Gene list
Applied filters:
Genomic element: GAOABQK02IO52T
Number of genes found: 324
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium lacteum | ||||||||
---|---|---|---|---|---|---|---|---|
Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
NA | DLA_11872 | tRNA-Glu | GAOABQK02IO52T | tRNA | 15376 | 72 | - | 0.527778 |
NA | DLA_11873 | tRNA-Pseudo | GAOABQK02IO52T | tRNA | 408508 | 71 | + | 0.507042 |
g6089 | DLA_06778 | GAOABQK02IO52T | CDS | 2675 | 1566 | + | 0.265006 | |
g6090 | DLA_06779 | GAOABQK02IO52T | CDS | 4517 | 837 | + | 0.261649 | |
g6091 | DLA_11668 | GAOABQK02IO52T | CDS | 5975 | 2301 | + | 0.262495 | |
g6092 | DLA_06780 | GAOABQK02IO52T | CDS | 8543 | 894 | + | 0.253915 | |
g6093 | DLA_06783 | GAOABQK02IO52T | CDS | 11210 | 693 | - | 0.233766 | |
g6094 | DLA_06786 | glycoside hydrolase family 25 (GH25) comprises enzymes with lysozyme (EC:3.2.1.17) activity contains a putative N-terminal signal peptide | GAOABQK02IO52T | CDS | 13496 | 840 | + | 0.35 |
g6095 | DLA_06788 | GAOABQK02IO52T | CDS | 16304 | 3150 | - | 0.235873 | |
g6096 | DLA_06789 | GAOABQK02IO52T | CDS | 19727 | 582 | - | 0.441581 | |
g6097 | DLA_06790 | GAOABQK02IO52T | CDS | 20587 | 1419 | + | 0.251586 | |
g6098 | DLA_06791 | GAOABQK02IO52T | CDS | 22177 | 2427 | + | 0.233622 | |
g6099 | DLA_06792 | GAOABQK02IO52T | CDS | 24816 | 2145 | + | 0.307692 | |
g6100 | DLA_06793 | GAOABQK02IO52T | CDS | 27199 | 414 | + | 0.350242 | |
g6101 | DLA_06794 | GAOABQK02IO52T | CDS | 27816 | 1317 | - | 0.290053 | |
g6102 | DLA_06795 | GAOABQK02IO52T | CDS | 30437 | 1989 | + | 0.306184 | |
g6103 | DLA_06796 | GAOABQK02IO52T | CDS | 32661 | 1725 | + | 0.292174 | |
g6104 | DLA_06797 | GAOABQK02IO52T | CDS | 34493 | 996 | - | 0.365462 | |
g6105 | DLA_06798 | GAOABQK02IO52T | CDS | 35913 | 1800 | + | 0.297222 | |
g6106 | DLA_06799 | GAOABQK02IO52T | CDS | 37861 | 609 | + | 0.311987 | |
g6107 | DLA_06800 | conserved protein involved in contractile vacuole discharge upon osmotic stressbr bNomenclature conflict: b Do not confuse this gene with phg1a encoding the putative phagocytic receptor 1a or with the phgA locus ( | GAOABQK02IO52T | CDS | 38525 | 978 | - | 0.340491 |
g6108 | DLA_06801 | GAOABQK02IO52T | CDS | 39597 | 843 | - | 0.342823 | |
g6109 | DLA_06802 | GAOABQK02IO52T | CDS | 40992 | 801 | - | 0.337079 | |
g6110 | DLA_06803 | GAOABQK02IO52T | CDS | 41983 | 1542 | + | 0.286641 | |
g6111 | DLA_06804 | GAOABQK02IO52T | CDS | 43669 | 4935 | - | 0.358865 | |
g6112 | DLA_06805 | functions in nuclear protein import via a substrate-importin alpha-beta transport complex that passes though the nuclear pore complexes (NPC) contains a N-terminal importin beta binding domain (IBB domain) | GAOABQK02IO52T | CDS | 49054 | 1587 | + | 0.360428 |
g6113 | DLA_06806 | GAOABQK02IO52T | CDS | 51884 | 1800 | + | 0.324444 | |
g6114 | DLA_06808 | GAOABQK02IO52T | CDS | 54390 | 1089 | + | 0.331497 | |
g6115 | DLA_06810 | GAOABQK02IO52T | CDS | 55740 | 309 | - | 0.346278 | |
g6116 | DLA_06811 | GAOABQK02IO52T | CDS | 56795 | 1080 | + | 0.383333 | |
g6117 | DLA_06812 | GAOABQK02IO52T | CDS | 58106 | 1263 | + | 0.355503 | |
g6118 | DLA_06813 | GAOABQK02IO52T | CDS | 59682 | 489 | - | 0.364008 | |
g6119 | DLA_06814 | GAOABQK02IO52T | CDS | 60772 | 1845 | + | 0.299729 | |
g6120 | DLA_06815 | GAOABQK02IO52T | CDS | 63029 | 1314 | + | 0.352359 | |
g6121 | DLA_06816 | GAOABQK02IO52T | CDS | 64421 | 1767 | - | 0.301075 | |
g6122 | DLA_06817 | GAOABQK02IO52T | CDS | 66465 | 2757 | - | 0.328255 | |
g6123 | DLA_06819 | GAOABQK02IO52T | CDS | 69545 | 2439 | + | 0.339073 | |
g6124 | DLA_06820 | GAOABQK02IO52T | CDS | 72537 | 1269 | + | 0.325453 | |
g6125 | DLA_06821 | GAOABQK02IO52T | CDS | 73832 | 1698 | - | 0.30212 | |
g6126 | DLA_06822 | GAOABQK02IO52T | CDS | 75745 | 2961 | - | 0.342452 | |
g6127 | DLA_06823 | GAOABQK02IO52T | CDS | 78960 | 3399 | - | 0.293027 | |
g6128 | DLA_06825 | GAOABQK02IO52T | CDS | 83539 | 417 | + | 0.333333 | |
g6129 | DLA_06826 | GAOABQK02IO52T | CDS | 84324 | 870 | - | 0.309195 | |
g6130 | DLA_06827 | member of the patatin family of glycoproteins which are storage proteins but also possess lipase activity contains a predicted signal peptide | GAOABQK02IO52T | CDS | 85422 | 891 | - | 0.352413 |
g6131 | DLA_06828 | GAOABQK02IO52T | CDS | 86744 | 4974 | - | 0.334942 | |
g6132 | DLA_06830 | GAOABQK02IO52T | CDS | 92613 | 2925 | - | 0.285128 | |
g6133 | DLA_06832 | GAOABQK02IO52T | CDS | 95848 | 2091 | - | 0.313726 | |
g6134 | DLA_06833 | GAOABQK02IO52T | CDS | 97950 | 240 | - | 0.25 | |
g6135 | DLA_06834 | GAOABQK02IO52T | CDS | 98563 | 3009 | - | 0.306414 | |
g6136 | DLA_06835 | member of the TKL (tyrosine kinase-like) group and the ARK (ankyrin repeat-containing kinase) family kinase activity stimulated by hyperosmolarity and heat shock there is a second copy of this gene | GAOABQK02IO52T | CDS | 102489 | 4140 | - | 0.322947 |
g6137 | DLA_06836 | GAOABQK02IO52T | CDS | 107367 | 3732 | - | 0.353966 | |
g6138 | DLA_06837 | GAOABQK02IO52T | CDS | 111590 | 1314 | - | 0.354642 | |
g6139 | DLA_06838 | GAOABQK02IO52T | CDS | 113411 | 1434 | + | 0.281729 | |
g6140 | DLA_06839 | GAOABQK02IO52T | CDS | 114984 | 2319 | + | 0.336783 | |
g6141 | DLA_06840 | GAOABQK02IO52T | CDS | 117375 | 1032 | + | 0.295543 | |
g6142 | DLA_06841 | GAOABQK02IO52T | CDS | 118547 | 3090 | - | 0.303883 | |
g6143 | DLA_06842 | GAOABQK02IO52T | CDS | 122493 | 1692 | + | 0.287825 | |
g6144 | DLA_06843 | GAOABQK02IO52T | CDS | 124233 | 2037 | - | 0.309278 | |
g6145 | DLA_06844 | GAOABQK02IO52T | CDS | 126540 | 999 | + | 0.378378 | |
g6146 | DLA_06845 | GAOABQK02IO52T | CDS | 127874 | 1875 | + | 0.314133 | |
g6147 | DLA_06847 | GAOABQK02IO52T | CDS | 130231 | 789 | + | 0.269962 | |
g6148 | DLA_06848 | GAOABQK02IO52T | CDS | 131650 | 6594 | + | 0.327571 | |
g6149 | DLA_06849 | GAOABQK02IO52T | CDS | 138582 | 3204 | + | 0.334582 | |
g6150 | DLA_06852 | GAOABQK02IO52T | CDS | 142304 | 1197 | + | 0.333333 | |
g6151 | DLA_06853 | GAOABQK02IO52T | CDS | 143752 | 1821 | - | 0.343767 | |
g6152 | DLA_06854 | GAOABQK02IO52T | CDS | 146019 | 2202 | + | 0.310173 | |
g6153 | DLA_06855 | GAOABQK02IO52T | CDS | 148438 | 1251 | - | 0.309353 | |
g6154 | DLA_06856 | GAOABQK02IO52T | CDS | 149796 | 1230 | + | 0.303252 | |
g6155 | DLA_06857 | conserved hypothetical protein similar to esophageal cancer associated protein there is a second copy of this gene | GAOABQK02IO52T | CDS | 151129 | 2898 | - | 0.31677 |
g6156 | DLA_06858 | GAOABQK02IO52T | CDS | 154724 | 480 | - | 0.316667 | |
g6157 | DLA_06859 | GAOABQK02IO52T | CDS | 155969 | 2106 | - | 0.315764 | |
g6158 | DLA_06860 | GAOABQK02IO52T | CDS | 158498 | 702 | + | 0.306268 | |
g6159 | DLA_06861 | GAOABQK02IO52T | CDS | 159354 | 393 | - | 0.284987 | |
g6160 | DLA_06863 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form | GAOABQK02IO52T | CDS | 160544 | 2301 | - | 0.348979 |
g6161 | DLA_06864 | GAOABQK02IO52T | CDS | 163473 | 2073 | + | 0.327062 | |
g6162 | DLA_06865 | GAOABQK02IO52T | CDS | 165952 | 1149 | + | 0.318538 | |
g6163 | DLA_06866 | GAOABQK02IO52T | CDS | 167124 | 1911 | - | 0.323391 | |
g6164 | DLA_06867 | GAOABQK02IO52T | CDS | 169190 | 2802 | + | 0.275161 | |
g6165 | DLA_06869 | GAOABQK02IO52T | CDS | 172244 | 540 | - | 0.368519 | |
g6166 | DLA_06870 | GAOABQK02IO52T | CDS | 173040 | 726 | + | 0.30854 | |
g6167 | DLA_06871 | ortholog of the magnesium transporter MMGT1 contains a putative signal sequence and one transmembrane domain | GAOABQK02IO52T | CDS | 173974 | 291 | - | 0.237113 |
g6168 | DLA_06872 | GAOABQK02IO52T | CDS | 174537 | 270 | + | 0.296296 | |
g6169 | DLA_11669 | GAOABQK02IO52T | CDS | 175395 | 651 | - | 0.347158 | |
g6170 | DLA_06873 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | GAOABQK02IO52T | CDS | 176715 | 450 | - | 0.333333 |
g6171 | DLA_06874 | GAOABQK02IO52T | CDS | 177709 | 2208 | - | 0.319746 | |
g6172 | DLA_06875 | GAOABQK02IO52T | CDS | 180700 | 1071 | + | 0.325864 | |
g6173 | DLA_06878 | GAOABQK02IO52T | CDS | 182524 | 528 | + | 0.304924 | |
g6174 | DLA_06879 | GAOABQK02IO52T | CDS | 184321 | 615 | - | 0.338211 | |
g6175 | DLA_06883 | GAOABQK02IO52T | CDS | 187216 | 1746 | - | 0.313288 | |
g6176 | DLA_06884 | GAOABQK02IO52T | CDS | 189381 | 3627 | + | 0.27764 | |
g6177 | DLA_06885 | GAOABQK02IO52T | CDS | 193209 | 540 | - | 0.272222 | |
g6178 | DLA_06886 | GAOABQK02IO52T | CDS | 193948 | 900 | + | 0.286667 | |
g6179 | DLA_06887 | GAOABQK02IO52T | CDS | 195119 | 1185 | + | 0.278481 | |
g6180 | DLA_06888 | GAOABQK02IO52T | CDS | 196483 | 1353 | + | 0.280857 | |
g6181 | DLA_06891 | GAOABQK02IO52T | CDS | 198295 | 1560 | - | 0.373077 | |
g6182 | DLA_06892 | GAOABQK02IO52T | CDS | 200784 | 1593 | + | 0.313873 | |
g6183 | DLA_06893 | GAOABQK02IO52T | CDS | 203312 | 987 | + | 0.300912 | |
g6184 | DLA_06894 | GAOABQK02IO52T | CDS | 205344 | 4128 | + | 0.341328 | |
g6185 | DLA_06895 | ortholog of Huntington's disease protein Huntingtin (HTT not to be confused with the human serotonin transporter now named SLC6A4) in Dictyostelium regulates myosin II phosphorylation through phosphatase PP2A affecting chemotaxis and cytokinesis also involved in osmoregulation bivalent cation maintenance with effects on development including presporespore differentiation | GAOABQK02IO52T | CDS | 210495 | 8700 | + | 0.330115 |
g6186 | DLA_06896 | catalyzes the reaction D-ribose-5-phosphate D-xylulose-5-phosphate D-sedoheptulose-7-phosphate D-glyceraldehyde-3-phosphate there is a second copy of this gene | GAOABQK02IO52T | CDS | 219448 | 1983 | - | 0.395865 |
g6187 | DLA_11670 | GAOABQK02IO52T | CDS | 221715 | 2754 | - | 0.306826 | |
g6188 | DLA_06897 | GAOABQK02IO52T | CDS | 224860 | 951 | - | 0.320715 | |
g6189 | DLA_06898 | GAOABQK02IO52T | CDS | 226095 | 837 | - | 0.322581 | |
g6190 | DLA_06899 | GAOABQK02IO52T | CDS | 227597 | 2031 | + | 0.321516 | |
g6191 | DLA_06900 | GAOABQK02IO52T | CDS | 230165 | 2697 | + | 0.311828 | |
g6192 | DLA_06901 | putative Ras guanine nucleotide exchange factor promotes the exchange of GDP for GTP on Ras small GTPases thus converting them into the active form similar to son of sevenless | GAOABQK02IO52T | CDS | 233724 | 3675 | + | 0.323265 |
g6193 | DLA_06904 | GAOABQK02IO52T | CDS | 238698 | 2793 | - | 0.324024 | |
g6194 | DLA_06905 | component of the gamma-secretase complex which executes the intramembrane proteolysis of type I integral membrane proteins | GAOABQK02IO52T | CDS | 241828 | 999 | - | 0.309309 |
g6195 | DLA_06906 | GAOABQK02IO52T | CDS | 243026 | 1500 | + | 0.308 | |
g6196 | DLA_06907 | GAOABQK02IO52T | CDS | 244624 | 1221 | - | 0.314496 | |
g6197 | DLA_06908 | GAOABQK02IO52T | CDS | 246045 | 954 | - | 0.272537 | |
g6198 | DLA_06909 | GAOABQK02IO52T | CDS | 247376 | 1623 | + | 0.32101 | |
g6199 | DLA_06910 | GAOABQK02IO52T | CDS | 249203 | 426 | - | 0.384977 | |
g6200 | DLA_06911 | GAOABQK02IO52T | CDS | 250152 | 288 | + | 0.291667 | |
g6201 | DLA_06912 | GAOABQK02IO52T | CDS | 251039 | 330 | - | 0.348485 | |
g6202 | DLA_06913 | GAOABQK02IO52T | CDS | 251587 | 1764 | - | 0.325964 | |
g6203 | DLA_06914 | GAOABQK02IO52T | CDS | 258001 | 2196 | + | 0.362022 | |
g6204 | DLA_06915 | GAOABQK02IO52T | CDS | 260528 | 1869 | + | 0.326378 | |
g6205 | DLA_06916 | GAOABQK02IO52T | CDS | 262549 | 783 | - | 0.296296 | |
g6206 | DLA_11671 | GAOABQK02IO52T | CDS | 263677 | 567 | + | 0.310406 | |
g6207 | DLA_06917 | GAOABQK02IO52T | CDS | 265073 | 4674 | + | 0.345315 | |
g6208 | DLA_06918 | GAOABQK02IO52T | CDS | 270258 | 1809 | + | 0.347706 | |
g6209 | DLA_06919 | GAOABQK02IO52T | CDS | 272235 | 678 | + | 0.30531 | |
g6210 | DLA_06920 | belongs to the Sec7 superfamily involved in phagocytosis and cell motility | GAOABQK02IO52T | CDS | 273684 | 2421 | + | 0.344486 |
g6211 | DLA_06921 | GAOABQK02IO52T | CDS | 276308 | 543 | + | 0.335175 | |
g6212 | DLA_06922 | GAOABQK02IO52T | CDS | 277059 | 1482 | - | 0.357625 | |
g6213 | DLA_06923 | GAOABQK02IO52T | CDS | 279060 | 1587 | + | 0.31821 | |
g6214 | DLA_06924 | GAOABQK02IO52T | CDS | 280771 | 573 | + | 0.326353 | |
g6215 | DLA_06925 | GAOABQK02IO52T | CDS | 281483 | 1110 | - | 0.328829 | |
g6216 | DLA_06926 | GAOABQK02IO52T | CDS | 282728 | 1095 | - | 0.309589 | |
g6217 | DLA_06927 | GAOABQK02IO52T | CDS | 284074 | 1239 | - | 0.330105 | |
g6218 | DLA_06929 | GAOABQK02IO52T | CDS | 286642 | 1476 | + | 0.348916 | |
g6219 | DLA_06930 | GAOABQK02IO52T | CDS | 288711 | 1182 | + | 0.27665 | |
g6220 | DLA_06931 | GAOABQK02IO52T | CDS | 290009 | 1014 | - | 0.311637 | |
g6221 | DLA_06932 | GAOABQK02IO52T | CDS | 291490 | 1233 | + | 0.300892 | |
g6222 | DLA_06933 | GAOABQK02IO52T | CDS | 292942 | 504 | - | 0.28373 | |
g6223 | DLA_06934 | GAOABQK02IO52T | CDS | 293652 | 1794 | - | 0.330546 | |
g6224 | DLA_06936 | GAOABQK02IO52T | CDS | 296793 | 2274 | - | 0.346966 | |
g6225 | DLA_06937 | GAOABQK02IO52T | CDS | 300296 | 543 | + | 0.267035 | |
g6226 | DLA_06938 | GAOABQK02IO52T | CDS | 301000 | 1266 | - | 0.345182 | |
g6227 | DLA_06939 | GAOABQK02IO52T | CDS | 302551 | 2001 | + | 0.30085 | |
g6228 | DLA_06940 | GAOABQK02IO52T | CDS | 304716 | 1059 | + | 0.303116 | |
g6229 | DLA_06941 | GAOABQK02IO52T | CDS | 306315 | 834 | + | 0.322542 | |
g6230 | DLA_06942 | GAOABQK02IO52T | CDS | 307606 | 831 | + | 0.32852 | |
g6231 | DLA_06943 | contains one C2 domain one MHD1 (Munc13-homology) domain and one MHD2 domain | GAOABQK02IO52T | CDS | 308697 | 3792 | + | 0.314873 |
g6232 | DLA_06945 | GAOABQK02IO52T | CDS | 312965 | 1083 | - | 0.289935 | |
g6233 | DLA_06946 | GAOABQK02IO52T | CDS | 314692 | 1926 | + | 0.363448 | |
g6234 | DLA_06947 | GAOABQK02IO52T | CDS | 316825 | 2715 | - | 0.331492 | |
g6235 | DLA_06948 | GAOABQK02IO52T | CDS | 320800 | 555 | + | 0.403604 | |
g6236 | DLA_06949 | GAOABQK02IO52T | CDS | 322203 | 915 | - | 0.353005 | |
g6237 | DLA_06950 | GAOABQK02IO52T | CDS | 324527 | 1281 | + | 0.282592 | |
g6238 | DLA_06951 | GAOABQK02IO52T | CDS | 326148 | 726 | + | 0.319559 | |
g6239 | DLA_06952 | GAOABQK02IO52T | CDS | 326950 | 5052 | - | 0.321853 | |
g6240 | DLA_06953 | GAOABQK02IO52T | CDS | 332362 | 1953 | + | 0.315412 | |
g6241 | DLA_06954 | GAOABQK02IO52T | CDS | 334461 | 1596 | - | 0.295739 | |
g6242 | DLA_06956 | GAOABQK02IO52T | CDS | 337730 | 426 | - | 0.284038 | |
g6243 | DLA_11672 | GAOABQK02IO52T | CDS | 338424 | 426 | - | 0.319249 | |
g6244 | DLA_06957 | GAOABQK02IO52T | CDS | 338974 | 1620 | - | 0.29321 | |
g6245 | DLA_06958 | GAOABQK02IO52T | CDS | 340681 | 270 | + | 0.277778 | |
g6246 | DLA_06959 | GAOABQK02IO52T | CDS | 341219 | 1992 | - | 0.318775 | |
g6247 | DLA_06961 | GAOABQK02IO52T | CDS | 344194 | 1281 | + | 0.293521 | |
g6248 | DLA_06962 | GAOABQK02IO52T | CDS | 346923 | 2586 | + | 0.338747 | |
g6249 | DLA_06963 | GAOABQK02IO52T | CDS | 349959 | 5151 | + | 0.317608 | |
g6250 | DLA_06964 | GAOABQK02IO52T | CDS | 356092 | 636 | + | 0.366352 | |
g6251 | DLA_06965 | GAOABQK02IO52T | CDS | 356924 | 708 | + | 0.289548 | |
g6252 | DLA_06966 | GAOABQK02IO52T | CDS | 357817 | 3051 | + | 0.303507 | |
g6253 | DLA_06967 | subunit of the 20S proteasome (macropain) the endopeptidase complex involved in an ATPubiquitin-dependent nonlysosomal proteolytic pathway in eukaryotes composed of up to 28 subunits which form a highly ordered ring-shaped structure (20S ring) | GAOABQK02IO52T | CDS | 361252 | 696 | - | 0.341954 |
g6254 | DLA_06968 | GAOABQK02IO52T | CDS | 362243 | 2244 | + | 0.295009 | |
g6255 | DLA_06969 | GAOABQK02IO52T | CDS | 364514 | 789 | - | 0.258555 | |
g6256 | DLA_06970 | GAOABQK02IO52T | CDS | 365848 | 1383 | + | 0.340564 | |
g6257 | DLA_06971 | GAOABQK02IO52T | CDS | 367324 | 2175 | - | 0.329655 | |
g6258 | DLA_06972 | GAOABQK02IO52T | CDS | 370044 | 384 | + | 0.382812 | |
g6259 | DLA_06973 | GAOABQK02IO52T | CDS | 370784 | 1821 | + | 0.315761 | |
g6260 | DLA_06974 | GAOABQK02IO52T | CDS | 373105 | 1275 | + | 0.294902 | |
g6261 | DLA_06975 | GAOABQK02IO52T | CDS | 374940 | 633 | + | 0.301738 | |
g6262 | DLA_06976 | GAOABQK02IO52T | CDS | 376039 | 981 | + | 0.331295 | |
g6263 | DLA_06977 | GAOABQK02IO52T | CDS | 377430 | 3825 | - | 0.324444 | |
g6264 | DLA_06978 | GAOABQK02IO52T | CDS | 381832 | 300 | - | 0.303333 | |
g6265 | DLA_06979 | GAOABQK02IO52T | CDS | 382382 | 1770 | + | 0.311299 | |
g6266 | DLA_06980 | GAOABQK02IO52T | CDS | 384308 | 1248 | - | 0.339744 | |
g6267 | DLA_06981 | GAOABQK02IO52T | CDS | 386011 | 360 | + | 0.291667 | |
g6268 | DLA_06982 | GAOABQK02IO52T | CDS | 386719 | 1077 | - | 0.301764 | |
g6269 | DLA_06985 | GAOABQK02IO52T | CDS | 390510 | 1839 | - | 0.353997 | |
g6270 | DLA_06986 | GAOABQK02IO52T | CDS | 394984 | 4206 | + | 0.362102 | |
g6271 | DLA_06987 | GAOABQK02IO52T | CDS | 399341 | 414 | - | 0.333333 | |
g6272 | DLA_06988 | GAOABQK02IO52T | CDS | 400319 | 231 | + | 0.320346 | |
g6273 | DLA_11673 | GAOABQK02IO52T | CDS | 400817 | 816 | + | 0.430147 | |
g6274 | DLA_06989 | GAOABQK02IO52T | CDS | 401737 | 2016 | - | 0.323909 | |
g6275 | DLA_06990 | GAOABQK02IO52T | CDS | 404089 | 1203 | + | 0.334996 | |
g6276 | DLA_06991 | GAOABQK02IO52T | CDS | 405378 | 1617 | - | 0.31107 | |
g6277 | DLA_11674 | GAOABQK02IO52T | CDS | 407984 | 390 | + | 0.312821 | |
g6278 | DLA_06992 | GAOABQK02IO52T | CDS | 408495 | 3780 | + | 0.298413 | |
g6279 | DLA_06993 | GAOABQK02IO52T | CDS | 413957 | 3456 | - | 0.303241 | |
g6280 | DLA_06994 | GAOABQK02IO52T | CDS | 417905 | 2673 | - | 0.295922 | |
g6281 | DLA_06996 | GAOABQK02IO52T | CDS | 422502 | 1737 | + | 0.315486 | |
g6282 | DLA_11675 | GAOABQK02IO52T | CDS | 425969 | 1512 | + | 0.417328 | |
g6283 | DLA_06997 | GAOABQK02IO52T | CDS | 427854 | 981 | + | 0.377166 | |
g6284 | DLA_06998 | GAOABQK02IO52T | CDS | 429085 | 2832 | + | 0.322034 | |
g6285 | DLA_06999 | GAOABQK02IO52T | CDS | 432203 | 1323 | + | 0.298564 | |
g6286 | DLA_07000 | ATP-dependent DNA ligase required for the ligation of Okazaki fragments during lagging-strand DNA synthesis | GAOABQK02IO52T | CDS | 433888 | 2760 | + | 0.334058 |
g6287 | DLA_07001 | GAOABQK02IO52T | CDS | 436769 | 1008 | - | 0.286706 | |
g6288 | DLA_07002 | GAOABQK02IO52T | CDS | 437914 | 1413 | + | 0.319887 | |
g6289 | DLA_07004 | GAOABQK02IO52T | CDS | 440071 | 1605 | - | 0.302804 | |
g6290 | DLA_07005 | GAOABQK02IO52T | CDS | 441759 | 897 | + | 0.284281 | |
g6291 | DLA_07006 | GAOABQK02IO52T | CDS | 442754 | 867 | - | 0.348328 | |
g6292 | DLA_07007 | GAOABQK02IO52T | CDS | 443936 | 1296 | + | 0.296296 | |
g6293 | DLA_07008 | GAOABQK02IO52T | CDS | 445389 | 702 | - | 0.324786 | |
g6294 | DLA_07009 | GAOABQK02IO52T | CDS | 446926 | 1887 | + | 0.326444 | |
g6295 | DLA_11676 | GAOABQK02IO52T | CDS | 448967 | 1152 | - | 0.283854 | |
g6296 | DLA_07010 | GAOABQK02IO52T | CDS | 450270 | 2373 | - | 0.282343 | |
g6297 | DLA_07011 | GAOABQK02IO52T | CDS | 453002 | 726 | + | 0.312672 | |
g6298 | DLA_07012 | GAOABQK02IO52T | CDS | 453969 | 1053 | - | 0.323837 | |
g6299 | DLA_07013 | GAOABQK02IO52T | CDS | 455960 | 2673 | + | 0.325103 | |
g6300 | DLA_07014 | GAOABQK02IO52T | CDS | 458766 | 2121 | + | 0.30976 | |
g6301 | DLA_07015 | GAOABQK02IO52T | CDS | 461803 | 660 | - | 0.343939 | |
g6302 | DLA_11677 | GAOABQK02IO52T | CDS | 462919 | 357 | - | 0.291317 | |
g6303 | DLA_07016 | GAOABQK02IO52T | CDS | 463490 | 1251 | - | 0.253397 | |
g6304 | DLA_07018 | GAOABQK02IO52T | CDS | 465283 | 2589 | - | 0.312476 | |
g6305 | DLA_07021 | conserved eukaryotic kinase (human MVK yeast ERG12) that plays a role in the synthesis of isopentanyl pyrophosphate a common intermediate in pathways including cholesterol biosynthesis | GAOABQK02IO52T | CDS | 470082 | 1155 | + | 0.341991 |
g6306 | DLA_07022 | GAOABQK02IO52T | CDS | 471770 | 1680 | - | 0.28869 | |
g6307 | DLA_07023 | GAOABQK02IO52T | CDS | 473753 | 1464 | + | 0.295765 | |
g6308 | DLA_07025 | GAOABQK02IO52T | CDS | 475447 | 3846 | - | 0.326573 | |
g6309 | DLA_07026 | GAOABQK02IO52T | CDS | 479637 | 3696 | - | 0.325216 | |
g6310 | DLA_07028 | GAOABQK02IO52T | CDS | 484023 | 546 | + | 0.326007 | |
g6311 | DLA_07030 | GAOABQK02IO52T | CDS | 485155 | 2169 | - | 0.339327 | |
g6312 | DLA_07031 | GAOABQK02IO52T | CDS | 488247 | 294 | + | 0.401361 | |
g6313 | DLA_07032 | GAOABQK02IO52T | CDS | 489254 | 885 | - | 0.353672 | |
g6314 | DLA_07033 | catalyzes the reaction D-glyceraldehyde 3-phosphate glycerone phosphate defects in human TPI1 are the cause of triosephosphate isomerase deficiency severe clinical disorder of glycolysis | GAOABQK02IO52T | CDS | 490529 | 777 | - | 0.365508 |
g6315 | DLA_07034 | GAOABQK02IO52T | CDS | 491546 | 1056 | + | 0.322917 | |
g6316 | DLA_07035 | GAOABQK02IO52T | CDS | 492988 | 1053 | - | 0.283951 | |
g6317 | DLA_07036 | homolog of human HMGCS1 catalyzes the reaction acetyl-CoA H2O acetoacetyl-CoA (S)-3-hydroxy-3-methylglutaryl-CoA CoA contains a predicted peroxisomal targeting signal | GAOABQK02IO52T | CDS | 495479 | 1401 | + | 0.356888 |
g6318 | DLA_07037 | GAOABQK02IO52T | CDS | 497222 | 2205 | - | 0.317914 | |
g6319 | DLA_07039 | GAOABQK02IO52T | CDS | 501910 | 1596 | - | 0.31391 | |
g6320 | DLA_07040 | GAOABQK02IO52T | CDS | 503740 | 2217 | + | 0.341001 | |
g6321 | DLA_07041 | catalyzes the reaction geranylgeranyl diphosphate protein-cysteine S-geranylgeranyl-protein diphosphate | GAOABQK02IO52T | CDS | 506221 | 1083 | + | 0.34903 |
g6322 | DLA_07042 | GAOABQK02IO52T | CDS | 507413 | 5760 | - | 0.312153 | |
g6323 | DLA_07043 | GAOABQK02IO52T | CDS | 513590 | 2301 | + | 0.317253 | |
g6324 | DLA_07044 | GAOABQK02IO52T | CDS | 516261 | 2535 | + | 0.321105 | |
g6325 | DLA_07045 | GAOABQK02IO52T | CDS | 518831 | 3597 | - | 0.318599 | |
g6326 | DLA_07046 | GAOABQK02IO52T | CDS | 523045 | 1407 | + | 0.316987 | |
g6327 | DLA_07047 | underexpressed in | GAOABQK02IO52T | CDS | 524724 | 888 | + | 0.337838 |
g6328 | DLA_07048 | GAOABQK02IO52T | CDS | 525873 | 879 | + | 0.336746 | |
g6329 | DLA_07049 | GAOABQK02IO52T | CDS | 526971 | 2703 | - | 0.337403 | |
g6330 | DLA_11678 | GAOABQK02IO52T | CDS | 530240 | 618 | - | 0.331715 | |
g6331 | DLA_07050 | GAOABQK02IO52T | CDS | 531352 | 918 | + | 0.339869 | |
g6332 | DLA_07051 | GAOABQK02IO52T | CDS | 532386 | 837 | + | 0.321386 | |
g6333 | DLA_07052 | GAOABQK02IO52T | CDS | 533333 | 498 | - | 0.307229 | |
g6334 | DLA_07053 | GAOABQK02IO52T | CDS | 534110 | 3546 | + | 0.319515 | |
g6335 | DLA_07054 | GAOABQK02IO52T | CDS | 537757 | 378 | - | 0.298942 | |
g6336 | DLA_07055 | GAOABQK02IO52T | CDS | 538454 | 375 | - | 0.328 | |
g6337 | DLA_07056 | GAOABQK02IO52T | CDS | 540651 | 1158 | + | 0.309154 | |
g6338 | DLA_07057 | GAOABQK02IO52T | CDS | 541977 | 474 | - | 0.2827 | |
g6339 | DLA_07058 | GAOABQK02IO52T | CDS | 542749 | 483 | + | 0.296066 | |
g6340 | DLA_07059 | GAOABQK02IO52T | CDS | 543681 | 1629 | + | 0.368324 | |
g6341 | DLA_07060 | GAOABQK02IO52T | CDS | 545602 | 2247 | + | 0.336894 | |
g6342 | DLA_07061 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H4 | GAOABQK02IO52T | CDS | 548163 | 414 | + | 0.39372 |
g6343 | DLA_07062 | ortholog of S. cerevisiae URA1 and human DPYD defects in DPYD cause dihydropyrimidine dehydrogenase deficiency catalyzes the reaction 56-dihydrouracil NADP uracil NADPH H | GAOABQK02IO52T | CDS | 549158 | 3054 | + | 0.384741 |
g6344 | DLA_07063 | GAOABQK02IO52T | CDS | 552777 | 5415 | + | 0.328901 | |
g6345 | DLA_07064 | GAOABQK02IO52T | CDS | 558791 | 2451 | - | 0.314565 | |
g6346 | DLA_07065 | GAOABQK02IO52T | CDS | 561324 | 1548 | - | 0.313953 | |
g6347 | DLA_07066 | ortholog of human CRIP1 contains 1 zinc-binding LIM domain LIM domains are found in proteins with differing functions including gene expression and cytoskeleton organisation and development | GAOABQK02IO52T | CDS | 563122 | 264 | - | 0.382576 |
g6348 | DLA_07067 | GAOABQK02IO52T | CDS | 563828 | 606 | - | 0.232673 | |
g6349 | DLA_07069 | GAOABQK02IO52T | CDS | 564818 | 2496 | + | 0.314103 | |
g6350 | DLA_07070 | GAOABQK02IO52T | CDS | 567474 | 3417 | - | 0.321042 | |
g6351 | DLA_07071 | GAOABQK02IO52T | CDS | 571269 | 531 | - | 0.335217 | |
g6352 | DLA_07072 | GAOABQK02IO52T | CDS | 572541 | 891 | + | 0.276094 | |
g6353 | DLA_07073 | GAOABQK02IO52T | CDS | 573795 | 1047 | + | 0.369628 | |
g6354 | DLA_07074 | GAOABQK02IO52T | CDS | 575157 | 1287 | + | 0.309246 | |
g6355 | DLA_07075 | GAOABQK02IO52T | CDS | 576512 | 4257 | - | 0.322293 | |
g6356 | DLA_07076 | GAOABQK02IO52T | CDS | 581262 | 1839 | - | 0.363785 | |
g6357 | DLA_07077 | GAOABQK02IO52T | CDS | 583246 | 1563 | - | 0.337172 | |
g6358 | DLA_07078 | GAOABQK02IO52T | CDS | 585242 | 423 | + | 0.288416 | |
g6359 | DLA_07079 | GAOABQK02IO52T | CDS | 586217 | 231 | + | 0.30303 | |
g6360 | DLA_07080 | involved in phagocytosis and substrate adhesion controls the levels of SibA adhesion molecules at the cell surface as well as the intracellular transport and stability of the SibA protein also involved in the intracellular killing of bacteria by determining the stability and cellular amount of the sulfotransferase Kil1br bNomenclature conflict: b Do not confuse this gene with phgA encoding drainin or with the phgA locus ( | GAOABQK02IO52T | CDS | 586782 | 1893 | - | 0.368199 |
g6361 | DLA_07081 | GAOABQK02IO52T | CDS | 589090 | 270 | - | 0.296296 | |
g6362 | DLA_07082 | GAOABQK02IO52T | CDS | 589566 | 1362 | - | 0.422173 | |
g6363 | DLA_07083 | GAOABQK02IO52T | CDS | 591815 | 1098 | + | 0.32969 | |
g6364 | DLA_07084 | GAOABQK02IO52T | CDS | 593010 | 2448 | - | 0.329657 | |
g6365 | DLA_07085 | GAOABQK02IO52T | CDS | 595945 | 1101 | - | 0.315168 | |
g6366 | DLA_07086 | GAOABQK02IO52T | CDS | 600546 | 1707 | + | 0.357352 | |
g6367 | DLA_07087 | putative protein serinethreonine kinase belongs to the PAKL subfamily of protein kinases the kinase domain is similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase | GAOABQK02IO52T | CDS | 603199 | 2982 | + | 0.346412 |
g6368 | DLA_07088 | GAOABQK02IO52T | CDS | 606292 | 1755 | - | 0.283191 | |
g6369 | DLA_07089 | GAOABQK02IO52T | CDS | 609130 | 2634 | + | 0.329916 | |
g6370 | DLA_07090 | GAOABQK02IO52T | CDS | 612055 | 615 | + | 0.317073 | |
g6371 | DLA_07091 | GAOABQK02IO52T | CDS | 612802 | 1539 | - | 0.339181 | |
g6372 | DLA_07092 | GAOABQK02IO52T | CDS | 614911 | 2685 | + | 0.347114 | |
g6373 | DLA_07093 | GAOABQK02IO52T | CDS | 617780 | 627 | - | 0.370016 | |
g6374 | DLA_07094 | GAOABQK02IO52T | CDS | 619195 | 1515 | - | 0.305611 | |
g6375 | DLA_07095 | GAOABQK02IO52T | CDS | 621953 | 1251 | + | 0.308553 | |
g6376 | DLA_07096 | belongs to a gene family conserved in amoeba contains a putative metal-binding domain | GAOABQK02IO52T | CDS | 625710 | 1059 | + | 0.326723 |
g6377 | DLA_07097 | GAOABQK02IO52T | CDS | 627094 | 2634 | - | 0.314351 | |
g6378 | DLA_07098 | GAOABQK02IO52T | CDS | 629988 | 903 | + | 0.314507 | |
g6379 | DLA_07099 | GAOABQK02IO52T | CDS | 631298 | 1080 | - | 0.356481 | |
g6380 | DLA_07100 | GAOABQK02IO52T | CDS | 632667 | 2820 | + | 0.30922 | |
g6381 | DLA_07101 | GAOABQK02IO52T | CDS | 635945 | 4212 | + | 0.328348 | |
g6382 | DLA_07102 | GAOABQK02IO52T | CDS | 640401 | 1662 | - | 0.295427 | |
g6383 | DLA_07103 | GAOABQK02IO52T | CDS | 642277 | 1752 | - | 0.304224 | |
g6384 | DLA_07105 | GAOABQK02IO52T | CDS | 644577 | 1728 | - | 0.302662 | |
g6385 | DLA_07106 | GAOABQK02IO52T | CDS | 646704 | 1536 | + | 0.314453 | |
g6386 | DLA_07107 | GAOABQK02IO52T | CDS | 648464 | 762 | - | 0.353018 | |
g6387 | DLA_07108 | GAOABQK02IO52T | CDS | 649858 | 747 | + | 0.348059 | |
g6388 | DLA_07109 | GAOABQK02IO52T | CDS | 650898 | 396 | - | 0.313131 | |
g6389 | DLA_07110 | GAOABQK02IO52T | CDS | 651734 | 1254 | + | 0.296651 | |
g6390 | DLA_07111 | GAOABQK02IO52T | CDS | 653197 | 660 | - | 0.359091 | |
g6391 | DLA_07112 | GAOABQK02IO52T | CDS | 654391 | 933 | + | 0.301179 | |
g6392 | DLA_07113 | ortholog of S. cerevisiae TFB1 subunit of TFIIH and nucleotide excision repair factor 3 complexes required for nucleotide excision repair target for transcriptional activators | GAOABQK02IO52T | CDS | 655521 | 1926 | + | 0.350987 |
g6393 | DLA_07114 | putative protein serinethreonine kinase N-terminus similar to mammalian STK3 and STK4 (MST) kinases and other STE20-like kinases stress-responsive kinase C-terminal half belongs to the peptidase C2 family contains 4 calpain III domains and has similarity to calpain-like cysteine protease | GAOABQK02IO52T | CDS | 657826 | 3318 | + | 0.347499 |
g6394 | DLA_07115 | GAOABQK02IO52T | CDS | 661516 | 1122 | - | 0.309269 | |
g6395 | DLA_07116 | GAOABQK02IO52T | CDS | 662877 | 534 | - | 0.277154 | |
g6396 | DLA_07117 | controls RNA polymerase II activity by phosphorylating the carboxy terminal domain (CTD) of the largest subunit predicted to interact with | GAOABQK02IO52T | CDS | 663556 | 1113 | + | 0.343217 |
g6397 | DLA_07118 | GAOABQK02IO52T | CDS | 664722 | 1782 | - | 0.306397 | |
g6398 | DLA_07119 | GAOABQK02IO52T | CDS | 666791 | 1806 | + | 0.295681 | |
g6399 | DLA_07121 | GAOABQK02IO52T | CDS | 668752 | 2100 | - | 0.33381 | |
g6400 | DLA_07122 | GAOABQK02IO52T | CDS | 671553 | 909 | - | 0.349835 | |
g6401 | DLA_07123 | GAOABQK02IO52T | CDS | 673443 | 2532 | - | 0.317536 | |
g6402 | DLA_07124 | GAOABQK02IO52T | CDS | 676808 | 228 | - | 0.27193 | |
g6403 | DLA_07125 | GAOABQK02IO52T | CDS | 677804 | 2007 | + | 0.308919 | |
g6404 | DLA_07126 | GAOABQK02IO52T | CDS | 680176 | 900 | - | 0.322222 | |
g6405 | DLA_07127 | GAOABQK02IO52T | CDS | 681179 | 1026 | - | 0.302144 | |
g6406 | DLA_07128 | GAOABQK02IO52T | CDS | 683154 | 1290 | - | 0.317829 | |
g6407 | DLA_07130 | GAOABQK02IO52T | CDS | 684776 | 2007 | - | 0.310414 | |
g6408 | DLA_07132 | GAOABQK02IO52T | CDS | 687639 | 2376 | - | 0.323653 | |
g6409 | DLA_07133 | GAOABQK02IO52T | CDS | 690319 | 3717 | - | 0.379338 | |
g6410 | DLA_07135 | GAOABQK02IO52T | CDS | 695459 | 18697 | + | 0.365246 |