Gene list
Applied filters:
COG category: General function prediction only
Organism: Dictyostelium discoideum AX4, AX4
Number of genes found: 1370
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium discoideum AX4, AX4 | ||||||||
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Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
DDB_G0267514 | DDB_G0267514 | DDB0232428 | CDS | 259066 | 2751 | - | 0.28426 | |
DDB_G0267566 | DDB_G0267566 | putative protein serinethreonine kinase contains an ankyrin repeat domain similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232428 | CDS | 343868 | 2535 | - | 0.244181 |
DDB_G0267592 | DDB_G0267592 | DDB0232428 | CDS | 383616 | 1596 | + | 0.309524 | |
DDB_G0267632 | DDB_G0267632 | DDB0232428 | CDS | 445092 | 1230 | - | 0.202439 | |
DDB_G0267686 | DDB_G0267686 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats contains an RGS (Regulator of G protein Signaling) domain | DDB0232428 | CDS | 564277 | 6693 | - | 0.276109 |
DDB_G0267732 | DDB_G0267732 | DDB0232428 | CDS | 723287 | 6147 | - | 0.252969 | |
DDB_G0267880 | DDB_G0267880 | similar to bacterial and fungal acetyltransferases member of the GNAT family | DDB0232428 | CDS | 1028328 | 570 | + | 0.233333 |
DDB_G0267904 | DDB_G0267904 | putative ortholog of Xenopus AND-1 (Acidic Nucleoplasmic DNA-binding protein 1) that participates in loading the MCM2-7 helicase complex at the initiation of DNA replication brbr bCommunity annotation:b DDB G0267904 is a wd-repeat protein with moderate similarity to AND-1 also known as CTF4 a wd40 and HMG-box containing protein originally discovered in Xenopus. (see Franke et al AND-1 a natural chimeric DNA-binding protein combines an HMG-box with regulatory WD-repeats.Journal of Cell Science 110 1051-1062) AND-1CTF4 participates in loading the MCM2-7 helicase complex at the initiation of DNA replication (see Zhu et al Genes and Development 21 2288-2299 (2007) also Tanaka et al Genes to Cells 14 807-20 (2009). Recent work suggests that AND-1CTF4 links sister chromatid cohesion with DNA replication(see Tanaka et al Genes to Cells 14 991-1001 (2009).br DDB G0267904 is overexpressed 12-fold [1299 hits to 99 p1e-210] in a Dicty strain lacking the retinoblastoma-like gene rblA. Most genes a | DDB0232428 | CDS | 1077141 | 3267 | - | 0.285277 |
DDB_G0267954 | DDB_G0267954 | contains a C-terminal Bicoid-interacting 3 domain which occurs in methyltransferases that modify RNA-binding proteins has similarity to mammalian 7SK snRNA methylphosphate capping enzyme | DDB0232428 | CDS | 1175758 | 1302 | + | 0.195853 |
DDB_G0268018 | DDB_G0268018 | DDB0232428 | CDS | 1314808 | 1596 | + | 0.280702 | |
DDB_G0268064 | DDB_G0268064 | DDB0232428 | CDS | 1393387 | 669 | - | 0.281016 | |
DDB_G0268078 | DDB_G0268078 | DDB0232428 | CDS | 1417972 | 1524 | + | 0.281496 | |
DDB_G0268116 | DDB_G0268116 | similarity to Xenopus F8A1 protein human Factor VIII intron 22 protein | DDB0232428 | CDS | 1479679 | 1113 | - | 0.238095 |
DDB_G0268132 | DDB_G0268132 | contains a SET domain involved in histone methylation an AWS (Associated With SET) domain and a post-SET zinc-binding domain | DDB0232428 | CDS | 1516724 | 2697 | + | 0.269559 |
DDB_G0268222 | DDB_G0268222 | belongs to the metallophosphoesterase superfamily similar to human PAPL (Ironzinc purple acid phosphatase-like protein) contains a predicted signal peptide | DDB0232428 | CDS | 1715767 | 1479 | - | 0.323191 |
DDB_G0268230 | DDB_G0268230 | DDB0232428 | CDS | 1727069 | 1764 | + | 0.265306 | |
DDB_G0268288 | DDB_G0268288 | DDB0232428 | CDS | 386296 | 3792 | - | 0.238397 | |
DDB_G0268322 | DDB_G0268322 | DDB0232428 | CDS | 659396 | 1008 | - | 0.340278 | |
DDB_G0268336 | DDB_G0268336 | DDB0232428 | CDS | 731136 | 792 | - | 0.268939 | |
DDB_G0268346 | DDB_G0268346 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232428 | CDS | 866636 | 1269 | + | 0.266351 |
DDB_G0268384 | DDB_G0268384 | DDB0232428 | CDS | 1085918 | 2886 | + | 0.30492 | |
DDB_G0268386 | DDB_G0268386 | similar to D. purpureum protein contains one SET domain and one tetratricopeptide repeat (TPR) region | DDB0232428 | CDS | 1104198 | 2031 | - | 0.232398 |
DDB_G0268462 | DDB_G0268462 | DDB0232428 | CDS | 1630091 | 1890 | + | 0.292064 | |
DDB_G0268486_ps | DDB_G0268486 | putative pseudogene contains protein kinase domain | DDB0232428 | CDS | 498516 | 2820 | - | 0.22305 |
DDB_G0268492 | DDB_G0268492 | DDB0232428 | CDS | 520101 | 2007 | - | 0.247135 | |
DDB_G0268504 | DDB_G0268504 | contains two putative coiled-coil domains conserved in Dictyostelium and Polysphondylium | DDB0232428 | CDS | 642853 | 15879 | + | 0.239688 |
DDB_G0268566 | DDB_G0268566 | DDB0232428 | CDS | 1378934 | 1701 | + | 0.188713 | |
DDB_G0268656 | DDB_G0268656 | highly similar to human ULK (Unc51-like kinase) does not contain the full consensus sequence required for kinase function | DDB0232428 | CDS | 1863917 | 954 | - | 0.220126 |
DDB_G0268786 | DDB_G0268786 | DDB0232428 | CDS | 2108112 | 1965 | - | 0.243766 | |
DDB_G0268824 | DDB_G0268824 | DDB0232428 | CDS | 2182743 | 1299 | - | 0.254811 | |
DDB_G0268826 | DDB_G0268826 | DDB0232428 | CDS | 2184410 | 3060 | - | 0.203595 | |
DDB_G0268876 | DDB_G0268876 | member of the TKL (tyrosine kinase-like) group of protein kinases contains filamin repeat similar to ABP120 | DDB0232428 | CDS | 2297918 | 4158 | - | 0.279702 |
DDB_G0268980_ps | DDB_G0268980 | putative pseudogene fragment very similar to parts of DDB_G0268948 a putative SAM dependent methyltransferase | DDB0232428 | CDS | 2065538 | 243 | - | 0.288066 |
DDB_G0268990 | DDB_G0268990 | DDB0232428 | CDS | 2079025 | 1308 | + | 0.249235 | |
DDB_G0269052 | DDB_G0269052 | DDB0232428 | CDS | 1898794 | 1815 | - | 0.230854 | |
DDB_G0269272 | DDB_G0269272 | DDB0232428 | CDS | 2434615 | 3645 | + | 0.257064 | |
DDB_G0269294 | DDB_G0269294 | DDB0232428 | CDS | 2471481 | 2553 | - | 0.224442 | |
DDB_G0269340 | DDB_G0269340 | DDB0232428 | CDS | 2565964 | 834 | + | 0.29976 | |
DDB_G0269344 | DDB_G0269344 | DDB0232428 | CDS | 2568156 | 1203 | - | 0.307564 | |
DDB_G0269348 | DDB_G0269348 | DDB0232428 | CDS | 2570683 | 1911 | - | 0.244898 | |
DDB_G0269356 | DDB_G0269356 | DDB0232428 | CDS | 2583576 | 819 | + | 0.246642 | |
DDB_G0269358 | DDB_G0269358 | DDB0232428 | CDS | 2584566 | 969 | - | 0.281734 | |
DDB_G0269370 | DDB_G0269370 | very similar to the human 25 kDa cleavage and polyadenylation specificity factor component of the cleavage factor Im (CFIm) complex that plays a key role in pre-mRNA 3' processing | DDB0232428 | CDS | 2630812 | 603 | + | 0.288557 |
DDB_G0269430 | DDB_G0269430 | Sel1-like repeats are tetratricopeptide repeat sequences originally identified in a C. elegans receptor molecule which is a key negative regulator of the Notch pathway Dictyostelium like mammals has two sel1-like proteins which are located next to each other | DDB0232428 | CDS | 2753471 | 2895 | + | 0.308463 |
DDB_G0269432 | DDB_G0269432 | Sel1-like repeats are tetratricopeptide repeat sequences originally identified in a C. elegans receptor molecule which is a key negative regulator of the Notch pathway Dictyostelium like mammals has two sel1-like proteins which are located next to each other | DDB0232428 | CDS | 2756997 | 3183 | + | 0.270814 |
DDB_G0269442 | DDB_G0269442 | DDB0232428 | CDS | 2784673 | 2772 | - | 0.240981 | |
DDB_G0269448 | DDB_G0269448 | DDB0232428 | CDS | 2791078 | 3879 | - | 0.267079 | |
DDB_G0269452 | DDB_G0269452 | DDB0232428 | CDS | 2799520 | 2991 | - | 0.248412 | |
DDB_G0269460 | DDB_G0269460 | DDB0232428 | CDS | 2818161 | 6666 | - | 0.271377 | |
DDB_G0269462 | DDB_G0269462 | large protein containing two ubiquitin domains has no ortholog in other organisms | DDB0232428 | CDS | 2825931 | 7014 | + | 0.286142 |
DDB_G0269514 | DDB_G0269514 | DDB0232428 | CDS | 2909436 | 1113 | - | 0.221024 | |
DDB_G0269546 | DDB_G0269546 | DDB0232428 | CDS | 2969017 | 4641 | + | 0.290239 | |
DDB_G0269560 | DDB_G0269560 | DDB0232428 | CDS | 2996712 | 1728 | - | 0.219329 | |
DDB_G0269614 | DDB_G0269614 | DDB0232428 | CDS | 3146250 | 1311 | + | 0.357742 | |
DDB_G0269628 | DDB_G0269628 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232428 | CDS | 3183487 | 2214 | - | 0.303975 |
DDB_G0269644 | DDB_G0269644 | DDB0232428 | CDS | 3214845 | 1650 | + | 0.258182 | |
DDB_G0269658 | DDB_G0269658 | DDB0232428 | CDS | 3247871 | 813 | + | 0.268143 | |
DDB_G0269686 | DDB_G0269686 | DDB0232428 | CDS | 3319946 | 2688 | - | 0.289062 | |
DDB_G0269722 | DDB_G0269722 | belongs to the methyltransferase superfamily ortholog of human WBSCR22 an uncharacterized methyltransferase associated with Williams-Beuren syndrome | DDB0232428 | CDS | 3414230 | 864 | + | 0.340278 |
DDB_G0269732 | DDB_G0269732 | DDB0232428 | CDS | 3443410 | 2439 | + | 0.357524 | |
DDB_G0269754 | DDB_G0269754 | DDB0232428 | CDS | 3484288 | 1062 | + | 0.211864 | |
DDB_G0269778 | DDB_G0269778 | DDB0232428 | CDS | 3547267 | 1083 | + | 0.290859 | |
DDB_G0269800 | DDB_G0269800 | putative ortholog of the conserved chromatin assembly factor 1 (CAF1) subunit Bbr bNote:b Do not confuse this gene with | DDB0232428 | CDS | 3628624 | 2115 | - | 0.274704 |
DDB_G0269836 | DDB_G0269836 | DDB0232428 | CDS | 3688411 | 786 | - | 0.229008 | |
DDB_G0269888 | DDB_G0269888 | DDB0232428 | CDS | 3802780 | 810 | + | 0.188889 | |
DDB_G0269898 | DDB_G0269898 | DDB0232428 | CDS | 3820454 | 2829 | + | 0.298339 | |
DDB_G0269936 | DDB_G0269936 | DDB0232428 | CDS | 3903678 | 1053 | + | 0.235518 | |
DDB_G0269952 | DDB_G0269952 | DDB0232428 | CDS | 3922020 | 795 | - | 0.208805 | |
DDB_G0269964 | DDB_G0269964 | DDB0232428 | CDS | 3938864 | 1998 | + | 0.285285 | |
DDB_G0269982 | DDB_G0269982 | similar to human TBC1D22B S. pombe gyp1 | DDB0232428 | CDS | 3972852 | 1635 | - | 0.292966 |
DDB_G0270016 | DDB_G0270016 | DDB0232428 | CDS | 4029381 | 909 | - | 0.225523 | |
DDB_G0270018 | DDB_G0270018 | DDB0232428 | CDS | 4030543 | 942 | - | 0.291932 | |
DDB_G0270096 | DDB_G0270096 | DDB0232428 | CDS | 4205387 | 2373 | - | 0.292035 | |
DDB_G0270146 | DDB_G0270146 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis | DDB0232428 | CDS | 4304005 | 1908 | - | 0.287212 |
DDB_G0270206 | DDB_G0270206 | DDB0232428 | CDS | 4404424 | 3465 | + | 0.223954 | |
DDB_G0270220 | DDB_G0270220 | DDB0232428 | CDS | 4432689 | 2520 | + | 0.314683 | |
DDB_G0270262 | DDB_G0270262 | DDB0232428 | CDS | 4528758 | 627 | + | 0.23764 | |
DDB_G0270284 | DDB_G0270284 | contains an N-terminal DOMON domain as it occurs in dopamine beta-monooxygenases the Dictyostelium protein is followed by a cytochrome b561 domain which contains 5 putative transmembrane regions in addition the protein contains a putative signal peptide | DDB0232428 | CDS | 4579488 | 1173 | + | 0.277067 |
DDB_G0270304 | DDB_G0270304 | DDB0232428 | CDS | 4607306 | 630 | - | 0.284127 | |
DDB_G0270324 | DDB_G0270324 | similar to N-myc downstream regulated gene 1 (NDRG1) defects in NDRG1 are the cause of Charcot-Marie-Tooth disease type 4D (CMT4D) also known as hereditary motor and sensory neuropathy Lom type (HMSNL) | DDB0232428 | CDS | 4644690 | 981 | + | 0.275229 |
DDB_G0270378 | DDB_G0270378 | similar to human TTC39C matches PFAM outer membrane protein IML2 mitochondrialtetratricopeptide repeat protein 39 | DDB0232428 | CDS | 4727960 | 1596 | + | 0.311404 |
DDB_G0270436 | DDB_G0270436 | DDB0232428 | CDS | 4873137 | 1566 | - | 0.297573 | |
DDB_G0270552 | DDB_G0270552 | contains one C2H2-type zinc finger motif and 2 ankyrin repeats contains 2 predicted coiled-coil domains | DDB0232428 | CDS | 2951187 | 2364 | + | 0.301184 |
DDB_G0270618 | DDB_G0270618 | DDB0232428 | CDS | 3364045 | 1233 | + | 0.281427 | |
DDB_G0270634 | DDB_G0270634 | similar to TNRC4 (TriNucleotide Repeat Containing 4 protein) and Bruno-like proteins contains 3 RRM domains | DDB0232428 | CDS | 3530459 | 1107 | + | 0.317073 |
DDB_G0270652 | DDB_G0270652 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232428 | CDS | 3647265 | 1122 | + | 0.266488 |
DDB_G0270692 | DDB_G0270692 | contains 6 ankyrin repeats contains one VPS9 (vacuolar sorting protein 9) domain similar to D. purpureum protein | DDB0232428 | CDS | 3887599 | 3024 | - | 0.276786 |
DDB_G0270720 | DDB_G0270720 | DDB0232428 | CDS | 4125800 | 1560 | + | 0.239744 | |
DDB_G0270746 | DDB_G0270746 | putative ortholog of H. sapiens transducin beta-like 2 (TBL2) deleted in patients with Williams-Beuren syndrome (WBS) | DDB0232428 | CDS | 4336075 | 1377 | - | 0.257807 |
DDB_G0270766 | DDB_G0270766 | DDB0232428 | CDS | 4499254 | 2994 | + | 0.257515 | |
DDB_G0270856 | DDB_G0270856 | DDB0232428 | CDS | 2591243 | 2496 | + | 0.271635 | |
DDB_G0270878 | DDB_G0270878 | DDB0232428 | CDS | 2931465 | 987 | - | 0.256332 | |
DDB_G0270920 | DDB_G0270920 | DDB0232428 | CDS | 3375140 | 3339 | - | 0.262953 | |
DDB_G0270932 | DDB_G0270932 | DDB0232428 | CDS | 3418520 | 3039 | + | 0.29253 | |
DDB_G0271270 | DDB_G0271270 | DDB0232429 | CDS | 179519 | 1080 | - | 0.287963 | |
DDB_G0271316 | DDB_G0271316 | DDB0232429 | CDS | 120793 | 657 | - | 0.231355 | |
DDB_G0271376 | DDB_G0271376 | DDB0232429 | CDS | 144988 | 762 | + | 0.295276 | |
DDB_G0271402 | DDB_G0271402 | DDB0232429 | CDS | 241165 | 2298 | + | 0.309835 | |
DDB_G0271484 | DDB_G0271484 | DDB0232429 | CDS | 427690 | 1485 | + | 0.256566 | |
DDB_G0271538 | DDB_G0271538 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family expressed in pstO cells | DDB0232429 | CDS | 568653 | 1584 | - | 0.285985 |
DDB_G0271550 | DDB_G0271550 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | DDB0232429 | CDS | 634463 | 1179 | + | 0.267176 |
DDB_G0271680 | DDB_G0271680 | DDB0232429 | CDS | 796698 | 1008 | + | 0.324405 | |
DDB_G0271682 | DDB_G0271682 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats contains two kinase domains one of which is predicted to be inactive | DDB0232429 | CDS | 792553 | 3075 | + | 0.247154 |
DDB_G0271720 | DDB_G0271720 | almost identical to | DDB0232429 | CDS | 843067 | 1029 | - | 0.290573 |
DDB_G0271730 | DDB_G0271730 | DDB0232429 | CDS | 868232 | 3978 | + | 0.311714 | |
DDB_G0271740 | DDB_G0271740 | DDB0232429 | CDS | 897538 | 1008 | + | 0.329365 | |
DDB_G0271748_ps | DDB_G0271748 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232429 | CDS | 711253 | 876 | + | 0.261416 |
DDB_G0271780 | DDB_G0271780 | DDB0232429 | CDS | 899784 | 1026 | + | 0.312865 | |
DDB_G0271802 | DDB_G0271802 | DDB0232429 | CDS | 783832 | 954 | + | 0.267296 | |
DDB_G0271820 | DDB_G0271820 | almost identical to | DDB0232429 | CDS | 837872 | 1035 | - | 0.284058 |
DDB_G0271884 | DDB_G0271884 | conserved putative quinone oxidoreductase belongs to the broader superfamily of zinc-dependent alcohol dehydrogenases | DDB0232429 | CDS | 973836 | 996 | - | 0.358434 |
DDB_G0272020 | DDB_G0272020 | contains an N-terminal F-box domain a central SH2 domain and C-terminal ankyrin repeats | DDB0232429 | CDS | 1179282 | 2412 | + | 0.246269 |
DDB_G0272064 | DDB_G0272064 | DDB0232429 | CDS | 1150556 | 8169 | + | 0.281307 | |
DDB_G0272092 | DDB_G0272092 | 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 | DDB0232429 | CDS | 1251605 | 2961 | - | 0.296184 |
DDB_G0272128 | DDB_G0272128 | 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 | DDB0232429 | CDS | 1375029 | 795 | + | 0.328302 |
DDB_G0272154 | DDB_G0272154 | DDB0232429 | CDS | 1594214 | 906 | - | 0.378587 | |
DDB_G0272180 | DDB_G0272180 | DDB0232429 | CDS | 1518514 | 1008 | + | 0.240079 | |
DDB_G0272184 | DDB_G0272184 | very conserved protein among bacteria and fungi zinc-binding ADH's are dimeric or tetrameric enzymes that bind two atoms of zinc per subunit | DDB0232429 | CDS | 1513508 | 966 | - | 0.385093 |
DDB_G0272186 | DDB_G0272186 | DDB0232429 | CDS | 1509530 | 3153 | - | 0.292103 | |
DDB_G0272192 | DDB_G0272192 | DDB0232429 | CDS | 1412468 | 1497 | + | 0.329993 | |
DDB_G0272206 | DDB_G0272206 | DDB0232429 | CDS | 1658418 | 5340 | + | 0.265169 | |
DDB_G0272254 | DDB_G0272254 | member of the TKL (tyrosine kinase-like) group contains a galactose oxidase central domain and three Kelch motifs | DDB0232429 | CDS | 1396081 | 3996 | - | 0.264765 |
DDB_G0272282 | DDB_G0272282 | member of the AGC kinase group similar to kinase domains of NDR (nuclear Dbf2-related) and MAST (microtubule-associated serinethreonine kinase) | DDB0232429 | CDS | 1572926 | 6309 | + | 0.272468 |
DDB_G0272356 | DDB_G0272356 | DDB0232429 | CDS | 1290469 | 1914 | - | 0.372518 | |
DDB_G0272440 | DDB_G0272440 | very similar to the H. sapiens tumor protein p53-inducible protein 3 (TP53I3) belongs to the broader superfamily of zinc-dependent alcohol dehydrogenases | DDB0232429 | CDS | 1596579 | 1008 | - | 0.340278 |
DDB_G0272466 | DDB_G0272466 | DDB0232429 | CDS | 1706359 | 867 | - | 0.304498 | |
DDB_G0272484 | DDB_G0272484 | 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 | DDB0232429 | CDS | 1760557 | 1545 | - | 0.297735 |
DDB_G0272628 | DDB_G0272628 | underexpressed in | DDB0232429 | CDS | 2278778 | 1023 | - | 0.333333 |
DDB_G0272666 | DDB_G0272666 | DDB0232429 | CDS | 1858373 | 3930 | + | 0.265903 | |
DDB_G0272797 | DDB_G0272797 | similar to cyclin dependent protein kinases there is a second copy of this gene | DDB0232429 | CDS | 2368968 | 2043 | - | 0.313754 |
DDB_G0272839 | DDB_G0272839 | has a short region of similarity to aprataxin a Hint related protein that is mutated in individuals with ataxia with oculomotor apraxia | DDB0232429 | CDS | 2148504 | 1173 | + | 0.224211 |
DDB_G0272913 | DDB_G0272913 | DDB0232429 | CDS | 1908716 | 762 | + | 0.26378 | |
DDB_G0272953 | DDB_G0272953 | DDB0232429 | CDS | 1904183 | 1545 | + | 0.212945 | |
DDB_G0273101 | DDB_G0273101 | there is a second copy of this gene | DDB0232429 | CDS | 2569065 | 6147 | + | 0.284041 |
DDB_G0273155 | DDB_G0273155 | there is a second copy of this gene | DDB0232429 | CDS | 2472439 | 1011 | - | 0.346192 |
DDB_G0273195 | DDB_G0273195 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 2690707 | 1764 | - | 0.294218 |
DDB_G0273301 | DDB_G0273301 | there is a second copy of this gene | DDB0232429 | CDS | 2668726 | 1926 | - | 0.323988 |
DDB_G0273413 | DDB_G0273413 | there is a second copy of this gene | DDB0232429 | CDS | 2940321 | 1371 | + | 0.243618 |
DDB_G0273417 | DDB_G0273417 | similar to bacterial S-adenosyl-L-methionine (SAM) methyltransferases similar to D. purpureum protein there is a second copy of this gene | DDB0232429 | CDS | 2943449 | 1407 | + | 0.25231 |
DDB_G0273477 | DDB_G0273477 | there is a second copy of this gene | DDB0232429 | CDS | 2933551 | 1509 | - | 0.204109 |
DDB_G0273547 | DDB_G0273547 | similar to bacterial S-adenosyl-L-methionine (SAM) methyltransferases similar to D. purpureum protein there is a second copy of this gene | DDB0232429 | CDS | 3086765 | 1407 | - | 0.25231 |
DDB_G0273551 | DDB_G0273551 | there is a second copy of this gene | DDB0232429 | CDS | 3090095 | 1371 | - | 0.243618 |
DDB_G0273557 | DDB_G0273557 | there is a second copy of this gene | DDB0232429 | CDS | 3096406 | 1509 | + | 0.204109 |
DDB_G0273735 | DDB_G0273735 | member of the major facilitator superfamily (MFS) expressed in upper cup during culmination there is a second copy of this gene | DDB0232429 | CDS | 3339316 | 1764 | + | 0.294218 |
DDB_G0273753 | DDB_G0273753 | there is a second copy of this gene | DDB0232429 | CDS | 3360515 | 1926 | + | 0.323988 |
DDB_G0273831 | DDB_G0273831 | there is a second copy of this gene | DDB0232429 | CDS | 3456169 | 6147 | - | 0.284041 |
DDB_G0273855 | DDB_G0273855 | there is a second copy of this gene | DDB0232429 | CDS | 3486160 | 915 | + | 0.243716 |
DDB_G0273921 | DDB_G0273921 | there is a second copy of this gene | DDB0232429 | CDS | 3558114 | 1011 | + | 0.346192 |
DDB_G0274007 | DDB_G0274007 | similar to cyclin dependent protein kinases there is a second copy of this gene | DDB0232429 | CDS | 3660427 | 2043 | + | 0.313754 |
DDB_G0274085 | DDB_G0274085 | underexpressed in | DDB0232429 | CDS | 3751889 | 1023 | + | 0.333333 |
DDB_G0274185 | DDB_G0274185 | contains an N-terminal oxidoreductase domain and a partial C-terminal oxidoreductase domain the GfoIdhMocA family proteins utilize NADP or NAD | DDB0232429 | CDS | 4815159 | 1293 | - | 0.336427 |
DDB_G0274199 | DDB_G0274199 | DDB0232429 | CDS | 4796097 | 1281 | + | 0.291179 | |
DDB_G0274201 | DDB_G0274201 | DDB0232429 | CDS | 4797968 | 951 | + | 0.268139 | |
DDB_G0274251 | DDB_G0274251 | DDB0232429 | CDS | 4152834 | 1077 | + | 0.226555 | |
DDB_G0274265 | DDB_G0274265 | DDB0232429 | CDS | 4139227 | 1803 | - | 0.291736 | |
DDB_G0274273 | DDB_G0274273 | DDB0232429 | CDS | 4010059 | 963 | - | 0.36864 | |
DDB_G0274283 | DDB_G0274283 | DDB0232429 | CDS | 4044553 | 1179 | - | 0.310433 | |
DDB_G0274293 | DDB_G0274293 | DDB0232429 | CDS | 4065363 | 1497 | + | 0.281229 | |
DDB_G0274433 | DDB_G0274433 | bCommunity annotation:b DDB G0274433 is weakly similar to SDS23 and SDS24 of budding yeast which are themselves homologues of sds23 from fission yeast. The fission yeast gene interacts with the anaphase promoting complex in a manner which is not understood molecularly. The APC must be dephosphoryated by PPI for normal mitosis and sds23 overexpressers bypass the requirement for PPI (Ishii et al EMBO Journal 15 6629-6640 (1996). Deletion of sds23 gives very slowly growing cells with multiple nuclei and extremely prolonged anaphase. In budding yeast however the double deletion is viable with changes mainly in the size of the vacuole. In Dicty a role of DDB_G0274433 in cell cycle control is suggested by the gene's fivefold overexpression in a Dicty strain deficient in the Dictyostelium | DDB0232429 | CDS | 4606302 | 1062 | + | 0.29661 |
DDB_G0274499 | DDB_G0274499 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity contains a predicted signal peptide | DDB0232429 | CDS | 4386087 | 942 | + | 0.316348 |
DDB_G0274505 | DDB_G0274505 | DDB0232429 | CDS | 4376727 | 1509 | - | 0.297548 | |
DDB_G0274527 | DDB_G0274527 | DDB0232429 | CDS | 4275808 | 1428 | - | 0.298319 | |
DDB_G0274613 | DDB_G0274613 | kinase domain similar to mitogen-activated protein kinases does not contain the consensus sequences known to be required for kinase function contains a RING zinc finger domain | DDB0232429 | CDS | 4893134 | 2496 | - | 0.260417 |
DDB_G0274663 | DDB_G0274663 | similar to human PRSS16 (thymus-specific serine protease) contains a putative signal peptide | DDB0232429 | CDS | 4408799 | 1464 | - | 0.347678 |
DDB_G0274739 | DDB_G0274739 | DDB0232429 | CDS | 3941346 | 1341 | + | 0.226696 | |
DDB_G0274781 | DDB_G0274781 | 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 | DDB0232429 | CDS | 3825256 | 678 | + | 0.29646 |
DDB_G0274801 | DDB_G0274801 | DDB0232429 | CDS | 3911402 | 2562 | - | 0.369243 | |
DDB_G0274807 | DDB_G0274807 | DDB0232429 | CDS | 3946871 | 1851 | - | 0.222582 | |
DDB_G0274821 | DDB_G0274821 | DDB0232429 | CDS | 3992986 | 2565 | - | 0.181287 | |
DDB_G0274911_ps | DDB_G0274911 | putative pseudogene fragment similar to D. discoideum gene | DDB0232429 | CDS | 4421760 | 1470 | - | 0.182993 |
DDB_G0274975 | DDB_G0274975 | DDB0232429 | CDS | 4730779 | 4398 | - | 0.31105 | |
DDB_G0275027 | DDB_G0275027 | DDB0232429 | CDS | 5323069 | 276 | - | 0.297101 | |
DDB_G0275041 | DDB_G0275041 | DDB0232429 | CDS | 5273798 | 1026 | + | 0.220273 | |
DDB_G0275049 | DDB_G0275049 | DDB0232429 | CDS | 5249449 | 924 | + | 0.313853 | |
DDB_G0275057 | DDB_G0275057 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | DDB0232429 | CDS | 5089988 | 1050 | + | 0.33619 |
DDB_G0275075 | DDB_G0275075 | ortholog of mammalian NARG1 and yeast NAT1 part of a complex that displays alpha (N-terminal) acetyltransferase activity | DDB0232429 | CDS | 5130987 | 2445 | + | 0.285072 |
DDB_G0275097 | DDB_G0275097 | DDB0232429 | CDS | 5060014 | 2256 | + | 0.321809 | |
DDB_G0275149 | DDB_G0275149 | similar to S. cerevisiae AKR1 (palmitoyltransferase AKR1) contains 5 ankyrin repeats and 1 zinc finger DHHC domain contains 6 putative transmembrane domains | DDB0232429 | CDS | 4965140 | 2097 | + | 0.299475 |
DDB_G0275165 | DDB_G0275165 | DDB0232429 | CDS | 5143836 | 2766 | - | 0.298988 | |
DDB_G0275195 | DDB_G0275195 | DDB0232429 | CDS | 5206472 | 3642 | - | 0.31933 | |
DDB_G0275203 | DDB_G0275203 | DDB0232429 | CDS | 5105558 | 1707 | + | 0.176333 | |
DDB_G0275205 | DDB_G0275205 | DDB0232429 | CDS | 5081463 | 1533 | - | 0.270711 | |
DDB_G0275215 | DDB_G0275215 | DDB0232429 | CDS | 5007231 | 2076 | - | 0.244701 | |
DDB_G0275289 | DDB_G0275289 | DDB0232429 | CDS | 5225979 | 2826 | - | 0.209837 | |
DDB_G0275345 | DDB_G0275345 | DDB0232429 | CDS | 5397156 | 2109 | + | 0.266477 | |
DDB_G0275351 | DDB_G0275351 | contains 1 C2H2-type zinc finger homolog of human ZNF593 and S. cerevisiae BUD20 (bud site selection protein 20) | DDB0232429 | CDS | 5402357 | 426 | + | 0.293427 |
DDB_G0275389 | DDB_G0275389 | DDB0232429 | CDS | 5493095 | 1608 | + | 0.298507 | |
DDB_G0275421 | DDB_G0275421 | contains 2 GRAM domains one RabGAPTBC domain and one EF hand domain | DDB0232429 | CDS | 5459788 | 3672 | + | 0.232026 |
DDB_G0275457 | DDB_G0275457 | DDB0232429 | CDS | 6112474 | 780 | + | 0.284615 | |
DDB_G0275459 | DDB_G0275459 | DDB0232429 | CDS | 6113524 | 900 | + | 0.428889 | |
DDB_G0275507 | DDB_G0275507 | similar to bacterial acetyltransferases homolog of E. coli maa (maltose O-acetyltransferase) | DDB0232429 | CDS | 6022499 | 591 | - | 0.314721 |
DDB_G0275529 | DDB_G0275529 | DDB0232429 | CDS | 5892491 | 4269 | - | 0.223003 | |
DDB_G0275559 | DDB_G0275559 | underexpressed in | DDB0232429 | CDS | 5618738 | 873 | + | 0.316151 |
DDB_G0275581 | DDB_G0275581 | DDB0232429 | CDS | 5550573 | 2736 | - | 0.299708 | |
DDB_G0275591 | DDB_G0275591 | DDB0232429 | CDS | 5562777 | 2082 | + | 0.304995 | |
DDB_G0275593 | DDB_G0275593 | DDB0232429 | CDS | 5568361 | 1221 | - | 0.232596 | |
DDB_G0275605_ps | DDB_G0275605 | putative pseudogene similar to gene | DDB0232429 | CDS | 5585797 | 1407 | - | 0.329069 |
DDB_G0275671 | DDB_G0275671 | putative serine esterase similar to hypothetical proteins in plants and yeast | DDB0232429 | CDS | 5687040 | 1239 | + | 0.268765 |
DDB_G0275793 | DDB_G0275793 | DDB0232429 | CDS | 5611769 | 1593 | - | 0.2285 | |
DDB_G0275913 | DDB_G0275913 | similar to bacterial acetyltransferases homolog of E. coli maa (maltose O-acetyltransferase) similar to D. purpureum protein | DDB0232429 | CDS | 6029488 | 573 | - | 0.340314 |
DDB_G0275951 | DDB_G0275951 | DDB0232429 | CDS | 5814130 | 711 | + | 0.341772 | |
DDB_G0275953 | DDB_G0275953 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232429 | CDS | 6210610 | 1044 | - | 0.272031 |
DDB_G0275971 | DDB_G0275971 | DDB0232429 | CDS | 6175233 | 2100 | + | 0.335714 | |
DDB_G0275993 | DDB_G0275993 | DDB0232429 | CDS | 6150629 | 687 | - | 0.227074 | |
DDB_G0276007 | DDB_G0276007 | DDB0232429 | CDS | 6178436 | 639 | + | 0.27543 | |
DDB_G0276013 | DDB_G0276013 | DDB0232429 | CDS | 6191275 | 2247 | - | 0.304406 | |
DDB_G0276017 | DDB_G0276017 | DDB0232429 | CDS | 6201276 | 1317 | + | 0.23918 | |
DDB_G0276031 | DDB_G0276031 | similar human THO complex subunit 3 (THOC3) although D. discoideum seems to be lacking THOC4 and THOC5 | DDB0232429 | CDS | 6461770 | 1437 | + | 0.302714 |
DDB_G0276037 | DDB_G0276037 | DDB0232429 | CDS | 6539160 | 1020 | + | 0.269608 | |
DDB_G0276117 | DDB_G0276117 | DDB0232429 | CDS | 6262508 | 615 | - | 0.21626 | |
DDB_G0276181 | DDB_G0276181 | member of the TKL (tyrosine kinase-like) group of protein kinases contains a PH (pleckstrin homology) domain | DDB0232429 | CDS | 6410071 | 4668 | - | 0.262853 |
DDB_G0276227 | DDB_G0276227 | DDB0232429 | CDS | 6222654 | 2514 | + | 0.239061 | |
DDB_G0276237 | DDB_G0276237 | DDB0232429 | CDS | 6306373 | 1077 | + | 0.275766 | |
DDB_G0276251 | DDB_G0276251 | similar to H. sapiens GP17 involved in modification of glycosylphosphatidylinositol contains 16 transmembrane domains | DDB0232429 | CDS | 6500338 | 4329 | + | 0.260799 |
DDB_G0276271 | DDB_G0276271 | DDB0232429 | CDS | 6637140 | 1641 | - | 0.203534 | |
DDB_G0276281 | DDB_G0276281 | DDB0232429 | CDS | 6608304 | 1032 | - | 0.223837 | |
DDB_G0276293 | DDB_G0276293 | DDB0232429 | CDS | 6559102 | 1473 | - | 0.304141 | |
DDB_G0276297 | DDB_G0276297 | DDB0232429 | CDS | 6556293 | 1056 | + | 0.294508 | |
DDB_G0276429 | DDB_G0276429 | DDB0232429 | CDS | 6932540 | 1422 | - | 0.270042 | |
DDB_G0276461 | DDB_G0276461 | putative protein serinethreonine kinase similar to the kinase domains of AAK1 (AP2 associated kinase) and BMP-inducible protein kinase (BIKe) | DDB0232429 | CDS | 6904331 | 2397 | - | 0.267418 |
DDB_G0276531 | DDB_G0276531 | similar to elaC and TRZ a zinc phosphodiesterase with tRNA 3'-processing endonuclease activity and probably involved in tRNA maturation by removing a 3'-trailer from precursor tRNAbrbr bCommunity annotation:b similar to elaC an endoribonuclease conserved from bacteria to humans sequence variants of which are associated with aggressive prostate cancer. Nothing seems to be known about the connection between elaC and cell proliferation. The possible involvement of the Dicty gene in cell cycle control is suggested by its 34-fold overexpression in a Dicty strain lacking the retinoblastoma like gene | DDB0232429 | CDS | 6795915 | 2871 | - | 0.27621 |
DDB_G0276545 | DDB_G0276545 | DDB0232429 | CDS | 6829983 | 1032 | - | 0.293605 | |
DDB_G0276623 | DDB_G0276623 | DDB0232429 | CDS | 7051390 | 537 | - | 0.320298 | |
DDB_G0276633 | DDB_G0276633 | DDB0232429 | CDS | 7061709 | 2496 | + | 0.262019 | |
DDB_G0276725 | DDB_G0276725 | DDB0232429 | CDS | 7175956 | 237 | + | 0.265823 | |
DDB_G0276811 | DDB_G0276811 | DDB0232429 | CDS | 7386858 | 2736 | + | 0.26462 | |
DDB_G0276815 | DDB_G0276815 | 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 | DDB0232429 | CDS | 7390722 | 1338 | - | 0.309417 |
DDB_G0276855 | DDB_G0276855 | DDB0232429 | CDS | 7489987 | 2193 | + | 0.300958 | |
DDB_G0276897 | DDB_G0276897 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232429 | CDS | 7267534 | 1494 | + | 0.299197 |
DDB_G0276961 | DDB_G0276961 | C-terminus similar to Arabidopsis thaliana plant adhesion molecule 1 Drosophila melanogaster extracellular matrix adhesion protein Pollux and human rab6 GTPase activating protein GAPCENA | DDB0232429 | CDS | 7212385 | 1536 | - | 0.266927 |
DDB_G0276997 | DDB_G0276997 | DDB0232429 | CDS | 7293362 | 1305 | + | 0.276628 | |
DDB_G0277007 | DDB_G0277007 | homolog of human SLC35C1 (GDP-fucose transporter 1) defects in human SLC35C1 are the cause of leukocyte adhesion deficiency type II contains 10 putative transmembrane domains | DDB0232429 | CDS | 7200459 | 1107 | + | 0.272809 |
DDB_G0277025 | DDB_G0277025 | DDB0232429 | CDS | 7262534 | 714 | + | 0.257703 | |
DDB_G0277031 | DDB_G0277031 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232429 | CDS | 7281651 | 1533 | - | 0.297456 |
DDB_G0277043 | DDB_G0277043 | structural similarity to Zn-dependent peptidases contains a a predicted signal anchor sequence and 4 putative transmembrane domains | DDB0232429 | CDS | 7322606 | 2187 | - | 0.288523 |
DDB_G0277149 | DDB_G0277149 | contains 3 TPR domains homolog of human TTC35 (tetratricopeptide repeat protein 35) | DDB0232429 | CDS | 7777377 | 969 | + | 0.26935 |
DDB_G0277151 | DDB_G0277151 | DDB0232429 | CDS | 7889956 | 1455 | - | 0.22543 | |
DDB_G0277165 | DDB_G0277165 | CAMKL family protein kinase the protein kinase domain is similar to those of the CAMKLBRSK subfamily which are named based on brain-specific expression in human and neuronal expression in worm | DDB0232429 | CDS | 7893420 | 2502 | - | 0.271783 |
DDB_G0277167 | DDB_G0277167 | DDB0232429 | CDS | 7668593 | 1392 | + | 0.257902 | |
DDB_G0277249 | DDB_G0277249 | DDB0232429 | CDS | 7817927 | 849 | - | 0.34629 | |
DDB_G0277257 | DDB_G0277257 | DDB0232429 | CDS | 7833225 | 1404 | - | 0.340456 | |
DDB_G0277337 | DDB_G0277337 | DDB0232429 | CDS | 7774136 | 2658 | - | 0.307374 | |
DDB_G0277427 | DDB_G0277427 | DDB0232429 | CDS | 8043662 | 1911 | + | 0.299843 | |
DDB_G0277449 | DDB_G0277449 | member of the AGC kinase group similar to kinase domains of SGK (serum and glucocorticoid responsive kinase) AktPKB and RSK (ribosomal S6 kinase) family members | DDB0232429 | CDS | 8121319 | 1371 | + | 0.300511 |
DDB_G0277471 | DDB_G0277471 | homolog of human PAAF1 (proteasomal ATPase-associated factor 1) which inhibits proteasome 26S assembly and activity contains 3 WD repeats | DDB0232429 | CDS | 8143567 | 1278 | - | 0.305164 |
DDB_G0277533 | DDB_G0277533 | similar to human WDR48 a WD repeat endosomal protein | DDB0232429 | CDS | 7976869 | 3519 | - | 0.24524 |
DDB_G0277539 | DDB_G0277539 | putative protein tyrosine kinase similar to human wee1 inhibitor of mitosis through phosphorylation of cdc2 | DDB0232429 | CDS | 8010617 | 2997 | - | 0.248248 |
DDB_G0277573 | DDB_G0277573 | DDB0232429 | CDS | 8170344 | 1017 | + | 0.277286 | |
DDB_G0277575 | DDB_G0277575 | DDB0232429 | CDS | 8169746 | 387 | - | 0.271318 | |
DDB_G0277655_ps | DDB_G0277655 | putative pseudogene very similar to neighboring genes that belong to a large D. discoideum protein family of unknown function many clustered on chr 2 | DDB0232429 | CDS | 8243854 | 3055 | + | 0.235025 |
DDB_G0277679 | DDB_G0277679 | DDB0232429 | CDS | 8347286 | 1101 | + | 0.257039 | |
DDB_G0277685 | DDB_G0277685 | DDB0232429 | CDS | 8335817 | 6561 | + | 0.299192 | |
DDB_G0277745 | DDB_G0277745 | DDB0232429 | CDS | 8419128 | 882 | - | 0.290249 | |
DDB_G0277941 | DDB_G0277941 | similar to HIRA histone cell cycle regulation defective homolog A | DDB0232430 | CDS | 39336 | 1431 | + | 0.288609 |
DDB_G0277967 | DDB_G0277967 | DDB0232430 | CDS | 72018 | 3144 | + | 0.26145 | |
DDB_G0277999 | DDB_G0277999 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232430 | CDS | 144948 | 1182 | - | 0.265651 |
DDB_G0278059 | DDB_G0278059 | similar to the human acetyl-coenzyme A transporter 1 contains 10 putative transmembrane domains | DDB0232430 | CDS | 207407 | 1857 | - | 0.234787 |
DDB_G0278087_ps | DDB_G0278087 | putative pseudogene containing a partial protein kinase domain and a partial ankyrin repeat | DDB0232430 | CDS | 256195 | 1557 | - | 0.285806 |
DDB_G0278111 | DDB_G0278111 | DDB0232430 | CDS | 294308 | 354 | - | 0.327684 | |
DDB_G0278113 | DDB_G0278113 | similar to protein-tyrosine phosphatases but probably not catalytically active due to lack of conservation of active site residues similar to human PTPLA (protein-tyrosine phosphatase-like member A) contains 4 putative transmembrane domains | DDB0232430 | CDS | 295249 | 678 | - | 0.297935 |
DDB_G0278151 | DDB_G0278151 | DDB0232430 | CDS | 372488 | 1455 | - | 0.294845 | |
DDB_G0278181 | DDB_G0278181 | DDB0232430 | CDS | 405756 | 2802 | + | 0.283726 | |
DDB_G0278229 | DDB_G0278229 | DDB0232430 | CDS | 512537 | 2673 | - | 0.263749 | |
DDB_G0278239 | DDB_G0278239 | DDB0232430 | CDS | 533251 | 1263 | - | 0.231987 | |
DDB_G0278253 | DDB_G0278253 | DDB0232430 | CDS | 566464 | 1710 | - | 0.27076 | |
DDB_G0278281 | DDB_G0278281 | DDB0232430 | CDS | 614554 | 1194 | - | 0.247069 | |
DDB_G0278297 | DDB_G0278297 | DDB0232430 | CDS | 639451 | 1203 | - | 0.270989 | |
DDB_G0278303_ps | DDB_G0278303 | putative pseudogene beta-ketoacyl synthase family protein | DDB0232430 | CDS | 652045 | 2175 | - | 0.243678 |
DDB_G0278327 | DDB_G0278327 | DDB0232430 | CDS | 707798 | 1677 | + | 0.268933 | |
DDB_G0278373 | DDB_G0278373 | at the N-terminus very similar to human ATPBD4 (ATP binding domain 4) also similar to plant and fungal endoribonuclease L-PSP family proteins | DDB0232430 | CDS | 771365 | 2259 | - | 0.232846 |
DDB_G0278415 | DDB_G0278415 | DDB0232430 | CDS | 857716 | 945 | + | 0.295238 | |
DDB_G0278427 | DDB_G0278427 | DDB0232430 | CDS | 870597 | 666 | + | 0.268769 | |
DDB_G0278453 | DDB_G0278453 | contains 5 coiled-coil domains highly repetitive glutamine and glutamic acid-rich protein | DDB0232430 | CDS | 901380 | 2472 | + | 0.330097 |
DDB_G0278473 | DDB_G0278473 | DDB0232430 | CDS | 929409 | 1995 | - | 0.277694 | |
DDB_G0278487 | DDB_G0278487 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases belongs to the CMGC group of protein kinases | DDB0232430 | CDS | 959760 | 1911 | + | 0.288854 |
DDB_G0278509 | DDB_G0278509 | DDB0232430 | CDS | 984753 | 3747 | + | 0.238858 | |
DDB_G0278521 | DDB_G0278521 | member of the TKL (tyrosine kinase-like) group the MLK (mixed lineage kinase) family and the HH498 subfamily contains an ankyrin repeat | DDB0232430 | CDS | 1000912 | 2727 | - | 0.226989 |
DDB_G0278535 | DDB_G0278535 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family contains an ankyrin repeat region and a SAM (Sterile alpha motif) domain | DDB0232430 | CDS | 1034770 | 2547 | + | 0.329407 |
DDB_G0278597 | DDB_G0278597 | DDB0232430 | CDS | 287423 | 831 | - | 0.305656 | |
DDB_G0278655 | DDB_G0278655 | DDB0232430 | CDS | 672611 | 867 | + | 0.302191 | |
DDB_G0278661 | DDB_G0278661 | DDB0232430 | CDS | 695788 | 4023 | - | 0.316182 | |
DDB_G0278665 | DDB_G0278665 | DDB0232430 | CDS | 753135 | 3273 | - | 0.31103 | |
DDB_G0278675 | DDB_G0278675 | DDB0232430 | CDS | 789665 | 1752 | - | 0.261986 | |
DDB_G0278683 | DDB_G0278683 | DDB0232430 | CDS | 839543 | 570 | + | 0.280702 | |
DDB_G0278759 | DDB_G0278759 | DDB0232430 | CDS | 1128110 | 2484 | + | 0.231079 | |
DDB_G0278793 | DDB_G0278793 | DDB0232430 | CDS | 1186077 | 690 | + | 0.350725 | |
DDB_G0278819 | DDB_G0278819 | ortholog of human CRNKL1 (crooked neck-like) involved in pre-mRNA splicing contains 11 HAT (Half A TPR) repeats | DDB0232430 | CDS | 1238183 | 2118 | + | 0.283758 |
DDB_G0278845 | DDB_G0278845 | member of the AGC kinase group similar to kinase domains of NDR (nuclear Dbf2-related) family members | DDB0232430 | CDS | 1269374 | 4053 | - | 0.265976 |
DDB_G0278851 | DDB_G0278851 | bCommunity annotation:b DDB G0278851 is similar to the rik1-associated factor raf1 of S. pombe. Raf1 (as well as rik1) participates in the Clr4 methyltransferase complex (see Horn et al Genes and Development 19 1705-1714) which methylates H3K9 important in silencing centromeric and telomeric repeats. It has recently been shown that these repeats are transcribed for a limited period during S-phase (Chen et al Nature 451 734-737 (2008) that this transcription is essential for RNA-interference mediated heterochromatin assembly and that the repeats are transcriptionally repressed outside of S-phase.br DDB_G0278851 and a second member of the Clr4 complex the methyl transferase clr4suvA are both overexpressed about threefold (p2e-63) in a Dicty strain in which the retinoblastoma-like protein rblA has been disrupted. Most genes associated with S-phase or mitosis are overexpressed in this strain. The activity of the clr4 complex is thus likely to be S-phase associated. All these observations a | DDB0232430 | CDS | 1278474 | 2757 | - | 0.318099 |
DDB_G0278901 | DDB_G0278901 | DDB0232430 | CDS | 1361340 | 4488 | - | 0.282308 | |
DDB_G0278909 | DDB_G0278909 | member of the TKL (tyrosine kinase-like) group and the ARMK (armadillo repeat-containing kinase) family contains an N-terminal LRR and a C-terminal armadillobeta-catenin repeat unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232430 | CDS | 1376167 | 5811 | + | 0.293581 |
DDB_G0278945 | DDB_G0278945 | DDB0232430 | CDS | 1251221 | 960 | + | 0.292708 | |
DDB_G0278953 | DDB_G0278953 | contains four CBS domains similar to protein kinase 5'AMP activated gamma subunit expressed in prespore cells | DDB0232430 | CDS | 1335145 | 1080 | - | 0.312963 |
DDB_G0279003 | DDB_G0279003 | DDB0232430 | CDS | 1503809 | 2328 | + | 0.334192 | |
DDB_G0279019 | DDB_G0279019 | DDB0232430 | CDS | 1519155 | 885 | + | 0.250847 | |
DDB_G0279043 | DDB_G0279043 | DDB0232430 | CDS | 1548959 | 603 | + | 0.310116 | |
DDB_G0279107 | DDB_G0279107 | DDB0232430 | CDS | 1638888 | 3717 | - | 0.283562 | |
DDB_G0279139 | DDB_G0279139 | homolog of human ANKRD29 contains 8 ankyrin repeats | DDB0232430 | CDS | 1678974 | 1143 | + | 0.297463 |
DDB_G0279179 | DDB_G0279179 | DDB0232430 | CDS | 1715076 | 2779 | + | 0.348687 | |
DDB_G0279241 | DDB_G0279241 | DDB0232430 | CDS | 1814829 | 2760 | - | 0.236594 | |
DDB_G0279259 | DDB_G0279259 | DDB0232430 | CDS | 1848643 | 2526 | + | 0.266825 | |
DDB_G0279261 | DDB_G0279261 | DDB0232430 | CDS | 1855053 | 1911 | + | 0.22449 | |
DDB_G0279275 | DDB_G0279275 | DDB0232430 | CDS | 1874332 | 1704 | + | 0.286385 | |
DDB_G0279355 | DDB_G0279355 | DDB0232430 | CDS | 1981638 | 1146 | + | 0.283595 | |
DDB_G0279363 | DDB_G0279363 | DDB0232430 | CDS | 1987447 | 516 | - | 0.244186 | |
DDB_G0279395 | DDB_G0279395 | DDB0232430 | CDS | 1853231 | 1341 | - | 0.247576 | |
DDB_G0279405 | DDB_G0279405 | CAMKL family protein kinase the protein kinase domain has similarity to those of calciumcalmodulin-dependent protein kinase kinases (CAMKK) that belong to a proposed calcium-triggered signaling cascade involved in a number of cellular processes | DDB0232430 | CDS | 1975813 | 2088 | + | 0.290709 |
DDB_G0279431 | DDB_G0279431 | DDB0232430 | CDS | 2040372 | 1581 | - | 0.251107 | |
DDB_G0279459 | DDB_G0279459 | bCommunity Annotationb DDB G0279459 contains a forkhead-associated domain which is similar to the corresponding domain in the KI-67 antigen a very widely used clinical proliferation marker and is the only hit when the KI-67 sequence is blasted against Dicty proteins. Direct comparison of the Dd sequence with KI-67 by Blast2Sequences identifies two regions of homology and gives an expected value of 4e-08 suggesting that the similarity may be real. The KI-67 antigen in humans is nuclear and present throughout the cell cycle in proliferating cells but undetectable in cells in G0. Recent work suggests that the protein is involved in ribosomal RNA synthesis ((Bullwinkel et al J Cell Physiology 206 624-635 (2005) Rahmanzadeh et al Cell and Molecular Biology 40 422-430 (2007). A role in chromatin compaction has also been ascribed to KI-67 (Kametaka et al Genes Cells 7 1231-42 (2002) but this appears to involve the C-terminus. The Dicty protein is significantly shorter than the human protein a | DDB0232430 | CDS | 2077799 | 3099 | - | 0.310745 |
DDB_G0279511 | DDB_G0279511 | DDB0232430 | CDS | 2181977 | 3690 | + | 0.263957 | |
DDB_G0279545 | DDB_G0279545 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232430 | CDS | 2237325 | 879 | - | 0.290102 |
DDB_G0279589 | DDB_G0279589 | DDB0232430 | CDS | 2089639 | 453 | + | 0.280353 | |
DDB_G0279675 | DDB_G0279675 | belongs to the carbon-nitrogen hydrolase family similar to human VNN1 (pantetheine hydrolase) contains a predicted signal anchor sequence | DDB0232430 | CDS | 2426331 | 1623 | - | 0.262477 |
DDB_G0279679 | DDB_G0279679 | DDB0232430 | CDS | 2429651 | 855 | - | 0.226901 | |
DDB_G0279695 | DDB_G0279695 | similar D. melanogaster ORF CG8021 and the RRM domain is similar to that of human RBM3 | DDB0232430 | CDS | 2457402 | 255 | + | 0.298039 |
DDB_G0279719 | DDB_G0279719 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232430 | CDS | 2480611 | 2829 | - | 0.265111 |
DDB_G0279783 | DDB_G0279783 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232430 | CDS | 2546062 | 888 | - | 0.240991 |
DDB_G0279807 | DDB_G0279807 | DDB0232430 | CDS | 2563367 | 1908 | - | 0.321803 | |
DDB_G0279821 | DDB_G0279821 | DDB0232430 | CDS | 2586560 | 1749 | - | 0.263579 | |
DDB_G0279823 | DDB_G0279823 | DDB0232430 | CDS | 2588778 | 2685 | - | 0.299814 | |
DDB_G0279831 | DDB_G0279831 | putative protein serinethreonine kinase CAMK group the protein kinase domain is similar to those of mammalian CAM kinase I | DDB0232430 | CDS | 2602496 | 2787 | + | 0.267671 |
DDB_G0279851 | DDB_G0279851 | putative histone acetyltransferase highly similar to bacterial GCN5-related N-acetyltransferase (GNAT) | DDB0232430 | CDS | 2640159 | 516 | - | 0.284884 |
DDB_G0279943 | DDB_G0279943 | belongs to the major facilitator superefamily contains 12 putative transmembrane domains | DDB0232430 | CDS | 2721717 | 1488 | - | 0.309812 |
DDB_G0279965 | DDB_G0279965 | members of the NAD-dependent epimerasedehydratase family use nucleotide-sugar substrates for a variety of chemical reactions contains a putative signal peptide | DDB0232430 | CDS | 2775437 | 1203 | - | 0.305902 |
DDB_G0279987 | DDB_G0279987 | DDB0232430 | CDS | 2820923 | 675 | + | 0.216296 | |
DDB_G0280019 | DDB_G0280019 | conserved in bacteria and fungi similar to S. cerevisiae HSP31 (heat shock protein 31) a putative protease | DDB0232430 | CDS | 2796272 | 702 | + | 0.339031 |
DDB_G0280111 | DDB_G0280111 | putative protein serinethreonine kinase similar to the kinase domains of AAK1 (AP2 associated kinase) and BMP-inducible protein kinase (BIKe) | DDB0232430 | CDS | 2948944 | 3381 | - | 0.280982 |
DDB_G0280123 | DDB_G0280123 | DDB0232430 | CDS | 2978017 | 708 | + | 0.262712 | |
DDB_G0280131 | DDB_G0280131 | member of the TKL (tyrosine kinase-like) group and the ARMK (armadillo repeat-containing kinase) family contains armadillobeta-catenin-like repeats unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232430 | CDS | 2985578 | 3579 | - | 0.308187 |
DDB_G0280133 | DDB_G0280133 | CAMK family protein kinase protein kinase domain similar to those of mammalian SNF1 like kinases | DDB0232430 | CDS | 2991402 | 4518 | + | 0.285967 |
DDB_G0280181 | DDB_G0280181 | contains three ankyrin repeats and an RA domain which plays a role in RasGTP activation in mammals and mating in yeast highly similar to | DDB0232430 | CDS | 3067276 | 1002 | - | 0.278443 |
DDB_G0280191 | DDB_G0280191 | DDB0232430 | CDS | 3082696 | 1323 | - | 0.230537 | |
DDB_G0280203_ps | DDB_G0280203 | putative pseudogene similar to pirin family proteins especially to DDB_G0281115 and DDB_G0280725 | DDB0232430 | CDS | 3101331 | 654 | + | 0.314985 |
DDB_G0280221 | DDB_G0280221 | DDB0232430 | CDS | 3129179 | 6531 | - | 0.27469 | |
DDB_G0280261 | DDB_G0280261 | contains one LisH domain and 7 WD40 domains similar to human TBL1X (F-box-likeWD repeat-containing protein) which plays a role in transcription activation mediated by nuclear receptors | DDB0232430 | CDS | 3178567 | 1743 | - | 0.324154 |
DDB_G0280289 | DDB_G0280289 | DDB0232430 | CDS | 3208817 | 2961 | - | 0.333671 | |
DDB_G0280329 | DDB_G0280329 | DDB0232430 | CDS | 3262966 | 1128 | + | 0.221631 | |
DDB_G0280367 | DDB_G0280367 | DDB0232430 | CDS | 2917996 | 909 | + | 0.190319 | |
DDB_G0280369 | DDB_G0280369 | DDB0232430 | CDS | 2942956 | 4443 | - | 0.244655 | |
DDB_G0280385 | DDB_G0280385 | DDB0232430 | CDS | 3156312 | 1332 | + | 0.294294 | |
DDB_G0280437 | DDB_G0280437 | DDB0232430 | CDS | 3353124 | 897 | - | 0.222965 | |
DDB_G0280461 | DDB_G0280461 | DDB0232430 | CDS | 3391535 | 1257 | - | 0.24105 | |
DDB_G0280549 | DDB_G0280549 | DDB0232430 | CDS | 3481319 | 1116 | + | 0.269713 | |
DDB_G0280557 | DDB_G0280557 | similar to erkA and erkB and other MAP kinases does not contain the consensus sequences required for kinase function | DDB0232430 | CDS | 3496721 | 1383 | + | 0.237889 |
DDB_G0280581 | DDB_G0280581 | DDB0232430 | CDS | 3524824 | 2070 | - | 0.20628 | |
DDB_G0280643 | DDB_G0280643 | similar to many CMGC family members including several MAPKs | DDB0232430 | CDS | 3598294 | 1329 | - | 0.261851 |
DDB_G0280717 | DDB_G0280717 | member of the AGC kinase group similar to the kinase domains of PKC (protein kinase C) and MAST (microtubule-associated serinethreonine kinase) | DDB0232430 | CDS | 3670258 | 1236 | - | 0.258091 |
DDB_G0280725 | DDB_G0280725 | almost identical to | DDB0232430 | CDS | 3688197 | 888 | - | 0.335586 |
DDB_G0280729_ps | DDB_G0280729 | putative pseudogene belongs to the pirin family | DDB0232430 | CDS | 3691400 | 840 | - | 0.333333 |
DDB_G0280735_ps | DDB_G0280735 | putative pseudogene predicted translation contains the C-terminal domain of pirin a nuclear protein of unknown function | DDB0232430 | CDS | 3696501 | 207 | + | 0.357488 |
DDB_G0280767 | DDB_G0280767 | DDB0232430 | CDS | 3718300 | 1269 | + | 0.312057 | |
DDB_G0280801 | DDB_G0280801 | DDB0232430 | CDS | 3766917 | 3807 | + | 0.328343 | |
DDB_G0280805 | DDB_G0280805 | homolog of human and S. cerevisiae KRR1 (KRR-R motif-containing protein) contains one RNA-binding KH domain S. cerevisiae KRR1 is required for 40S ribosome biogenesis | DDB0232430 | CDS | 3779782 | 1125 | - | 0.277333 |
DDB_G0280825 | DDB_G0280825 | similar to bacterial acetyltransferases homolog of E. coli maa (maltose O-acetyltransferase) similar to D. purpureum protein | DDB0232430 | CDS | 1441074 | 576 | + | 0.326389 |
DDB_G0280845 | DDB_G0280845 | DDB0232430 | CDS | 1421922 | 2185 | + | 0.279634 | |
DDB_G0280855 | DDB_G0280855 | similar to erkA and erkB and other MAP kinases unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232430 | CDS | 3794487 | 1179 | + | 0.25106 |
DDB_G0280895 | DDB_G0280895 | has the same domain composition as fbxA and | DDB0232430 | CDS | 3841507 | 4506 | - | 0.264536 |
DDB_G0280923 | DDB_G0280923 | DDB0232430 | CDS | 3886092 | 282 | + | 0.326241 | |
DDB_G0280955 | DDB_G0280955 | GTPase activator for rab8A involved in the regulation of contractile vacuole function during hypoosmotic stress | DDB0232430 | CDS | 3904017 | 2202 | - | 0.262489 |
DDB_G0280997 | DDB_G0280997 | DDB0232430 | CDS | 3926681 | 1029 | - | 0.295432 | |
DDB_G0281059 | DDB_G0281059 | DDB0232430 | CDS | 3994227 | 1068 | + | 0.256554 | |
DDB_G0281083 | DDB_G0281083 | DDB0232430 | CDS | 4029591 | 1737 | - | 0.312608 | |
DDB_G0281115 | DDB_G0281115 | almost identical to | DDB0232430 | CDS | 4078245 | 888 | + | 0.323198 |
DDB_G0281119_ps | DDB_G0281119 | putative pseudogene similar to pirin family proteins especially to parts of DDB_G0281115 and DDB_G0280725 | DDB0232430 | CDS | 4081406 | 591 | + | 0.329949 |
DDB_G0281123_ps | DDB_G0281123 | putative pseudogene similar to Dictyostelium genes | DDB0232430 | CDS | 4083976 | 387 | + | 0.307494 |
DDB_G0281137 | DDB_G0281137 | DDB0232430 | CDS | 4091325 | 1794 | + | 0.240245 | |
DDB_G0281155 | DDB_G0281155 | putative sugar transporter contains 12 putative transmembrane domains | DDB0232430 | CDS | 4113808 | 1614 | + | 0.29368 |
DDB_G0281259 | DDB_G0281259 | similar to the DREV (DORA reverse strand) protein found in other eukaryotes believed to be a methyltransferase but is of unknown function | DDB0232430 | CDS | 4305745 | 1230 | + | 0.243089 |
DDB_G0281283 | DDB_G0281283 | DDB0232430 | CDS | 4337681 | 660 | + | 0.283333 | |
DDB_G0281309 | DDB_G0281309 | DDB0232430 | CDS | 4120970 | 603 | - | 0.296849 | |
DDB_G0281333 | DDB_G0281333 | DDB0232430 | CDS | 4318553 | 2700 | - | 0.266667 | |
DDB_G0281359 | DDB_G0281359 | DDB0232430 | CDS | 4401226 | 1032 | + | 0.251938 | |
DDB_G0281505 | DDB_G0281505 | DDB0232430 | CDS | 4641293 | 1014 | - | 0.287968 | |
DDB_G0281589 | DDB_G0281589 | very similar to mammalian CBWD1 and CBWD2 ubiquitiously expressed COBW domain-containing proteins prokaryotic CobW involved in cobalamin (vitamin B12) biosynthesis | DDB0232430 | CDS | 4676319 | 1191 | - | 0.246012 |
DDB_G0281603 | DDB_G0281603 | DDB0232430 | CDS | 4698687 | 1926 | + | 0.246106 | |
DDB_G0281633_ps | DDB_G0281633 | putative pseudogene fragment similar to pirin family proteins especially to the C-terminal half of DDB_G0281115 and DDB_G0280725 | DDB0232430 | CDS | 4738827 | 327 | + | 0.299694 |
DDB_G0281671 | DDB_G0281671 | DDB0232430 | CDS | 4794386 | 4170 | - | 0.243885 | |
DDB_G0281673 | DDB_G0281673 | DDB0232430 | CDS | 4799865 | 822 | + | 0.290754 | |
DDB_G0281745 | DDB_G0281745 | DDB0232430 | CDS | 4910382 | 1794 | + | 0.337793 | |
DDB_G0281751 | DDB_G0281751 | DDB0232430 | CDS | 4916395 | 822 | - | 0.287105 | |
DDB_G0281807_ps | DDB_G0281807 | putative pseudogene fragment similar to pirin family protein | DDB0232430 | CDS | 4741312 | 333 | + | 0.321321 |
DDB_G0281831 | DDB_G0281831 | conserved in bacteria a member of the NK (nucleosidenucleotide kinase) superfamily also belongs to the zeta toxin family which in bacteria is a component of a postregulational killing system | DDB0232430 | CDS | 4993575 | 507 | - | 0.262327 |
DDB_G0281839 | DDB_G0281839 | DDB0232430 | CDS | 4997894 | 2502 | + | 0.328937 | |
DDB_G0281903 | DDB_G0281903 | DDB0232430 | CDS | 5094433 | 1218 | + | 0.254516 | |
DDB_G0281909 | DDB_G0281909 | DDB0232430 | CDS | 5103620 | 1836 | - | 0.289216 | |
DDB_G0281917 | DDB_G0281917 | DDB0232430 | CDS | 5121103 | 954 | + | 0.29979 | |
DDB_G0281927 | DDB_G0281927 | DDB0232430 | CDS | 5152552 | 942 | + | 0.272824 | |
DDB_G0282005 | DDB_G0282005 | DDB0232430 | CDS | 5234911 | 681 | + | 0.30837 | |
DDB_G0282127 | DDB_G0282127 | DDB0232430 | CDS | 5429045 | 1038 | + | 0.220617 | |
DDB_G0282135 | DDB_G0282135 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232430 | CDS | 5405787 | 1551 | + | 0.283688 |
DDB_G0282157 | DDB_G0282157 | DDB0232430 | CDS | 5467686 | 1668 | + | 0.209832 | |
DDB_G0282213 | DDB_G0282213 | DDB0232430 | CDS | 5526720 | 1464 | - | 0.239071 | |
DDB_G0282233 | DDB_G0282233 | DDB0232430 | CDS | 5550968 | 1707 | + | 0.322203 | |
DDB_G0282303 | DDB_G0282303 | DDB0232430 | CDS | 5610805 | 2364 | - | 0.249154 | |
DDB_G0282311 | DDB_G0282311 | DDB0232430 | CDS | 5621318 | 1992 | + | 0.314759 | |
DDB_G0282393 | DDB_G0282393 | DDB0232430 | CDS | 5695519 | 699 | + | 0.276109 | |
DDB_G0282407 | DDB_G0282407 | DDB0232430 | CDS | 5710802 | 2262 | - | 0.376658 | |
DDB_G0282429 | DDB_G0282429 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | DDB0232430 | CDS | 5758659 | 939 | - | 0.312034 |
DDB_G0282477 | DDB_G0282477 | DDB0232430 | CDS | 5822316 | 267 | + | 0.318352 | |
DDB_G0282487 | DDB_G0282487 | DDB0232430 | CDS | 5834821 | 936 | + | 0.185897 | |
DDB_G0282573 | DDB_G0282573 | DDB0232430 | CDS | 5953713 | 1227 | + | 0.294214 | |
DDB_G0282575 | DDB_G0282575 | DDB0232430 | CDS | 5957238 | 3585 | + | 0.278661 | |
DDB_G0282603 | DDB_G0282603 | DDB0232430 | CDS | 5993046 | 600 | + | 0.261667 | |
DDB_G0282673 | DDB_G0282673 | DDB0232430 | CDS | 6100946 | 1533 | + | 0.300065 | |
DDB_G0282711 | DDB_G0282711 | contains a plant homeodomain (PHD) finger a C4HC3 zinc-finger-like motif found in nuclear proteins thought to be involved in chromatin-mediated transcriptional regulation | DDB0232430 | CDS | 6179495 | 4086 | - | 0.263338 |
DDB_G0282765 | DDB_G0282765 | DDB0232430 | CDS | 5832783 | 915 | + | 0.254645 | |
DDB_G0282779_ps | DDB_G0282779 | putative pseudogene similar to D. discoideum genes | DDB0232430 | CDS | 5911017 | 2427 | - | 0.261228 |
DDB_G0282823 | DDB_G0282823 | DDB0232430 | CDS | 6262357 | 2712 | - | 0.272493 | |
DDB_G0282875 | DDB_G0282875 | DDB0232430 | CDS | 6329217 | 729 | + | 0.242798 | |
DDB_G0282885 | DDB_G0282885 | DDB0232430 | CDS | 6339466 | 1203 | + | 0.23192 | |
DDB_G0282895 | DDB_G0282895 | member of the TKL (tyrosine kinase-like) group contains three N-terminal MORN (Membrane Occupation and Recognition Nexus) repeats | DDB0232430 | CDS | 6249781 | 4905 | + | 0.262385 |
DDB_G0282945 | DDB_G0282945 | DDB0232431 | CDS | 31559 | 2010 | - | 0.280597 | |
DDB_G0282963 | DDB_G0282963 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats | DDB0232431 | CDS | 60445 | 5286 | + | 0.265796 |
DDB_G0283017 | DDB_G0283017 | DDB0232431 | CDS | 164286 | 2676 | + | 0.246637 | |
DDB_G0283039 | DDB_G0283039 | DDB0232431 | CDS | 196663 | 1341 | - | 0.222968 | |
DDB_G0283065 | DDB_G0283065 | putative eukaryotic translation initiation factor 2 alpha (eIF2alpha) kinase putative protein serinethreonine kinase related to the GCN2 (general control non-derepressible) family of protein kinases that phosphorylate the alpha subunit of eIF2 | DDB0232431 | CDS | 122741 | 1914 | - | 0.242424 |
DDB_G0283191 | DDB_G0283191 | DDB0232431 | CDS | 394762 | 1695 | + | 0.277286 | |
DDB_G0283211_ps | DDB_G0283211 | putative pseudogene belongs to the large D. discoideum zinc-containing alcohol dehydrogenase (ADH) family | DDB0232431 | CDS | 368141 | 768 | - | 0.272135 |
DDB_G0283291 | DDB_G0283291 | DDB0232431 | CDS | 467526 | 1092 | - | 0.271978 | |
DDB_G0283301 | DDB_G0283301 | DDB0232431 | CDS | 480042 | 1992 | + | 0.254016 | |
DDB_G0283337 | DDB_G0283337 | DDB0232431 | CDS | 491931 | 3387 | - | 0.219368 | |
DDB_G0283397 | DDB_G0283397 | DDB0232431 | CDS | 606939 | 2757 | - | 0.283642 | |
DDB_G0283399 | DDB_G0283399 | DDB0232431 | CDS | 609993 | 504 | - | 0.18254 | |
DDB_G0283451 | DDB_G0283451 | DDB0232431 | CDS | 712043 | 1215 | - | 0.33251 | |
DDB_G0283495 | DDB_G0283495 | DDB0232431 | CDS | 611003 | 2319 | + | 0.337214 | |
DDB_G0283535 | DDB_G0283535 | similar to H. sapiens DMXL1 and DMXL2 and D. melanogaster DmX REMI mutant fails to aggregate see | DDB0232431 | CDS | 837650 | 8379 | - | 0.297291 |
DDB_G0283551 | DDB_G0283551 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity highly similar to neighboring gene | DDB0232431 | CDS | 810010 | 3975 | - | 0.255597 |
DDB_G0283553 | DDB_G0283553 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity highly similar to neighboring gene | DDB0232431 | CDS | 815506 | 4545 | - | 0.252805 |
DDB_G0283565 | DDB_G0283565 | DDB0232431 | CDS | 833347 | 3024 | - | 0.305886 | |
DDB_G0283595 | DDB_G0283595 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232431 | CDS | 805455 | 3873 | - | 0.251743 |
DDB_G0283649 | DDB_G0283649 | similar to the S. cerevisiae LOT6 a FMN-dependent NAD(P)H:quinone reductase that may be involved in quinone detoxification | DDB0232431 | CDS | 910617 | 600 | - | 0.301667 |
DDB_G0283677 | DDB_G0283677 | DDB0232431 | CDS | 963963 | 882 | + | 0.217687 | |
DDB_G0283687 | DDB_G0283687 | similar to CC1-like splicing factors characterized by an N-terminal arginine-rich low complexity domain followed by three RNA recognition domains similar to human RBM23 and RBM39 | DDB0232431 | CDS | 982205 | 2184 | + | 0.330586 |
DDB_G0283697 | DDB_G0283697 | DDB0232431 | CDS | 992255 | 2562 | + | 0.276347 | |
DDB_G0283727 | DDB_G0283727 | DDB0232431 | CDS | 1038776 | 756 | + | 0.376984 | |
DDB_G0283793 | DDB_G0283793 | DDB0232431 | CDS | 1114386 | 2136 | - | 0.305243 | |
DDB_G0283799 | DDB_G0283799 | DDB0232431 | CDS | 1120333 | 1098 | - | 0.211293 | |
DDB_G0283803 | DDB_G0283803 | DDB0232431 | CDS | 1122911 | 582 | + | 0.298969 | |
DDB_G0283817 | DDB_G0283817 | DDB0232431 | CDS | 1149949 | 882 | + | 0.314059 | |
DDB_G0283821 | DDB_G0283821 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis | DDB0232431 | CDS | 1155677 | 2826 | - | 0.295824 |
DDB_G0283859 | DDB_G0283859 | DDB0232431 | CDS | 1066871 | 5037 | + | 0.289458 | |
DDB_G0283915 | DDB_G0283915 | DDB0232431 | CDS | 1270973 | 702 | + | 0.337607 | |
DDB_G0283927 | DDB_G0283927 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232431 | CDS | 1307685 | 1458 | - | 0.226337 |
DDB_G0283935 | DDB_G0283935 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232431 | CDS | 1333704 | 942 | + | 0.284501 |
DDB_G0283949 | DDB_G0283949 | DDB0232431 | CDS | 1350512 | 1398 | - | 0.268956 | |
DDB_G0283977 | DDB_G0283977 | DDB0232431 | CDS | 1409294 | 2622 | - | 0.217391 | |
DDB_G0283985 | DDB_G0283985 | DDB0232431 | CDS | 1263489 | 1608 | + | 0.250622 | |
DDB_G0283991 | DDB_G0283991 | DDB0232431 | CDS | 1287653 | 1092 | + | 0.308608 | |
DDB_G0284055 | DDB_G0284055 | DDB0232431 | CDS | 1474815 | 1335 | - | 0.270412 | |
DDB_G0284079 | DDB_G0284079 | contains two ankyrin repeats and an RA domain which plays a role in RasGTP activation in mammals and mating in yeast highly similar to | DDB0232431 | CDS | 1538387 | 912 | + | 0.291667 |
DDB_G0284083 | DDB_G0284083 | DDB0232431 | CDS | 1548205 | 999 | + | 0.209209 | |
DDB_G0284085 | DDB_G0284085 | DDB0232431 | CDS | 1549462 | 1098 | + | 0.175774 | |
DDB_G0284091 | DDB_G0284091 | DDB0232431 | CDS | 1556685 | 723 | - | 0.337483 | |
DDB_G0284157 | DDB_G0284157 | DDB0232431 | CDS | 1583322 | 3426 | + | 0.28955 | |
DDB_G0284167 | DDB_G0284167 | DDB0232431 | CDS | 1610129 | 882 | - | 0.422902 | |
DDB_G0284207 | DDB_G0284207 | DDB0232431 | CDS | 1688943 | 858 | + | 0.284382 | |
DDB_G0284209 | DDB_G0284209 | DDB0232431 | CDS | 1690478 | 876 | - | 0.280822 | |
DDB_G0284211_ps | DDB_G0284211 | putative pseudogene belonging to the short-chain dehydrogenasereductase (SDR) familybrbr bCommunity annotation:b probably a recent pseudogene of the short-chain dehydrogenase family including DDB0185894. The coding sequence share high level of homology with DDB0185894 before and after the stop codon resulting in a truncated and probably non functional protein if that gene is still transcribed. Christophe Anjard May 2007 | DDB0232431 | CDS | 1692886 | 738 | + | 0.298103 |
DDB_G0284223 | DDB_G0284223 | DDB0232431 | CDS | 1712491 | 1641 | - | 0.322364 | |
DDB_G0284239 | DDB_G0284239 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232431 | CDS | 1731488 | 2031 | + | 0.356475 |
DDB_G0284251 | DDB_G0284251 | kinase domain similar to those of mitogen-activated protein kinases similar to the STE20 family | DDB0232431 | CDS | 1754346 | 1491 | - | 0.273642 |
DDB_G0284277 | DDB_G0284277 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232431 | CDS | 1821556 | 870 | - | 0.314943 |
DDB_G0284289 | DDB_G0284289 | DDB0232431 | CDS | 1835474 | 2166 | - | 0.262696 | |
DDB_G0284351 | DDB_G0284351 | DDB0232431 | CDS | 1869385 | 735 | + | 0.287075 | |
DDB_G0284365 | DDB_G0284365 | DDB0232431 | CDS | 1895020 | 681 | + | 0.287812 | |
DDB_G0284429 | DDB_G0284429 | DDB0232431 | CDS | 1981059 | 864 | - | 0.261574 | |
DDB_G0284485 | DDB_G0284485 | DDB0232431 | CDS | 2034779 | 846 | - | 0.321513 | |
DDB_G0284539 | DDB_G0284539 | DDB0232431 | CDS | 2152696 | 2997 | - | 0.242576 | |
DDB_G0284565 | DDB_G0284565 | DDB0232431 | CDS | 2142583 | 4788 | - | 0.267126 | |
DDB_G0284603 | DDB_G0284603 | DDB0232431 | CDS | 2211789 | 1413 | + | 0.208068 | |
DDB_G0284661 | DDB_G0284661 | putative protein serinethreonine kinase CAMK group kinase domain similar to mammalian CAM kinase I | DDB0232431 | CDS | 2309177 | 1446 | - | 0.304288 |
DDB_G0284701 | DDB_G0284701 | DDB0232431 | CDS | 2371416 | 1314 | - | 0.269406 | |
DDB_G0284727 | DDB_G0284727 | DDB0232431 | CDS | 2313169 | 2424 | + | 0.288779 | |
DDB_G0284741 | DDB_G0284741 | DDB0232431 | CDS | 2402392 | 4188 | - | 0.298472 | |
DDB_G0284919 | DDB_G0284919 | similar to human DHRSX (dehydrogenasereductase SDR family member on chromosome X) and retinol dehydrogenase | DDB0232431 | CDS | 2646442 | 990 | - | 0.233333 |
DDB_G0284937 | DDB_G0284937 | DDB0232431 | CDS | 2665360 | 1026 | + | 0.287524 | |
DDB_G0284969 | DDB_G0284969 | DDB0232431 | CDS | 2719814 | 1764 | + | 0.272676 | |
DDB_G0284995 | DDB_G0284995 | DDB0232431 | CDS | 2782622 | 873 | + | 0.252005 | |
DDB_G0285011 | DDB_G0285011 | similar to the fungi mitochondrial transferase caf17 a mitochondrial matrix protein involved in the incorporation of iron-sulfur clusters into mitochondrial aconitase-type proteins | DDB0232431 | CDS | 2814046 | 1227 | - | 0.295029 |
DDB_G0285033 | DDB_G0285033 | belongs to the short-chain dehydrogenasereductase family | DDB0232431 | CDS | 2839925 | 786 | + | 0.307888 |
DDB_G0285095 | DDB_G0285095 | DDB0232431 | CDS | 2804851 | 792 | - | 0.306818 | |
DDB_G0285127 | DDB_G0285127 | DDB0232431 | CDS | 2886739 | 1101 | - | 0.217984 | |
DDB_G0285209 | DDB_G0285209 | DDB0232431 | CDS | 2951533 | 810 | + | 0.261728 | |
DDB_G0285265 | DDB_G0285265 | contains one EF hand similar to calmodulin | DDB0232431 | CDS | 3032493 | 420 | - | 0.292857 |
DDB_G0285351 | DDB_G0285351 | DDB0232431 | CDS | 3146811 | 1365 | - | 0.267399 | |
DDB_G0285411 | DDB_G0285411 | DDB0232431 | CDS | 3189133 | 4317 | + | 0.217049 | |
DDB_G0285445 | DDB_G0285445 | has the same domain composition as fbxA and | DDB0232431 | CDS | 3230059 | 3537 | - | 0.271699 |
DDB_G0285463 | DDB_G0285463 | member of the TKL (tyrosine kinase-like) group and the CZAK (C-terminal domain of ZakA) family contains 7 putative transmembrane domains | DDB0232431 | CDS | 3259648 | 2076 | - | 0.308285 |
DDB_G0285467 | DDB_G0285467 | DDB0232431 | CDS | 3266519 | 1398 | + | 0.326896 | |
DDB_G0285511 | DDB_G0285511 | DDB0232431 | CDS | 3331170 | 1683 | - | 0.322638 | |
DDB_G0285529 | DDB_G0285529 | DDB0232431 | CDS | 3346712 | 1149 | + | 0.252393 | |
DDB_G0285531 | DDB_G0285531 | DDB0232431 | CDS | 3348010 | 1200 | + | 0.245833 | |
DDB_G0285587 | DDB_G0285587 | DDB0232431 | CDS | 3413814 | 1170 | - | 0.275214 | |
DDB_G0285645 | DDB_G0285645 | DDB0232431 | CDS | 3531932 | 957 | - | 0.256008 | |
DDB_G0285663 | DDB_G0285663 | conserved protozoa protein that are putative permeases involved in the transport of lipids contains 10 putative transmembrane domains | DDB0232431 | CDS | 3554545 | 3456 | - | 0.308738 |
DDB_G0285753_ps | DDB_G0285753 | putative pseudogene similar to a family of D. discoideum genes including | DDB0232431 | CDS | 3388026 | 975 | + | 0.29641 |
DDB_G0285755_ps | DDB_G0285755 | putative pseudogene similar to cyclin-like F-box containing proteins | DDB0232431 | CDS | 3393941 | 645 | - | 0.317829 |
DDB_G0285803 | DDB_G0285803 | belongs to the GNAT family homolog of S. cerevisiae MAK3 (maintenance of killer protein 3) | DDB0232431 | CDS | 3673056 | 558 | + | 0.250896 |
DDB_G0285823 | DDB_G0285823 | DDB0232431 | CDS | 3703536 | 1521 | + | 0.331361 | |
DDB_G0285827 | DDB_G0285827 | DDB0232431 | CDS | 3706474 | 1002 | + | 0.251497 | |
DDB_G0285831 | DDB_G0285831 | DDB0232431 | CDS | 3709396 | 522 | + | 0.260536 | |
DDB_G0285837 | DDB_G0285837 | DDB0232431 | CDS | 3674059 | 6603 | - | 0.283356 | |
DDB_G0285897 | DDB_G0285897 | DDB0232431 | CDS | 3798877 | 1701 | + | 0.280423 | |
DDB_G0285903 | DDB_G0285903 | DDB0232431 | CDS | 3808445 | 792 | - | 0.27399 | |
DDB_G0285905 | DDB_G0285905 | DDB0232431 | CDS | 3809647 | 843 | - | 0.204033 | |
DDB_G0285969 | DDB_G0285969 | putative cysteine protease member of the DJ-1ThiJPfpI family which includes human PARK7 associated with Parkinson's disease | DDB0232431 | CDS | 3885433 | 618 | - | 0.305825 |
DDB_G0285973 | DDB_G0285973 | DDB0232431 | CDS | 3894503 | 1404 | + | 0.289174 | |
DDB_G0285989 | DDB_G0285989 | DDB0232431 | CDS | 3911476 | 3705 | + | 0.239676 | |
DDB_G0285991 | DDB_G0285991 | DDB0232431 | CDS | 3915272 | 882 | - | 0.25737 | |
DDB_G0286067 | DDB_G0286067 | DDB0232431 | CDS | 4019113 | 3573 | + | 0.240974 | |
DDB_G0286073 | DDB_G0286073 | DDB0232431 | CDS | 4028900 | 1638 | + | 0.281441 | |
DDB_G0286129 | DDB_G0286129 | similar to mammalian F-boxWD repeat-containing protein 7 which is part to the E3 ubiquitin-protein ligase complex | DDB0232431 | CDS | 4060377 | 2220 | + | 0.263514 |
DDB_G0286167 | DDB_G0286167 | DDB0232431 | CDS | 4119612 | 1410 | - | 0.312057 | |
DDB_G0286201_ps | DDB_G0286201 | putative pseudogene similar to a Dictyostelid family of oxidoreductases including | DDB0232431 | CDS | 4168246 | 846 | + | 0.239953 |
DDB_G0286203 | DDB_G0286203 | DDB0232431 | CDS | 4169821 | 1026 | + | 0.24269 | |
DDB_G0286223 | DDB_G0286223 | contains up to 13 WD40 repeats very similar to D. purpureum protein | DDB0232431 | CDS | 4210540 | 2304 | + | 0.291667 |
DDB_G0286239 | DDB_G0286239 | DDB0232431 | CDS | 4234344 | 1080 | + | 0.316667 | |
DDB_G0286243 | DDB_G0286243 | DDB0232431 | CDS | 4239634 | 3012 | + | 0.285193 | |
DDB_G0286283 | DDB_G0286283 | DDB0232431 | CDS | 4297454 | 924 | + | 0.199134 | |
DDB_G0286297 | DDB_G0286297 | DDB0232431 | CDS | 4322636 | 354 | - | 0.251412 | |
DDB_G0286305 | DDB_G0286305 | DDB0232431 | CDS | 4332234 | 1017 | - | 0.360865 | |
DDB_G0286309 | DDB_G0286309 | DDB0232431 | CDS | 4335795 | 1026 | + | 0.337232 | |
DDB_G0286311 | DDB_G0286311 | DDB0232431 | CDS | 4337464 | 4422 | + | 0.313433 | |
DDB_G0286325_ps | DDB_G0286325 | putative pseudogene similar to D. discoideum gene | DDB0232431 | CDS | 4171531 | 354 | + | 0.262712 |
DDB_G0286397 | DDB_G0286397 | DDB0232431 | CDS | 4407676 | 1281 | - | 0.225605 | |
DDB_G0286443 | DDB_G0286443 | DDB0232431 | CDS | 4513273 | 675 | - | 0.244444 | |
DDB_G0286481 | DDB_G0286481 | putative protein serinethreonine kinase similar to casein kinase II the alpha chain of a ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | DDB0232431 | CDS | 4514745 | 1818 | - | 0.264026 |
DDB_G0286513 | DDB_G0286513 | DDB0232431 | CDS | 4577203 | 1683 | + | 0.236482 | |
DDB_G0286527_ps | DDB_G0286527 | putative pseudogene similar to a Dictyostelid family of putative SAM-dependent methyltransferases including | DDB0232431 | CDS | 4594246 | 561 | - | 0.247772 |
DDB_G0286575 | DDB_G0286575 | similar to retinol dehydrogenase and eukaryotic proteins of the short chain dehydrogenasesreductases family | DDB0232431 | CDS | 4647468 | 873 | + | 0.218786 |
DDB_G0286581 | DDB_G0286581 | DDB0232431 | CDS | 4651768 | 915 | + | 0.285246 | |
DDB_G0286625 | DDB_G0286625 | conserved hyphothetical protein similar to AprA an autocrine repressor of proliferation | DDB0232431 | CDS | 4749168 | 1566 | - | 0.308429 |
DDB_G0286627 | DDB_G0286627 | putative protein serinethreonine kinase belongs to the STE group the kinase domain is similar to yeast BCK1 a mitogen-activated protein (MAP) kinase kinase kinase | DDB0232431 | CDS | 4756048 | 2016 | - | 0.251984 |
DDB_G0286641 | DDB_G0286641 | putative GTPase that has high similarity to NOG1GTPBP4 GTPases which in S. cerevisiae associates with free 60S ribosomal subunits in the nucleolus this D. discoideumprotein is only about half the length and lacks the NOG1 C-terminal domain | DDB0232431 | CDS | 4774707 | 1044 | + | 0.198276 |
DDB_G0286691 | DDB_G0286691 | DDB0232431 | CDS | 4852997 | 408 | + | 0.25 | |
DDB_G0286713 | DDB_G0286713 | DDB0232431 | CDS | 4882439 | 693 | - | 0.277056 | |
DDB_G0286735 | DDB_G0286735 | DDB0232431 | CDS | 4909097 | 2085 | + | 0.317026 | |
DDB_G0286841 | DDB_G0286841 | member of the AGC kinase group similar to the kinase domains of MAST kinases (Microtubule-Associated SerineThreonine kinase) | DDB0232431 | CDS | 4966020 | 1389 | - | 0.218143 |
DDB_G0286845 | DDB_G0286845 | DDB0232431 | CDS | 4972112 | 885 | + | 0.277966 | |
DDB_G0286849 | DDB_G0286849 | similar to bacterial short-chain dehydrogenasereductase family proteins and human RDH8 (retinol dehydrogenase 8) | DDB0232431 | CDS | 4977120 | 870 | - | 0.28046 |
DDB_G0286861 | DDB_G0286861 | DDB0232431 | CDS | 4978558 | 885 | + | 0.275706 | |
DDB_G0286883 | DDB_G0286883 | DDB0232431 | CDS | 5022922 | 573 | - | 0.277487 | |
DDB_G0286947 | DDB_G0286947 | DDB0232431 | CDS | 5126978 | 5022 | + | 0.258662 | |
DDB_G0286979 | DDB_G0286979 | DDB0232431 | CDS | 5150412 | 1884 | - | 0.277601 | |
DDB_G0287001 | DDB_G0287001 | member of the TKL (tyrosine kinase-like) group contains zinc-binding LIM domain | DDB0232431 | CDS | 5188585 | 1953 | - | 0.28213 |
DDB_G0287003 | DDB_G0287003 | DDB0232431 | CDS | 5191304 | 1254 | - | 0.334928 | |
DDB_G0287013 | DDB_G0287013 | DDB0232431 | CDS | 5205106 | 1026 | - | 0.346979 | |
DDB_G0287017 | DDB_G0287017 | belongs to the HAD-like hydrolase superfamily similar to human HDHD3 (haloacid dehalogenase-like hydrolase domain-containing protein 3) | DDB0232431 | CDS | 5207898 | 858 | - | 0.221445 |
DDB_G0287037 | DDB_G0287037 | DDB0232431 | CDS | 5215181 | 978 | + | 0.274029 | |
DDB_G0287067 | DDB_G0287067 | DDB0232431 | CDS | 5289082 | 393 | - | 0.29771 | |
DDB_G0287081 | DDB_G0287081 | DDB0232431 | CDS | 5304055 | 840 | - | 0.24881 | |
DDB_G0287151 | DDB_G0287151 | similar to retinol dehydrogenase and eukaryotic short chain dehydrogenasesreductases family proteins | DDB0232431 | CDS | 5393798 | 930 | - | 0.224731 |
DDB_G0287193 | DDB_G0287193 | DDB0232431 | CDS | 5388100 | 3177 | + | 0.251495 | |
DDB_G0287305 | DDB_G0287305 | DDB0232432 | CDS | 110292 | 543 | - | 0.246777 | |
DDB_G0287309 | DDB_G0287309 | DDB0232432 | CDS | 112586 | 600 | + | 0.26 | |
DDB_G0287319 | DDB_G0287319 | similar to human SLC35E2 (solute carrier family 35 member E2) contains 10 putative transmembrane domains | DDB0232432 | CDS | 129877 | 1047 | + | 0.30468 |
DDB_G0287323 | DDB_G0287323 | contains an N-terminal oxidoreductase domain and a partial C-terminal oxidoreductase domain the GfoIdhMocA family proteins utilize NADP or NAD | DDB0232432 | CDS | 133013 | 1293 | + | 0.28925 |
DDB_G0287331 | DDB_G0287331 | DDB0232432 | CDS | 144715 | 2136 | + | 0.267322 | |
DDB_G0287335 | DDB_G0287335 | has similarity to human cold inducible RNA binding protein (CIRBP) however it is considreably shorter | DDB0232432 | CDS | 148219 | 276 | + | 0.344203 |
DDB_G0287379 | DDB_G0287379 | DDB0232432 | CDS | 233763 | 3231 | + | 0.320644 | |
DDB_G0287407 | DDB_G0287407 | similar to nephrocystin 3 Grp94 neighboring nucleotidase and other TPR repeat-containing proteins | DDB0232432 | CDS | 263392 | 4992 | + | 0.313902 |
DDB_G0287541 | DDB_G0287541 | DDB0232432 | CDS | 397759 | 2010 | + | 0.21592 | |
DDB_G0287617 | DDB_G0287617 | similar to Bax inhibitor 1 that may have a role in inhibition of apoptosis contains 7 transmembrane domains | DDB0232432 | CDS | 479630 | 765 | + | 0.284967 |
DDB_G0287679 | DDB_G0287679 | DDB0232432 | CDS | 545368 | 3369 | - | 0.290591 | |
DDB_G0287729 | DDB_G0287729 | DDB0232432 | CDS | 613467 | 2121 | + | 0.296558 | |
DDB_G0287843 | DDB_G0287843 | DDB0232432 | CDS | 806278 | 1923 | - | 0.333853 | |
DDB_G0287909 | DDB_G0287909 | DDB0232432 | CDS | 833953 | 3585 | - | 0.271409 | |
DDB_G0287929 | DDB_G0287929 | DDB0232432 | CDS | 861720 | 1377 | + | 0.302832 | |
DDB_G0287961 | DDB_G0287961 | DDB0232432 | CDS | 894476 | 5595 | - | 0.27328 | |
DDB_G0288005 | DDB_G0288005 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232432 | CDS | 962125 | 960 | - | 0.314583 |
DDB_G0288011 | DDB_G0288011 | DDB0232432 | CDS | 974125 | 780 | + | 0.305128 | |
DDB_G0288029 | DDB_G0288029 | member of the aspartateglutamateuridylate kinase family similar to glutamate 5-kinase | DDB0232432 | CDS | 994876 | 891 | - | 0.243547 |
DDB_G0288039 | DDB_G0288039 | DDB0232432 | CDS | 1009340 | 771 | + | 0.268482 | |
DDB_G0288069 | DDB_G0288069 | DDB0232432 | CDS | 1045172 | 3249 | + | 0.271776 | |
DDB_G0288147 | DDB_G0288147 | member of the tyrosine kinase-like (TKL) group similar to plant serinethreonine kinases contains a phorbol esterdiacylglycerol-binding domain | DDB0232432 | CDS | 1147360 | 4044 | + | 0.271513 |
DDB_G0288155 | DDB_G0288155 | DDB0232432 | CDS | 1159975 | 741 | - | 0.333333 | |
DDB_G0288165 | DDB_G0288165 | sulfurates the molybdenum cofactor which is essential for xanthine dehydrogenase and aldehyde oxidase | DDB0232432 | CDS | 1172053 | 1116 | - | 0.292115 |
DDB_G0288201 | DDB_G0288201 | DDB0232432 | CDS | 1230521 | 942 | - | 0.266454 | |
DDB_G0288255 | DDB_G0288255 | very similar to bacterial ribosomal RNA large subunit methyltransferase Nalso known as radical SAM protein or Cfr family protein | DDB0232432 | CDS | 1294679 | 1224 | - | 0.287582 |
DDB_G0288263 | DDB_G0288263 | DDB0232432 | CDS | 1310716 | 1266 | - | 0.226698 | |
DDB_G0288279 | DDB_G0288279 | DDB0232432 | CDS | 1332303 | 747 | + | 0.253012 | |
DDB_G0288291 | DDB_G0288291 | contains 1 RRM (RNA recognition motif) domain similar to the RRM domain of eukaryotic peptidyl-prolyl cis-trans isomerase E | DDB0232432 | CDS | 1356313 | 372 | + | 0.266129 |
DDB_G0288395 | DDB_G0288395 | DDB0232432 | CDS | 1489692 | 339 | - | 0.247788 | |
DDB_G0288405 | DDB_G0288405 | DDB0232432 | CDS | 1502693 | 2202 | + | 0.265668 | |
DDB_G0288429 | DDB_G0288429 | belongs to the short-chain dehydrogenasesreductases (SDR) family | DDB0232432 | CDS | 1527197 | 993 | + | 0.281974 |
DDB_G0288441 | DDB_G0288441 | DDB0232432 | CDS | 1540991 | 804 | + | 0.263682 | |
DDB_G0288453 | DDB_G0288453 | DDB0232432 | CDS | 1521809 | 2913 | - | 0.270855 | |
DDB_G0288465 | DDB_G0288465 | converts pantetheine 4'-phosphate to 3'-dephospho-CoA in other organisms this activity is part of a bifunctional enzyme that also has dephospho-CoA kinase activity in Dictyostelium the latter activity is encoded by | DDB0232432 | CDS | 1558211 | 1230 | - | 0.233333 |
DDB_G0288525 | DDB_G0288525 | DDB0232432 | CDS | 1644947 | 1674 | - | 0.247909 | |
DDB_G0288529 | DDB_G0288529 | DDB0232432 | CDS | 1628807 | 1587 | + | 0.267171 | |
DDB_G0288531 | DDB_G0288531 | DDB0232432 | CDS | 1649759 | 2196 | + | 0.255009 | |
DDB_G0288535 | DDB_G0288535 | DDB0232432 | CDS | 1660756 | 1395 | - | 0.235842 | |
DDB_G0288547 | DDB_G0288547 | DDB0232432 | CDS | 1676407 | 1038 | - | 0.259152 | |
DDB_G0288559 | DDB_G0288559 | DDB0232432 | CDS | 1685010 | 1650 | + | 0.303636 | |
DDB_G0288591 | DDB_G0288591 | DDB0232432 | CDS | 1726934 | 861 | + | 0.293844 | |
DDB_G0288597 | DDB_G0288597 | DDB0232432 | CDS | 1732418 | 1926 | - | 0.226895 | |
DDB_G0288625 | DDB_G0288625 | DDB0232432 | CDS | 1759888 | 2316 | - | 0.295337 | |
DDB_G0288651 | DDB_G0288651 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232432 | CDS | 1782938 | 1353 | - | 0.317812 |
DDB_G0288669 | DDB_G0288669 | DDB0232432 | CDS | 1797088 | 930 | - | 0.230108 | |
DDB_G0288729 | DDB_G0288729 | ortholog of the mammalian reticulon-4-interacting protein 1 a zinc-containing alcohol dehydrogenase | DDB0232432 | CDS | 1887042 | 1059 | - | 0.249292 |
DDB_G0288779 | DDB_G0288779 | DDB0232432 | CDS | 1950277 | 1482 | + | 0.212551 | |
DDB_G0288795 | DDB_G0288795 | putative protein serinethreonine kinase AGC group similar to the kinase domains of mammalian AKTPKB similar to yeast protein kinases GAD8 and SCH9 | DDB0232432 | CDS | 1975761 | 1926 | - | 0.317757 |
DDB_G0288811 | DDB_G0288811 | very similar to TBC1 domain family member 15 proteins and yeast GYP7 TBC domain-containing proteins in yeast are GTPase activator proteins | DDB0232432 | CDS | 2006806 | 2490 | + | 0.284739 |
DDB_G0288865 | DDB_G0288865 | DDB0232432 | CDS | 1959111 | 486 | - | 0.257202 | |
DDB_G0288917 | DDB_G0288917 | similar to retinol dehydrogenase and eukaryotic proteins of the short chain dehydrogenasesreductases family | DDB0232432 | CDS | 2119308 | 954 | + | 0.240042 |
DDB_G0288949 | DDB_G0288949 | DDB0232432 | CDS | 2101452 | 1392 | - | 0.236351 | |
DDB_G0288981 | DDB_G0288981 | DDB0232432 | CDS | 2203346 | 441 | - | 0.206349 | |
DDB_G0289031 | DDB_G0289031 | ortholog of the conserved spastic paraplegia 21 (SPG21) also known as Maspardin defects in human SPG21 are the cause of the neurodegenerative disorder spastic paraplegia also known as Mast syndrome | DDB0232432 | CDS | 2258354 | 1155 | - | 0.256277 |
DDB_G0289057 | DDB_G0289057 | DDB0232432 | CDS | 2307545 | 936 | + | 0.238248 | |
DDB_G0289059 | DDB_G0289059 | DDB0232432 | CDS | 2308883 | 996 | + | 0.252008 | |
DDB_G0289061 | DDB_G0289061 | DDB0232432 | CDS | 2310384 | 1002 | + | 0.257485 | |
DDB_G0289111 | DDB_G0289111 | DDB0232432 | CDS | 2353928 | 942 | + | 0.335456 | |
DDB_G0289127 | DDB_G0289127 | DDB0232432 | CDS | 2385358 | 861 | - | 0.304297 | |
DDB_G0289129 | DDB_G0289129 | DDB0232432 | CDS | 2386701 | 885 | - | 0.310734 | |
DDB_G0289167 | DDB_G0289167 | similar to bacterial short-chain dehydrogenasereductase family proteins and human RDH8 (retinol dehydrogenase 8) | DDB0232432 | CDS | 2441551 | 972 | - | 0.244856 |
DDB_G0289235 | DDB_G0289235 | DDB0232432 | CDS | 2524160 | 2523 | + | 0.266746 | |
DDB_G0289259 | DDB_G0289259 | similar to bacterial fungal and plant proteins from the short-chain dehydrogenasereductase family | DDB0232432 | CDS | 2556391 | 879 | - | 0.265074 |
DDB_G0289335 | DDB_G0289335 | DDB0232432 | CDS | 2652694 | 2064 | - | 0.28876 | |
DDB_G0289349 | DDB_G0289349 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity also contains an N-terminal transmembrane domain | DDB0232432 | CDS | 2670443 | 1479 | + | 0.279919 |
DDB_G0289355 | DDB_G0289355 | DDB0232432 | CDS | 2681578 | 1893 | + | 0.216587 | |
DDB_G0289403 | DDB_G0289403 | DDB0232432 | CDS | 2749137 | 966 | - | 0.315735 | |
DDB_G0289439 | DDB_G0289439 | DDB0232432 | CDS | 2778983 | 405 | + | 0.367901 | |
DDB_G0289581 | DDB_G0289581 | DDB0232432 | CDS | 2997750 | 741 | - | 0.237517 | |
DDB_G0289609 | DDB_G0289609 | contains two CBS domains expressed in pstAO cells and in upper cup during culmination | DDB0232432 | CDS | 3019826 | 438 | - | 0.296804 |
DDB_G0289669 | DDB_G0289669 | DDB0232432 | CDS | 3069414 | 1626 | - | 0.264453 | |
DDB_G0289671 | DDB_G0289671 | similar to human ABHD13 (Abhydrolase domain-containing protein 13) and S. pombe bem46 contains one putative transmembrane domain | DDB0232432 | CDS | 3072697 | 864 | + | 0.280093 |
DDB_G0289703 | DDB_G0289703 | DDB0232432 | CDS | 3127157 | 2931 | + | 0.247015 | |
DDB_G0289735 | DDB_G0289735 | DDB0232432 | CDS | 3179530 | 1626 | + | 0.245387 | |
DDB_G0290127 | DDB_G0290127 | DDB0232432 | CDS | 3689897 | 1950 | + | 0.212308 | |
DDB_G0290139 | DDB_G0290139 | DDB0232432 | CDS | 3695903 | 1431 | + | 0.331936 | |
DDB_G0290181 | DDB_G0290181 | similar to S.cerevisiae RRP5 and animal PDCD11 (Programmed cell death protein 11) | DDB0232432 | CDS | 3746723 | 2730 | - | 0.25641 |
DDB_G0290199 | DDB_G0290199 | DDB0232432 | CDS | 3783788 | 651 | - | 0.241167 | |
DDB_G0290225 | DDB_G0290225 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity enriched in gametes | DDB0232432 | CDS | 3824091 | 1212 | - | 0.287954 |
DDB_G0290307 | DDB_G0290307 | contains three RRM domains homolog of ELAVL1 (embryonic lethal abnormal vision-like 1) | DDB0232432 | CDS | 3938585 | 1380 | + | 0.300725 |
DDB_G0290311 | DDB_G0290311 | DDB0232432 | CDS | 3942085 | 1086 | - | 0.300184 | |
DDB_G0290329 | DDB_G0290329 | DDB0232432 | CDS | 3968559 | 906 | - | 0.335541 | |
DDB_G0290369 | DDB_G0290369 | DDB0232432 | CDS | 3976953 | 5661 | + | 0.242183 | |
DDB_G0290415 | DDB_G0290415 | DDB0232432 | CDS | 4053731 | 3303 | + | 0.277929 | |
DDB_G0290423 | DDB_G0290423 | DDB0232432 | CDS | 4067949 | 1743 | + | 0.242111 | |
DDB_G0290427 | DDB_G0290427 | DDB0232432 | CDS | 4113138 | 963 | - | 0.311526 | |
DDB_G0290449 | DDB_G0290449 | DDB0232432 | CDS | 4015567 | 924 | - | 0.238095 | |
DDB_G0290471 | DDB_G0290471 | member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats does not contain the consensus sequences required for kinase function | DDB0232432 | CDS | 4105828 | 1059 | - | 0.234183 |
DDB_G0290521 | DDB_G0290521 | DDB0232432 | CDS | 4200324 | 1293 | - | 0.354988 | |
DDB_G0290605 | DDB_G0290605 | DDB0232432 | CDS | 4356438 | 1155 | + | 0.27619 | |
DDB_G0290621 | DDB_G0290621 | DDB0232432 | CDS | 4383355 | 2904 | - | 0.22865 | |
DDB_G0290623 | DDB_G0290623 | DDB0232432 | CDS | 4387215 | 2436 | + | 0.2578 | |
DDB_G0290689 | DDB_G0290689 | homolog of E. coli rppH very similar to | DDB0232432 | CDS | 4419333 | 552 | - | 0.278986 |
DDB_G0290771 | DDB_G0290771 | DDB0232432 | CDS | 4578736 | 5247 | - | 0.27673 | |
DDB_G0290827 | DDB_G0290827 | DDB0232432 | CDS | 4603659 | 753 | - | 0.200531 | |
DDB_G0290859 | DDB_G0290859 | member of the AGC kinase group similar to NDR (nuclear Dbf2-related) and RSK (ribosomal S6 kinase) family members | DDB0232432 | CDS | 4688665 | 1260 | + | 0.307143 |
DDB_G0290877 | DDB_G0290877 | DDB0232432 | CDS | 4704549 | 2475 | - | 0.288081 | |
DDB_G0290983 | DDB_G0290983 | DDB0232432 | CDS | 4844885 | 4008 | - | 0.221307 | |
DDB_G0291003 | DDB_G0291003 | DDB0232432 | CDS | 4876763 | 2598 | - | 0.299461 | |
DDB_G0291013 | DDB_G0291013 | DDB0232432 | CDS | 4889905 | 1149 | + | 0.302872 | |
DDB_G0291059 | DDB_G0291059 | contains two ankyrin repeats and two K homology (KH) domains similar to high density lipoprotein-binding protein (vigilin) | DDB0232432 | CDS | 4839561 | 1155 | + | 0.303896 |
DDB_G0291133 | DDB_G0291133 | putative protein tyrosine kinase similar to S. pombe wee1 inhibitor of mitosis through phosphorylation of cdc2 | DDB0232432 | CDS | 5030354 | 2337 | + | 0.26059 |
DDB_G0291149 | DDB_G0291149 | DDB0232432 | CDS | 5052148 | 1569 | - | 0.251115 | |
DDB_G0291167 | DDB_G0291167 | DDB0232432 | CDS | 5083393 | 681 | - | 0.251101 | |
DDB_G0291195 | DDB_G0291195 | DDB0232432 | CDS | 5092325 | 792 | + | 0.294192 | |
DDB_G0291205 | DDB_G0291205 | DDB0232432 | CDS | 5120775 | 2727 | + | 0.268794 | |
DDB_G0291336 | DDB_G0291336 | DDB0232433 | CDS | 134282 | 834 | - | 0.2494 | |
DDB_G0291338 | DDB_G0291338 | DDB0232433 | CDS | 135540 | 657 | + | 0.219178 | |
DDB_G0291350 | DDB_G0291350 | putative protein serinethreonine kinase similar to mammalian MPSK (myristoylated and palmitoylated serinethreonine kinase) a kinase involved in transcriptional regulation and protein phosphorylation may be an intermediary in the TGF-beta signaling pathway | DDB0232433 | CDS | 162730 | 1110 | - | 0.245045 |
DDB_G0291402 | DDB_G0291402 | DDB0232433 | CDS | 257921 | 447 | - | 0.306488 | |
DDB_G0291444 | DDB_G0291444 | DDB0232433 | CDS | 320738 | 1344 | + | 0.287946 | |
DDB_G0291468 | DDB_G0291468 | DDB0232433 | CDS | 378403 | 1608 | + | 0.264303 | |
DDB_G0291472 | DDB_G0291472 | DDB0232433 | CDS | 381635 | 1221 | - | 0.290745 | |
DDB_G0291476 | DDB_G0291476 | DDB0232433 | CDS | 396540 | 726 | + | 0.316804 | |
DDB_G0291486 | DDB_G0291486 | similar to CUGBP proteins and Bruno-like proteins human CUGBP1 regulates splicing and translation of various RNAs contains 3 RRM domains | DDB0232433 | CDS | 413873 | 1470 | + | 0.348299 |
DDB_G0291538 | DDB_G0291538 | similar to bacterial acetyltransferases homolog of E. coli maa (maltose O-acetyltransferase) contains a predicted peroxisomal targeting signal | DDB0232433 | CDS | 533329 | 546 | + | 0.322344 |
DDB_G0291578 | DDB_G0291578 | member of a small Dictyostelium gene family missing the carboxyl half compared to related proteins | DDB0232433 | CDS | 571007 | 486 | + | 0.195473 |
DDB_G0291664 | DDB_G0291664 | highly similar to | DDB0232433 | CDS | 338918 | 2880 | + | 0.291319 |
DDB_G0291674 | DDB_G0291674 | similar to bacterial short-chain dehydrogenasereductase family proteins and human RDH8 (retinol dehydrogenase 8) | DDB0232433 | CDS | 431044 | 951 | - | 0.281809 |
DDB_G0291676 | DDB_G0291676 | similar to bacterial short-chain dehydrogenasereductase family proteins | DDB0232433 | CDS | 432569 | 903 | - | 0.282392 |
DDB_G0291716 | DDB_G0291716 | DDB0232433 | CDS | 726193 | 2322 | - | 0.251938 | |
DDB_G0291720 | DDB_G0291720 | DDB0232433 | CDS | 721305 | 1278 | - | 0.311424 | |
DDB_G0291722 | DDB_G0291722 | DDB0232433 | CDS | 719367 | 1344 | - | 0.233631 | |
DDB_G0291726 | DDB_G0291726 | DDB0232433 | CDS | 716979 | 690 | - | 0.356522 | |
DDB_G0291758 | DDB_G0291758 | DDB0232433 | CDS | 697440 | 1194 | + | 0.273869 | |
DDB_G0291796 | DDB_G0291796 | DDB0232433 | CDS | 757607 | 2541 | + | 0.284534 | |
DDB_G0291824 | DDB_G0291824 | DDB0232433 | CDS | 827281 | 1878 | - | 0.300319 | |
DDB_G0291842 | DDB_G0291842 | putative protein tyrosine kinase similar to S. pombe WEE1 inhibitor of mitosis through phosphorylation of cdc2 | DDB0232433 | CDS | 822502 | 1059 | - | 0.351275 |
DDB_G0291886_ps | DDB_G0291886 | similar to | DDB0232433 | CDS | 881755 | 2151 | + | 0.248257 |
DDB_G0291888 | DDB_G0291888 | DDB0232433 | CDS | 886219 | 1416 | + | 0.214689 | |
DDB_G0291896 | DDB_G0291896 | weakly similar to mammalian NASP (Nuclear Autoantigenic Sperm Protein) a histone chaperone required for DNA replication normal cell cycle progression and cell proliferationbrbr bCommunity annotation:b DDB G0291896 is similar (first blast hit both ways) to the N1N2 protein of Xenopus in humans known as NASP (nuclear autoantigenic sperm protein) a histone chaperone found in all dividing cells and implicated in chromatin assembly (see Wang et al NAR 36 5763-5772 (2008). NASP is required for cell cycle progression and is upregulated in a variety of cancers (see Alekseev et al Reproductive Biology and Endocrinology 7 45 2009).br DDB_G0291896 is overexpressed threefold (p2e-72) in a Dicty strain in which the retinoblastoma-like protein rblA has been disrupted. Most genes with functions in cell cycle progression are overexpressed in this strain and most overexpressed genes have identifiable cell cycle functions (Doquang et al. in preparation) these include other genes involved in chromatin as | DDB0232433 | CDS | 904350 | 1503 | + | 0.314039 |
DDB_G0291918 | DDB_G0291918 | putative protein serinethreonine kinase CAMK group kinase domain is similar to those of mammalian death-associated protein kinases (DAPK) | DDB0232433 | CDS | 943654 | 2010 | + | 0.287065 |
DDB_G0291926 | DDB_G0291926 | weakly similar ro S. cerevisiae Arc1 a protein that binds tRNA and methionyl- and glutamyl-tRNA synthetases delivering tRNA to them stimulating catalysis and ensuring their localization to the cytoplasm | DDB0232433 | CDS | 959253 | 1092 | - | 0.282967 |
DDB_G0292006 | DDB_G0292006 | DDB0232433 | CDS | 1004992 | 966 | + | 0.247412 | |
DDB_G0292056 | DDB_G0292056 | DDB0232433 | CDS | 1115547 | 5472 | + | 0.272844 | |
DDB_G0292110 | DDB_G0292110 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232433 | CDS | 1201167 | 1053 | + | 0.253561 |
DDB_G0292116 | DDB_G0292116 | belongs to the short-chain dehydrogenasesreductases family similar to human HSDL2 (Hydroxysteroid dehydrogenase-like protein 2) | DDB0232433 | CDS | 1219275 | 849 | - | 0.328622 |
DDB_G0292298 | DDB_G0292298 | DDB0232433 | CDS | 1424473 | 501 | - | 0.307385 | |
DDB_G0292312 | DDB_G0292312 | DDB0232433 | CDS | 1454104 | 1593 | - | 0.287508 | |
DDB_G0292332 | DDB_G0292332 | DDB0232433 | CDS | 1500852 | 561 | + | 0.210339 | |
DDB_G0292350 | DDB_G0292350 | DDB0232433 | CDS | 1496951 | 3675 | + | 0.270204 | |
DDB_G0292354 | DDB_G0292354 | putative protein serinethreonine kinase TTBK family similar to casein kinase similar to mammalian tau-tubulin kinase (TTBK) which phosphorylates the microtubule-associated protein tau implicated in Alzheimer's disease | DDB0232433 | CDS | 1420214 | 1488 | + | 0.30578 |
DDB_G0292410 | DDB_G0292410 | similar to H. sapiens zinc finger CCCH-type containing 15 and M. musculus immediate early response erythropoietin 4 | DDB0232433 | CDS | 1561008 | 1122 | - | 0.336898 |
DDB_G0292424 | DDB_G0292424 | DDB0232433 | CDS | 1593747 | 1017 | + | 0.285152 | |
DDB_G0292430 | DDB_G0292430 | DDB0232433 | CDS | 1609068 | 1323 | - | 0.249433 | |
DDB_G0292432 | DDB_G0292432 | DDB0232433 | CDS | 1610862 | 1815 | - | 0.293113 | |
DDB_G0292494 | DDB_G0292494 | similar to human TTC39A and TTC39B matches PFAM outer membrane protein IML2 mitochondrialtetratricopeptide repeat protein 39 | DDB0232433 | CDS | 1739944 | 2388 | - | 0.220268 |
DDB_G0292528 | DDB_G0292528 | DDB0232433 | CDS | 1616689 | 897 | - | 0.331104 | |
DDB_G0292530 | DDB_G0292530 | DDB0232433 | CDS | 1625548 | 2967 | + | 0.276373 | |
DDB_G0292550 | DDB_G0292550 | DDB0232433 | CDS | 1642791 | 4194 | - | 0.223891 | |
DDB_G0292570 | DDB_G0292570 | DDB0232433 | CDS | 1784981 | 522 | - | 0.254789 | |
DDB_G0292574 | DDB_G0292574 | DDB0232433 | CDS | 1791327 | 870 | + | 0.270115 | |
DDB_G0292602 | DDB_G0292602 | DDB0232433 | CDS | 1827272 | 879 | - | 0.31058 | |
DDB_G0292624 | DDB_G0292624 | protein serinethreonine kinase CAMK group CAMK1 family similar to the Dictyostelium myosin light chain kinase (mlkA) and mammalian CAM kinases | DDB0232433 | CDS | 1864394 | 942 | + | 0.298301 |
DDB_G0292698 | DDB_G0292698 | DDB0232433 | CDS | 1997307 | 921 | - | 0.365907 | |
DDB_G0292700 | DDB_G0292700 | DDB0232433 | CDS | 1999329 | 894 | - | 0.241611 | |
DDB_G0292714 | DDB_G0292714 | DDB0232433 | CDS | 1780390 | 4446 | + | 0.234818 | |
DDB_G0292746 | DDB_G0292746 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity also contains a PH domain involved in intracellular signaling | DDB0232433 | CDS | 2069434 | 2898 | + | 0.327467 |
DDB_G0292774 | DDB_G0292774 | DDB0232433 | CDS | 2013605 | 1098 | + | 0.270492 | |
DDB_G0292834 | DDB_G0292834 | DDB0232433 | CDS | 2130562 | 1710 | - | 0.29883 | |
DDB_G0292852 | DDB_G0292852 | ortholog of human LACE1 an AFG1-like ATPase and similar to yeast AFG1 family of proteins contains a P-loop motif and are predicted to be ATPases | DDB0232433 | CDS | 2099022 | 1584 | + | 0.279672 |
DDB_G0292960 | DDB_G0292960 | DDB0232433 | CDS | 2129207 | 1173 | + | 0.225916 | |
DDB_G0293032 | DDB_G0293032 | DDB0232433 | CDS | 2351624 | 4698 | - | 0.270115 | |
DDB_G0293034 | DDB_G0293034 | DDB0232433 | CDS | 2371825 | 942 | - | 0.33121 | |
DDB_G0293062 | DDB_G0293062 | conserved in plants and bacteria predicted to have a structural domain found in several acyl-CoA acyltransferase enzymes | DDB0232433 | CDS | 2415200 | 246 | + | 0.313008 |
DDB_G0293070 | DDB_G0293070 | putative ortholog of H. sapiens TEP1 a component of the telomerase ribonucleoprotein complex involved in replication of chromosome termini | DDB0232433 | CDS | 2426564 | 7293 | - | 0.319896 |
DDB_G0293072 | DDB_G0293072 | DDB0232433 | CDS | 2434758 | 1701 | - | 0.258083 | |
DDB_G0293170 | DDB_G0293170 | DDB0232433 | CDS | 2392178 | 3165 | + | 0.222749 | |
DDB_G0293174 | DDB_G0293174 | DDB0232433 | CDS | 2473465 | 3810 | + | 0.246194 | |
DDB_G0293184 | DDB_G0293184 | kinase domain similar to S. pombe cdc7 cell division control protein 7 which plays a role in cytokinesis contains RhoGAP domain found in the Rho family of small G proteins unlikely to function as a kinase as it does not contain a catalytic aspartate | DDB0232433 | CDS | 2540484 | 3561 | + | 0.281382 |
DDB_G0293234 | DDB_G0293234 | ortholog of the conserved non-catalytic N-acetyltransferase that catalyzes the transfer of an acetyl group to the N-terminal residue of a protein that contains a Met-Glu Met-Asp Met-Asn or Met-Met N-terminus ortholog of S. cerevisiae MDM20 the N-terminal acetyltransferase B (NatB) complex subunit | DDB0232433 | CDS | 2661843 | 2814 | - | 0.27221 |
DDB_G0293276 | DDB_G0293276 | member of the AGC kinase group similar to kinase domains of AktPKB and MAST (microtubule-associated serinethreonine kinase) family members | DDB0232433 | CDS | 2701490 | 1551 | - | 0.246937 |
DDB_G0293292 | DDB_G0293292 | putative protein serinethreonine kinase N-terminal kinase domain similar to vertebrate Nek kinases which are involved in regulation of mitosis C-terminal kinase domain weakly similar to ULK (Unc-51-like kinase) | DDB0232433 | CDS | 2647324 | 4116 | + | 0.234208 |
DDB_G0293392 | DDB_G0293392 | conserved protein mammalian orthologs are predicted Zn-dependent hydrolases of the beta-lactamase fold | DDB0232433 | CDS | 2830538 | 1110 | + | 0.282883 |
DDB_G0293412 | DDB_G0293412 | DDB0232433 | CDS | 2844115 | 2010 | + | 0.30199 | |
DDB_G0293460 | DDB_G0293460 | DDB0232433 | CDS | 2919081 | 1275 | + | 0.287843 | |
DDB_G0293514 | DDB_G0293514 | DDB0232433 | CDS | 2984590 | 492 | + | 0.292683 | |
DDB_G0293562 | DDB_G0293562 | DDB0232433 | CDS | 3048907 | 1584 | + | 0.289141 | |
DDB_G0293592 | DDB_G0293592 | DDB0232433 | CDS | 3100713 | 483 | + | 0.277433 | |
DDB_G0293594 | DDB_G0293594 | DDB0232433 | CDS | 3101875 | 492 | + | 0.264228 | |
DDB_G0293604 | DDB_G0293604 | DDB0232433 | CDS | 3126896 | 897 | - | 0.248606 | |
DDB_G0293658 | DDB_G0293658 | DDB0232433 | CDS | 3221806 | 1245 | - | 0.258635 | |
DDB_G0293668 | DDB_G0293668 | DDB0232433 | CDS | 3238981 | 909 | + | 0.20242 | |
DDB_G0293670 | DDB_G0293670 | DDB0232433 | CDS | 3241196 | 792 | + | 0.224747 | |
DDB_G0293714 | DDB_G0293714 | DDB0232433 | CDS | 3102749 | 504 | + | 0.281746 | |
DDB_G0293718 | DDB_G0293718 | DDB0232433 | CDS | 3104858 | 483 | + | 0.318841 | |
DDB_G0293862 | DDB_G0293862 | DDB0232433 | CDS | 3396260 | 750 | - | 0.309333 | |
DDB_G0293864 | DDB_G0293864 | DDB0232433 | CDS | 3398572 | 1527 | + | 0.251473 | |
DDB_G0293868 | DDB_G0293868 | DDB0232433 | CDS | 3402442 | 1638 | - | 0.230159 | |
DDB_G0293930 | DDB_G0293930 | similar to human ZDHHC16 (zinc finger DHHC domain-containing protein 16) contains 4 putative transmembrane domains | DDB0232433 | CDS | 3510935 | 960 | - | 0.258333 |
DDB_G0293956 | DDB_G0293956 | DDB0232433 | CDS | 3572844 | 354 | - | 0.30226 | |
DDB_G0293958 | DDB_G0293958 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis | DDB0232433 | CDS | 3460612 | 4779 | + | 0.208203 |
DDB_G0293976 | DDB_G0293976 | DDB0232433 | CDS | 3485736 | 1347 | - | 0.200445 | |
DDB_G0294292 | DDB_G0294292 | similar to S. cerevisiae Lgs1 a putative GTPase involved in 60S ribosomal subunit biogenesis | DDB0232429 | CDS | 8123 | 2025 | + | 0.304198 |
DDB_G0294571 | DDB_G0294571 | DDB0232432 | CDS | 4610784 | 612 | - | 0.28268 | |
DDB_G0294583 | DDB_G0294583 | DDB0232429 | CDS | 1122814 | 705 | + | 0.229787 | |
DDB_G0294585 | DDB_G0294585 | contains a domain found in the family of Major Royal Jelly Proteins constituting 82-90 | DDB0232430 | CDS | 3552325 | 4941 | - | 0.277069 |
DDB_G0294589 | DDB_G0294589 | DDB0232431 | CDS | 4603487 | 882 | + | 0.276644 | |
DDB_G0294595 | DDB_G0294595 | multi-domain protein the TPR superhelical structures present a surface that is well suited to binding large substrates such as proteins and nucleic acids | DDB0232431 | CDS | 1785353 | 1542 | + | 0.217899 |
DDB_G0294621 | DDB_G0294621 | contains three Sel1-like repeats which are related to tetratricopeptide (TPR) repeats | DDB0232431 | CDS | 86151 | 1854 | + | 0.304207 |
DDB_G0294629 | DDB_G0294629 | DDB0232433 | CDS | 1603469 | 1785 | - | 0.285154 | |
DDB_G0295481_ps | DDB_G0295481 | putative pseudogene fragment very similar to Dictyostelium ppiD | DDB0232431 | CDS | 944514 | 243 | + | 0.283951 |
DDB_G0295691 | DDB_G0295691 | shares a region of similarity with proteins of unknown functions contains eight predicted transmembrane domains | DDB0232433 | CDS | 883760 | 1164 | + | 0.256873 |
DDB_G0295717 | DDB_G0295717 | DDB0232431 | CDS | 2373104 | 2466 | - | 0.242092 | |
DDB_G0295731 | DDB_G0295731 | DDB0232430 | CDS | 2424448 | 1680 | + | 0.192857 | |
DDB_G0295739 | DDB_G0295739 | DDB0232432 | CDS | 3772467 | 999 | - | 0.309309 | |
DDB_G0295781 | DDB_G0295781 | weakly similar to S. cerevisiae DUG3 involved in degradation of glutathione (GSH) and other peptides containing a gamma-glu-X bond in an alternative pathway to GSH degradation by gamma-glutamyl transpeptidase | DDB0232431 | CDS | 4542261 | 1125 | - | 0.330667 |
DDB_G0295793 | DDB_G0295793 | DDB0232433 | CDS | 2856788 | 1974 | + | 0.340426 | |
DDB_G0295807 | DDB_G0295807 | DDB0232429 | CDS | 986307 | 912 | - | 0.302632 | |
DDB_G0295833 | DDB_G0295833 | there is a second copy of this gene | DDB0232429 | CDS | 2544712 | 915 | - | 0.243716 |
DDB_G0295847 | DDB_G0295847 | DDB0232428 | CDS | 585586 | 4029 | - | 0.275503 | |
DDB_G0295849 | DDB_G0295849 | DDB0232430 | CDS | 5349087 | 1470 | + | 0.353061 | |
DDB_G0304561 | DDB_G0304561 | similar to solute carrier family 35 member E4 (SLC35E4) proteins contains 10 predicted transmembrane domains | DDB0232431 | CDS | 2797226 | 1476 | + | 0.278455 |
DDB_G0348940 | DDB_G0348940 | DDB0232429 | CDS | 7403620 | 1473 | + | 0.220638 | |
DDB_G0349043 | DDB_G0349043 | DDB0232432 | CDS | 1336627 | 1767 | - | 0.271647 | |
DDB_G0349375 | DDB_G0349375 | DDB0232429 | CDS | 5604371 | 612 | + | 0.267974 | |
DG1091 | DDB_G0289175 | DDB0232432 | CDS | 2479410 | 5478 | - | 0.220701 | |
abcD1 | DDB_G0279917 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232430 | CDS | 2772102 | 2205 | - | 0.247166 |
abcD2 | DDB_G0293194 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232433 | CDS | 2712310 | 2226 | + | 0.32929 |
abcD3 | DDB_G0279919 | half transporter consisting of one ABC domain and one transmembrane domain | DDB0232430 | CDS | 2769281 | 2253 | - | 0.246338 |
abcE1 | DDB_G0290483 | DDB0232432 | CDS | 4209815 | 1812 | - | 0.34989 | |
abcF1 | DDB_G0285997 | DDB0232431 | CDS | 3922084 | 2127 | - | 0.381758 | |
abcF2 | DDB_G0284047 | DDB0232431 | CDS | 1542455 | 1782 | - | 0.335578 | |
abcF3 | DDB_G0275637 | DDB0232429 | CDS | 6056870 | 1959 | - | 0.325166 | |
abcF4 | DDB_G0267436 | DDB0232428 | CDS | 1263019 | 3429 | + | 0.31846 | |
abhd | DDB_G0289723 | DDB0232432 | CDS | 3165541 | 1188 | - | 0.289562 | |
abkA | DDB_G0288749 | 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 | DDB0232432 | CDS | 1916080 | 1698 | - | 0.246761 |
abkB | DDB_G0281799 | 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 | DDB0232430 | CDS | 4693676 | 2007 | - | 0.255107 |
abkC | DDB_G0267774 | 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 | DDB0232428 | CDS | 825289 | 2070 | - | 0.246377 |
abkD | DDB_G0284897 | 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 | DDB0232431 | CDS | 2611033 | 2088 | - | 0.273946 |
acmsd | DDB_G0286525 | catalyzes the reaction: 2-amino-3-(3-oxoprop-1-en-1-yl)but-2-enedioate 2-aminomuconate semialdehyde CO2 | DDB0232431 | CDS | 4592587 | 1080 | + | 0.340741 |
aco | DDB_G0277497 | bNomenclature conflict:b Do not confuse this gene with acoA the acyl-CoA oxidase or aco1 and aco2 the aconitases | DDB0232429 | CDS | 8019782 | 1107 | + | 0.29991 |
adcB | DDB_G0274395 | DDB0232429 | CDS | 4691677 | 1854 | - | 0.288565 | |
agtA | DDB_G0283005 | likely catalyzes the alpha addition of galactose to Fuc-Gal-GlcNAc-HyPro143-Skp1 (FpaAFpaB) | DDB0232431 | CDS | 143819 | 1947 | - | 0.214689 |
aif | DDB_G0288247 | involved in caspase-independent mitochondrial cell death similar to H. sapiens AIFM1 the mitochondrial Apoptosis-Inducing Factor 1 | DDB0232432 | CDS | 1306170 | 1599 | - | 0.317699 |
aip1 | DDB_G0278733 | conserved protein containing WD40 repeats involved in actin-dependent processes such as endocytosis cytokinesis and motility interacts genetically with nhe1 and suppresses nhe1- mutant phenotypes | DDB0232430 | CDS | 1283399 | 1794 | + | 0.377926 |
alg9 | DDB_G0279349 | CAZy family GT22 catalyzes N-linked mannosylation | DDB0232430 | CDS | 1972184 | 1950 | + | 0.232308 |
alrA | DDB_G0293850 | involved in regulation of aggregate size member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232433 | CDS | 3404974 | 894 | + | 0.325503 |
alrB | DDB_G0285053 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2618768 | 936 | - | 0.318376 |
alrC | DDB_G0268058 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232428 | CDS | 1371493 | 966 | - | 0.258799 |
alrD | DDB_G0285027 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2833891 | 873 | - | 0.266896 |
alrE | DDB_G0285025 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2832495 | 870 | - | 0.301149 |
alrF | DDB_G0285023 | member of aldo-keto reductase family which reduces CO to C-OH in aldehydes and ketones | DDB0232431 | CDS | 2831142 | 918 | - | 0.238562 |
alr_ps | DDB_G0268562 | putative pseudogene similar to aldo-keto reductases alrA-F | DDB0232428 | CDS | 1373976 | 462 | - | 0.248918 |
anapc3 | DDB_G0288223 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232432 | CDS | 1273822 | 2913 | - | 0.278064 |
anapc6 | DDB_G0286233 | putative ortholog of cdc16 a conserved protein containing several TPRs (tetratrico peptide repeats) | DDB0232431 | CDS | 4222260 | 2598 | - | 0.234411 |
anapc7 | DDB_G0292470 | component of the anaphase-promoting complexcyclosome (APCC) a cell cycle-regulated ubiquitin ligase that controls progression through the cell cycle | DDB0232433 | CDS | 1686299 | 1743 | + | 0.243259 |
anapc8 | DDB_G0272775 | DDB0232429 | CDS | 2162746 | 1779 | - | 0.323215 | |
ankrd39 | DDB_G0287345 | DDB0232432 | CDS | 159445 | 525 | - | 0.266667 | |
aprA | DDB_G0281663 | secreted protein that exists in a 150 kDa complex repressor of cell proliferation | DDB0232430 | CDS | 4787137 | 1485 | + | 0.334007 |
arcA | DDB_G0277825 | component of the Dictyostelium Arp2Arp3 complex | DDB0232430 | CDS | 304397 | 1110 | - | 0.396396 |
arfA | DDB_G0289173 | DDB0232432 | CDS | 2516577 | 549 | + | 0.35337 | |
arfrp1 | DDB_G0283631 | DDB0232431 | CDS | 888563 | 651 | + | 0.271889 | |
arkA | DDB_G0289555 | suppressor of spalten (spnA) mutant member of the TKL (tyrosine kinase-like) group and ARK (ankyrin repeat-containing kinase) family | DDB0232432 | CDS | 2941850 | 4383 | + | 0.300707 |
arl1 | DDB_G0288163 | DDB0232432 | CDS | 1170444 | 552 | - | 0.304348 | |
arl2 | DDB_G0281307 | DDB0232430 | CDS | 4073757 | 555 | + | 0.261261 | |
arl5 | DDB_G0271942 | DDB0232429 | CDS | 1019381 | 552 | - | 0.293478 | |
arl8 | DDB_G0283525 | DDB0232431 | CDS | 729167 | 558 | + | 0.284946 | |
arrA | DDB_G0282457 | DDB0232430 | CDS | 5783278 | 594 | - | 0.210438 | |
arrB | DDB_G0274445 | DDB0232429 | CDS | 4578208 | 540 | - | 0.244444 | |
arrC | DDB_G0271792 | DDB0232429 | CDS | 729816 | 603 | + | 0.26534 | |
arrD | DDB_G0289069 | DDB0232432 | CDS | 2306273 | 651 | + | 0.265745 | |
arrE | DDB_G0280479 | DDB0232430 | CDS | 3427999 | 594 | - | 0.287879 | |
arrF | DDB_G0289435 | DDB0232432 | CDS | 2746763 | 573 | + | 0.273997 | |
arrH | DDB_G0288015 | bCommunity annotations: b The arrH arrJ and arrK genes and no others of the arrX group are strongly (6 to 30-fold) overexpressed in a Dictyostelium strain in which the retinoblastoma-like gene rblA has been disrupted. Most of the genes overexpressed in this strain are associated with cell cycle progression and this suggests that the main role of the corresponding proteins is in S-phase or mitosis. Human Arf1 has been reported to be essential for Golgi complex fragmentation during mitosis (Tang et al JBC 283 6085-94 (2008) Xiang et al JBC 282 21829-37 (2007). It thus seems possible that ArrH ArrJ and ArrK are involved in this process in Dicty. Harry MacWilliams September 2009brbr We have found very similar results including human C. elegans and D. melanogaster sequences in the set of proteins used for the tree. See Weeks G Gaudet P and Insall RH. (2005) The small GTPase superfamily. in Dictyostelium Genomics. Horizon Bioscience. Pascale Gaudet October 2009br | DDB0232432 | CDS | 977719 | 570 | + | 0.282456 |
arrI_ps | DDB_G0280687 | putative pseudogene ADP-ribosylation factor family protein | DDB0232430 | CDS | 3629662 | 234 | + | 0.286325 |
arrJ | DDB_G0280621 | DDB0232430 | CDS | 3577717 | 567 | + | 0.282187 | |
arrK | DDB_G0280633 | DDB0232430 | CDS | 3586248 | 567 | + | 0.280423 | |
arrL | DDB_G0278057 | DDB0232430 | CDS | 206243 | 588 | + | 0.267007 | |
ascc3 | DDB_G0290389 | ortholog of human ASCC3 part of the TRIP4 complex that enhances activation of NF-kappa-B SRF and AP1 | DDB0232432 | CDS | 4020336 | 6588 | - | 0.307377 |
ascc3l | DDB_G0270042 | putative RNA helicase involved in the second step of RNA splicing ortholog of human ASCC3L1 and yeast BRR2 | DDB0232428 | CDS | 4082408 | 6714 | - | 0.320077 |
atg1 | DDB_G0292390 | Dictyostelium homolog of yeast atg1 belongs to the ULK (Unc-51-like kinase) family of kinases required for macroautophagy | DDB0232433 | CDS | 1694801 | 2007 | + | 0.255605 |
aurK | DDB_G0279343 | putative protein serinethreonine kinase Aur family associates with the mitotic spindle and plays a key role in mitosis the single Dictyostelium aurora kinase has properties of both aurora A and B kinases in other organisms | DDB0232430 | CDS | 1959552 | 1155 | - | 0.30303 |
bub2 | DDB_G0268794 | putative ortholog of S. cerevisiae BUB2 a mitotic checkpoint protein | DDB0232428 | CDS | 2123318 | 1101 | + | 0.269755 |
bub3 | DDB_G0292134 | ortholog of BUB3 a mitotic checkpoint protein in human a kinetochore protein that interacts with BUB1 | DDB0232433 | CDS | 1247461 | 996 | - | 0.346386 |
cak1-1 | DDB_G0273059 | 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 | DDB0232429 | CDS | 2688821 | 1281 | + | 0.320062 |
cak1-2 | DDB_G0273737 | 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 | DDB0232429 | CDS | 3341355 | 1281 | - | 0.320062 |
calA | DDB_G0279407 | calcium-dependent regulatory protein involved in cytokinesis regulated by cytosolic Ca2 fluxes allowing differential binding to target CaM binding proteins (CaMBPs) binds several proteins among them nuclear NumA and Cdk5 | DDB0232430 | CDS | 2244074 | 459 | - | 0.35512 |
calB | DDB_G0269104 | DDB0232428 | CDS | 2981116 | 450 | + | 0.275556 | |
casK | DDB_G0276885 | CK2 family protein kinase a ubiquitious serinethreonine protein kinase in eukaryotic cells that phosphorylates many protein substrates in addition to casein | DDB0232429 | CDS | 7370887 | 1014 | + | 0.310651 |
cbpL | DDB_G0288785 | putative Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232432 | CDS | 1964055 | 576 | + | 0.258681 |
cbpM | DDB_G0286371 | putative Ca2-binding protein with 4 putative EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232431 | CDS | 4370399 | 552 | - | 0.277174 |
cdc20 | DDB_G0285601 | ortholog of CDC20 a cell-cycle regulated activator of anaphase-promoting complexcyclosome (APCC) which is required for metaphaseanaphase transition directs ubiquitination of mitotic cyclins | DDB0232431 | CDS | 3433247 | 1500 | + | 0.346 |
cdc40 | DDB_G0289501 | conserved splicing factor S. cerevisiae cdc40 is important for catalytic step II of pre-mRNA splicing and plays a role in cell cycle progression | DDB0232432 | CDS | 2860682 | 1788 | + | 0.319351 |
cdc7 | DDB_G0292152 | similar to S. cerevisiae cell division control protein 7 (CDC7) a serinethreonine kinase required for mitosis and meiosis | DDB0232433 | CDS | 1294776 | 3186 | + | 0.23666 |
cdh1 | DDB_G0287259 | ortholog of FZR1CDH1 that regulates the ubiquitin ligase activity of the anaphase promoting complexcyclosome (APCC) which directs ubiquitination of cyclins resulting in mitotic exit related to cdc20 | DDB0232432 | CDS | 54882 | 2265 | - | 0.284768 |
cdk1 | DDB_G0272813 | similar to CDK1 and CDK2 cell cycle CAK (CDK-activating kinase) kinases predicted to activate SG2 cyclins cyclin A B and D | DDB0232429 | CDS | 2216835 | 891 | + | 0.331089 |
cdk10 | DDB_G0268480 | putative cell division cycle 2 (CDC2)-like protein kinase has similarity to PITSLRE proteins and other cyclin-dependent kinase 2 kinases | DDB0232428 | CDS | 294048 | 1101 | - | 0.256131 |
cdk11 | DDB_G0283279 | very similar to human CDL1 (PITSLRE serinethreonine-protein kinase CDC2L1) which appears to play multiple roles in cell cycle progression cytokinesis and apoptosis predicted to interact with | DDB0232431 | CDS | 446640 | 1077 | - | 0.338904 |
cdk5 | DDB_G0288677 | CMGC group protein kinase highly similar to mammalian cdk5 localizes to the nucleus and shuttles to the cytoplasm during late mitosis binds calmodulin PsaA | DDB0232432 | CDS | 1885785 | 879 | + | 0.302617 |
cdk7 | DDB_G0285417 | putative ortholog of CDK7 and CTK1 which phosphorylates the C-terminal repeated domain of the RNA polymerase II large subunit predicted to be activated by | DDB0232431 | CDS | 3627427 | 1083 | + | 0.307479 |
cdk8 | DDB_G0267442 | controls RNA polymerase II activity by phosphorylating the carboxy terminal domain (CTD) of the largest subunit predicted to interact with | DDB0232428 | CDS | 1582311 | 1143 | - | 0.314961 |
cdk9-1 | DDB_G0273207 | 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 | DDB0232429 | CDS | 2708039 | 2085 | + | 0.282974 |
cdk9-2 | DDB_G0273721 | 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 | DDB0232429 | CDS | 3321422 | 2085 | - | 0.282974 |
celA | DDB_G0271134 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | DDB0232429 | CDS | 58680 | 2118 | - | 0.36119 |
cenA | DDB_G0288427 | similar to human Centrin 2 EF-hand protein localizes to the centromer from which it dissociates during mitosis | DDB0232432 | CDS | 1525659 | 456 | + | 0.245614 |
cenB | DDB_G0279151 | centrin required for nuclear and centrosome stability localizes to the nucleus in interphase but not during mitosis and is involved in the centrosome cycle | DDB0232430 | CDS | 1697579 | 453 | - | 0.258278 |
chid1 | DDB_G0290417 | DDB0232432 | CDS | 4060970 | 1158 | - | 0.244387 | |
ciao1 | DDB_G0269728 | 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 | DDB0232428 | CDS | 3427650 | 1002 | + | 0.284431 |
clkA | DDB_G0281179 | similar to cyclin-like kinases (CLK) putative dual specifity kinase | DDB0232430 | CDS | 4167312 | 2799 | + | 0.215077 |
cln3 | DDB_G0291157 | ortholog of Cln3 responsible for Batten's disease a juvenile neurological disorder | DDB0232432 | CDS | 5060161 | 1266 | - | 0.313586 |
cnbA | DDB_G0267446 | regulatory subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase contains an EF-hand calcium binding motif | DDB0232428 | CDS | 816934 | 1041 | - | 0.26513 |
cnbB | DDB_G0285999 | contains 3 EF-hands similar to calcineurin B (cnbA) the regulatory subunit of the Ca2calmodulin-dependent serinethreonine protein phosphatase | DDB0232431 | CDS | 3918232 | 552 | + | 0.269928 |
cnrF | DDB_G0276119 | DDB0232429 | CDS | 6259472 | 2961 | + | 0.280986 | |
cnrM | DDB_G0288307 | DDB0232432 | CDS | 1376942 | 4920 | - | 0.293089 | |
comB | DDB_G0281825 | DDB0232430 | CDS | 5112758 | 6324 | - | 0.278937 | |
comD | DDB_G0283345 | similar to drug resistance transporters contains 14 transmembrane domains | DDB0232431 | CDS | 539820 | 3528 | + | 0.291667 |
copA | DDB_G0267982 | contains five WD40 repeats alpha subunit of the coatomer complex essential for the secretory pathway | DDB0232428 | CDS | 1232234 | 3666 | + | 0.331969 |
copB2 | DDB_G0278285 | contains six WD40 repeats beta prime subunit of the coatomer complex essential for the secretory pathway | DDB0232430 | CDS | 618891 | 3018 | - | 0.333996 |
copE | DDB_G0267950 | DDB0232428 | CDS | 1172814 | 903 | + | 0.272425 | |
corA | DDB_G0267382 | actin binding protein regulating actin nucleation involved in cytokinesis and cell motility | DDB0232428 | CDS | 943374 | 1338 | - | 0.400598 |
corB | DDB_G0269388 | 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 | DDB0232428 | CDS | 2678066 | 2889 | + | 0.32918 |
cpras1 | DDB_G0277381 | DDB0232429 | CDS | 7946446 | 2529 | - | 0.316726 | |
cpras2 | DDB_G0293376 | contains a circularly permuted GTPase domain with the conserved motifs G1-G2 lying downstream of the G3-G4-G5 motifs large protein of unknown function whose domain composition is not conserved a closely related ortholog is found in D. purpureum | DDB0232433 | CDS | 2805934 | 11802 | - | 0.295543 |
cpsf4 | DDB_G0270148 | ortholog of the human CPSF4 and yeast YTH1 the 30 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs human CPSF4 binds RNA polymers with a preference for poly(U) | DDB0232428 | CDS | 4311820 | 1119 | + | 0.324397 |
csn5 | DDB_G0284597 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | DDB0232431 | CDS | 2205667 | 999 | - | 0.304304 |
cstf1 | DDB_G0278769 | component of the CSTF complex which in mammalian is required for polyadenylation and 3'-end cleavage of pre-mRNAs | DDB0232430 | CDS | 1141749 | 1521 | + | 0.302433 |
cstf2 | DDB_G0280529 | component of the CSTF complex which in mammalian is required for polyadenylation and 3'-end cleavage of pre-mRNAs | DDB0232430 | CDS | 3461453 | 1626 | + | 0.305043 |
ctbsA | DDB_G0274233 | 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 | DDB0232429 | CDS | 4699494 | 1158 | + | 0.310881 |
ctbsB | DDB_G0276795 | 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 | DDB0232429 | CDS | 7316822 | 1122 | + | 0.294118 |
ctr9 | DDB_G0277841 | component of the conserved Paf1 complex a multifunctional complex involved in histone methylation and plays a role in RNA elongation and processing REMI mutant forms aberrant fruiting bodies see | DDB0232430 | CDS | 746082 | 3321 | + | 0.308341 |
dcp2 | DDB_G0283315 | ortholog of the conserved mRNA-decapping enzyme 2 necessary for the degradation of mRNAs | DDB0232431 | CDS | 515744 | 1863 | + | 0.31723 |
dcp2_ps | DDB_G0283809 | putative pseudogene similar to | DDB0232431 | CDS | 1130346 | 258 | - | 0.325581 |
dduA | DDB_G0282559 | downregulated in the uninfected | DDB0232430 | CDS | 5934889 | 1296 | - | 0.278549 |
dgkA | DDB_G0277223 | dgkA corresponds to a previously reported myosin II heavy chain kinase designated myosin heavy chain-protein kinase C (MHC-PKC) recent research shows the protein does not contain a protein kinase domain but a diacylglycerol kinase domain | DDB0232429 | CDS | 7741603 | 2664 | + | 0.28003 |
dhkG | DDB_G0284045 | DDB0232431 | CDS | 1509861 | 10299 | - | 0.239441 | |
dicA | DDB_G0280849 | DDB0232430 | CDS | 3856978 | 1965 | - | 0.337405 | |
dmtA | DDB_G0289329 | DDB0232432 | CDS | 2694067 | 1092 | - | 0.271978 | |
drg1 | DDB_G0289317 | ortholog of human DRG1 which may be involved in cell proliferation differentiation and death highly conserved in eukaryotes belongs to the GTP1OBG family | DDB0232432 | CDS | 2634493 | 1113 | - | 0.337826 |
drg2 | DDB_G0279451 | ortholog of human DRG2 which may be involved in cell proliferation differentiation and death highly conserved in eukaryotes belongs to the GTP1OBG family | DDB0232430 | CDS | 2066556 | 1095 | - | 0.305023 |
drkA | DDB_G0289791 | DDB0232432 | CDS | 3144874 | 1929 | + | 0.276827 | |
drkB | DDB_G0289709 | DDB0232432 | CDS | 3147575 | 2073 | + | 0.2904 | |
drkC | DDB_G0281899 | tyrosine kinase member of the TKL (tyrosine kinase-like) group and the DRK (Dictyostelium receptor-like kinase) subfamily involved in phagocytosis and late phagosomelysosome fusion enriched in S cells in slugs | DDB0232430 | CDS | 5088116 | 2250 | - | 0.305778 |
drkD | DDB_G0281557 | member of the TKL (tyrosine kinase-like) group and the DRK (Dictyostelium receptor-like kinase) subfamily contains a leucine-rich repeat (LRR) region | DDB0232430 | CDS | 4777368 | 3867 | + | 0.334885 |
dst1 | DDB_G0274593 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232429 | CDS | 3862026 | 2214 | + | 0.289521 |
dst2 | DDB_G0267730 | putative protein serinethreonine kinase the kinase domain is similar to mitogen-activated protein kinases and other STE20-like kinases stress-responsive kinase | DDB0232428 | CDS | 719427 | 3429 | + | 0.33275 |
dst3 | DDB_G0291267 | putative protein serinethreonine kinase the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232433 | CDS | 35064 | 1689 | - | 0.351095 |
dst4 | DDB_G0288071 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232432 | CDS | 1048762 | 1458 | - | 0.325789 |
dupA | DDB_G0277071 | contains both a kinase domain and a phosphatase domain similar to MAP kinase phosphatase in plants and dual-specificty phosphatase 19 in mammals regulates the MAP Kinase response to Legionella pneumophila infection in Dictyostelium | DDB0232429 | CDS | 7439874 | 7365 | - | 0.295995 |
dymA | DDB_G0277849 | DDB0232430 | CDS | 252381 | 2562 | - | 0.330211 | |
dymB | DDB_G0277851 | DDB0232430 | CDS | 1081009 | 2763 | - | 0.279045 | |
dynE | DDB_G0278579 | DDB0232430 | CDS | 1102831 | 597 | + | 0.269682 | |
dyrk1 | DDB_G0277485 | DDB0232429 | CDS | 7981156 | 2511 | + | 0.249303 | |
dyrk2 | DDB_G0293750 | DDB0232433 | CDS | 3272270 | 2748 | + | 0.306405 | |
eIF2a | DDB_G0284267 | EIF2A ortholog the eukaryotic initiation factor 2A that binds Met-tRNA | DDB0232431 | CDS | 1799493 | 1827 | - | 0.363437 |
egeA | DDB_G0272002 | DDB0232429 | CDS | 1164190 | 765 | - | 0.300654 | |
egeB | DDB_G0269164 | highly similar to EgeA required for aggregation | DDB0232428 | CDS | 4173872 | 1278 | + | 0.309859 |
eif3B | DDB_G0283597 | EIF3B ortholog the eukaryotic initiation factor eta subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232431 | CDS | 847464 | 2013 | + | 0.350224 |
eif3I | DDB_G0285683 | EIF3I ortholog the eukaryotic initiation factor beta subunit In human binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA is composed of at least 12 different subunits | DDB0232431 | CDS | 3586013 | 996 | - | 0.348394 |
elmoD | DDB_G0280943 | DDB0232430 | CDS | 3852474 | 3804 | + | 0.253943 | |
elof1 | DDB_G0287203 | ortholog of the conserved elongation factor 1 a transcription elongation factor that contains a conserved zinc finger domain implicated in chromatin structure maintenance in actively transcribed regions in S. cerevisiae | DDB0232431 | CDS | 5404659 | 243 | - | 0.366255 |
elp2 | DDB_G0275651 | similar to S. cerevisiae ELP2 subunit of the RNA polymerase II elongator complex | DDB0232429 | CDS | 5847867 | 2706 | - | 0.318182 |
eral1 | DDB_G0288609 | DDB0232432 | CDS | 1740020 | 1197 | - | 0.3066 | |
ercc8 | DDB_G0276481 | ortholog of S. cerevisiae RAD26 and H. sapiens ERCC8 (CSA) involved in Cockayne syndrome | DDB0232429 | CDS | 6778627 | 1542 | + | 0.284695 |
eriA | DDB_G0283113 | similar to C. elegans eri-1 RNA exonuclease that acts as a negative regulator of RNA interference (RNAi) contains one exonuclease domainbrbr bCommunity annotation:b EriA codes for a multifunctional RNA exonuclease which has been identified with negative regulation of RNAi and in processing the 5.8s ribosomal RNA. The gene is nearly 8-fold overexpressed in a Dicty strain in which the retinoblastoma-like gene rblA is disrupted. Other genes overexpressed in this strain include virtually all those with unique or major functions in S-phase or mitosis. Neither RNAi nor ribosomal processing obviously fits into this class. However it has recently been shown in mammalian cells that eriA under the pseudonym 3'hExo stably associates with histone pre-mRNAs and participates in a complex that determines the site of their cleavage (see Yang et al Mol Cell Biol 29 4045-4056 (2009). Another protein in this complex is the histone stem-loop binding protein DDB_G0277383 which is threefold upregulated in t | DDB0232431 | CDS | 263707 | 663 | + | 0.273002 |
erkA | DDB_G0286353 | DDB0232431 | CDS | 4355028 | 1590 | + | 0.303774 | |
erkB | DDB_G0283903 | DDB0232431 | CDS | 1385123 | 1110 | - | 0.323423 | |
esd | DDB_G0283037 | very similar to human ESD and to S. cerevisiae S-formylglutathione hydrolase (YJL068C) which seems to be involved in formaldehyde detoxification | DDB0232431 | CDS | 192516 | 858 | + | 0.264569 |
exoc5 | DDB_G0287881 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | DDB0232432 | CDS | 652393 | 2937 | - | 0.290092 |
fbxA | DDB_G0276887 | F-box and WD40 domains containing protein part of a complex that targets proteins for ubiquination has the same domain composition as | DDB0232429 | CDS | 7333559 | 3744 | + | 0.311165 |
fcf1 | DDB_G0267606 | DDB0232428 | CDS | 408722 | 585 | + | 0.261538 | |
fdxr | DDB_G0287353 | catlyzes the reaction: reduced ferredoxin NADP oxidized ferredoxin NADPH H | DDB0232432 | CDS | 169845 | 1548 | - | 0.26292 |
fhit | DDB_G0274257 | 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 | DDB0232429 | CDS | 4124527 | 450 | - | 0.311111 |
fhkA | DDB_G0293656 | 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 | DDB0232433 | CDS | 3219230 | 1782 | - | 0.231201 |
fhkB | DDB_G0280599 | CAMK group RAD53 family protein kinase the protein kinase domain is similar to those of mammalian cell cycle checkpoint kinases chk2 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteins | DDB0232430 | CDS | 3548058 | 3429 | - | 0.26305 |
fhkC | DDB_G0281567 | CAMK group RAD53 family protein kinase similar to mammalian cell cycle checkpoint kinases chk2 and yeast RAD53 contains a forkhead-associated (FHA) domain a phosphopeptide recognition domain found in many regulatory proteins | DDB0232430 | CDS | 4871788 | 1788 | + | 0.291387 |
fhkD | DDB_G0285963 | 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 proteins | DDB0232431 | CDS | 3876403 | 2250 | - | 0.286667 |
fhkE | DDB_G0280321 | 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 proteins | DDB0232430 | CDS | 3257414 | 2139 | + | 0.257597 |
flpA | DDB_G0286549 | DDB0232431 | CDS | 4784977 | 2148 | + | 0.268622 | |
fnkA | DDB_G0275561 | protein kinase STE group | DDB0232429 | CDS | 5624593 | 2382 | + | 0.283375 |
fnkB | DDB_G0267934 | DDB0232428 | CDS | 1147906 | 1593 | - | 0.251726 | |
fnkE | DDB_G0275879 | protein kinase domain similar to those of the mitogen-activated protein kinases which belong to the STE20 family contains two protein kinase domains one of which is predicted to be inactive contains several FNIP repeats | DDB0232429 | CDS | 5838829 | 3966 | + | 0.2824 |
fnkF_ps | DDB_G0275183 | putative pseudogene STEFNIP protein kinase family | DDB0232429 | CDS | 5290527 | 2628 | - | 0.270548 |
fray1 | DDB_G0278863 | kinase domain similar to 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 | DDB0232430 | CDS | 1298188 | 1725 | - | 0.338551 |
fray2 | DDB_G0276577 | 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 | DDB0232429 | CDS | 6994954 | 3087 | - | 0.339164 |
fslB | DDB_G0270730 | similar to the G-protein coupled receptors contains 7 putative transmembrane domains and a potential signal sequence | DDB0232428 | CDS | 4235323 | 1929 | - | 0.258683 |
fuk | DDB_G0269678 | catalyzes the reaction: ATP L-fucose ADP beta-L-fucose 1-phosphate | DDB0232428 | CDS | 3301231 | 4215 | - | 0.288493 |
gacX | DDB_G0288205 | DDB0232432 | CDS | 1235608 | 1692 | + | 0.309693 | |
gbpC | DDB_G0291079 | member of the TKL (tyrosine kinase-like) group and ROCO family of protein kinases belongs to the LRRK family of protein kinases contains LRR Roc COR RasGEF protein kinase DEP cyclic nucleotide-binding and GRAM domains involved in cGMP-mediated chemotaxis catalyzes GDP to GTP exchange on its own Roc domain translocates from cytoplasm to cell cortex after cAMP stimulation GRAM domain binds directly to plasma membrane | DDB0232432 | CDS | 4959991 | 7896 | + | 0.333967 |
gdap2 | DDB_G0284349 | ortholog of the human GDAP2 protein contains an Appr-1-p processing domain and a C-terminal cellular retinaldehyde-bindingtriple function domain | DDB0232431 | CDS | 1866926 | 1707 | - | 0.246632 |
gdt2 | DDB_G0270666 | member of the TKL (tyrosine kinase-like) group and the GDT family putative transmembrane protein | DDB0232428 | CDS | 3713353 | 4914 | - | 0.252747 |
gdt3_ps | DDB_G0285891 | putative pseudogene member of the TKL (tyrosine kinase-like) group and the GDT family belongs to the MLK protein kinase family | DDB0232431 | CDS | 3781232 | 5880 | - | 0.234014 |
gdt4 | DDB_G0270550 | member of the TKL (tyrosine kinase-like) group and the GDT family putative transmembrane protein | DDB0232428 | CDS | 2926042 | 4863 | + | 0.265474 |
gdt6 | DDB_G0270544 | member of the TKL (tyrosine kinase-like) group and the GDT family unlikely to function as a kinase as it does not contain a catalytic aspartate putative transmembrane protein | DDB0232428 | CDS | 2913781 | 4359 | + | 0.274145 |
gdt8 | DDB_G0270668 | member of the TKL (tyrosine kinase-like) group and the GDT family putative transmembrane protein | DDB0232428 | CDS | 3723386 | 3981 | - | 0.283848 |
gdt9 | DDB_G0278879 | DDB0232430 | CDS | 1327589 | 4734 | + | 0.274398 | |
gefX | DDB_G0269298 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family contains RasGEF nucleotide exchange factor domain | DDB0232428 | CDS | 2476607 | 2883 | - | 0.312522 |
gemA | DDB_G0267830 | simlar to M. musculus mitochondrial Rho1 and S. cerevisiae GEM1 a conserved tail-anchored outer mitochondrial membrane GTPase contains two GTP-binding domains two EF hand domains and a C-terminal transmembrane domain | DDB0232428 | CDS | 929880 | 1977 | - | 0.265048 |
gemin5 | DDB_G0288425 | ortholog of Gemin 5 a component of Cajal bodies (CBs) and Gems nuclear organelles responsible for spliceosomal small nuclear ribonucleoprotein (snRNP) biogenesis | DDB0232432 | CDS | 1517710 | 3831 | + | 0.257113 |
gerE | DDB_G0286551 | contains numerous TETP repeats expressed specifically in spores | DDB0232431 | CDS | 4754201 | 1374 | - | 0.306405 |
glkA | DDB_G0270218 | putative protein serinethreonine kinase GSK family member of the CMGC kinase group similar to Drosophila shaggy and other glycogen synthase kinases | DDB0232428 | CDS | 4429657 | 1422 | + | 0.23699 |
glnA3 | DDB_G0279591 | catalyzes the reaction ATP L-glutamate ammonia ADP phosphate L-glutamine | DDB0232430 | CDS | 2109355 | 2208 | - | 0.352355 |
gloB1 | DDB_G0285717 | catalyzes the reaction S-lactoyl-glutathione H2O reduced glutathione D-lactate | DDB0232431 | CDS | 3631211 | 807 | - | 0.275093 |
gloB2 | DDB_G0291482 | catalyzes the reaction S-lactoyl-glutathione H2O reduced glutathione D-lactate | DDB0232433 | CDS | 411372 | 879 | + | 0.335609 |
gna1 | DDB_G0279475 | gna bGblucosamibNbe-6-phosphate bAbcetyltransferase | DDB0232430 | CDS | 2113626 | 474 | - | 0.242616 |
gnb1l | DDB_G0289181 | ortholog of the mammalian GNB1L contains several WD-40 repeats | DDB0232432 | CDS | 2444140 | 1080 | + | 0.234259 |
gnl1 | DDB_G0285371 | DDB0232431 | CDS | 3179167 | 2541 | - | 0.283747 | |
gnl3 | DDB_G0287147 | similar to the conserved guanine nucleotide-binding protein-like 3 also called nucleostemin in mammals a protein in the nucleolus of most stem cells and many tumor cells involved in cell-cycle progression | DDB0232431 | CDS | 5379967 | 1848 | - | 0.318182 |
gpbA | DDB_G0277143 | DDB0232429 | CDS | 7812708 | 1044 | - | 0.3659 | |
gpbB | DDB_G0275045 | DDB0232429 | CDS | 5266629 | 990 | + | 0.419192 | |
gpn1 | DDB_G0293220 | DDB0232433 | CDS | 2684279 | 1191 | + | 0.309824 | |
gpn2 | DDB_G0281787 | DDB0232430 | CDS | 4982225 | 948 | + | 0.256329 | |
gpn3 | DDB_G0285197 | DDB0232431 | CDS | 2952647 | 858 | + | 0.29021 | |
gppA | DDB_G0267398 | DDB0232428 | CDS | 1607815 | 1635 | - | 0.285015 | |
grlA | DDB_G0271684 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature plays a role in sporulation | DDB0232429 | CDS | 779738 | 2397 | - | 0.278264 |
grlB | DDB_G0271686 | DDB0232429 | CDS | 776318 | 2268 | - | 0.283069 | |
grlC | DDB_G0282461 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232430 | CDS | 5789478 | 2403 | + | 0.27965 |
grlD | DDB_G0286895 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232431 | CDS | 5037852 | 2376 | + | 0.280724 |
grlF | DDB_G0282175 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232430 | CDS | 5487367 | 2313 | + | 0.272806 |
grlG | DDB_G0272244 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232429 | CDS | 1741474 | 2319 | - | 0.292799 |
grlH | DDB_G0282459 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232430 | CDS | 5785479 | 2295 | + | 0.300218 |
grlJ | DDB_G0272150 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232429 | CDS | 1600728 | 2352 | + | 0.278061 |
grlK | DDB_G0269386 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232428 | CDS | 2668447 | 2115 | - | 0.327187 |
grlL | DDB_G0281211 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232430 | CDS | 4210774 | 2127 | + | 0.316408 |
grlM | DDB_G0286643 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232431 | CDS | 4778203 | 2250 | + | 0.317333 |
grlO | DDB_G0271688 | metabotropic glutamate receptors are coupled to G-proteins and stimulate the inositol phosphateCa2 intracellular signaling pathway distinctive '7TM' signature | DDB0232429 | CDS | 773062 | 2460 | - | 0.239837 |
grwd1 | DDB_G0291566 | ortholog of the mammalian GRWD1 contains several WD-40 repeats | DDB0232433 | CDS | 556339 | 1449 | - | 0.354727 |
gskA | DDB_G0272110 | 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 | DDB0232429 | CDS | 1334436 | 1404 | - | 0.324786 |
gtf3C3 | DDB_G0278321 | DDB0232430 | CDS | 689224 | 2994 | + | 0.289579 | |
gtpA | DDB_G0275441 | DDB0232429 | CDS | 5822886 | 1350 | - | 0.347407 | |
gtpbp1 | DDB_G0292538 | ortholog of the mammalian GTPBP1 and very similar to GTPBP2 contains a translation elongation factor EFTuEF1A domain 2 and C-terminal domain | DDB0232433 | CDS | 1635942 | 2034 | + | 0.357915 |
gtpbp3 | DDB_G0270228 | ortholog of the mammalian GTPBP3 and S. cerevisiae MSS1 GTPases responsible for the 5-carboxymethylaminomethyl modification of the wobble uridine base in mitochondrial tRNAs | DDB0232428 | CDS | 4442110 | 1539 | + | 0.250162 |
gtpbp5 | DDB_G0277801 | similar to human GTPBP5 GTP1OBG family protein involved in the ribosome maturation process | DDB0232429 | CDS | 8429520 | 1887 | - | 0.254902 |
guaD | DDB_G0277743 | catalyzes the reaction guanine Hsub2subO xanthine NHsub3sub | DDB0232429 | CDS | 8417392 | 1353 | + | 0.311899 |
gxcA | DDB_G0277987 | Rac guanyl-nucleotide exchange factor involved in chemotaxis and development there are two transcripts for this gene that seem to be differentially expressed during development with the shorter isoform expressed in vegetative cells and the longer isoform during development | DDB0232430 | CDS | 114291 | 6117 | - | 0.297695 |
hddc2 | DDB_G0290795 | conserved protein HD domains occur in a superfamily of enzymes with a predicted or known phosphohydrolase activity | DDB0232432 | CDS | 4613721 | 573 | - | 0.279232 |
hira | DDB_G0276423 | ortholog of yeast HIR1 a transcriptional corepressor involved in the cell cycle-regulated transcription of histone H2A H2B H3 and H4 genes | DDB0232429 | CDS | 6881531 | 3345 | - | 0.30852 |
hpd | DDB_G0277511 | catalyzes the reaction 4-hydroxyphenylpyruvate Osub2sub homogentisate COsub2sub | DDB0232429 | CDS | 8032217 | 2214 | + | 0.342367 |
hpdl-1 | DDB_G0273429 | catalyzes the reaction 4-hydroxyphenylpyruvate Osub2sub homogentisate COsub2sub there is a second copy of this gene | DDB0232429 | CDS | 2988290 | 1485 | + | 0.227609 |
hpdl-2 | DDB_G0273513 | catalyzes the reaction 4-hydroxyphenylpyruvate Osub2sub homogentisate COsub2sub there is a second copy of this gene | DDB0232429 | CDS | 3041831 | 1485 | - | 0.227609 |
iksA | DDB_G0283109 | similar to fungal kinases contains an IQ calmodulin-binding region | DDB0232431 | CDS | 257953 | 2940 | + | 0.272449 |
iliQ | DDB_G0292926 | contains a large ankyrin repeat region induced by Legionella pneumophila infection | DDB0232433 | CDS | 2280235 | 2490 | + | 0.214458 |
ireA | DDB_G0267650 | 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 | DDB0232428 | CDS | 495110 | 2955 | + | 0.237902 |
irlA | DDB_G0272987 | DDB0232429 | CDS | 2020830 | 4296 | + | 0.26513 | |
irlB-1 | DDB_G0273333 | 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 | DDB0232429 | CDS | 2539802 | 4347 | - | 0.216931 |
irlB-2 | DDB_G0273857 | 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 | DDB0232429 | CDS | 3487559 | 4347 | + | 0.216931 |
irlC | DDB_G0270894 | the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy contains a SWIM Zn-finger domain | DDB0232428 | CDS | 3195968 | 4335 | + | 0.231834 |
irlD | DDB_G0269632 | DDB0232428 | CDS | 3190841 | 4518 | + | 0.261399 | |
irlE | DDB_G0288803 | putative protein serinethreonine kinase the kinase domain is similar to yeast IRE1 kinase required for inositol phototrophy | DDB0232432 | CDS | 1985593 | 4053 | + | 0.237602 |
kinX | DDB_G0283391 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family similar to LIM kinases which regulate actin dynamics | DDB0232431 | CDS | 749416 | 3285 | + | 0.312329 |
kinY | DDB_G0289661 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family similar to LIM kinases which regulate actin dynamics | DDB0232432 | CDS | 3255902 | 1740 | + | 0.251149 |
krsA | DDB_G0284181 | putative protein serinethreonine kinase belongs to the protein kinase MST subfamily similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase involved in signal transduction and hyperosmotic response | DDB0232431 | CDS | 1697612 | 1386 | - | 0.313853 |
krsB | DDB_G0267978 | 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 | DDB0232428 | CDS | 1220851 | 3318 | + | 0.331826 |
ksrA-1 | DDB_G0272883 | catalyzes the reduction of sphinganine to 3-dehydrosphinganine in glycosphingolipid metabolism there is a second copy of this gene | DDB0232429 | CDS | 2361855 | 1005 | - | 0.311443 |
ksrA-2 | DDB_G0274015 | catalyzes the reduction of sphinganine to 3-dehydrosphinganine in glycosphingolipid metabolism there is a second copy of this gene | DDB0232429 | CDS | 3668724 | 1005 | + | 0.311443 |
kxcA | DDB_G0289859 | member of the TKL (tyrosine kinase-like) group and the LISK (LIM domain and testis-specific kinase) family contains calmodulin-binding RhoGEF and pleckstrin homology (PH) domains | DDB0232432 | CDS | 3309104 | 3936 | + | 0.256352 |
kxcB | DDB_G0293124 | kinase domain similar to those of stress-induced STK kinases contains a DH (Dbl homology) domain followed by a PH (pleckstrin homology) domain found in proteins shown to encode a GEF activity specific for Rho family members | DDB0232433 | CDS | 2557594 | 3378 | - | 0.301066 |
l2hgdh | DDB_G0267656 | ortholog of the H. sapiens L2HGDH which when defective causes L-2-hydroxyglutaric aciduria-a rare autosomal recessive disorder | DDB0232428 | CDS | 518710 | 1341 | + | 0.282625 |
ldhA | DDB_G0281101 | DDB0232430 | CDS | 4061672 | 1023 | - | 0.314761 | |
lip1 | DDB_G0268966 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | DDB0232428 | CDS | 2042126 | 1245 | + | 0.306827 |
lip5 | DDB_G0277723 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | DDB0232429 | CDS | 8375987 | 1809 | - | 0.317302 |
lis1 | DDB_G0288375 | dynein regulator associated with centrosomes and microtubules functionally interacts with dcx in cAMP signalling | DDB0232432 | CDS | 1452516 | 1260 | + | 0.35 |
lkb1 | DDB_G0279629 | CAMK group CAMKL family kinase protein kinase involved in regulating both development and the stress response | DDB0232430 | CDS | 2335074 | 1761 | - | 0.294719 |
lst8 | DDB_G0292592 | component of the TORC2 (Tor complex 2) with Tor Rip3 and PiaA that plays a role in regulation of adenylate cyclase (ACA) and protein kinase B (PKB) activation during aggregation | DDB0232433 | CDS | 1819608 | 915 | - | 0.338798 |
lvsA | DDB_G0269150 | DDB0232428 | CDS | 3119127 | 10860 | - | 0.304236 | |
lvsB | DDB_G0271504 | DDB0232429 | CDS | 668886 | 12357 | + | 0.254916 | |
lvsC | DDB_G0280971 | DDB0232430 | CDS | 4286715 | 7476 | + | 0.290931 | |
lvsE | DDB_G0282925 | DDB0232431 | CDS | 90982 | 6579 | + | 0.286518 | |
lvsF | DDB_G0284333 | similar to mammalian FAN human LYST and mouse Beige proteins | DDB0232431 | CDS | 1946519 | 3465 | - | 0.278788 |
lvsG | DDB_G0268088 | protein with a beigeBEACH domain a weak protein kinase domain and N-terminal WD40 repeats does not contain the consensus sequences required for kinase function | DDB0232428 | CDS | 1432947 | 6540 | - | 0.272018 |
mak16l | DDB_G0269642 | ortholog of S. cerevisiae MAK16 and mammalian RBM13 inyeast an essential nuclear protein constituent of 66S pre-ribosomal particles | DDB0232428 | CDS | 3206739 | 930 | + | 0.307527 |
mdn1 | DDB_G0295765 | 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. | DDB0232429 | CDS | 5627352 | 17703 | - | 0.282438 |
mecr | DDB_G0278095 | ortholog of the mammalian MECR and S. cerevisiae ETR1 a mitochondrial 2-enoyl thioester reductase that belongs to the zinc-containing alcohol dehydrogenase family | DDB0232430 | CDS | 262493 | 1053 | - | 0.358025 |
med31 | DDB_G0285221 | ortholog of the mediator of RNA polymerase II transcription subunit 31 the mediator complex functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery | DDB0232431 | CDS | 2996613 | 531 | - | 0.265537 |
mekA | DDB_G0269152 | 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 | DDB0232428 | CDS | 4015409 | 1983 | - | 0.252143 |
memo1 | DDB_G0284869 | ortholog of the H. sapiens MEMO1 a mediator of ErbB2-driven cell motility | DDB0232431 | CDS | 2629450 | 873 | - | 0.293242 |
mettl1 | DDB_G0276491 | ortholog of the conserved methyltransferase-like 1 (METTL1) which in H. sapiens forms a complex with WDR4 catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | DDB0232429 | CDS | 6855520 | 837 | + | 0.309438 |
mfeA | DDB_G0291247 | DDB0232433 | CDS | 383676 | 1326 | - | 0.390649 | |
mfsd1 | DDB_G0289201 | ortholog of the human MSFD1 also knon as SMAP-4 (Smooth Muscle cell-Associated Protein 4) contains 10 putative transmembrane domains and an additional potential signal peptide | DDB0232432 | CDS | 2461603 | 1521 | - | 0.336621 |
mgp2 | DDB_G0270024 | DDB0232428 | CDS | 4042887 | 2634 | - | 0.31549 | |
mhkA | DDB_G0291231 | myosin II heavy chain kinase is an atypical protein serinethreonine kinase in the Alpha kinase group phosphorylates the myosin II heavy chain and drives myosin II disassembly | DDB0232433 | CDS | 65139 | 3441 | + | 0.334496 |
mhkB | DDB_G0289115 | myosin heavy chain kinase an atypical protein serinethreonine kinase in the Alpha kinase group participates in the regulation of myosin II assembly into the cytoskeleton | DDB0232432 | CDS | 2375954 | 2199 | + | 0.289677 |
mhkC | DDB_G0290687 | myosin heavy chain kinase an atypical protein serinethreonine kinase in the Alpha kinase group drives the disassembly of myosin II filaments for efficient cytokinesis REMI mutant forms aberrant fruiting bodies see | DDB0232432 | CDS | 4426907 | 2343 | - | 0.349979 |
mhkD | DDB_G0282489 | belongs to the Atypical Alpha protein kinases highly similar to Dictyostelium mhkA contains N-terminal predicted coiled-coil domain contains C-terminal G-protein beta WD-40 repeats | DDB0232430 | CDS | 5835955 | 2826 | - | 0.279193 |
mkcA | DDB_G0285427 | similar to MAP cascade kinases belonging to the PAK sub-family of the STE20 serinethreonine kinases partial suppressor of tagB mutation | DDB0232431 | CDS | 3440715 | 2583 | - | 0.275648 |
mkcB | DDB_G0290723 | similar to Dictyostelium mkcA and other mitogen-activated protein kinases (Ste20PAK family) REMI mutant forms aberrant fruiting bodies see | DDB0232432 | CDS | 4499748 | 2145 | + | 0.332867 |
mkcC | DDB_G0287853 | kinase domain very similar to those of Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) | DDB0232432 | CDS | 826726 | 2676 | + | 0.342302 |
mkcD | DDB_G0277413 | similar to Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) | DDB0232429 | CDS | 7960057 | 1959 | + | 0.291986 |
mkcE | DDB_G0281649 | kinase domain similar to those of Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) | DDB0232430 | CDS | 4757942 | 2148 | + | 0.271881 |
mkcF | DDB_G0270102 | similar to Dictyostelium mkcA and mkcB and other mitogen-activated protein kinases (Ste20PAK family) contains one SH3 (src Homology-3) domain | DDB0232428 | CDS | 4222376 | 2034 | - | 0.319076 |
mkkA | DDB_G0283265 | developmentally regulated MEKK | DDB0232431 | CDS | 530684 | 3804 | + | 0.287066 |
mlcC | DDB_G0289563 | light chain that binds to the neck region of myoC contains two calcium-binding EF-hand motifs but does not bind calcium | DDB0232432 | CDS | 2954406 | 225 | - | 0.311111 |
mlcD | DDB_G0277917 | DDB0232430 | CDS | 607477 | 444 | + | 0.304054 | |
mlcE | DDB_G0277859 | component of actin-based molecular motor myosin II (conventional myosin) component | DDB0232430 | CDS | 76885 | 453 | + | 0.364238 |
mlcR | DDB_G0276077 | component of actin-based molecular motor myosin II (conventional myosin) component | DDB0232429 | CDS | 6426413 | 486 | + | 0.31893 |
mlkA | DDB_G0279925 | CAMK1 family protein kinase phosphorylates the myosin II regulatory light chain at S13 is not regulated by Ca2calmodulin | DDB0232430 | CDS | 2752719 | 888 | - | 0.317568 |
mnd1 | DDB_G0291750 | DDB0232433 | CDS | 686426 | 666 | - | 0.252252 | |
morg1 | DDB_G0289711 | ortholog of MORG1 a molecular scaffold protein that acts as a module in the assembly of a multicomponent scaffold for the ERK (extracellular signal-regulated kinase) pathway contains 7 WD40 repeats | DDB0232432 | CDS | 3150155 | 978 | - | 0.260736 |
mpdu1 | DDB_G0295677 | contains at least three transmembrane domains ortholog of mannose-P-dolichol utilization defect 1 protein MPDU1 | DDB0232428 | CDS | 3914310 | 708 | + | 0.286723 |
mppA1 | DDB_G0274809 | part of a complex that removes the transit peptide from the precursor form of proteins imported from the cytoplasm across the mitochondrial inner membrane consists of an alpha and a beta ( | DDB0232429 | CDS | 3949604 | 1965 | + | 0.279389 |
mppA2 | DDB_G0290997 | the mitochondrial processing peptidase removes the transit peptide from the precursor form of proteins imported from the cytoplasm across the mitochondrial inner membrane consists of an alpha and a beta ( | DDB0232432 | CDS | 4869039 | 1338 | - | 0.35725 |
mppB | DDB_G0288777 | removes the transit peptide from the precursor form of proteins imported from the cytoplasm across the mitochondrial inner membrane consists of an alpha ( | DDB0232432 | CDS | 1942737 | 1410 | - | 0.358156 |
mps1 | DDB_G0280995 | putative protein threoninetyrosine kinase similar to yeast and zebrafish mps1 (monopolar spindle) kinase a threoninetyrosine kinase | DDB0232430 | CDS | 3923506 | 2952 | + | 0.289295 |
mrd1 | DDB_G0284663 | ortholog of yeast MRD1 and mammalian RBM19 yeast MRD1 binds to the 35S pre-rRNA and the U3 snoRNA and is involved in pre-rRNA processing contains 5 RRM domains | DDB0232431 | CDS | 2315842 | 2688 | - | 0.278646 |
mrkA | DDB_G0292304 | CAMKL family protein kinase similar to MARK kinases SNF1 kinases and AMPK kinases contains 1 kinase-associated (KA1) domain and 1 UBA domain | DDB0232433 | CDS | 1433748 | 3183 | - | 0.286836 |
mrkB | DDB_G0285643 | CAMKL family protein kinase similar to SNF1 kinases MARK kinases and AMPK kinases | DDB0232431 | CDS | 3523048 | 2148 | - | 0.284916 |
mrkC | DDB_G0281895 | CAMKL family protein kinase similar to MARK kinases SNF1 kinases and AMPK kinases contains C-terminal kinase associated domain 1 | DDB0232430 | CDS | 5083659 | 2322 | + | 0.295866 |
mtpn | DDB_G0268038 | Ortholog of metazoan myotrophin (MTPN) which might be involved in cerebellar morphogenesis and cardiac hypertrophy contains 2 ankyrin repeats | DDB0232428 | CDS | 1344276 | 363 | + | 0.30854 |
naa20 | DDB_G0276345 | ortholog of the conserved catalytic subunit of the NatB N-terminal acetyltransferase (NAA20) which in yeast catalyzes the transfer of an acetyl group to the N-terminal residue of a protein that contains a Met-Glu Met-Asp Met-Asn or Met-Met N-terminus | DDB0232429 | CDS | 6679320 | 522 | + | 0.293103 |
naa50 | DDB_G0295721 | highly conserved protein ortholog of human NAA50 and yeast Mak3 | DDB0232430 | CDS | 183263 | 510 | - | 0.258824 |
nat10 | DDB_G0268868 | highly conserved protein ortholog of human NAT10 and yeast KRE33 predicted to localize to the nucleolus | DDB0232428 | CDS | 2281503 | 3174 | - | 0.290485 |
nat9 | DDB_G0272710 | DDB0232429 | CDS | 1909663 | 639 | - | 0.256651 | |
natA | DDB_G0275449 | DDB0232429 | CDS | 5856743 | 612 | - | 0.276144 | |
ncbp2 | DDB_G0287197 | ortholog of mammalian NCPB2 and yeast CBP2 small subunit of the heterodimeric cap binding complex involved in mediating U snRNA export from the nucleus | DDB0232431 | CDS | 5395993 | 705 | + | 0.299291 |
ncfA | DDB_G0288773 | homolog of the essential mammalian neutrophil cytosolic factor p67 that functions as an NADPH oxidase activator contains N-terminal TPR repeats and a C-terminal WW domain | DDB0232432 | CDS | 2003648 | 1815 | - | 0.32011 |
ncsA | DDB_G0275931 | contains four EF-hands belongs to the frequenins a family of myristoyl-switch calcium-binding proteins | DDB0232429 | CDS | 6088223 | 561 | - | 0.279857 |
ndrA | DDB_G0278457 | member of the AGC kinases NDR group localizes to centrosomes and to the spindle during prometaphase and is involved in phagocytosis | DDB0232430 | CDS | 907158 | 1593 | + | 0.344633 |
ndrB | DDB_G0288753 | member of the AGC kinase group similar to NDR protein kinases including yeast morphogenesis proteins ORB6 and CBK1 | DDB0232432 | CDS | 1909293 | 1629 | - | 0.324125 |
ndrC | DDB_G0284839 | member of the AGC kinase group NDR family related to mammalian LATS1 and LATS2 (LArge Tumor Suppressor homolog) kinases | DDB0232431 | CDS | 2493584 | 3939 | + | 0.307692 |
ndrD | DDB_G0289543 | member of the AGC kinase group NDR family related to mammalian LATS1 and LATS2 (LArge Tumor Suppressor homolog) kinases | DDB0232432 | CDS | 2920470 | 6339 | + | 0.255088 |
ndufaf5 | DDB_G0287769 | conserved mitochondrial complex I (CI) assembly factor which when mutated in human leads to mitochondrial disease in Dictyostelium mutations in the ndufaf5 gene cause defects in growth and development and autophagy is increased. | DDB0232432 | CDS | 675763 | 1311 | - | 0.254767 |
nek2 | DDB_G0270814 | protein serinethreonine kinase homologous to human Nek2 kinase involved in formation of microtubule-organizing centers (MTOCs) | DDB0232428 | CDS | 4847143 | 1257 | - | 0.258552 |
nek3 | DDB_G0275241 | putative protein serinethreonine kinase similar to vertebrate Nek kinases which are involved in regulation of mitosis not a human Nek3 homolog | DDB0232429 | CDS | 4983790 | 3372 | - | 0.269276 |
nek4 | DDB_G0289277 | similar to vertebrate Nek kinases which are involved in regulation of mitosis most similar to Nek4 | DDB0232432 | CDS | 2561379 | 1494 | - | 0.222222 |
nit1-1 | DDB_G0273457 | similar to mammalian NIT1 there is a second copy of this gene | DDB0232429 | CDS | 2982881 | 876 | - | 0.289954 |
nit1-2 | DDB_G0273519 | similar to mammalian NIT1 there is a second copy of this gene | DDB0232429 | CDS | 3048030 | 876 | + | 0.289954 |
nit2 | DDB_G0287939 | DDB0232432 | CDS | 872348 | 987 | - | 0.274569 | |
nle1 | DDB_G0295761 | DDB0232428 | CDS | 2884549 | 1524 | - | 0.330052 | |
nog1 | DDB_G0285465 | very similar to NOG1GTPBP4 GTPases which in S. cerevisiae associates with free 60S ribosomal subunits in the nucleolus and is involved in their biogenesis | DDB0232431 | CDS | 3263032 | 2025 | - | 0.342222 |
nol9 | DDB_G0277945 | ortholog of H. sapiens NOL9 similar to S. cerevisiae GRC3 believed to be involved in rRNA processing | DDB0232430 | CDS | 44863 | 2052 | + | 0.20614 |
npcA | DDB_G0269158 | one of two orthologs of NPC1 (with | DDB0232428 | CDS | 4862383 | 4029 | + | 0.336808 |
npcB | DDB_G0276657 | one of two orthologs of NPC1 (with | DDB0232429 | CDS | 7081017 | 4194 | - | 0.284454 |
nup43 | DDB_G0277955 | component of the nuclear pore complex contains four WD40 repeats | DDB0232430 | CDS | 60115 | 1254 | - | 0.22807 |
nup62 | DDB_G0274587 | ortholog of the 62 kDa nucleoporin an essential component of the nuclear pore complex | DDB0232429 | CDS | 3866512 | 2130 | + | 0.378404 |
omt1 | DDB_G0271590 | DDB0232429 | CDS | 696177 | 756 | + | 0.244709 | |
omt11 | DDB_G0293886 | similar to plant and bacterial O-methyltransferases expressed in pstO cells during culmination | DDB0232433 | CDS | 3424368 | 996 | + | 0.247992 |
omt12 | DDB_G0293888 | highly similar to plant and bacterial O-methyltransferases expressed in pstA cells | DDB0232433 | CDS | 3426309 | 1110 | + | 0.243243 |
omt3 | DDB_G0274197 | DDB0232429 | CDS | 4793181 | 1314 | - | 0.267884 | |
omt4 | DDB_G0275013 | DDB0232429 | CDS | 5190004 | 1017 | - | 0.26057 | |
omt5 | DDB_G0275499 | DDB0232429 | CDS | 6014515 | 693 | + | 0.307359 | |
omt6 | DDB_G0275501 | DDB0232429 | CDS | 6015883 | 696 | + | 0.304598 | |
omt7 | DDB_G0282591 | DDB0232430 | CDS | 5980059 | 1020 | - | 0.221569 | |
omt9 | DDB_G0289823 | DDB0232432 | CDS | 3290073 | 1074 | - | 0.286778 | |
pARTg | DDB_G0271766 | DDB0232429 | CDS | 860066 | 4857 | - | 0.224212 | |
pXi | DDB_G0289119 | CAMK group protein serinethreonine kinase | DDB0232432 | CDS | 2420542 | 2076 | - | 0.25289 |
pabpc1A | DDB_G0293558 | similar to mammalian PABPC1 involved in cytoplasmic regulatory processes of mRNA metabolism binding the poly(A) tail of mRNA | DDB0232433 | CDS | 3041877 | 1698 | + | 0.415783 |
pabpc1B | DDB_G0290745 | similar to mammalian PABPC1 involved in cytoplasmic regulatory processes of mRNA metabolism binding the poly(A) tail of mRNA contains an additional N-terminal H-rich domain | DDB0232432 | CDS | 4494408 | 2445 | + | 0.325153 |
pabpn1 | DDB_G0277371 | similar to human PABPN1 (PAB2) which is involved in the 3'-end formation of mRNA precursors (pre-mRNA) by the addition of a poly(A) tail defects in PABPN1 may be the cause of an autosomal dominant oculopharyngeal muscular dystrophy | DDB0232429 | CDS | 7899822 | 669 | - | 0.327354 |
pakA | DDB_G0269166 | 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 | DDB0232428 | CDS | 3436536 | 3594 | + | 0.33222 |
pakB | DDB_G0276459 | protein serinethreonine kinase that phosphorylates myoD (myosin ID) and myoK (myosin IK) heavy chains similar to p21-activated kinase belongs to the STE20 family PAKA subfamily of protein kinases | DDB0232429 | CDS | 6847900 | 2559 | - | 0.339195 |
pakC | DDB_G0267450 | STE20PAK protein kinase required for normal chemotaxis contains PAK-boxP21-Rho-binding (CRIB) domain and pleckstrin homology (PH) domain | DDB0232428 | CDS | 229145 | 1434 | - | 0.33682 |
pakD | DDB_G0269696 | 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 | DDB0232428 | CDS | 3345400 | 5037 | + | 0.25273 |
pakE | DDB_G0293932 | 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 | DDB0232433 | CDS | 3512665 | 2781 | + | 0.270766 |
pakF | DDB_G0274409 | putative protein serinethreonine kinase belongs to the protein kinase PAKL subfamily the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232429 | CDS | 4648326 | 3531 | - | 0.282073 |
pakG | DDB_G0282891 | putative protein serinethreonine kinase belongs to the protein kinase PAKL subfamily the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | DDB0232430 | CDS | 6346144 | 3540 | + | 0.284181 |
pakH-1 | DDB_G0273121 | putative protein serinethreonine kinase similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases belongs to the PAKL subfamily stress-responsive kinase there is a second copy of this gene | DDB0232429 | CDS | 2532742 | 1542 | + | 0.282101 |
pakH-2 | DDB_G0273865 | 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 | DDB0232429 | CDS | 3497296 | 1542 | - | 0.282101 |
pats1 | DDB_G0269250 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR WD40 and protein kinase domains | DDB0232428 | CDS | 2657392 | 9555 | - | 0.289901 |
pdkA | DDB_G0281471 | member of the AGC kinase group similar to mammalian PDK (phosphoinositide-dependent protein kinase) known to phosphorylate AktPKB | DDB0232430 | CDS | 4550105 | 2061 | - | 0.273654 |
pdkB | DDB_G0284489 | member of the AGC kinase group similar to mammalian PDK (phosphoinositide-dependent protein kinase) known to phosphorylate AktPKB | DDB0232431 | CDS | 2038480 | 2727 | + | 0.260726 |
pelo | DDB_G0280447 | ortholog of the conserved D. melanogaster protein pelota which is required for spindle formation and nuclear envelope breakdown during spermatogenesis and is proposed to act in protein translation. | DDB0232430 | CDS | 3368362 | 1326 | - | 0.295626 |
pex7 | DDB_G0279801 | ortholog of peroxin 7 binds the peroxisome targeting signal type 2 (PTS2) contains 6 WD40 repeats mutations in human homolog cause a variety of peroxisomal disorders | DDB0232430 | CDS | 2554628 | 951 | + | 0.31756 |
pfp1 | DDB_G0276405 | putative cysteine protease member of the DJ-1ThiJPfpI family which includes human PARK7 associated with Parkinson's disease | DDB0232429 | CDS | 6818286 | 585 | - | 0.317949 |
phg2 | DDB_G0283699 | serinethreonine kinase regulating cell substrate adhesion phagocytosis motility and actin organization member of the TKL (tyrosine kinase-like) group belongs to the ARK (ankyrin repeat-containing kinase) family although it does not contain ankyrin repeats | DDB0232431 | CDS | 995559 | 4164 | - | 0.304275 |
phgA | DDB_G0269130 | 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 ( | DDB0232428 | CDS | 3817626 | 1317 | - | 0.347001 |
pigN | DDB_G0279313 | highly conserved protein involved in GPI anchor biosynthesis ortholog of yeast MCD4 | DDB0232430 | CDS | 1921668 | 3099 | + | 0.308809 |
pigO | DDB_G0278687 | putative transferase involved in GPI biosynthesis functions with PigF to transfer ethanolamine phosphate to the third mannose of GPI (glycosylphosphatidylinositol) | DDB0232430 | CDS | 887014 | 3363 | + | 0.223015 |
pitrm1 | DDB_G0271506 | DDB0232429 | CDS | 455398 | 3201 | - | 0.282099 | |
pkaC | DDB_G0283907 | AGC group PKA family protein kinase protein serinethreonine kinase regulates spore cell differentiation | DDB0232431 | CDS | 1394958 | 1947 | + | 0.333847 |
pkaD | DDB_G0277145 | DDB0232429 | CDS | 7643321 | 2145 | - | 0.253613 | |
pkbA | DDB_G0268620 | 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 | DDB0232428 | CDS | 1977388 | 1335 | + | 0.357303 |
pkgA | DDB_G0276157 | serinethreonine protein kinase of the MAST (Microtubule Associated SerineThreonine kinase) family | DDB0232429 | CDS | 6275918 | 4104 | - | 0.287037 |
pkgB | DDB_G0290157 | AGC group protein serinethreonine kinase cAMP-activated protein kinase involved in morphogenesis during multicellular development | DDB0232432 | CDS | 3717777 | 1440 | - | 0.324306 |
pkgC | DDB_G0286125 | serinethreonine protein kinase of the AGC group similar to mammalian ribosomal protein S6 kinase | DDB0232431 | CDS | 4067973 | 2733 | - | 0.312843 |
pkgD | DDB_G0284029 | AGC group protein serinethreonine kinase similar to cAMP-activated protein kinase catalytic subunits | DDB0232431 | CDS | 1459718 | 2979 | - | 0.28231 |
pkgE_ps | DDB_G0280981 | putative pseudogene similar to AGC protein kinases of the AKT family | DDB0232430 | CDS | 3912677 | 1095 | + | 0.343379 |
pkiA | DDB_G0289391 | DDB0232432 | CDS | 2783089 | 384 | + | 0.351562 | |
pksB | DDB_G0282357 | ortholog of E. coli ydfG and S. cerevisiae TMA29 that have NADP-dependent L-serine dehydrogenase activity also acts on other amino acids such as D-threonine and L-allo-threonine homotetramer | DDB0232430 | CDS | 6131868 | 783 | + | 0.303959 |
plaA | DDB_G0278525 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity | DDB0232430 | CDS | 1019968 | 1161 | - | 0.289406 |
plk | DDB_G0274503 | putative protein serinethreonine kinase similar to yeast CDC5 Drosophila polo and mammalian PLK which play a role in mitosis and localize to the centrosomes | DDB0232429 | CDS | 4379150 | 2937 | - | 0.280899 |
plrg1 | DDB_G0279507 | DDB0232430 | CDS | 2174875 | 1551 | + | 0.317215 | |
pmmA | DDB_G0279289 | catalyzes the reaction alpha-D-mannose 1-phosphate D-mannose 6-phosphate | DDB0232430 | CDS | 1893937 | 750 | - | 0.262667 |
pmmB | DDB_G0272781 | catalyzes the reaction alpha-D-mannose 1-phosphate D-mannose 6-phosphate | DDB0232429 | CDS | 2170341 | 750 | - | 0.268 |
pno1 | DDB_G0287557 | conserved protein in S. cerevisiae a nucleolar protein required for pre-18S rRNA processing | DDB0232432 | CDS | 417964 | 720 | + | 0.290278 |
ppme1 | DDB_G0281651 | similar to H. sapiens PPME1 which demethylates proteins that have been reversibly carboxymethylated | DDB0232430 | CDS | 4760769 | 966 | + | 0.272257 |
prkag | DDB_G0272542 | non-catalytic subunit of the AMP-activated protein kinase (AMPK) complex contains two CBS domains | DDB0232429 | CDS | 1788557 | 1734 | - | 0.277393 |
prmt1 | DDB_G0291556 | DDB0232433 | CDS | 504463 | 1026 | - | 0.287524 | |
prmt2 | DDB_G0289445 | DDB0232432 | CDS | 2803733 | 1539 | - | 0.275504 | |
prosc | DDB_G0278713 | highly similar to mammalian PROSC a homolog of a bacterial gene co-transcribed with proline synthetase | DDB0232430 | CDS | 1087624 | 768 | - | 0.24349 |
prp19 | DDB_G0276803 | 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 | DDB0232429 | CDS | 7360384 | 1545 | - | 0.337864 |
prpD | DDB_G0288681 | DDB0232432 | CDS | 1873609 | 1479 | + | 0.354293 | |
prpf4 | DDB_G0287635 | ortholog of the prp4 splicing factor component of the U4U6-U5 snRNP complex contains 7 WD repeats and a splicing factor motif | DDB0232432 | CDS | 533367 | 1803 | - | 0.297837 |
prpf4B | DDB_G0279703 | protein serinethreonine kinase DYRK family member of the CMGC kinase group similar to mammalian pre-mRNA processing factor PRP4 kinase and DYRK kinases | DDB0232430 | CDS | 2466144 | 2436 | + | 0.296388 |
prpf6 | DDB_G0272374 | component of the U5 sRNP complex may act in the tri-snRNP complex as a bridging factor between U5 and U4U6 snRNPs | DDB0232429 | CDS | 1378065 | 3045 | + | 0.324138 |
psmD10 | DDB_G0289189 | DDB0232432 | CDS | 2453090 | 699 | - | 0.304721 | |
psmD14 | DDB_G0272566 | DDB0232429 | CDS | 1896679 | 921 | + | 0.313789 | |
ptcA | DDB_G0293882 | DDB0232433 | CDS | 3419922 | 1518 | + | 0.216733 | |
ptcE | DDB_G0268718 | DDB0232428 | CDS | 1991527 | 2241 | - | 0.285141 | |
ptcI | DDB_G0275823 | DDB0232429 | CDS | 5546562 | 3492 | - | 0.269759 | |
pter | DDB_G0293394 | DDB0232433 | CDS | 2831683 | 1113 | - | 0.277628 | |
pwp1 | DDB_G0275073 | DDB0232429 | CDS | 5128411 | 1710 | + | 0.334503 | |
pwp2 | DDB_G0284621 | DDB0232431 | CDS | 2240813 | 2769 | - | 0.298664 | |
pyd1 | DDB_G0267966 | ortholog of S. cerevisiae URA1 and human DPYD defects in DPYD cause dihydropyrimidine dehydrogenase deficiency catalyzes the reaction 56-dihydrouracil NADP uracil NADPH H | DDB0232428 | CDS | 1202711 | 3030 | + | 0.367327 |
pyd3 | DDB_G0274123 | DDB0232429 | CDS | 4571492 | 1176 | + | 0.333333 | |
pyk3 | DDB_G0289001 | member of the TKL (tyrosine kinase-like) group and the DPYK (Dictyostelium protein tyrosine kinase) family of protein kinases contains two kinase domains one of which is predicted to be inactive the C-terminal kinase domain has tyrosine kinase activitybr bCommunity annotation:b Pyk3 appears to be involved in differentiation pathway choice as the KO shows reduced pstO differentiation and compensatory expansion of the prespore region. Pyk3 has been proposed to act in a pathway involving ptpC and statC effectively potentiating the action of DIF-1. One of the factors that influences pathway choice is cell cycle position classic experiments show that cold-synchronized cells which enter development shortly after warming prefer the stalk pathway. This is due to an increased DIF sensitivity. New results (Strasser Tsang and MacWilliams in preparation) now show that the pyk3 transcript is upregulated roughly fivefold after cold synchronization at a time when cells show strong stalk preference (p | DDB0232432 | CDS | 2269413 | 4017 | - | 0.283047 |
pyroxd1 | DDB_G0289727 | DDB0232432 | CDS | 3170582 | 1641 | + | 0.233394 | |
qdpr | DDB_G0272684 | 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 | DDB0232429 | CDS | 1985270 | 696 | - | 0.329023 |
qkgA-1 | DDB_G0273259 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains there is a second copy of this gene | DDB0232429 | CDS | 2831844 | 4662 | + | 0.27885 |
qkgA-2 | DDB_G0273635 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains there is a second copy of this gene | DDB0232429 | CDS | 3195191 | 4662 | - | 0.27885 |
rab11A | DDB_G0269238 | DDB0232428 | CDS | 4269122 | 645 | - | 0.344186 | |
rab11B | DDB_G0287211 | DDB0232432 | CDS | 41773 | 663 | + | 0.235294 | |
rab11C | DDB_G0277101 | DDB0232429 | CDS | 7509311 | 675 | - | 0.317037 | |
rab14 | DDB_G0281337 | DDB0232430 | CDS | 4383385 | 621 | - | 0.339775 | |
rab18 | DDB_G0289827 | DDB0232432 | CDS | 3292859 | 609 | - | 0.287356 | |
rab1A | DDB_G0283757 | DDB0232431 | CDS | 1241175 | 609 | - | 0.326765 | |
rab1B | DDB_G0277867 | DDB0232430 | CDS | 743092 | 621 | - | 0.330113 | |
rab1C | DDB_G0269174 | DDB0232428 | CDS | 2911005 | 606 | - | 0.310231 | |
rab1D | DDB_G0284985 | DDB0232431 | CDS | 2756032 | 615 | - | 0.304065 | |
rab1E | DDB_G0275969 | DDB0232429 | CDS | 6179943 | 651 | + | 0.274962 | |
rab21 | DDB_G0286553 | DDB0232431 | CDS | 4804109 | 639 | + | 0.309859 | |
rab24 | DDB_G0268402 | DDB0232428 | CDS | 1157427 | 609 | - | 0.325123 | |
rab2A | DDB_G0292268 | DDB0232433 | CDS | 1422661 | 624 | + | 0.310897 | |
rab2B | DDB_G0272138 | DDB0232429 | CDS | 1483407 | 609 | + | 0.297209 | |
rab32A | DDB_G0283603 | DDB0232431 | CDS | 965063 | 660 | - | 0.309091 | |
rab32B | DDB_G0269416 | DDB0232428 | CDS | 2727197 | 783 | + | 0.265645 | |
rab32C | DDB_G0275675 | DDB0232429 | CDS | 5696031 | 675 | + | 0.302222 | |
rab32D | DDB_G0285051 | DDB0232431 | CDS | 2597422 | 687 | + | 0.263464 | |
rab4 | DDB_G0292406 | DDB0232433 | CDS | 1558648 | 618 | + | 0.302589 | |
rab5A | DDB_G0271984 | DDB0232429 | CDS | 1113320 | 606 | + | 0.328383 | |
rab5B | DDB_G0282847 | similar to rab5 but has a long amino extension and is missing two conserved cysteine residues at the carboxyl terminus | DDB0232430 | CDS | 6292039 | 645 | + | 0.311628 |
rab6 | DDB_G0268068 | DDB0232428 | CDS | 1398472 | 627 | + | 0.287081 | |
rab7A | DDB_G0269236 | rab family small GTPase involved in vesicle fusion during endocytosis there is another rab7 homolog rab7B | DDB0232428 | CDS | 2627248 | 612 | + | 0.348039 |
rab7B | DDB_G0287553 | there is another rab7 homolog rab7A | DDB0232432 | CDS | 408133 | 594 | - | 0.294613 |
rab8A | DDB_G0280043 | regulates contractile vacuole discharging in response to osmotic stress regulated by | DDB0232430 | CDS | 3266503 | 627 | + | 0.317384 |
rab8B | DDB_G0276399 | DDB0232429 | CDS | 6878753 | 612 | - | 0.328431 | |
rabA | DDB_G0291233 | DDB0232433 | CDS | 312209 | 606 | - | 0.268977 | |
rabC | DDB_G0271736 | DDB0232429 | CDS | 718547 | 591 | + | 0.291032 | |
rabF1-1 | DDB_G0272905 | there is a second copy of this gene | DDB0232429 | CDS | 2459564 | 573 | - | 0.277487 |
rabF1-2 | DDB_G0273935 | there is a second copy of this gene | DDB0232429 | CDS | 3571468 | 585 | + | 0.273504 |
rabG1 | DDB_G0291738 | DDB0232433 | CDS | 677353 | 591 | + | 0.323181 | |
rabG2 | DDB_G0290783 | DDB0232432 | CDS | 4595466 | 483 | + | 0.335404 | |
rabH | DDB_G0275955 | DDB0232429 | CDS | 6208676 | 597 | - | 0.211055 | |
rabJ | DDB_G0277441 | DDB0232429 | CDS | 8110957 | 771 | + | 0.273671 | |
rabK1 | DDB_G0290833 | DDB0232432 | CDS | 4609179 | 642 | - | 0.239875 | |
rabL | DDB_G0290779 | DDB0232432 | CDS | 4606115 | 615 | - | 0.297561 | |
rabM | DDB_G0290829 | DDB0232432 | CDS | 4605000 | 609 | - | 0.284072 | |
rabN1 | DDB_G0290789 | DDB0232432 | CDS | 4608094 | 651 | - | 0.254992 | |
rabN2 | DDB_G0290793 | DDB0232432 | CDS | 4612672 | 555 | - | 0.27027 | |
rabO | DDB_G0290407 | DDB0232432 | CDS | 4047054 | 657 | + | 0.232877 | |
rabP | DDB_G0290875 | DDB0232432 | CDS | 4703255 | 699 | + | 0.250358 | |
rabQ | DDB_G0268760 | DDB0232428 | CDS | 2054001 | 615 | + | 0.282927 | |
rabS | DDB_G0282537 | DDB0232430 | CDS | 5897353 | 666 | - | 0.234234 | |
rabT1 | DDB_G0268910 | DDB0232428 | CDS | 2365532 | 669 | + | 0.22571 | |
rabT2 | DDB_G0269262 | DDB0232428 | CDS | 2416810 | 657 | + | 0.235921 | |
rabU | DDB_G0291293 | DDB0232433 | CDS | 69908 | 585 | + | 0.268376 | |
rabV | DDB_G0282899 | DDB0232430 | CDS | 6281058 | 702 | + | 0.176638 | |
rabW | DDB_G0276295 | DDB0232429 | CDS | 6558113 | 657 | + | 0.226788 | |
rabY | DDB_G0282203 | DDB0232430 | CDS | 5519409 | 711 | - | 0.255977 | |
rabZ | DDB_G0286169 | DDB0232431 | CDS | 4062977 | 690 | - | 0.298551 | |
rac1A | DDB_G0277869 | DDB0232430 | CDS | 441220 | 585 | - | 0.358974 | |
rac1B | DDB_G0268622 | DDB0232428 | CDS | 2364212 | 585 | - | 0.317949 | |
rac1C | DDB_G0282365 | DDB0232430 | CDS | 6045140 | 582 | - | 0.324742 | |
racA | DDB_G0286555 | RhoBTB subfamily protein which have a unique domain architecture composed of a N-terminal GTPase domain two bric a brac domains (BTB and a conserved C-terminal domain there are orthoolgs in several eukaryotes including mammals but are absent from fungi and plants in Dictyostelium appears to be involved in the regulation of the actin cytoskeleton | DDB0232431 | CDS | 4692759 | 1797 | - | 0.327212 |
racB | DDB_G0279605 | DDB0232430 | CDS | 2370154 | 588 | - | 0.323129 | |
racC | DDB_G0293526 | DDB0232433 | CDS | 3000314 | 579 | + | 0.322971 | |
racD | DDB_G0291976 | DDB0232433 | CDS | 1210911 | 765 | + | 0.32549 | |
racE | DDB_G0280975 | interacts with gxcT rgaA and darA acts together with fttB (14-3-3) to regulate the cortical cytoskeleton and cleavage furrow progression during cytokinesis | DDB0232430 | CDS | 4354163 | 672 | - | 0.360119 |
racF1 | DDB_G0269176 | DDB0232428 | CDS | 3007465 | 582 | + | 0.271478 | |
racF2 | DDB_G0276967 | DDB0232429 | CDS | 7215630 | 582 | - | 0.274914 | |
racG | DDB_G0269178 | DDB0232428 | CDS | 3735334 | 606 | - | 0.250825 | |
racH | DDB_G0269240 | DDB0232428 | CDS | 3360340 | 603 | + | 0.325041 | |
racI | DDB_G0277897 | DDB0232430 | CDS | 93233 | 618 | - | 0.273463 | |
racJ | DDB_G0292560 | DDB0232433 | CDS | 1884330 | 618 | + | 0.263754 | |
racL | DDB_G0292816 | DDB0232433 | CDS | 2181555 | 591 | + | 0.279188 | |
racM | DDB_G0289103 | DDB0232432 | CDS | 2368291 | 570 | - | 0.27193 | |
racN | DDB_G0278009 | DDB0232430 | CDS | 154173 | 660 | + | 0.259091 | |
racO | DDB_G0277791 | DDB0232429 | CDS | 8401462 | 831 | + | 0.202166 | |
racP | DDB_G0285453 | DDB0232431 | CDS | 3245052 | 1131 | + | 0.312113 | |
racQ | DDB_G0278011 | DDB0232430 | CDS | 155490 | 558 | + | 0.256272 | |
rae1 | DDB_G0283835 | DDB0232431 | CDS | 1191439 | 1029 | + | 0.308066 | |
ragA | DDB_G0288701 | ortholog of S. cerevisiae GTR1 and H. sapiens RagA and RagB a cytoplasmic GTP binding protein | DDB0232432 | CDS | 1844809 | 906 | + | 0.296909 |
ranA | DDB_G0291235 | DDB0232433 | CDS | 78789 | 639 | + | 0.363067 | |
ranB | DDB_G0274943 | DDB0232429 | CDS | 4583590 | 2265 | - | 0.316998 | |
rapA | DDB_G0291237 | DDB0232433 | CDS | 98914 | 561 | + | 0.354724 | |
rapB | DDB_G0272857 | DDB0232429 | CDS | 2094380 | 618 | - | 0.305825 | |
rapC | DDB_G0270340 | DDB0232428 | CDS | 4670322 | 837 | + | 0.296296 | |
raptor | DDB_G0270398 | putative Raptor protein ortholog a component of the TORC1 complex in yeasts with Lst8 and Tor does not co-immunoprecipitate with the TORC2 complex | DDB0232428 | CDS | 4758927 | 4530 | - | 0.330905 |
rasB | DDB_G0292998 | nuclear Ras that may have a role in cell division andor nuclear division expressed throughout growth and development | DDB0232433 | CDS | 2415988 | 594 | - | 0.3367 |
rasC | DDB_G0281385 | Ras protein required for aggregation activated by rasGEF GefA enriched in prestalk cellsbr bCommunity annotation:b Gene expression is greatly perturbed in vegetative rasC-rasG- double null mutants and in early development a subset of important signalling genes are not induced adequately. Notable among these early genes are acaA dagA erkA erkB gpaB and csbA. The discoidin I genes are also underexpresed. The expression of most of these genes (not the discoidins) is rescued when carA is overexpressed in the double null line. Most remarkably the overall profile of gene expression changes in vegetative double null mutants compared to the parent strain is highly similar to that of wild-type cells six hours after infection with Legionella pneumophila compared to uninfected cells (in terms of gene expression changes correlation coefficient 0.61) (Li et al 2009) making this strain phenocopy the Legionella-resistant dupA mutant to some extent (correlation coefficient 0.49). Of 55 genes overe | DDB0232430 | CDS | 4519070 | 570 | + | 0.333333 |
rasD | DDB_G0292996 | DDB0232433 | CDS | 2530991 | 564 | - | 0.294326 | |
rasG | DDB_G0293434 | maximally expressed during growth activated by rasGEF GefRbr bCommunity annotation:b Gene expression is greatly perturbed in vegetative rasC-rasG- double null mutants and in early development a subset of important signalling genes are not induced adequately. Notable among these early genes are acaA dagA erkA erkB gpaB and csbA. The discoidin I genes are also underexpresed. The expression of most of these genes (not the discoidins) is rescued when carA is overexpressed in the double null line. Most remarkably the overall profile of gene expression changes in vegetative double null mutants compared to the parent strain is highly similar to that of wild-type cells six hours after infection with Legionella pneumophila compared to uninfected cells (correlation coefficient 0.61) (Li et al 2009) making this strain partially phenocopy the Legionella-resistant dupA mutant (in terms of gene expression changes correlation coefficient 0.49). Of 55 genes overexpressed at least 4-fold in the veget | DDB0232433 | CDS | 2877682 | 570 | - | 0.368421 |
rasS | DDB_G0283537 | DDB0232431 | CDS | 849934 | 585 | - | 0.305983 | |
rasU | DDB_G0270138 | DDB0232428 | CDS | 4299011 | 642 | + | 0.253894 | |
rasV | DDB_G0270736 | DDB0232428 | CDS | 4279831 | 690 | - | 0.234783 | |
rasW | DDB_G0270122 | DDB0232428 | CDS | 4277085 | 651 | - | 0.282642 | |
rasX | DDB_G0270124 | DDB0232428 | CDS | 4281896 | 642 | - | 0.267913 | |
rasY | DDB_G0270126 | DDB0232428 | CDS | 4283626 | 651 | - | 0.282642 | |
rasZ | DDB_G0270140 | DDB0232428 | CDS | 4300316 | 645 | + | 0.272868 | |
rbbD | DDB_G0282529 | similar to H. sapiens Retinoblastoma binding proteins RBBP4 and RBBP7 and S. cerevisiae HAT2 a subunit of the HAT1HAT2 histone acetyltransferase complex | DDB0232430 | CDS | 5888997 | 1272 | - | 0.331761 |
rbbE | DDB_G0285847 | DDB0232431 | CDS | 3858078 | 1578 | + | 0.292142 | |
rbm8A | DDB_G0286007 | conserved protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance the human ortholog has been shown to interact with | DDB0232431 | CDS | 3939784 | 564 | - | 0.281915 |
rckA | DDB_G0278737 | member of the TKL (tyrosine kinase-like) group contains an RGS (Regulator of G protein Signaling) domain | DDB0232430 | CDS | 1218919 | 3378 | + | 0.261693 |
rheb | DDB_G0277041 | DDB0232429 | CDS | 7321470 | 558 | + | 0.28853 | |
rliA | DDB_G0272783 | twelve transmembrane domain protein that may act as a transporter repressed after Legionella pneumophila infection | DDB0232429 | CDS | 2172067 | 1416 | + | 0.267655 |
rmd5 | DDB_G0274829 | ortholog of the conserved RMD5 which in yeast has has an E3-like ubiquitin ligase activity | DDB0232429 | CDS | 4057449 | 1335 | - | 0.262921 |
rnf113 | DDB_G0267870 | DDB0232428 | CDS | 995736 | 1068 | + | 0.251873 | |
rnf160 | DDB_G0274875 | DDB0232429 | CDS | 4311743 | 5595 | - | 0.235746 | |
roco11 | DDB_G0268636 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains | DDB0232428 | CDS | 2199646 | 4464 | + | 0.267473 |
roco4 | DDB_G0288251 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR and protein kinase domains | DDB0232432 | CDS | 1284583 | 5181 | + | 0.332947 |
roco5 | DDB_G0294533 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains RhoGEF PH LRR Roc COR and protein kinase domains | DDB0232432 | CDS | 1439427 | 8403 | - | 0.309413 |
roco6 | DDB_G0279417 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains LRR Roc COR WD40 PH and protein kinase domains | DDB0232430 | CDS | 2094570 | 6444 | + | 0.293451 |
roco7 | DDB_G0267472 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains Roc COR WD40 and protein kinase domains related to LRR-containing kinases but does not contain an LRR domain | DDB0232428 | CDS | 628403 | 7848 | - | 0.293833 |
roco8 | DDB_G0286127 | member of the TKL (tyrosine kinase-like) group and the ROCO family of protein kinases contains DEP LRR Roc COR and protein kinase domains | DDB0232431 | CDS | 4112361 | 5604 | - | 0.267131 |
roco9 | DDB_G0288183 | member of the TKL (tyrosine kinase-like) group and ROCO family of protein kinases contains RhoGAP LRR Roc Cor and protein kinase domains | DDB0232432 | CDS | 1219231 | 10098 | - | 0.264706 |
rsc11-1 | DDB_G0272791 | conserved protein of unknown function there is a second copy of this gene | DDB0232429 | CDS | 2268088 | 1731 | + | 0.306759 |
rsc11-2 | DDB_G0295699 | conserved protein of unknown function there is a second copy of this gene | DDB0232429 | CDS | 3761741 | 1731 | - | 0.306759 |
rsmA | DDB_G0283547 | DDB0232431 | CDS | 800136 | 660 | + | 0.260606 | |
rsmB | DDB_G0281253 | DDB0232430 | CDS | 4295825 | 783 | + | 0.219668 | |
rsmC | DDB_G0278449 | DDB0232430 | CDS | 896854 | 723 | + | 0.236515 | |
rsmD | DDB_G0292318 | DDB0232433 | CDS | 1471614 | 684 | + | 0.19152 | |
rsmE-1 | DDB_G0273099 | there is a second copy of this gene | DDB0232429 | CDS | 2580465 | 663 | + | 0.205128 |
rsmE-2 | DDB_G0273825 | there is a second copy of this gene | DDB0232429 | CDS | 3450554 | 663 | - | 0.205128 |
rsmF | DDB_G0278389 | DDB0232430 | CDS | 814663 | 627 | + | 0.239234 | |
rsmG | DDB_G0278717 | DDB0232430 | CDS | 501817 | 609 | - | 0.192118 | |
rsmH | DDB_G0278403 | DDB0232430 | CDS | 825274 | 819 | + | 0.229548 | |
rsmK | DDB_G0278217 | DDB0232430 | CDS | 491519 | 588 | + | 0.19898 | |
rsmM | DDB_G0292300 | DDB0232433 | CDS | 1426160 | 645 | + | 0.308527 | |
samkA | DDB_G0269876 | DDB0232428 | CDS | 3775693 | 1923 | + | 0.228289 | |
samkB | DDB_G0284859 | putative protein kinase containing a SAM (sterile alpha motif) homology domain a putative protein interaction module | DDB0232431 | CDS | 2549067 | 1782 | + | 0.251403 |
samkB_ps1 | DDB_G0270988 | putative pseudogene SAMK (SAM domain-containing kinase) family | DDB0232428 | CDS | 3791042 | 1593 | - | 0.264909 |
samkC | DDB_G0270678 | putative protein kinase containing a SAM (sterile alpha motif) homology domain a putative protein interaction module | DDB0232428 | CDS | 3778203 | 2628 | + | 0.251903 |
samkD | DDB_G0270680 | similar to SNF1-like kinases unlikely to function as a kinase as it lacks the catalytic aspartate | DDB0232428 | CDS | 3781297 | 1662 | + | 0.197954 |
samkE_ps1 | DDB_G0283165 | putative pseudogene SAMK (SAM domain-containing kinase) family | DDB0232431 | CDS | 352482 | 1272 | - | 0.26022 |
sarA | DDB_G0272296 | similar to budding yeast Sar1 a 21 kDa GTP- binding protein involved in vesicular transport between the endoplasmic reticulum and the Golgi | DDB0232429 | CDS | 1644732 | 567 | - | 0.33157 |
sarB | DDB_G0278477 | weakly similar to budding yeast Sar1 a 21 kDa GTP- binding protein involved in vesicular transport between the endoplasmic reticulum and the Golgi | DDB0232430 | CDS | 934441 | 585 | - | 0.268376 |
sdrA | DDB_G0290659 | DDB0232432 | CDS | 4286973 | 873 | + | 0.290951 | |
sec13 | DDB_G0292052 | DDB0232433 | CDS | 1099513 | 906 | + | 0.34106 | |
sec31 | DDB_G0270992 | DDB0232428 | CDS | 3837509 | 4068 | + | 0.346853 | |
sec7 | DDB_G0272486 | belongs to the Sec7 superfamily involved in phagocytosis and cell motility | DDB0232429 | CDS | 1791640 | 2796 | - | 0.299714 |
secG | DDB_G0287459 | Arf-guanyl-nucleotide exchange factor of the cytohesin family involved in chemotaxis to cAMP during development and substrate adhesion | DDB0232432 | CDS | 318028 | 2961 | - | 0.372847 |
sepA | DDB_G0276465 | plays a role in the regulation of cleavage furrow formation similar to S. pombe cdc7 | DDB0232429 | CDS | 6942806 | 3504 | + | 0.32363 |
set1 | DDB_G0289257 | DDB0232432 | CDS | 2551579 | 4461 | + | 0.297467 | |
sf3b4 | DDB_G0267714 | DDB0232428 | CDS | 676187 | 1080 | - | 0.333333 | |
sgkA | DDB_G0272522 | homolog of human Sphk1 phosphorylates sphinganine to sphinganine 1-phosphate | DDB0232429 | CDS | 1846158 | 1875 | + | 0.3088 |
sgkB | DDB_G0284545 | homolog of human Sphk2 phosphorylates sphinganine to sphinganine 1-phosphate | DDB0232431 | CDS | 2087340 | 2283 | + | 0.251862 |
sgkC | DDB_G0272350 | DDB0232429 | CDS | 1700447 | 2178 | + | 0.344812 | |
sgkD | DDB_G0289343 | DDB0232432 | CDS | 2664172 | 2052 | + | 0.203704 | |
sgtA | DDB_G0280345 | DDB0232430 | CDS | 3286144 | 1005 | - | 0.311443 | |
shkA | DDB_G0283267 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain negative regulator of phosphoinositol signaling | DDB0232431 | CDS | 438511 | 1584 | + | 0.318182 |
shkB | DDB_G0288617 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232432 | CDS | 1745652 | 1962 | - | 0.331295 |
shkC | DDB_G0278409 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232430 | CDS | 836437 | 1521 | - | 0.332676 |
shkD | DDB_G0281343 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232430 | CDS | 4376038 | 2235 | + | 0.314541 |
shkE | DDB_G0290451 | member of the TKL (tyrosine kinase-like) group and the SHK (SH2-domain containing kinase) subfamily contains a C-terminal SH2 (Src homology 2) domain | DDB0232432 | CDS | 4058161 | 2133 | + | 0.284107 |
sigI | DDB_G0275177 | DDB0232429 | CDS | 5054068 | 915 | - | 0.27541 | |
sky1 | DDB_G0275627 | similar to SRPKs (Serinearginine-Rich Protein specific Kinases) serinethreonine kinases that specifically phosphoryate arginine-serine rich domains found in the SR family of splicing factors | DDB0232429 | CDS | 5951942 | 1971 | - | 0.318113 |
slc35b2 | DDB_G0269602 | belongs to the drugmetabolite transporter (DMT) superfamily similar to D. melanogaster sll human SLC35B2 contains 8 predicted transmembrane domains | DDB0232428 | CDS | 3110201 | 1080 | - | 0.297222 |
smu1 | DDB_G0278353 | DDB0232430 | CDS | 737677 | 1593 | - | 0.266164 | |
snfA | DDB_G0277905 | CAMKL family protein kinase catalytic subunit of the AMP-activated protein kinase (AMPK) complex similar to SNF1 kinases and AMPK experiments in Dictyostelium show that AMPK signaling plays an important role in mitochondrial disease. | DDB0232430 | CDS | 589784 | 2184 | + | 0.250458 |
snpA | DDB_G0285111 | DDB0232431 | CDS | 2863727 | 876 | - | 0.3379 | |
spg1 | DDB_G0291269 | DDB0232433 | CDS | 37774 | 612 | + | 0.338235 | |
spkA-1 | DDB_G0273445 | 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 | DDB0232429 | CDS | 2969377 | 1917 | - | 0.310381 |
spkA-2 | DDB_G0273531 | 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 | DDB0232429 | CDS | 3060166 | 1917 | + | 0.310381 |
splA | DDB_G0283385 | dual-specificity protein kinase involved in spore coat formation and morphogenesis member of the TKL (tyrosine kinase-like) group and the CZAK (C-terminal domain of ZakA) family | DDB0232431 | CDS | 623097 | 7233 | + | 0.323655 |
splB | DDB_G0285321 | member of the TKL (tyrosine kinase-like) group activates the transcriptional regulator STATc | DDB0232431 | CDS | 3131349 | 3468 | + | 0.27797 |
sqrdl | DDB_G0292250 | ortholog of the conserved sulfide quinone reductase-like protein in S. pombe this oxidoreductase is involved in mitochondrial sulfide oxidation | DDB0232433 | CDS | 1300465 | 1359 | - | 0.341428 |
sr | DDB_G0290009 | catalyzes the reaction 78-dihydrobiopterin NADPsupsup sepiapterin NADPH Hsupsup the final step in L-erythro-tetrahydrobiopterin (BH4) biosynthesis a cofactor for aromatic amino acid oxidationbr | DDB0232432 | CDS | 3552302 | 804 | + | 0.238806 |
srp72 | DDB_G0291412 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | DDB0232433 | CDS | 275731 | 2019 | - | 0.270926 |
srpRB | DDB_G0278543 | DDB0232430 | CDS | 1043259 | 873 | + | 0.269187 | |
sti1 | DDB_G0292404 | DDB0232433 | CDS | 1556012 | 1695 | - | 0.362242 | |
strap | DDB_G0286457 | ortholog of the serine-threonine kinase receptor-associated protein STRAP an inhibitor of TGF-beta signaling contains 7 WD40 repeats | DDB0232431 | CDS | 4462466 | 882 | - | 0.349206 |
strn | DDB_G0288327 | homolog of mammalians striatins calmodulin-binding proteins expressed in the central nervous system and Drosophila Cka involved in the Jun kinase pathway | DDB0232432 | CDS | 1395012 | 2484 | + | 0.288647 |
stt3 | DDB_G0285159 | CAZy family GT66 subunit of the oligosaccharyltransferase complex which catalyzes asparagine-linked glycosylation of newly synthesized proteins in the ER lumen ortholog of S. cerevisiae OST1 contains 13 transmembrane domains | DDB0232431 | CDS | 2899851 | 2145 | + | 0.359441 |
sugt1 | DDB_G0269292 | ortholog of S. cerevisiae SGT1 and mammalian SUGT1 associated with the SCF (Skp1pCdc53pF box protein) ubiquitin ligase complex | DDB0232428 | CDS | 2470067 | 1164 | + | 0.293814 |
sunB | DDB_G0285925 | SUN-like protein with a centrally located domain contains a predicted N-terminal signal sequence | DDB0232431 | CDS | 3835569 | 3837 | + | 0.250195 |
suox | DDB_G0278893 | catalyzes the reaction sulfite Osub2sub Hsub2subO sulfate Hsub2subOsub2subbr ortholog of H. sapiens SUOX of which defects cause isolated sulfite oxidase deficiency (ISOD) characterized by neurological abnormalities requires molybdopterin cofactor | DDB0232430 | CDS | 1346298 | 1197 | - | 0.324144 |
suvA | DDB_G0269554 | the D. melanogaster ortholog su(var)3-9 has a central role in heterochromatin-induced gene silencing | DDB0232428 | CDS | 2983180 | 4605 | + | 0.283388 |
svkA | DDB_G0286359 | very similar to mammalian ST25 kinase (SOK1) and other STE20-like kinases stress-responsive kinase phosphorylates severin essential for cell separation during cytokinesis | DDB0232431 | CDS | 4476218 | 1437 | + | 0.343076 |
symA | DDB_G0292814 | DDB0232433 | CDS | 2158906 | 1371 | - | 0.33698 | |
taf5 | DDB_G0287337 | subunit of TFIID and SAGA complexes involved in RNA polymerase II transcription initiation and in chromatin modification | DDB0232432 | CDS | 150447 | 2847 | + | 0.316473 |
tbck | DDB_G0267760 | 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 | DDB0232428 | CDS | 792299 | 3102 | + | 0.275306 |
thoc6 | DDB_G0287653 | ortholog of THOC6 which exists in the THO complex required for transcriptional elongation | DDB0232432 | CDS | 441079 | 1440 | + | 0.271528 |
tipD | DDB_G0275323 | 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 | DDB0232429 | CDS | 5406103 | 1839 | + | 0.334965 |
tkrA | DDB_G0292104 | catalyzes the reaction D-gluconate NADPsupsup 2-dehydro-D-gluconate NADPH Hsupsup | DDB0232433 | CDS | 1190069 | 1005 | + | 0.300498 |
tmem115 | DDB_G0278061 | DDB0232430 | CDS | 209901 | 867 | - | 0.262976 | |
tmem20 | DDB_G0292606 | putative drugmetabolite transporter containing 10 predicted transmembrane domains | DDB0232433 | CDS | 1830985 | 2097 | + | 0.311874 |
tra1 | DDB_G0281947 | atypical protein kinase belongs to the PIKK family of protein kinases similar to transformationtranscription domain-associated protein (TRRAP) | DDB0232430 | CDS | 5137846 | 13749 | + | 0.291294 |
tra2 | DDB_G0278349 | similar to the conserved Tra2 proteins (including human TRA2A TRA2B and SFRS10) that have splicing regulatory function involved in sex-determination in Drosophila | DDB0232430 | CDS | 731119 | 981 | + | 0.415902 |
trfA | DDB_G0269194 | DDB0232428 | CDS | 3020703 | 4173 | - | 0.309609 | |
trmt5 | DDB_G0279739 | ortholog of the mammalian TRMT5 and the S. cerevisiae TRM5 tRNAmethyltransferase that methylates guanosine-37 in various tRNAs | DDB0232430 | CDS | 2486411 | 1383 | - | 0.253796 |
tssc1 | DDB_G0274279 | DDB0232429 | CDS | 4037996 | 1203 | + | 0.267664 | |
tsuA | DDB_G0267962 | putative protein serinethreonine kinase similar to mammalian STK36 and fly fused kinase (fu) a ST kinase involved in the hedgehog signal transduction pathway belongs to the ULK (Unc-51-like kinase) family of kinases | DDB0232428 | CDS | 1191800 | 6744 | + | 0.248517 |
ttc27 | DDB_G0293372 | DDB0232433 | CDS | 2801637 | 2562 | - | 0.296253 | |
ttc4 | DDB_G0286253 | DDB0232431 | CDS | 4254280 | 1194 | - | 0.278057 | |
tupA | DDB_G0282189 | DDB0232430 | CDS | 5574241 | 1740 | + | 0.331034 | |
u2af2 | DDB_G0286395 | large subunit of the U2 small nuclear ribonucleoprotein auxiliary factor (U2AF) which is a splicing factor that forms a heterodimer with | DDB0232431 | CDS | 4405482 | 2016 | + | 0.361607 |
utp13 | DDB_G0276283 | component of the small subunit (SSU) processome containing the U3 snoRNA involved in processing of pre-18S rRNA highly similar to H. sapiens transducin beta-like 3 (TBL3) | DDB0232429 | CDS | 6600384 | 2709 | + | 0.277593 |
utp15 | DDB_G0283581 | DDB0232431 | CDS | 863530 | 1590 | - | 0.3 | |
utp6 | DDB_G0279601 | DDB0232430 | CDS | 2214566 | 1830 | + | 0.227322 | |
vilA | DDB_G0288557 | DDB0232432 | CDS | 1709022 | 5115 | - | 0.324536 | |
vps15 | DDB_G0282627 | putative protein serinethreonine kinase similar to human PIK3R4 and yeast VPS15 which regulate the phosphatidylinositol 3 kinase VPS34 (hVps34) yeast VPS15VPS34 complex known to be involved in vacuolar protein sorting | DDB0232430 | CDS | 6019111 | 5901 | + | 0.306219 |
vps29 | DDB_G0288787 | ortholog of VPS29 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | DDB0232432 | CDS | 1965193 | 552 | - | 0.311594 |
vps5 | DDB_G0272989 | putative ortholog of mammalian sorting nexin and S. cerevisiae VPS5 a subunit of the membrane-associated retromer complex essential for endosome-to-Golgi retrograde transport | DDB0232429 | CDS | 2025586 | 1638 | - | 0.339438 |
vps8 | DDB_G0291606 | putative ortholog of VPS8 involved in vacuolar protein localization | DDB0232433 | CDS | 397697 | 5256 | + | 0.296233 |
wdr12 | DDB_G0279903 | DDB0232430 | CDS | 2678219 | 1392 | + | 0.30819 | |
wdr18 | DDB_G0288659 | DDB0232432 | CDS | 1790292 | 1683 | + | 0.273321 | |
wdr23 | DDB_G0291832 | DDB0232433 | CDS | 834929 | 1986 | - | 0.291541 | |
wdr24 | DDB_G0287817 | DDB0232432 | CDS | 760582 | 3072 | - | 0.277995 | |
wdr3 | DDB_G0282623 | DDB0232430 | CDS | 6010118 | 2829 | + | 0.308236 | |
wdr36 | DDB_G0277019 | 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) | DDB0232429 | CDS | 7238641 | 3081 | + | 0.278156 |
wdr4 | DDB_G0281061 | similar to H. sapiens WDR4 which is required for 7-methylguanosine modification of tRNA and forms a complex with METTL1 | DDB0232430 | CDS | 3999282 | 1404 | - | 0.254274 |
wdr45l | DDB_G0282581 | ortholog of the conserved WDR45 like protein that is up-regulated in a variety of human cancers contains 3 WD-40 repeats | DDB0232430 | CDS | 5969861 | 1053 | + | 0.304843 |
wdr46 | DDB_G0280489 | DDB0232430 | CDS | 3437042 | 1869 | + | 0.308186 | |
wdr5 | DDB_G0287273 | highly similar to WDR5 protein involved in histone H3 K4 methylation | DDB0232432 | CDS | 72820 | 1008 | + | 0.298611 |
wdr53 | DDB_G0293608 | DDB0232433 | CDS | 3130386 | 1107 | + | 0.226739 | |
wdr57 | DDB_G0271788 | ortholog of human WDR57 which binds PRP8 contains 7 WD40 repeats | DDB0232429 | CDS | 716526 | 1068 | + | 0.32397 |
wdr61 | DDB_G0282793 | DDB0232430 | CDS | 6064156 | 900 | + | 0.306667 | |
wdr68 | DDB_G0275925 | DDB0232429 | CDS | 6064231 | 978 | + | 0.312883 | |
wdr7 | DDB_G0272771 | putative ortholog of H. sapiens WDR7 also known as TGF-beta resistance-associated protein (TRAG) and rabconnectin-3 beta | DDB0232429 | CDS | 2154360 | 4029 | - | 0.327128 |
wdr89 | DDB_G0283635 | DDB0232431 | CDS | 891645 | 1080 | + | 0.285185 | |
wdr91 | DDB_G0268084 | DDB0232428 | CDS | 1428913 | 2301 | - | 0.263798 | |
xab2 | DDB_G0277977 | DDB0232430 | CDS | 88368 | 2553 | + | 0.278104 | |
yakA | DDB_G0283605 | belongs to the CMGC group of protein kinases putative protein serinethreonine kinase | DDB0232431 | CDS | 868454 | 4377 | + | 0.303404 |
zak2 | DDB_G0276187 | contains two kinase domains N-terminal kinase domain related to STE group C-terminal domain similar to TKL group highly similar to zakA and has overlapping function with zakA shown to be a tyrosine kinase and regulator of GSK3 also regulates pattern formation during development via dstC (STATc) signaling | DDB0232429 | CDS | 6396810 | 1908 | - | 0.253145 |
zakA | DDB_G0276025 | contains two kinase domains N-terminal kinase domain related to STE group C-terminal domain similar to TKL group | DDB0232429 | CDS | 6393550 | 2346 | - | 0.239983 |
zfand | DDB_G0270362 | DDB0232428 | CDS | 4713592 | 498 | + | 0.289157 | |
zpr1 | DDB_G0269438 | ortholog of ZPR1 a eukaryotic zinc finger protein | DDB0232428 | CDS | 2767401 | 1434 | - | 0.288703 |