPP2R4 (PTPA) that stimulates the phosphotyrosyl phosphatase activity of PP2A in the presence of ATP and Mg(2) in vitro | GAOABQK02GQAQJ | CDS | 604651 | 963 | - | 0.345794 |
g4149 | DLA_04597 | GAOABQK02GQAQJ | CDS | 611526 | 2625 | - | 0.32419 | |
g415 | DLA_00460 | contig05409_1.exp | CDS | 945875 | 1254 | + | 0.339713 | |
g4158 | DLA_04605 | GAOABQK02GQAQJ | CDS | 630116 | 7644 | + | 0.354003 | |
g4163 | DLA_04610 | GAOABQK02GQAQJ | CDS | 643235 | 2076 | - | 0.307803 | |
g4205 | DLA_04650 | contains a sac phosphatase domain similar to D. discoideum sac1 similar to D. purpureum protein | GAOABQK02GQAQJ | CDS | 723389 | 3156 | - | 0.295627 |
g4216 | DLA_04663 | GAOABQK02GQAQJ | CDS | 744357 | 2100 | + | 0.32 | |
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 |
g4225 | DLA_04672 | GAOABQK02GQAQJ | CDS | 770362 | 2007 | - | 0.337319 | |
g4234 | DLA_04682 | GAOABQK02GQAQJ | CDS | 789545 | 1029 | - | 0.316812 | |
g4271 | DLA_04716 | GAOABQK02GQAQJ | CDS | 869762 | 8682 | - | 0.349804 | |
g4293 | DLA_04739 | GAOABQK02GQAQJ | CDS | 925019 | 1179 | - | 0.318066 | |
g4303 | DLA_04749 | GAOABQK02GQAQJ | CDS | 952334 | 1602 | + | 0.338951 | |
g4315 | DLA_04763 | GAOABQK02GQAQJ | CDS | 981628 | 726 | + | 0.285124 | |
g4336 | DLA_04789 | GAOABQK02GQAQJ | CDS | 1046815 | 4053 | + | 0.339255 | |
g4361 | DLA_04820 | GAOABQK02GRIAE | CDS | 17839 | 2421 | - | 0.336225 | |
g4362 | DLA_04821 | GAOABQK02GRIAE | CDS | 20539 | 2247 | - | 0.315532 | |
g4412 | DLA_04878 | GAOABQK02GRIAE | CDS | 155358 | 4623 | + | 0.307376 | |
g446 | DLA_00493 | contig05409_1.exp | CDS | 1022388 | 2244 | - | 0.3418 | |
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 |
g4554 | DLA_05047 | GAOABQK02H81I9 | CDS | 260609 | 963 | - | 0.364486 | |
g4592 | DLA_05087 | GAOABQK02H81I9 | CDS | 346046 | 441 | + | 0.324263 | |
g4604 | DLA_05099 | GAOABQK02H81I9 | CDS | 375330 | 2349 | + | 0.325671 | |
g4618 | DLA_05115 | GAOABQK02H81I9 | CDS | 409558 | 4971 | - | 0.345001 | |
g4628 | DLA_05125 | GAOABQK02H81I9 | CDS | 434500 | 4944 | + | 0.344053 | |
g4629 | DLA_05126 | GAOABQK02H81I9 | CDS | 440362 | 2097 | - | 0.379113 | |
g4699 | DLA_05203 | GAOABQK02H81I9 | CDS | 597680 | 2328 | - | 0.341065 | |
g4769 | DLA_05278 | GAOABQK02H81I9 | CDS | 774378 | 2373 | - | 0.334598 | |
g4784 | DLA_05295 | GAOABQK02H81I9 | CDS | 806986 | 5853 | - | 0.320178 | |
g479 | DLA_00531 | contig05409_1.exp | CDS | 1098948 | 4128 | + | 0.349806 | |
g4811 | DLA_05328 | GAOABQK02H81I9 | CDS | 864922 | 1761 | + | 0.284497 | |
g4816 | DLA_05332 | GAOABQK02H81I9 | CDS | 873335 | 2250 | - | 0.326667 | |
g4855 | DLA_05376 | GAOABQK02HUB3S | CDS | 69940 | 2490 | + | 0.326908 | |
g4863 | DLA_05385 | GAOABQK02HUB3S | CDS | 82935 | 5202 | + | 0.328143 | |
g4886 | DLA_05410 | GAOABQK02HUB3S | CDS | 144754 | 3432 | + | 0.33042 | |
g4887 | DLA_05411 | GAOABQK02HUB3S | CDS | 148443 | 1041 | - | 0.329491 | |
g4888 | DLA_05412 | GAOABQK02HUB3S | CDS | 149655 | 492 | - | 0.302846 | |
g4925 | DLA_05453 | GAOABQK02HUB3S | CDS | 236552 | 2322 | - | 0.306632 | |
g4991 | DLA_05525 | GAOABQK02HUB3S | CDS | 383190 | 1203 | - | 0.320033 | |
g5001 | DLA_05538 | GAOABQK02HUB3S | CDS | 401139 | 1557 | + | 0.326268 | |
g501 | DLA_00554 | contig05409_1.exp | CDS | 1147813 | 1587 | + | 0.328923 | |
g5021 | DLA_05560 | GAOABQK02HUB3S | CDS | 434802 | 7788 | - | 0.351181 | |
g5059 | DLA_05599 | GAOABQK02HUB3S | CDS | 526810 | 1863 | - | 0.3489 | |
g5070 | DLA_05615 | GAOABQK02HUB3S | CDS | 553749 | 6030 | - | 0.315091 | |
g5073 | DLA_05618 | GAOABQK02HUB3S | CDS | 562805 | 2460 | - | 0.314634 | |
g5087 | DLA_05635 | GAOABQK02HUB3S | CDS | 593660 | 1707 | - | 0.313415 | |
g5108 | DLA_05657 | GAOABQK02HUB3S | CDS | 648858 | 2475 | - | 0.298586 | |
g5142 | DLA_05702 | GAOABQK02HUB3S | CDS | 733229 | 2988 | - | 0.282798 | |
g5200 | DLA_05772 | GAOABQK02HUB3S | CDS | 915455 | 2523 | + | 0.349187 | |
g5285 | DLA_05866 | GAOABQK02HUB3S | CDS | 1120661 | 2448 | - | 0.330474 | |
g529 | DLA_00582 | contig05409_1.exp | CDS | 1207838 | 4317 | + | 0.351633 | |
g5310 | DLA_05900 | GAOABQK02HUB3S | CDS | 1179641 | 2886 | + | 0.288635 | |
g5336 | DLA_05934 | GAOABQK02HUB3S | CDS | 1241031 | 3873 | + | 0.32662 | |
g5354 | DLA_05956 | contains a cyclase domain 7 transmembrane helices a histidine kinase domain and two receiver domains | GAOABQK02HUB3S | CDS | 1277865 | 4821 | - | 0.340178 |
g5417 | DLA_06029 | GAOABQK02HUB3S | CDS | 1428820 | 2505 | - | 0.30978 | |
g5428 | DLA_06042 | GAOABQK02HUB3S | CDS | 1453817 | 2178 | + | 0.305785 | |
g5433 | DLA_06049 | GAOABQK02HUB3S | CDS | 1461570 | 2115 | - | 0.340898 | |
g5445 | DLA_06065 | GAOABQK02HUB3S | CDS | 1494646 | 993 | + | 0.316213 | |
g5448 | DLA_06068 | GAOABQK02HUB3S | CDS | 1502068 | 3438 | - | 0.331006 | |
g5468 | DLA_06093 | GAOABQK02HUB3S | CDS | 1546733 | 414 | - | 0.330918 | |
g5536 | DLA_06168 | GAOABQK02HUB3S | CDS | 1705673 | 1164 | + | 0.311856 | |
g561 | DLA_00617 | contig05409_1.exp | CDS | 1280986 | 912 | - | 0.358553 | |
g5647 | DLA_06294 | GAOABQK02IBA3P | CDS | 85170 | 930 | - | 0.291398 | |
g5654 | DLA_06300 | GAOABQK02IBA3P | CDS | 100124 | 4236 | - | 0.344901 | |
g5666 | DLA_06312 | catalytic subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase | GAOABQK02IBA3P | CDS | 133718 | 1569 | + | 0.333971 |
g5752 | DLA_06415 | GAOABQK02IBA3P | CDS | 362764 | 1143 | - | 0.339458 | |
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 |
g5842 | DLA_06516 | GAOABQK02IBA3P | CDS | 553910 | 3255 | - | 0.349309 | |
g5959 | DLA_11661 | GAOABQK02IBA3P | CDS | 839364 | 762 | - | 0.368766 | |
g6002 | DLA_06684 | GAOABQK02IBA3P | CDS | 951201 | 2358 | - | 0.337574 | |
g6006 | DLA_06687 | GAOABQK02IBA3P | CDS | 962016 | 2868 | - | 0.331939 | |
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 |
g6066 | DLA_06753 | inositol 5-phosphatase similar to the human protein OCRL which when defect causes Lowe syndrome involved in Dictyostelium growth development and phagocytosis | GAOABQK02IBA3P | CDS | 1087916 | 2187 | + | 0.328761 |
g6079 | DLA_06767 | GAOABQK02IBA3P | CDS | 1121898 | 2040 | - | 0.323039 | |
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 | |
g6184 | DLA_06894 | GAOABQK02IO52T | CDS | 205344 | 4128 | + | 0.341328 | |
g6260 | DLA_06974 | GAOABQK02IO52T | CDS | 373105 | 1275 | + | 0.294902 | |
g6268 | DLA_06982 | GAOABQK02IO52T | CDS | 386719 | 1077 | - | 0.301764 | |
g6276 | DLA_06991 | GAOABQK02IO52T | CDS | 405378 | 1617 | - | 0.31107 | |
g6364 | DLA_07084 | GAOABQK02IO52T | CDS | 593010 | 2448 | - | 0.329657 | |
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 |
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 |
g6433 | DLA_07159 | GAOABQK02JBK0O | CDS | 45121 | 2970 | - | 0.306734 | |
g6466 | DLA_07195 | GAOABQK02JBK0O | CDS | 130705 | 501 | - | 0.315369 | |
g6497 | DLA_07234 | GAOABQK02JEBFV | CDS | 45755 | 2196 | - | 0.331056 | |
g651 | DLA_00720 | F4PJNLW01A00V1 | CDS | 34648 | 1248 | - | 0.309295 | |
g6524 | DLA_07265 | GAOABQK02JOCCH | CDS | 48097 | 3072 | + | 0.277995 | |
g6529 | DLA_07270 | GAOABQK02JOCCH | CDS | 58644 | 1905 | - | 0.290814 | |
g6566 | DLA_07317 | contains 5 transmembrane domains there is a second copy of this gene | GAOABQK02JOCCH | CDS | 152486 | 705 | + | 0.339007 |
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 | |
g6636 | DLA_07391 | GAOABQK02JOCCH | CDS | 319799 | 5493 | + | 0.298744 | |
g6674 | DLA_07435 | GAOABQK02JOCCH | CDS | 403183 | 3987 | + | 0.346627 | |
g6679 | DLA_07439 | GAOABQK02JOCCH | CDS | 414241 | 1386 | - | 0.368687 | |
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 | |
g6756 | DLA_07524 | GAOABQK02JOCCH | CDS | 588961 | 2115 | - | 0.336643 | |
g6857 | DLA_07643 | GAOABQK02JOCCH | CDS | 812714 | 6405 | - | 0.340515 | |
g6866 | DLA_07655 | GAOABQK02JOCCH | CDS | 839143 | 2553 | + | 0.302781 | |
g687 | DLA_00758 | F4PJNLW01A00V1 | CDS | 111311 | 2625 | + | 0.34781 | |
g6883 | DLA_07677 | GAOABQK02JOCCH | CDS | 880767 | 1194 | + | 0.326633 | |
g689 | DLA_00761 | F4PJNLW01A00V1 | CDS | 118427 | 1425 | + | 0.327719 | |
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 |
g6992 | DLA_07794 | GLQOFTK02FH5TG | CDS | 225458 | 534 | + | 0.327715 | |
g7011 | DLA_07814 | GLQOFTK02FH5TG | CDS | 269937 | 6186 | + | 0.35257 | |
g7012 | DLA_07815 | GLQOFTK02FH5TG | CDS | 276321 | 2337 | - | 0.344031 | |
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 | |
g705 | DLA_00778 | F4PJNLW01A00V1 | CDS | 153474 | 432 | - | 0.298611 | |
g7119 | DLA_07947 | GLQOFTK02FH5TG | CDS | 533740 | 2316 | + | 0.355786 | |
g713 | DLA_00785 | F4PJNLW01A00V1 | CDS | 167363 | 1281 | + | 0.323966 | |
g7217 | DLA_08053 | GLQOFTK02FH5TG | CDS | 742825 | 5442 | - | 0.34932 | |
g7222 | DLA_08062 | GLQOFTK02FH5TG | CDS | 759231 | 1590 | + | 0.284906 | |
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 | |
g7309 | DLA_08165 | similar to the cofilin phosphatase slingshot and to other dual-specificity phosphatasesbr there is a second copy of this gene | GLQOFTK02FH5TG | CDS | 948410 | 1101 | + | 0.322434 |
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 |
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 |
g7434 | DLA_08313 | GLQOFTK02FH5TG | CDS | 1251930 | 1500 | - | 0.29 | |
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 |
g7469 | DLA_08356 | GLQOFTK02FH5TG | CDS | 1335202 | 1944 | - | 0.308128 | |
g7498 | DLA_11717 | GLQOFTK02FH5TG | CDS | 1403137 | 438 | - | 0.276256 | |
g7533 | DLA_08427 | GLQOFTK02FH5TG | CDS | 1483060 | 3141 | + | 0.323464 | |
g754 | DLA_00830 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | F4PJNLW01A00V1 | CDS | 266491 | 2316 | - | 0.324698 |
g7666 | DLA_08571 | GLQOFTK02G2F2O | CDS | 229400 | 3729 | + | 0.335747 | |
g7724 | DLA_08642 | GLQOFTK02G2F2O | CDS | 383694 | 4512 | - | 0.359043 | |
g7748 | DLA_08663 | GLQOFTK02G2F2O | CDS | 439272 | 1941 | + | 0.296754 | |
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 |
g7812 | DLA_08732 | protein serinethreonine phosphatase required for chemotaxis and development suppresses the | GLQOFTK02G2F2O | CDS | 578711 | 918 | - | 0.360566 |
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 | |
g7939 | DLA_08873 | GLQOFTK02G2F2O | CDS | 845720 | 2619 | - | 0.316915 | |
g7953 | DLA_08888 | GLQOFTK02G2F2O | CDS | 886835 | 1737 | + | 0.35118 | |
g8077 | DLA_09028 | GLQOFTK02G2F2O | CDS | 1171541 | 1416 | + | 0.336158 | |
g8099 | DLA_09052 | GLQOFTK02G2F2O | CDS | 1220399 | 549 | + | 0.264117 | |
g8108 | DLA_09063 | GLQOFTK02G2F2O | CDS | 1245728 | 2325 | - | 0.32086 | |
g812 | DLA_00892 | F4PJNLW01A00V1 | CDS | 372454 | 2172 | + | 0.371547 | |
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 | |
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 |
g8298 | DLA_09259 | GLQOFTK02G2F2O | CDS | 1673495 | 3150 | + | 0.334603 | |
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 | |
g8368 | DLA_09334 | GLQOFTK02G2F2O | CDS | 1804605 | 483 | + | 0.337474 | |
g838 | DLA_00918 | phosphoinositide phosphatase with low specific activity compared to other known phosphoinositide phosphatases can dephosphorylate several phosphoinositide substrates with a preference for PI(5)P constitutively expressed putative ortholog of H. sapiens EPM2A involved in myoclonic epilepsy of Lafora | F4PJNLW01A00V1 | CDS | 439027 | 657 | - | 0.316591 |
g8396 | DLA_09365 | GLQOFTK02G2F2O | CDS | 1852909 | 447 | - | 0.317673 | |
g8403 | DLA_09372 | GLQOFTK02G2F2O | CDS | 1864027 | 1155 | + | 0.316883 | |
g8412 | DLA_09381 | GLQOFTK02G2F2O | CDS | 1880032 | 2088 | - | 0.357759 | |
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 |
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 |
g8558 | DLA_11779 | GLQOFTK02GHM7A | CDS | 154270 | 270 | + | 0.277778 | |
g8593 | DLA_09585 | GLQOFTK02GHM7A | CDS | 246755 | 4185 | + | 0.314934 | |
g8597 | DLA_09589 | GLQOFTK02GHM7A | CDS | 256496 | 2496 | - | 0.306891 | |
g8628 | DLA_09622 | GLQOFTK02GHM7A | CDS | 340924 | 834 | - | 0.266187 | |
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 | |
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 |
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 |
g8778 | DLA_09776 | GLQOFTK02GHM7A | CDS | 658485 | 1215 | + | 0.302058 | |
g8805 | DLA_09810 | GLQOFTK02GHM7A | CDS | 726834 | 1869 | + | 0.316212 | |
g8819 | DLA_09821 | GLQOFTK02GHM7A | CDS | 774623 | 1158 | - | 0.310881 | |
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 |
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 |
g8885 | DLA_09899 | GLQOFTK02GQ36N | CDS | 44251 | 708 | + | 0.323446 | |
g8896 | DLA_09914 | GLQOFTK02GQ36N | CDS | 80933 | 2232 | - | 0.336022 | |
g89 | DLA_00104 | contig05409_1.exp | CDS | 205615 | 3432 | + | 0.337121 | |
g8900 | DLA_09918 | GLQOFTK02GQ36N | CDS | 86387 | 2031 | - | 0.293451 | |
g8906 | DLA_09925 | GLQOFTK02GQ36N | CDS | 97926 | 1716 | - | 0.327506 | |
g8907 | DLA_09926 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | GLQOFTK02GQ36N | CDS | 100032 | 2586 | - | 0.310905 |
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 |
g8975 | DLA_09997 | GLQOFTK02GQ36N | CDS | 257526 | 2103 | - | 0.314788 | |
g9035 | DLA_10056 | GLQOFTK02GQ36N | CDS | 377200 | 1983 | + | 0.33535 | |
g9056 | DLA_10077 | GLQOFTK02GQ36N | CDS | 417938 | 447 | - | 0.288591 | |
g9075 | DLA_10099 | GLQOFTK02GQ36N | CDS | 469272 | 1191 | - | 0.275399 | |
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 |
g9120 | DLA_10154 | GLQOFTK02GQ36N | CDS | 597098 | 552 | - | 0.298913 | |
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 | |
g9312 | DLA_10379 | GLQOFTK02GUKFG | CDS | 381941 | 1743 | + | 0.325875 | |
g9327 | DLA_10395 | GLQOFTK02GUKFG | CDS | 404946 | 1500 | - | 0.340667 | |
g9335 | DLA_10408 | GLQOFTK02GUKFG | CDS | 428539 | 1335 | + | 0.310861 | |
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 |
g9445 | DLA_10523 | GLQOFTK02IIOHN | CDS | 85920 | 4386 | + | 0.332421 | |
g945 | DLA_01044 | F4PJNLW01A00V1 | CDS | 689006 | 3144 | - | 0.310433 | |
g9617 | DLA_10723 | GLQOFTK02IRMR1 | CDS | 31401 | 4668 | - | 0.336118 | |
g9624 | DLA_10729 | GLQOFTK02IRMR1 | CDS | 53933 | 4098 | + | 0.340898 | |
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 | |
g9657 | DLA_10770 | GLQOFTK02IRMR1 | CDS | 131584 | 1497 | + | 0.334001 | |
g9695 | DLA_10819 | homolog of S. cerevisiae CDC50 (cell division control protein 50) which is required for polarized cell growth contains two putative transmembrane domains | GLQOFTK02JCFFB | CDS | 13761 | 924 | - | 0.32684 |
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 | |
g9744 | DLA_10878 | GLQOFTK02JL55Q | CDS | 18609 | 327 | - | 0.33945 | |
g9853 | DLA_10997 | protein serinethreonine phosphatase required for chemotaxis and development suppresses the | GLQOFTK02JL55Q | CDS | 269264 | 924 | - | 0.338745 |
g9859 | DLA_11004 | GLQOFTK02JL55Q | CDS | 280021 | 1545 | - | 0.374757 | |
g986 | DLA_01096 | F4PJNLW01A00V1 | CDS | 794819 | 3531 | + | 0.353724 | |
g987 | DLA_11460 | F4PJNLW01A00V1 | CDS | 798527 | 3270 | + | 0.355352 | |
g9870 | DLA_11015 | GLQOFTK02JL55Q | CDS | 307354 | 3702 | + | 0.337655 | |
g9877 | DLA_11025 | GLQOFTK02JL55Q | CDS | 327533 | 1737 | + | 0.352332 | |
g9897 | DLA_11046 | GLQOFTK02JL55Q | CDS | 366394 | 2460 | - | 0.367886 | |
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 |
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 |