Gene list
Applied filters:
Genomic element: F4PJNLW01A00V1
Number of genes found: 640
Show UniProt / TrEMBL protein name | View in Fasta format (DNA) | View in Fasta format (Protein) | ||||
Dictyostelium lacteum | ||||||||
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Name | Locus tag | Product / Description | Genomic element | Type | Begin | Length | Strand | GC-content |
NA | DLA_11902 | tRNA-Gln | F4PJNLW01A00V1 | tRNA | 592539 | 72 | - | 0.402778 |
drnA | DLA_01047 | similar to the mammalian Dicer protein an RNase III protein that converts long dsRNA (double-stranded RNA) into siRNA (small interfering RNA) in Dictyostelium involved in RNA interference and microRNA processing | F4PJNLW01A00V1 | CDS | 697220 | 3645 | - | 0.314129 |
g1000 | DLA_01110 | F4PJNLW01A00V1 | CDS | 828964 | 1653 | - | 0.30127 | |
g1001 | DLA_01111 | component of the SCF ubiquitin ligase complex the fpaB gene encodes a protein almost identical to that of fpaA differing in one amino acid only series of glycosylation reactions attaches a pentasaccharide chain to HyPro143 there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 831508 | 483 | - | 0.339545 |
g1002 | DLA_01112 | F4PJNLW01A00V1 | CDS | 832593 | 3108 | - | 0.361647 | |
g1003 | DLA_01113 | F4PJNLW01A00V1 | CDS | 836642 | 957 | + | 0.339603 | |
g1004 | DLA_01114 | F4PJNLW01A00V1 | CDS | 837872 | 1662 | - | 0.342359 | |
g1005 | DLA_01115 | F4PJNLW01A00V1 | CDS | 840089 | 1410 | - | 0.311348 | |
g1006 | DLA_01116 | F4PJNLW01A00V1 | CDS | 841672 | 1410 | - | 0.370213 | |
g1007 | DLA_01117 | F4PJNLW01A00V1 | CDS | 843560 | 7092 | + | 0.326424 | |
g1008 | DLA_01118 | F4PJNLW01A00V1 | CDS | 851960 | 2121 | + | 0.286657 | |
g1009 | DLA_01120 | F4PJNLW01A00V1 | CDS | 854260 | 417 | + | 0.302158 | |
g1010 | DLA_01121 | F4PJNLW01A00V1 | CDS | 855110 | 2964 | + | 0.339406 | |
g1011 | DLA_01122 | F4PJNLW01A00V1 | CDS | 858219 | 1269 | - | 0.327029 | |
g1012 | DLA_01123 | 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) | F4PJNLW01A00V1 | CDS | 859752 | 708 | - | 0.323446 |
g1013 | DLA_11462 | F4PJNLW01A00V1 | CDS | 860814 | 426 | + | 0.262911 | |
g1014 | DLA_01124 | F4PJNLW01A00V1 | CDS | 861418 | 939 | + | 0.332268 | |
g1015 | DLA_01125 | F4PJNLW01A00V1 | CDS | 862685 | 960 | + | 0.291667 | |
g1016 | DLA_01126 | F4PJNLW01A00V1 | CDS | 864333 | 840 | + | 0.29881 | |
g1017 | DLA_01127 | F4PJNLW01A00V1 | CDS | 865535 | 759 | - | 0.280632 | |
g1018 | DLA_01128 | F4PJNLW01A00V1 | CDS | 866619 | 570 | + | 0.294737 | |
g1019 | DLA_01129 | F4PJNLW01A00V1 | CDS | 867408 | 1245 | - | 0.349398 | |
g1020 | DLA_01130 | F4PJNLW01A00V1 | CDS | 868852 | 1428 | - | 0.279412 | |
g1021 | DLA_01132 | F4PJNLW01A00V1 | CDS | 871920 | 336 | + | 0.297619 | |
g1022 | DLA_01133 | F4PJNLW01A00V1 | CDS | 872330 | 942 | - | 0.276008 | |
g1023 | DLA_01134 | F4PJNLW01A00V1 | CDS | 874184 | 2289 | + | 0.367409 | |
g1024 | DLA_01135 | F4PJNLW01A00V1 | CDS | 876685 | 699 | - | 0.273248 | |
g1025 | DLA_01136 | F4PJNLW01A00V1 | CDS | 877773 | 198 | + | 0.333333 | |
g1026 | DLA_01137 | F4PJNLW01A00V1 | CDS | 878684 | 1566 | - | 0.323755 | |
g1027 | DLA_01138 | F4PJNLW01A00V1 | CDS | 880585 | 786 | + | 0.321883 | |
g1028 | DLA_01139 | F4PJNLW01A00V1 | CDS | 881450 | 2721 | - | 0.314958 | |
g1029 | DLA_01140 | F4PJNLW01A00V1 | CDS | 884584 | 1035 | - | 0.320773 | |
g1030 | DLA_01141 | F4PJNLW01A00V1 | CDS | 885963 | 1764 | - | 0.328231 | |
g1031 | DLA_01142 | F4PJNLW01A00V1 | CDS | 888152 | 1965 | - | 0.347074 | |
g1032 | DLA_01143 | F4PJNLW01A00V1 | CDS | 891067 | 2724 | - | 0.318282 | |
g1033 | DLA_01144 | F4PJNLW01A00V1 | CDS | 893896 | 1710 | + | 0.307602 | |
g1034 | DLA_01145 | F4PJNLW01A00V1 | CDS | 895823 | 378 | + | 0.314815 | |
g1035 | DLA_01146 | F4PJNLW01A00V1 | CDS | 896334 | 2064 | + | 0.35126 | |
g1036 | DLA_01147 | F4PJNLW01A00V1 | CDS | 898949 | 288 | + | 0.298611 | |
g1037 | DLA_01148 | F4PJNLW01A00V1 | CDS | 899630 | 510 | + | 0.309804 | |
g1038 | DLA_01149 | F4PJNLW01A00V1 | CDS | 900466 | 948 | + | 0.295359 | |
g1039 | DLA_11463 | F4PJNLW01A00V1 | CDS | 901570 | 1158 | - | 0.351468 | |
g1040 | DLA_01150 | F4PJNLW01A00V1 | CDS | 904204 | 1107 | - | 0.31617 | |
g1041 | DLA_01151 | F4PJNLW01A00V1 | CDS | 908661 | 2589 | + | 0.3708 | |
g1042 | DLA_01152 | F4PJNLW01A00V1 | CDS | 911579 | 402 | - | 0.283582 | |
g1043 | DLA_01153 | F4PJNLW01A00V1 | CDS | 912269 | 1566 | + | 0.323116 | |
g1044 | DLA_01154 | F4PJNLW01A00V1 | CDS | 914257 | 897 | + | 0.391304 | |
g1045 | DLA_01155 | F4PJNLW01A00V1 | CDS | 915420 | 5451 | - | 0.335168 | |
g1046 | DLA_01156 | F4PJNLW01A00V1 | CDS | 921345 | 7026 | + | 0.322516 | |
g1047 | DLA_01157 | F4PJNLW01A00V1 | CDS | 928640 | 3351 | + | 0.314235 | |
g1048 | DLA_01158 | F4PJNLW01A00V1 | CDS | 932557 | 279 | + | 0.290323 | |
g1049 | DLA_01159 | F4PJNLW01A00V1 | CDS | 933048 | 1425 | - | 0.334035 | |
g1050 | DLA_01160 | F4PJNLW01A00V1 | CDS | 934640 | 2652 | - | 0.347285 | |
g1051 | DLA_01161 | F4PJNLW01A00V1 | CDS | 937679 | 1728 | - | 0.32581 | |
g1052 | DLA_01162 | F4PJNLW01A00V1 | CDS | 940052 | 603 | - | 0.273632 | |
g1053 | DLA_01163 | F4PJNLW01A00V1 | CDS | 940984 | 1425 | - | 0.263158 | |
g1054 | DLA_01164 | F4PJNLW01A00V1 | CDS | 942832 | 1635 | - | 0.327829 | |
g1055 | DLA_01165 | F4PJNLW01A00V1 | CDS | 945624 | 1398 | + | 0.329041 | |
g1056 | DLA_01166 | similar to the human lipase family catalyzes the reaction: Triacylglycerol Hsub2subO diacylglycerol a carboxylate | F4PJNLW01A00V1 | CDS | 947178 | 1215 | - | 0.365432 |
g1057 | DLA_01167 | F4PJNLW01A00V1 | CDS | 948652 | 1140 | + | 0.338596 | |
g1058 | DLA_01168 | F4PJNLW01A00V1 | CDS | 950617 | 2925 | + | 0.367863 | |
g1059 | DLA_01169 | F4PJNLW01A00V1 | CDS | 953771 | 1434 | - | 0.297071 | |
g1060 | DLA_11464 | F4PJNLW01A00V1 | CDS | 955280 | 339 | + | 0.286136 | |
g1061 | DLA_01170 | F4PJNLW01A00V1 | CDS | 956070 | 2178 | - | 0.374196 | |
g1062 | DLA_11465 | F4PJNLW01A00V1 | CDS | 959402 | 456 | - | 0.258772 | |
g1063 | DLA_01171 | F4PJNLW01A00V1 | CDS | 960216 | 393 | + | 0.318066 | |
g1064 | DLA_01172 | F4PJNLW01A00V1 | CDS | 961082 | 1116 | - | 0.329749 | |
g1065 | DLA_01173 | F4PJNLW01A00V1 | CDS | 962636 | 1800 | - | 0.364444 | |
g1066 | DLA_01174 | F4PJNLW01A00V1 | CDS | 965085 | 1551 | + | 0.317215 | |
g1067 | DLA_01175 | F4PJNLW01A00V1 | CDS | 966915 | 1383 | - | 0.339118 | |
g1068 | DLA_01176 | F4PJNLW01A00V1 | CDS | 968608 | 1041 | - | 0.335255 | |
g1069 | DLA_01177 | F4PJNLW01A00V1 | CDS | 970180 | 2199 | + | 0.313324 | |
g1070 | DLA_01178 | F4PJNLW01A00V1 | CDS | 972478 | 1959 | - | 0.335375 | |
g1071 | DLA_01179 | F4PJNLW01A00V1 | CDS | 974717 | 912 | + | 0.253289 | |
g1072 | DLA_01180 | F4PJNLW01A00V1 | CDS | 975804 | 453 | - | 0.379691 | |
g1073 | DLA_01182 | F4PJNLW01A00V1 | CDS | 977295 | 519 | - | 0.319846 | |
g1074 | DLA_01183 | F4PJNLW01A00V1 | CDS | 979121 | 1500 | - | 0.281333 | |
g1075 | DLA_01184 | F4PJNLW01A00V1 | CDS | 981106 | 906 | - | 0.343267 | |
g1076 | DLA_01186 | F4PJNLW01A00V1 | CDS | 983053 | 1326 | - | 0.306938 | |
g1077 | DLA_01188 | F4PJNLW01A00V1 | CDS | 985347 | 3480 | + | 0.310345 | |
g1078 | DLA_01190 | F4PJNLW01A00V1 | CDS | 989493 | 1569 | + | 0.342894 | |
g1079 | DLA_01192 | F4PJNLW01A00V1 | CDS | 991088 | 3372 | - | 0.283511 | |
g1080 | DLA_11466 | F4PJNLW01A00V1 | CDS | 995012 | 1251 | + | 0.297362 | |
g1081 | DLA_01193 | F4PJNLW01A00V1 | CDS | 997311 | 3690 | + | 0.325745 | |
g1082 | DLA_11467 | F4PJNLW01A00V1 | CDS | 1001283 | 936 | + | 0.311966 | |
g1083 | DLA_11468 | F4PJNLW01A00V1 | CDS | 1002670 | 2007 | + | 0.284504 | |
g1084 | DLA_01194 | F4PJNLW01A00V1 | CDS | 1005316 | 3210 | + | 0.350779 | |
g1085 | DLA_01195 | catalyzes the reaction CDP-choline 12-diacylglycerol CMP a phosphatidylcholine most similar to plant genes REMI mutant forms aberrant fruiting bodies see | F4PJNLW01A00V1 | CDS | 1008714 | 1191 | + | 0.311503 |
g1086 | DLA_01197 | F4PJNLW01A00V1 | CDS | 1010803 | 579 | + | 0.279793 | |
g1087 | DLA_01198 | F4PJNLW01A00V1 | CDS | 1011517 | 1935 | + | 0.327649 | |
g1088 | DLA_01200 | F4PJNLW01A00V1 | CDS | 1013662 | 2727 | - | 0.302164 | |
g1089 | DLA_01201 | F4PJNLW01A00V1 | CDS | 1020294 | 3582 | + | 0.357063 | |
g1090 | DLA_01202 | F4PJNLW01A00V1 | CDS | 1024145 | 489 | - | 0.327198 | |
g1091 | DLA_01205 | F4PJNLW01A00V1 | CDS | 1025608 | 480 | - | 0.408333 | |
g1092 | DLA_01206 | highly conserved protein containing an alkyl hydroperoxide reductasethiol specific antioxidantmal allergen domain identical to | F4PJNLW01A00V1 | CDS | 1027088 | 912 | + | 0.357456 |
g1093 | DLA_01208 | F4PJNLW01A00V1 | CDS | 1029214 | 396 | - | 0.30303 | |
g1094 | DLA_01210 | F4PJNLW01A00V1 | CDS | 1030016 | 585 | - | 0.382906 | |
g1095 | DLA_01211 | F4PJNLW01A00V1 | CDS | 1031188 | 1548 | + | 0.319767 | |
g1096 | DLA_01212 | F4PJNLW01A00V1 | CDS | 1033053 | 825 | + | 0.293333 | |
g1097 | DLA_01213 | F4PJNLW01A00V1 | CDS | 1034101 | 2148 | - | 0.366853 | |
g1098 | DLA_01214 | F4PJNLW01A00V1 | CDS | 1036723 | 1620 | - | 0.331481 | |
g1099 | DLA_01215 | F4PJNLW01A00V1 | CDS | 1038454 | 1191 | - | 0.345088 | |
g1100 | DLA_01216 | F4PJNLW01A00V1 | CDS | 1040176 | 4545 | + | 0.345215 | |
g1101 | DLA_01217 | F4PJNLW01A00V1 | CDS | 1044962 | 4236 | + | 0.333333 | |
g1102 | DLA_01218 | F4PJNLW01A00V1 | CDS | 1049434 | 4431 | + | 0.331302 | |
g1103 | DLA_01219 | F4PJNLW01A00V1 | CDS | 1054121 | 1938 | - | 0.389061 | |
g1104 | DLA_01220 | catalyzes the reaction: 3-hydroxy-2-methylpropanoyl-CoA H2O CoA 3-hydroxy-2-methylpropanoate ortholog of the mammalian HIBCH enzyme | F4PJNLW01A00V1 | CDS | 1056585 | 1152 | - | 0.358507 |
g1105 | DLA_01221 | F4PJNLW01A00V1 | CDS | 1057888 | 1659 | + | 0.306811 | |
g1106 | DLA_01222 | F4PJNLW01A00V1 | CDS | 1059567 | 6933 | - | 0.300303 | |
g1107 | DLA_01224 | F4PJNLW01A00V1 | CDS | 1068083 | 6939 | - | 0.300331 | |
g1108 | DLA_01225 | F4PJNLW01A00V1 | CDS | 1075598 | 1473 | - | 0.285132 | |
g1109 | DLA_01226 | F4PJNLW01A00V1 | CDS | 1077570 | 1770 | + | 0.389266 | |
g1110 | DLA_01227 | F4PJNLW01A00V1 | CDS | 1079405 | 1206 | - | 0.290216 | |
g1111 | DLA_01228 | F4PJNLW01A00V1 | CDS | 1080787 | 1110 | + | 0.311712 | |
g1112 | DLA_01229 | F4PJNLW01A00V1 | CDS | 1082234 | 2250 | - | 0.354222 | |
g1113 | DLA_01230 | F4PJNLW01A00V1 | CDS | 1086396 | 2109 | - | 0.308677 | |
g1114 | DLA_01231 | F4PJNLW01A00V1 | CDS | 1089808 | 2295 | + | 0.346405 | |
g1115 | DLA_01232 | F4PJNLW01A00V1 | CDS | 1092890 | 2142 | + | 0.332866 | |
g1116 | DLA_01233 | conserved protein of unknown function contains a putative signal peptide followed by a transmembrane domain | F4PJNLW01A00V1 | CDS | 1095509 | 222 | + | 0.396396 |
g1117 | DLA_01234 | F4PJNLW01A00V1 | CDS | 1096028 | 4542 | + | 0.337957 | |
g1118 | DLA_01235 | F4PJNLW01A00V1 | CDS | 1100695 | 1263 | - | 0.32304 | |
g1119 | DLA_01237 | F4PJNLW01A00V1 | CDS | 1102872 | 1176 | - | 0.320578 | |
g1120 | DLA_01238 | F4PJNLW01A00V1 | CDS | 1105141 | 2157 | + | 0.364395 | |
g1121 | DLA_01239 | 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) | F4PJNLW01A00V1 | CDS | 1108058 | 729 | + | 0.348422 |
g1122 | DLA_01240 | similar to D. purpureum protein contains one coiled-coil domain | F4PJNLW01A00V1 | CDS | 1109132 | 489 | - | 0.259714 |
g1123 | DLA_01241 | non-catalytic subunit of the AMP-activated protein kinase (AMPK) complex contains two CBS domains | F4PJNLW01A00V1 | CDS | 1109956 | 1629 | + | 0.333947 |
g1124 | DLA_01242 | F4PJNLW01A00V1 | CDS | 1111675 | 2160 | - | 0.307407 | |
g1125 | DLA_01243 | F4PJNLW01A00V1 | CDS | 1114056 | 4023 | - | 0.333333 | |
g1126 | DLA_11469 | F4PJNLW01A00V1 | CDS | 1118348 | 3996 | - | 0.318569 | |
g1127 | DLA_01244 | F4PJNLW01A00V1 | CDS | 1122642 | 4023 | - | 0.34079 | |
g1128 | DLA_01245 | F4PJNLW01A00V1 | CDS | 1127299 | 963 | - | 0.34891 | |
g1129 | DLA_01246 | F4PJNLW01A00V1 | CDS | 1128887 | 1311 | + | 0.334859 | |
g1130 | DLA_01247 | F4PJNLW01A00V1 | CDS | 1130542 | 1641 | + | 0.393053 | |
g1131 | DLA_01248 | F4PJNLW01A00V1 | CDS | 1132598 | 1683 | + | 0.382056 | |
g1132 | DLA_01249 | F4PJNLW01A00V1 | CDS | 1134624 | 1155 | + | 0.333333 | |
g1133 | DLA_01250 | F4PJNLW01A00V1 | CDS | 1135865 | 2100 | + | 0.345238 | |
g1134 | DLA_01251 | similar to the esterase encoded by | F4PJNLW01A00V1 | CDS | 1138000 | 1065 | - | 0.323005 |
g1135 | DLA_01252 | F4PJNLW01A00V1 | CDS | 1139362 | 1332 | - | 0.36036 | |
g1136 | DLA_01253 | F4PJNLW01A00V1 | CDS | 1141153 | 1866 | + | 0.338692 | |
g1137 | DLA_01255 | F4PJNLW01A00V1 | CDS | 1143780 | 1638 | + | 0.310745 | |
g1138 | DLA_01256 | F4PJNLW01A00V1 | CDS | 1145631 | 4023 | - | 0.323391 | |
g1139 | DLA_01257 | F4PJNLW01A00V1 | CDS | 1149950 | 1407 | - | 0.366027 | |
g1140 | DLA_01258 | superoxide dismutase of the SOD1 family expressed at constant levels throughout the life cycle and upregulated upon oxidative stress enriched in prespore cells | F4PJNLW01A00V1 | CDS | 1151652 | 459 | - | 0.407407 |
g1141 | DLA_01259 | F4PJNLW01A00V1 | CDS | 1152403 | 1476 | - | 0.402439 | |
g1142 | DLA_01260 | homolog of mammalian Rab GDP dissociation inhibitor alpha forms a soluble complex with Rab proteins thereby preventing exchange of GDP for GTP | F4PJNLW01A00V1 | CDS | 1154536 | 1356 | + | 0.377581 |
g1143 | DLA_01261 | bifunctional enolase-phosphatase that cleaves the substrates 23-diketo-5-methylthio-1-phosphopentane and 2-hydroxy-3-keto-5-methylthio-1-phosphopentene | F4PJNLW01A00V1 | CDS | 1156181 | 801 | + | 0.330836 |
g1144 | DLA_01262 | F4PJNLW01A00V1 | CDS | 1157028 | 3807 | - | 0.353297 | |
g1145 | DLA_01263 | F4PJNLW01A00V1 | CDS | 1161441 | 261 | + | 0.398467 | |
g1146 | DLA_01264 | F4PJNLW01A00V1 | CDS | 1161847 | 1629 | - | 0.300184 | |
g1147 | DLA_01265 | F4PJNLW01A00V1 | CDS | 1163534 | 1497 | + | 0.281897 | |
g1148 | DLA_01266 | F4PJNLW01A00V1 | CDS | 1165064 | 1224 | - | 0.295752 | |
g1149 | DLA_01267 | F4PJNLW01A00V1 | CDS | 1167153 | 6837 | + | 0.346204 | |
g1150 | DLA_11470 | F4PJNLW01A00V1 | CDS | 1174662 | 795 | + | 0.295597 | |
g1151 | DLA_01268 | F4PJNLW01A00V1 | CDS | 1176051 | 228 | - | 0.421053 | |
g1152 | DLA_01269 | F4PJNLW01A00V1 | CDS | 1177069 | 2502 | - | 0.323341 | |
g1153 | DLA_01270 | F4PJNLW01A00V1 | CDS | 1180005 | 4395 | - | 0.301479 | |
g1154 | DLA_01272 | F4PJNLW01A00V1 | CDS | 1185178 | 3942 | - | 0.341705 | |
g1155 | DLA_01273 | F4PJNLW01A00V1 | CDS | 1189694 | 2349 | + | 0.260962 | |
g1156 | DLA_01274 | F4PJNLW01A00V1 | CDS | 1192312 | 9372 | - | 0.330666 | |
g1157 | DLA_01275 | F4PJNLW01A00V1 | CDS | 1201874 | 1893 | - | 0.375066 | |
g1158 | DLA_01276 | F4PJNLW01A00V1 | CDS | 1204146 | 477 | + | 0.287212 | |
g1159 | DLA_01277 | F4PJNLW01A00V1 | CDS | 1205329 | 888 | - | 0.414414 | |
g1160 | DLA_01278 | F4PJNLW01A00V1 | CDS | 1207537 | 1776 | - | 0.377815 | |
g1161 | DLA_11471 | F4PJNLW01A00V1 | CDS | 1209647 | 3924 | - | 0.33104 | |
g1162 | DLA_01279 | F4PJNLW01A00V1 | CDS | 1214037 | 4026 | - | 0.328862 | |
g1163 | DLA_01280 | F4PJNLW01A00V1 | CDS | 1218879 | 3033 | + | 0.352456 | |
g1164 | DLA_01281 | F4PJNLW01A00V1 | CDS | 1221948 | 381 | - | 0.278215 | |
g1165 | DLA_01282 | F4PJNLW01A00V1 | CDS | 1222612 | 798 | + | 0.298246 | |
g1166 | DLA_01283 | F4PJNLW01A00V1 | CDS | 1223834 | 1074 | + | 0.296089 | |
g1167 | DLA_01284 | F4PJNLW01A00V1 | CDS | 1225330 | 4419 | - | 0.342838 | |
g1168 | DLA_01285 | F4PJNLW01A00V1 | CDS | 1231592 | 2397 | - | 0.380058 | |
g1169 | DLA_01286 | F4PJNLW01A00V1 | CDS | 1234840 | 2883 | - | 0.304544 | |
g1170 | DLA_01287 | C-terminus similar to Arabidopsis thaliana plant adhesion molecule 1 Drosophila melanogaster extracellular matrix adhesion protein Pollux and human rab6 GTPase activating protein GAPCENA | F4PJNLW01A00V1 | CDS | 1238303 | 1377 | + | 0.291213 |
g1171 | DLA_01288 | F4PJNLW01A00V1 | CDS | 1240312 | 1047 | - | 0.293219 | |
g1172 | DLA_01290 | F4PJNLW01A00V1 | CDS | 1243480 | 981 | + | 0.310907 | |
g1173 | DLA_01291 | F4PJNLW01A00V1 | CDS | 1244646 | 3147 | - | 0.307595 | |
g1174 | DLA_01292 | F4PJNLW01A00V1 | CDS | 1248592 | 477 | + | 0.312369 | |
g1175 | DLA_01293 | F4PJNLW01A00V1 | CDS | 1249088 | 1107 | + | 0.342367 | |
g1176 | DLA_01294 | F4PJNLW01A00V1 | CDS | 1250509 | 930 | + | 0.386021 | |
g1177 | DLA_01295 | F4PJNLW01A00V1 | CDS | 1251631 | 2424 | + | 0.314769 | |
g1178 | DLA_01296 | F4PJNLW01A00V1 | CDS | 1254097 | 3381 | - | 0.303461 | |
g1179 | DLA_01298 | F4PJNLW01A00V1 | CDS | 1258662 | 240 | + | 0.345833 | |
g1180 | DLA_01299 | F4PJNLW01A00V1 | CDS | 1259286 | 897 | - | 0.362319 | |
g1181 | DLA_01300 | F4PJNLW01A00V1 | CDS | 1260850 | 1074 | - | 0.353817 | |
g1182 | DLA_01301 | F4PJNLW01A00V1 | CDS | 1264254 | 1569 | + | 0.290631 | |
g1183 | DLA_01302 | F4PJNLW01A00V1 | CDS | 1266312 | 1134 | - | 0.329806 | |
g1184 | DLA_01303 | F4PJNLW01A00V1 | CDS | 1268220 | 1251 | - | 0.366906 | |
g1185 | DLA_01304 | F4PJNLW01A00V1 | CDS | 1269820 | 4548 | + | 0.335972 | |
g1186 | DLA_01305 | F4PJNLW01A00V1 | CDS | 1274982 | 663 | + | 0.276018 | |
g1187 | DLA_01306 | F4PJNLW01A00V1 | CDS | 1275687 | 543 | - | 0.27256 | |
g1188 | DLA_01307 | F4PJNLW01A00V1 | CDS | 1276398 | 531 | - | 0.280603 | |
g1189 | DLA_01308 | F4PJNLW01A00V1 | CDS | 1277198 | 840 | + | 0.3 | |
g1190 | DLA_01309 | F4PJNLW01A00V1 | CDS | 1278322 | 2439 | + | 0.291923 | |
g1191 | DLA_01310 | F4PJNLW01A00V1 | CDS | 1281598 | 1455 | + | 0.320962 | |
g1192 | DLA_01311 | F4PJNLW01A00V1 | CDS | 1283081 | 1686 | - | 0.288849 | |
g1193 | DLA_01312 | F4PJNLW01A00V1 | CDS | 1285676 | 1476 | + | 0.347561 | |
g1194 | DLA_11472 | F4PJNLW01A00V1 | CDS | 1287578 | 1254 | + | 0.363636 | |
g1195 | DLA_01313 | F4PJNLW01A00V1 | CDS | 1289060 | 1809 | - | 0.297402 | |
g1196 | DLA_01314 | F4PJNLW01A00V1 | CDS | 1291700 | 1485 | + | 0.319865 | |
g1197 | DLA_01315 | F4PJNLW01A00V1 | CDS | 1293838 | 1179 | + | 0.308736 | |
g1198 | DLA_01317 | F4PJNLW01A00V1 | CDS | 1295821 | 2256 | + | 0.277926 | |
g1199 | DLA_01318 | F4PJNLW01A00V1 | CDS | 1298155 | 2430 | - | 0.310288 | |
g1200 | DLA_01319 | F4PJNLW01A00V1 | CDS | 1300703 | 2397 | - | 0.285774 | |
g1201 | DLA_11473 | F4PJNLW01A00V1 | CDS | 1303164 | 2403 | - | 0.287973 | |
g1202 | DLA_01320 | F4PJNLW01A00V1 | CDS | 1305969 | 3759 | - | 0.3054 | |
g1203 | DLA_01321 | F4PJNLW01A00V1 | CDS | 1310522 | 621 | - | 0.380032 | |
g1204 | DLA_01322 | F4PJNLW01A00V1 | CDS | 1311871 | 774 | + | 0.316537 | |
g1205 | DLA_01323 | F4PJNLW01A00V1 | CDS | 1312839 | 1686 | - | 0.319098 | |
g1206 | DLA_01324 | F4PJNLW01A00V1 | CDS | 1314830 | 1323 | - | 0.30839 | |
g1207 | DLA_01325 | F4PJNLW01A00V1 | CDS | 1316373 | 2172 | - | 0.303867 | |
g1208 | DLA_01327 | F4PJNLW01A00V1 | CDS | 1319775 | 1596 | - | 0.285714 | |
g1209 | DLA_01329 | F4PJNLW01A00V1 | CDS | 1321589 | 1302 | - | 0.390169 | |
g1210 | DLA_01330 | F4PJNLW01A00V1 | CDS | 1324138 | 3057 | - | 0.33366 | |
g1211 | DLA_01331 | F4PJNLW01A00V1 | CDS | 1328706 | 1299 | - | 0.321786 | |
g1212 | DLA_01334 | F4PJNLW01A00V1 | CDS | 1332509 | 666 | + | 0.280781 | |
g1213 | DLA_01335 | F4PJNLW01A00V1 | CDS | 1333407 | 3303 | - | 0.339691 | |
g1214 | DLA_01336 | F4PJNLW01A00V1 | CDS | 1337969 | 3510 | + | 0.335613 | |
g1215 | DLA_01337 | F4PJNLW01A00V1 | CDS | 1341753 | 5667 | - | 0.341803 | |
g1216 | DLA_01338 | F4PJNLW01A00V1 | CDS | 1347722 | 882 | - | 0.300454 | |
g1217 | DLA_01341 | F4PJNLW01A00V1 | CDS | 1349717 | 4146 | + | 0.285576 | |
g1218 | DLA_11474 | F4PJNLW01A00V1 | CDS | 1354366 | 630 | + | 0.365079 | |
g1219 | DLA_01342 | F4PJNLW01A00V1 | CDS | 1355274 | 1449 | - | 0.278813 | |
g1220 | DLA_01343 | F4PJNLW01A00V1 | CDS | 1356994 | 2553 | - | 0.358402 | |
g1221 | DLA_01345 | F4PJNLW01A00V1 | CDS | 1361311 | 2187 | - | 0.34888 | |
g1222 | DLA_01346 | F4PJNLW01A00V1 | CDS | 1365312 | 1128 | + | 0.264184 | |
g1223 | DLA_01347 | F4PJNLW01A00V1 | CDS | 1366499 | 3003 | - | 0.298035 | |
g1224 | DLA_01348 | F4PJNLW01A00V1 | CDS | 1370261 | 2862 | + | 0.324249 | |
g1225 | DLA_01349 | F4PJNLW01A00V1 | CDS | 1374980 | 1335 | + | 0.301873 | |
g1226 | DLA_01350 | F4PJNLW01A00V1 | CDS | 1376663 | 435 | - | 0.416092 | |
g1227 | DLA_01351 | F4PJNLW01A00V1 | CDS | 1377733 | 1074 | - | 0.294227 | |
g1228 | DLA_01352 | F4PJNLW01A00V1 | CDS | 1379280 | 5112 | - | 0.333333 | |
g1229 | DLA_01353 | F4PJNLW01A00V1 | CDS | 1385049 | 1917 | + | 0.284298 | |
g1230 | DLA_01354 | F4PJNLW01A00V1 | CDS | 1387269 | 828 | + | 0.254831 | |
g1231 | DLA_01355 | F4PJNLW01A00V1 | CDS | 1389383 | 3114 | - | 0.274245 | |
g1232 | DLA_01356 | F4PJNLW01A00V1 | CDS | 1392693 | 3024 | - | 0.319775 | |
g1233 | DLA_01357 | F4PJNLW01A00V1 | CDS | 1396060 | 3738 | + | 0.266988 | |
g1234 | DLA_01358 | F4PJNLW01A00V1 | CDS | 1399984 | 1170 | + | 0.269231 | |
g1235 | DLA_11475 | F4PJNLW01A00V1 | CDS | 1401323 | 318 | - | 0.396226 | |
g1236 | DLA_01359 | protein serinethreonine kinase homologous to human Nek2 kinase involved in formation of microtubule-organizing centers (MTOCs) | F4PJNLW01A00V1 | CDS | 1401955 | 1134 | - | 0.308642 |
g1237 | DLA_01360 | component of the H2A-H2B-H3-H4 histone octamer dimerizes with histone H4 | F4PJNLW01A00V1 | CDS | 1403767 | 405 | + | 0.407407 |
g1238 | DLA_11476 | F4PJNLW01A00V1 | CDS | 1404591 | 942 | - | 0.323779 | |
g1239 | DLA_01361 | F4PJNLW01A00V1 | CDS | 1406049 | 3495 | - | 0.27382 | |
g1240 | DLA_01362 | putative Raptor protein ortholog a component of the TORC1 complex in yeasts with Lst8 and Tor does not co-immunoprecipitate with the TORC2 complex | F4PJNLW01A00V1 | CDS | 1410095 | 4344 | + | 0.350138 |
g1241 | DLA_01363 | F4PJNLW01A00V1 | CDS | 1415103 | 288 | + | 0.288194 | |
g1242 | DLA_01364 | F4PJNLW01A00V1 | CDS | 1415616 | 2718 | - | 0.278146 | |
g1243 | DLA_01365 | F4PJNLW01A00V1 | CDS | 1418602 | 504 | + | 0.257937 | |
g1244 | DLA_01366 | F4PJNLW01A00V1 | CDS | 1419396 | 3018 | + | 0.32273 | |
g1245 | DLA_01367 | F4PJNLW01A00V1 | CDS | 1422505 | 924 | - | 0.238095 | |
g1246 | DLA_01368 | F4PJNLW01A00V1 | CDS | 1424016 | 1647 | + | 0.298118 | |
g1247 | DLA_01369 | F4PJNLW01A00V1 | CDS | 1425667 | 2325 | - | 0.304086 | |
g1248 | DLA_01371 | conserved eukaryotic protein of unknown function ortholog of human SPATA20 (spermatogenesis associated 20) | F4PJNLW01A00V1 | CDS | 1428424 | 2304 | + | 0.311632 |
g1249 | DLA_01372 | 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) | F4PJNLW01A00V1 | CDS | 1430927 | 1035 | - | 0.311111 |
g1250 | DLA_01373 | similar to mammalian Nup54 component of the nuclear pore complex | F4PJNLW01A00V1 | CDS | 1432426 | 1329 | + | 0.327314 |
g1251 | DLA_01374 | members of this family are membrane proteins involved in long chain fatty acid elongation systems that produce 26-carbon precursors for ceramide and sphingolipid synthesis contains 7 putative transmembrane domains | F4PJNLW01A00V1 | CDS | 1434114 | 816 | + | 0.295343 |
g1252 | DLA_01375 | F4PJNLW01A00V1 | CDS | 1435351 | 843 | + | 0.301305 | |
g1253 | DLA_01376 | F4PJNLW01A00V1 | CDS | 1436456 | 330 | + | 0.381818 | |
g1254 | DLA_01377 | ortholog of human TSN DNA-binding protein that specifically recognizes consensus sequences at the breakpoint junctions in chromosomal translocations interacts with translin-associated protein X (TSNAX) | F4PJNLW01A00V1 | CDS | 1437077 | 714 | - | 0.2493 |
g1255 | DLA_01378 | F4PJNLW01A00V1 | CDS | 1438955 | 1689 | + | 0.281824 | |
g1256 | DLA_01379 | ortholog of the human CPSF2 and yeast CFT2 the 100 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF) complex required for 3' processing of mRNAs | F4PJNLW01A00V1 | CDS | 1441091 | 2268 | + | 0.307319 |
g1257 | DLA_01380 | F4PJNLW01A00V1 | CDS | 1443542 | 297 | - | 0.208754 | |
g1258 | DLA_01381 | F4PJNLW01A00V1 | CDS | 1444033 | 1494 | + | 0.281125 | |
g1259 | DLA_01382 | F4PJNLW01A00V1 | CDS | 1445702 | 1614 | - | 0.257745 | |
g1260 | DLA_01383 | F4PJNLW01A00V1 | CDS | 1447566 | 1953 | - | 0.321557 | |
g1261 | DLA_01384 | F4PJNLW01A00V1 | CDS | 1450299 | 2781 | + | 0.385113 | |
g1262 | DLA_01385 | catalyzes the reaction (S)-3-(5-oxo-45-dihydro-3H-imidazol-4-yl)propanoate H2O N-formimidoyl-L-glutamate H | F4PJNLW01A00V1 | CDS | 1453545 | 1272 | + | 0.30739 |
g1263 | DLA_01386 | F4PJNLW01A00V1 | CDS | 1455017 | 978 | - | 0.282209 | |
g1264 | DLA_01388 | F4PJNLW01A00V1 | CDS | 1456550 | 3531 | + | 0.34013 | |
g1265 | DLA_01389 | belongs to a family of short proteins that includes proteins from the NADH-ubiquinone oxidoreductase complex I named LYR after a highly conserved tripeptide motif | F4PJNLW01A00V1 | CDS | 1460431 | 417 | - | 0.263789 |
g1266 | DLA_01390 | F4PJNLW01A00V1 | CDS | 1460970 | 1641 | + | 0.255332 | |
g1267 | DLA_01391 | F4PJNLW01A00V1 | CDS | 1462912 | 306 | - | 0.323529 | |
g1268 | DLA_01392 | F4PJNLW01A00V1 | CDS | 1463356 | 258 | - | 0.321705 | |
g1269 | DLA_01393 | F4PJNLW01A00V1 | CDS | 1463729 | 489 | - | 0.345603 | |
g631 | DLA_00698 | F4PJNLW01A00V1 | CDS | 1 | 83 | - | 0.385542 | |
g632 | DLA_00700 | F4PJNLW01A00V1 | CDS | 1619 | 1938 | + | 0.31063 | |
g633 | DLA_00701 | F4PJNLW01A00V1 | CDS | 3780 | 1101 | - | 0.247956 | |
g634 | DLA_00702 | F4PJNLW01A00V1 | CDS | 4965 | 2502 | + | 0.278577 | |
g635 | DLA_00703 | catalyzes the reaction ATP L-glutamyl-tRNA(Gln) L-glutamine ADP phosphate L-glutaminyl-tRNA(Gln) L-glutamate | F4PJNLW01A00V1 | CDS | 7654 | 1668 | + | 0.291966 |
g636 | DLA_00704 | F4PJNLW01A00V1 | CDS | 9460 | 1839 | + | 0.256661 | |
g637 | DLA_00705 | F4PJNLW01A00V1 | CDS | 11526 | 2700 | + | 0.33 | |
g638 | DLA_00706 | F4PJNLW01A00V1 | CDS | 14437 | 2826 | - | 0.314225 | |
g639 | DLA_00707 | F4PJNLW01A00V1 | CDS | 17774 | 2130 | + | 0.349296 | |
g640 | DLA_00708 | F4PJNLW01A00V1 | CDS | 20157 | 486 | - | 0.320988 | |
g641 | DLA_00709 | F4PJNLW01A00V1 | CDS | 21016 | 525 | + | 0.413333 | |
g642 | DLA_00710 | F4PJNLW01A00V1 | CDS | 21765 | 522 | - | 0.277778 | |
g643 | DLA_00711 | F4PJNLW01A00V1 | CDS | 22496 | 918 | - | 0.302832 | |
g644 | DLA_00712 | F4PJNLW01A00V1 | CDS | 23588 | 1596 | - | 0.316416 | |
g645 | DLA_00713 | F4PJNLW01A00V1 | CDS | 25932 | 1755 | + | 0.317949 | |
g646 | DLA_00714 | conserved E2 ubiquitin-conjugating protein which catalyzes the covalent attachment of ubiquitin to other proteins | F4PJNLW01A00V1 | CDS | 28242 | 447 | + | 0.360179 |
g647 | DLA_00715 | F4PJNLW01A00V1 | CDS | 29125 | 1464 | + | 0.267076 | |
g648 | DLA_00717 | F4PJNLW01A00V1 | CDS | 31881 | 354 | - | 0.324859 | |
g649 | DLA_00718 | member of the histone H2A-H2B sub-family related to the NF-YB subunit of the CCAAT-binding activator NF-Y | F4PJNLW01A00V1 | CDS | 32467 | 417 | - | 0.275779 |
g650 | DLA_00719 | F4PJNLW01A00V1 | CDS | 33208 | 1356 | + | 0.262537 | |
g651 | DLA_00720 | F4PJNLW01A00V1 | CDS | 34648 | 1248 | - | 0.309295 | |
g652 | DLA_00721 | F4PJNLW01A00V1 | CDS | 38734 | 642 | - | 0.32866 | |
g653 | DLA_00722 | F4PJNLW01A00V1 | CDS | 39623 | 1137 | + | 0.350923 | |
g654 | DLA_00723 | RrmJFtsJ ribosomal RNA methyltransferase family member well conserved heat shock proteins present in prokaryotes archaea and eukaryotes similar to S. cerevisiae MRM2 required for methylation of U(2791) in 21S rRNA | F4PJNLW01A00V1 | CDS | 40896 | 978 | + | 0.271984 |
g655 | DLA_00724 | F4PJNLW01A00V1 | CDS | 41961 | 2124 | - | 0.281544 | |
g656 | DLA_00725 | F4PJNLW01A00V1 | CDS | 44689 | 2286 | - | 0.323272 | |
g657 | DLA_00726 | F4PJNLW01A00V1 | CDS | 47753 | 474 | + | 0.350211 | |
g658 | DLA_00727 | F4PJNLW01A00V1 | CDS | 48546 | 1665 | + | 0.307508 | |
g659 | DLA_00728 | F4PJNLW01A00V1 | CDS | 50300 | 1050 | - | 0.290476 | |
g660 | DLA_00729 | F4PJNLW01A00V1 | CDS | 51694 | 1098 | - | 0.282332 | |
g661 | DLA_00730 | F4PJNLW01A00V1 | CDS | 53130 | 1572 | + | 0.283715 | |
g662 | DLA_00731 | F4PJNLW01A00V1 | CDS | 55144 | 5109 | + | 0.315717 | |
g663 | DLA_00732 | F4PJNLW01A00V1 | CDS | 60841 | 852 | - | 0.319249 | |
g664 | DLA_00733 | F4PJNLW01A00V1 | CDS | 61950 | 2313 | - | 0.279291 | |
g665 | DLA_00735 | F4PJNLW01A00V1 | CDS | 65491 | 1167 | + | 0.353042 | |
g666 | DLA_00736 | F4PJNLW01A00V1 | CDS | 66823 | 444 | - | 0.331081 | |
g667 | DLA_00737 | F4PJNLW01A00V1 | CDS | 67871 | 738 | - | 0.390244 | |
g668 | DLA_00738 | F4PJNLW01A00V1 | CDS | 69380 | 1170 | + | 0.298291 | |
g669 | DLA_00739 | F4PJNLW01A00V1 | CDS | 70760 | 3471 | - | 0.312014 | |
g670 | DLA_00740 | F4PJNLW01A00V1 | CDS | 74728 | 1353 | + | 0.350333 | |
g671 | DLA_00741 | F4PJNLW01A00V1 | CDS | 76363 | 5484 | - | 0.30434 | |
g672 | DLA_11447 | F4PJNLW01A00V1 | CDS | 81977 | 1602 | - | 0.318352 | |
g673 | DLA_00742 | F4PJNLW01A00V1 | CDS | 83911 | 1125 | + | 0.304889 | |
g674 | DLA_00743 | F4PJNLW01A00V1 | CDS | 85489 | 1101 | - | 0.326975 | |
g675 | DLA_00744 | F4PJNLW01A00V1 | CDS | 86826 | 717 | + | 0.331939 | |
g676 | DLA_00745 | F4PJNLW01A00V1 | CDS | 87632 | 1698 | - | 0.312721 | |
g677 | DLA_00746 | subunit of the COP9 signalosome (CSN) a complex of the ubiquitin-proteasome pathway composed of eight subunits (CSN1-8) | F4PJNLW01A00V1 | CDS | 89633 | 792 | - | 0.301768 |
g678 | DLA_00748 | F4PJNLW01A00V1 | CDS | 91087 | 7068 | - | 0.317629 | |
g679 | DLA_00749 | F4PJNLW01A00V1 | CDS | 98677 | 858 | + | 0.342657 | |
g680 | DLA_00750 | F4PJNLW01A00V1 | CDS | 99661 | 993 | - | 0.352467 | |
g681 | DLA_00751 | F4PJNLW01A00V1 | CDS | 101167 | 666 | + | 0.348348 | |
g682 | DLA_00752 | F4PJNLW01A00V1 | CDS | 102369 | 1788 | + | 0.362975 | |
g683 | DLA_00753 | F4PJNLW01A00V1 | CDS | 104591 | 912 | - | 0.423246 | |
g684 | DLA_00754 | F4PJNLW01A00V1 | CDS | 105851 | 828 | - | 0.262077 | |
g685 | DLA_00755 | F4PJNLW01A00V1 | CDS | 106754 | 1449 | + | 0.289165 | |
g686 | DLA_00757 | F4PJNLW01A00V1 | CDS | 108444 | 1512 | - | 0.39418 | |
g687 | DLA_00758 | F4PJNLW01A00V1 | CDS | 111311 | 2625 | + | 0.34781 | |
g688 | DLA_00759 | F4PJNLW01A00V1 | CDS | 114128 | 3147 | - | 0.288529 | |
g689 | DLA_00761 | F4PJNLW01A00V1 | CDS | 118427 | 1425 | + | 0.327719 | |
g690 | DLA_00762 | F4PJNLW01A00V1 | CDS | 120103 | 282 | - | 0.368794 | |
g691 | DLA_00763 | F4PJNLW01A00V1 | CDS | 120597 | 2127 | + | 0.332863 | |
g692 | DLA_00764 | F4PJNLW01A00V1 | CDS | 123009 | 1257 | + | 0.412888 | |
g693 | DLA_00765 | F4PJNLW01A00V1 | CDS | 124627 | 1254 | + | 0.357257 | |
g694 | DLA_00766 | F4PJNLW01A00V1 | CDS | 125928 | 1743 | - | 0.292599 | |
g695 | DLA_00767 | F4PJNLW01A00V1 | CDS | 127817 | 5166 | - | 0.392373 | |
g696 | DLA_00769 | F4PJNLW01A00V1 | CDS | 134290 | 240 | + | 0.304167 | |
g697 | DLA_00770 | F4PJNLW01A00V1 | CDS | 134815 | 678 | + | 0.336283 | |
g698 | DLA_00771 | F4PJNLW01A00V1 | CDS | 136270 | 7062 | + | 0.323421 | |
g699 | DLA_00772 | F4PJNLW01A00V1 | CDS | 143489 | 1716 | - | 0.320513 | |
g700 | DLA_00773 | ortholog of vitellogenic carboxypeptidase a conserved serine carboxypeptidase expressed in mosquito ovaries contains a predicted signal peptide | F4PJNLW01A00V1 | CDS | 145541 | 1521 | - | 0.332676 |
g701 | DLA_00774 | F4PJNLW01A00V1 | CDS | 147285 | 1170 | - | 0.298291 | |
g702 | DLA_00775 | F4PJNLW01A00V1 | CDS | 149037 | 1473 | + | 0.30482 | |
g703 | DLA_00776 | F4PJNLW01A00V1 | CDS | 151130 | 1470 | + | 0.364626 | |
g704 | DLA_00777 | F4PJNLW01A00V1 | CDS | 152799 | 327 | + | 0.327217 | |
g705 | DLA_00778 | F4PJNLW01A00V1 | CDS | 153474 | 432 | - | 0.298611 | |
g706 | DLA_00779 | ortholog of the putative tumor suppressor candidate 4 protein (TUSC4) the nitrogen permease regulator 2 (NPR2) family of regulators are involved in post-translational control of nitrogen permease | F4PJNLW01A00V1 | CDS | 154243 | 1182 | - | 0.327411 |
g707 | DLA_11448 | F4PJNLW01A00V1 | CDS | 155658 | 453 | - | 0.452539 | |
g708 | DLA_00780 | F4PJNLW01A00V1 | CDS | 156871 | 2907 | + | 0.325421 | |
g709 | DLA_00781 | F4PJNLW01A00V1 | CDS | 159971 | 3423 | - | 0.315221 | |
g710 | DLA_00782 | F4PJNLW01A00V1 | CDS | 163745 | 399 | - | 0.390977 | |
g711 | DLA_00783 | F4PJNLW01A00V1 | CDS | 164811 | 894 | + | 0.369128 | |
g712 | DLA_00784 | subunit common to RNA polymerases I II and III ortholog of S. cerevisiae RPB10 | F4PJNLW01A00V1 | CDS | 165886 | 207 | - | 0.31401 |
g713 | DLA_00785 | F4PJNLW01A00V1 | CDS | 167363 | 1281 | + | 0.323966 | |
g714 | DLA_00786 | F4PJNLW01A00V1 | CDS | 168705 | 1512 | - | 0.342593 | |
g715 | DLA_00787 | F4PJNLW01A00V1 | CDS | 170363 | 2574 | - | 0.378399 | |
g716 | DLA_11449 | F4PJNLW01A00V1 | CDS | 173362 | 1539 | + | 0.332684 | |
g717 | DLA_00788 | F4PJNLW01A00V1 | CDS | 175851 | 861 | + | 0.326365 | |
g718 | DLA_00790 | F4PJNLW01A00V1 | CDS | 177891 | 606 | - | 0.334983 | |
g719 | DLA_00791 | F4PJNLW01A00V1 | CDS | 178857 | 1383 | - | 0.336226 | |
g720 | DLA_00792 | Ca2-binding protein with chaperone activity in the endoplasmic reticulum plays a role in phagocytosis | F4PJNLW01A00V1 | CDS | 180508 | 1608 | - | 0.393657 |
g721 | DLA_00793 | ortholog of MON2 in S. cerevisiae MON2 plays a a role in endocytosis and vacuole integrity | F4PJNLW01A00V1 | CDS | 182489 | 5205 | + | 0.360807 |
g722 | DLA_00794 | F4PJNLW01A00V1 | CDS | 188088 | 2253 | + | 0.340879 | |
g723 | DLA_00796 | F4PJNLW01A00V1 | CDS | 190893 | 4350 | + | 0.355632 | |
g724 | DLA_00797 | F4PJNLW01A00V1 | CDS | 195634 | 4053 | + | 0.303726 | |
g725 | DLA_00798 | F4PJNLW01A00V1 | CDS | 200058 | 3948 | + | 0.323961 | |
g726 | DLA_00799 | DEADDEAH box helicases are involved in various aspects of RNA metabolism | F4PJNLW01A00V1 | CDS | 204635 | 3465 | - | 0.361039 |
g727 | DLA_00800 | F4PJNLW01A00V1 | CDS | 208293 | 360 | - | 0.291667 | |
g728 | DLA_00801 | F4PJNLW01A00V1 | CDS | 209082 | 876 | + | 0.297945 | |
g729 | DLA_00802 | F4PJNLW01A00V1 | CDS | 212215 | 1983 | + | 0.348462 | |
g730 | DLA_00803 | F4PJNLW01A00V1 | CDS | 214464 | 1044 | - | 0.360153 | |
g731 | DLA_11450 | F4PJNLW01A00V1 | CDS | 215990 | 360 | + | 0.308333 | |
g732 | DLA_00804 | F4PJNLW01A00V1 | CDS | 216545 | 2196 | + | 0.338798 | |
g733 | DLA_00805 | F4PJNLW01A00V1 | CDS | 218912 | 471 | - | 0.271762 | |
g734 | DLA_00806 | F4PJNLW01A00V1 | CDS | 219784 | 3666 | + | 0.29078 | |
g735 | DLA_00807 | F4PJNLW01A00V1 | CDS | 223542 | 6822 | - | 0.340369 | |
g736 | DLA_00808 | similar to COG8 component of the conserved oligomeric Golgi complex which is composed of eight different subunits | F4PJNLW01A00V1 | CDS | 231513 | 2127 | + | 0.29055 |
g737 | DLA_00809 | F4PJNLW01A00V1 | CDS | 234799 | 387 | + | 0.374677 | |
g738 | DLA_00811 | F4PJNLW01A00V1 | CDS | 235608 | 1470 | + | 0.308163 | |
g739 | DLA_00812 | F4PJNLW01A00V1 | CDS | 237137 | 1650 | - | 0.306667 | |
g740 | DLA_00814 | similar to human EXOSC6 and S. pombe mtr3 which are components of the exosome a 3'-5' exoribonuclease complex involved in RNA processing | F4PJNLW01A00V1 | CDS | 239231 | 822 | + | 0.310219 |
g741 | DLA_00815 | F4PJNLW01A00V1 | CDS | 240411 | 1833 | - | 0.29569 | |
g742 | DLA_00816 | F4PJNLW01A00V1 | CDS | 242340 | 1851 | - | 0.311723 | |
g743 | DLA_00817 | F4PJNLW01A00V1 | CDS | 244268 | 1881 | - | 0.310473 | |
g744 | DLA_00819 | F4PJNLW01A00V1 | CDS | 247009 | 1746 | - | 0.338488 | |
g745 | DLA_00820 | catalyzes the reaction GTP oxaloacetate GDP phosphoenolpyruvate COsub2sub in gluconeogenesis and the TCA cycle | F4PJNLW01A00V1 | CDS | 249191 | 1887 | + | 0.397986 |
g746 | DLA_00821 | F4PJNLW01A00V1 | CDS | 251425 | 1431 | - | 0.34102 | |
g747 | DLA_00822 | F4PJNLW01A00V1 | CDS | 253903 | 207 | - | 0.318841 | |
g748 | DLA_00823 | F4PJNLW01A00V1 | CDS | 255007 | 1323 | + | 0.269085 | |
g749 | DLA_00824 | ortholog of the human G6PD defects in G6PD cause chronic non-spherocytic hemolytic anemia (CNSHA) catalyzes the reaction D-glucose 6-phosphate NADPsupsup D-glucono-15-lactone 6-phosphate NADPH Hsupsup there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 256464 | 1536 | - | 0.373047 |
g750 | DLA_00826 | F4PJNLW01A00V1 | CDS | 258630 | 1767 | + | 0.359932 | |
g751 | DLA_00827 | F4PJNLW01A00V1 | CDS | 260892 | 825 | + | 0.273939 | |
g752 | DLA_00828 | F4PJNLW01A00V1 | CDS | 262490 | 1920 | + | 0.411458 | |
g753 | DLA_00829 | putative ortholog of H. sapiens SHOC2 also known as Ras-binding protein Sur-8 | F4PJNLW01A00V1 | CDS | 264836 | 1536 | + | 0.350911 |
g754 | DLA_00830 | similar to mammalian XPR1 which may confer susceptibility to infection with murine leukaemia viruses also similar to yeast SYG1 a G-protein associated signal transduction protein and plant PHO1 that may be involved in phosphate transport | F4PJNLW01A00V1 | CDS | 266491 | 2316 | - | 0.324698 |
g755 | DLA_00831 | F4PJNLW01A00V1 | CDS | 269332 | 1707 | - | 0.326303 | |
g756 | DLA_00833 | F4PJNLW01A00V1 | CDS | 271654 | 753 | - | 0.361222 | |
g757 | DLA_00834 | F4PJNLW01A00V1 | CDS | 272712 | 912 | - | 0.246711 | |
g758 | DLA_00835 | F4PJNLW01A00V1 | CDS | 273958 | 909 | - | 0.330033 | |
g759 | DLA_00836 | F4PJNLW01A00V1 | CDS | 275234 | 381 | - | 0.291339 | |
g760 | DLA_00837 | F4PJNLW01A00V1 | CDS | 275914 | 1620 | + | 0.307407 | |
g761 | DLA_00838 | F4PJNLW01A00V1 | CDS | 277567 | 1449 | - | 0.310559 | |
g762 | DLA_11451 | F4PJNLW01A00V1 | CDS | 279080 | 1206 | + | 0.313433 | |
g763 | DLA_00839 | F4PJNLW01A00V1 | CDS | 280717 | 828 | + | 0.285024 | |
g764 | DLA_00841 | F4PJNLW01A00V1 | CDS | 282447 | 306 | - | 0.294118 | |
g765 | DLA_00842 | F4PJNLW01A00V1 | CDS | 283616 | 396 | + | 0.363636 | |
g766 | DLA_00843 | F4PJNLW01A00V1 | CDS | 284519 | 1326 | - | 0.293364 | |
g767 | DLA_00844 | F4PJNLW01A00V1 | CDS | 285946 | 957 | + | 0.345873 | |
g768 | DLA_00846 | F4PJNLW01A00V1 | CDS | 287419 | 987 | - | 0.331307 | |
g769 | DLA_00847 | F4PJNLW01A00V1 | CDS | 288983 | 5649 | + | 0.355815 | |
g770 | DLA_00848 | F4PJNLW01A00V1 | CDS | 294833 | 375 | - | 0.277333 | |
g771 | DLA_00849 | F4PJNLW01A00V1 | CDS | 295345 | 558 | - | 0.284946 | |
g772 | DLA_00850 | F4PJNLW01A00V1 | CDS | 296003 | 1506 | + | 0.286189 | |
g773 | DLA_00851 | ortholog of S. cerevisiae and H. sapiens EMG1 involved in 40S ribosome biogenesis | F4PJNLW01A00V1 | CDS | 297802 | 978 | - | 0.322086 |
g774 | DLA_00852 | similar to human LMAN1 (lectin mannose-binding protein 1) belongs to the legume-like lectin family contains 1 predicted transmembrane domain similar to D. purpureum protein | F4PJNLW01A00V1 | CDS | 299268 | 1593 | + | 0.327056 |
g775 | DLA_00854 | F4PJNLW01A00V1 | CDS | 303099 | 306 | - | 0.261438 | |
g776 | DLA_00855 | F4PJNLW01A00V1 | CDS | 303707 | 1491 | + | 0.315225 | |
g777 | DLA_00856 | F4PJNLW01A00V1 | CDS | 305305 | 3129 | + | 0.286353 | |
g778 | DLA_00858 | F4PJNLW01A00V1 | CDS | 308752 | 1359 | - | 0.303164 | |
g779 | DLA_00859 | F4PJNLW01A00V1 | CDS | 310297 | 1461 | + | 0.299795 | |
g780 | DLA_00860 | F4PJNLW01A00V1 | CDS | 311798 | 1473 | + | 0.281738 | |
g781 | DLA_00861 | F4PJNLW01A00V1 | CDS | 313355 | 942 | + | 0.283439 | |
g782 | DLA_11452 | F4PJNLW01A00V1 | CDS | 315214 | 459 | + | 0.300654 | |
g783 | DLA_00862 | F4PJNLW01A00V1 | CDS | 316270 | 3633 | + | 0.289017 | |
g784 | DLA_00863 | F4PJNLW01A00V1 | CDS | 320436 | 1503 | + | 0.298071 | |
g785 | DLA_00864 | F4PJNLW01A00V1 | CDS | 322040 | 351 | - | 0.307692 | |
g786 | DLA_00865 | F4PJNLW01A00V1 | CDS | 322782 | 3009 | - | 0.378863 | |
g787 | DLA_00866 | F4PJNLW01A00V1 | CDS | 326549 | 1014 | + | 0.361933 | |
g788 | DLA_00867 | F4PJNLW01A00V1 | CDS | 328013 | 1314 | - | 0.331811 | |
g789 | DLA_00868 | F4PJNLW01A00V1 | CDS | 329642 | 2184 | + | 0.325092 | |
g790 | DLA_00869 | F4PJNLW01A00V1 | CDS | 332134 | 2709 | - | 0.323736 | |
g791 | DLA_00870 | F4PJNLW01A00V1 | CDS | 335427 | 1572 | - | 0.370865 | |
g792 | DLA_00871 | conserved protein similar to yeast CWC22 an essential putative spliceosomal component | F4PJNLW01A00V1 | CDS | 337487 | 2142 | - | 0.352007 |
g793 | DLA_00872 | F4PJNLW01A00V1 | CDS | 339945 | 1755 | - | 0.317379 | |
g794 | DLA_00874 | F4PJNLW01A00V1 | CDS | 343306 | 312 | - | 0.294872 | |
g795 | DLA_00875 | F4PJNLW01A00V1 | CDS | 344010 | 1749 | + | 0.321326 | |
g796 | DLA_00876 | F4PJNLW01A00V1 | CDS | 345844 | 1503 | - | 0.323353 | |
g797 | DLA_00877 | F4PJNLW01A00V1 | CDS | 347714 | 684 | + | 0.346491 | |
g798 | DLA_00879 | F4PJNLW01A00V1 | CDS | 349371 | 1707 | + | 0.369654 | |
g799 | DLA_00880 | F4PJNLW01A00V1 | CDS | 351586 | 1113 | + | 0.362983 | |
g800 | DLA_00881 | F4PJNLW01A00V1 | CDS | 352956 | 1179 | + | 0.357082 | |
g801 | DLA_00882 | F4PJNLW01A00V1 | CDS | 354324 | 738 | - | 0.310298 | |
g802 | DLA_00883 | F4PJNLW01A00V1 | CDS | 355603 | 249 | + | 0.293173 | |
g803 | DLA_00884 | F4PJNLW01A00V1 | CDS | 356279 | 2874 | + | 0.376479 | |
g804 | DLA_00885 | belongs to the substrate carrier protein family involved in transport of molecules across the mitochondrial membrane regulated by the MADS-box transcription factor SrfA during development brbr bCommunity annotation:b Overview of the | F4PJNLW01A00V1 | CDS | 359397 | 1071 | - | 0.349206 |
g805 | DLA_00886 | F4PJNLW01A00V1 | CDS | 361091 | 987 | - | 0.368794 | |
g806 | DLA_11453 | F4PJNLW01A00V1 | CDS | 362755 | 603 | - | 0.313433 | |
g807 | DLA_00887 | F4PJNLW01A00V1 | CDS | 364301 | 1164 | + | 0.361684 | |
g808 | DLA_00888 | F4PJNLW01A00V1 | CDS | 365640 | 1284 | + | 0.285826 | |
g809 | DLA_00889 | catalyzes the reaction ATP L-arginine tRNAArg AMP diphosphate L-arginyl-tRNAArg | F4PJNLW01A00V1 | CDS | 367096 | 1872 | - | 0.367521 |
g810 | DLA_00890 | similar to mammalian NIT1 there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 369236 | 939 | + | 0.339723 |
g811 | DLA_00891 | F4PJNLW01A00V1 | CDS | 370322 | 1446 | - | 0.301521 | |
g812 | DLA_00892 | F4PJNLW01A00V1 | CDS | 372454 | 2172 | + | 0.371547 | |
g813 | DLA_00893 | F4PJNLW01A00V1 | CDS | 374770 | 1014 | - | 0.306706 | |
g814 | DLA_00894 | F4PJNLW01A00V1 | CDS | 376260 | 1614 | + | 0.282528 | |
g815 | DLA_00895 | F4PJNLW01A00V1 | CDS | 377913 | 1767 | - | 0.281834 | |
g816 | DLA_00896 | F4PJNLW01A00V1 | CDS | 380056 | 1344 | - | 0.28869 | |
g817 | DLA_00897 | F4PJNLW01A00V1 | CDS | 381894 | 1473 | + | 0.281059 | |
g818 | DLA_00898 | F4PJNLW01A00V1 | CDS | 383940 | 1785 | + | 0.285714 | |
g819 | DLA_00899 | F4PJNLW01A00V1 | CDS | 386130 | 1767 | + | 0.284097 | |
g820 | DLA_11454 | F4PJNLW01A00V1 | CDS | 388492 | 1764 | + | 0.287415 | |
g821 | DLA_00900 | F4PJNLW01A00V1 | CDS | 390582 | 1542 | + | 0.365759 | |
g822 | DLA_00901 | F4PJNLW01A00V1 | CDS | 392243 | 1842 | + | 0.286645 | |
g823 | DLA_00903 | F4PJNLW01A00V1 | CDS | 394407 | 1482 | - | 0.283401 | |
g824 | DLA_00904 | F4PJNLW01A00V1 | CDS | 396372 | 1326 | + | 0.340875 | |
g825 | DLA_00905 | F4PJNLW01A00V1 | CDS | 397716 | 2379 | - | 0.34174 | |
g826 | DLA_00906 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers br bNomenclature conflict:b Do not confuse this gene with clc also known as clcA encoding the clathrin light chain | F4PJNLW01A00V1 | CDS | 400235 | 2616 | - | 0.365443 |
g827 | DLA_00907 | F4PJNLW01A00V1 | CDS | 403659 | 1371 | + | 0.391685 | |
g828 | DLA_00908 | F4PJNLW01A00V1 | CDS | 405482 | 3894 | - | 0.357473 | |
g829 | DLA_00909 | F4PJNLW01A00V1 | CDS | 409957 | 3246 | + | 0.379544 | |
g830 | DLA_00910 | similar to Arabidopsis AMT1 involved in transporting ammonia in the environment into the cell contains 11 transmembrane domains | F4PJNLW01A00V1 | CDS | 413597 | 1302 | + | 0.361751 |
g831 | DLA_00911 | F4PJNLW01A00V1 | CDS | 415447 | 2505 | - | 0.390818 | |
g832 | DLA_00912 | similar to the cell division cycle 2-related protein kinase 7 (CRK7) and other cell division cycle 2-like protein kinases there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 418405 | 1833 | + | 0.355701 |
g833 | DLA_00913 | ortholog of the trafficking protein particle complex subunit 10 part of the multisubunit TRAPP (transport protein particle) complex there is a second copy of this gene | F4PJNLW01A00V1 | CDS | 420669 | 3933 | + | 0.33969 |
g834 | DLA_00914 | F4PJNLW01A00V1 | CDS | 424736 | 3198 | - | 0.258286 | |
g835 | DLA_00916 | F4PJNLW01A00V1 | CDS | 428746 | 1794 | - | 0.375697 | |
g836 | DLA_11455 | F4PJNLW01A00V1 | CDS | 432399 | 2580 | + | 0.324419 | |
g837 | DLA_00917 | F4PJNLW01A00V1 | CDS | 435856 | 2655 | + | 0.369492 | |
g838 | DLA_00918 | phosphoinositide phosphatase with low specific activity compared to other known phosphoinositide phosphatases can dephosphorylate several phosphoinositide substrates with a preference for PI(5)P constitutively expressed putative ortholog of H. sapiens EPM2A involved in myoclonic epilepsy of Lafora | F4PJNLW01A00V1 | CDS | 439027 | 657 | - | 0.316591 |
g839 | DLA_00919 | F4PJNLW01A00V1 | CDS | 439803 | 591 | - | 0.302876 | |
g840 | DLA_11456 | F4PJNLW01A00V1 | CDS | 440657 | 1554 | + | 0.301158 | |
g841 | DLA_00920 | F4PJNLW01A00V1 | CDS | 442743 | 3303 | + | 0.340599 | |
g842 | DLA_00921 | F4PJNLW01A00V1 | CDS | 446407 | 3276 | + | 0.320513 | |
g843 | DLA_00923 | F4PJNLW01A00V1 | CDS | 450368 | 1644 | + | 0.379562 | |
g844 | DLA_00924 | F4PJNLW01A00V1 | CDS | 452710 | 810 | - | 0.264198 | |
g845 | DLA_00925 | F4PJNLW01A00V1 | CDS | 453911 | 4515 | - | 0.341085 | |
g846 | DLA_00926 | F4PJNLW01A00V1 | CDS | 459261 | 1626 | + | 0.353014 | |
g847 | DLA_00927 | F4PJNLW01A00V1 | CDS | 461092 | 1266 | + | 0.300948 | |
g848 | DLA_00928 | F4PJNLW01A00V1 | CDS | 462535 | 369 | - | 0.319783 | |
g849 | DLA_00929 | F4PJNLW01A00V1 | CDS | 464441 | 2265 | - | 0.349669 | |
g850 | DLA_00930 | F4PJNLW01A00V1 | CDS | 467822 | 369 | - | 0.303523 | |
g851 | DLA_00931 | F4PJNLW01A00V1 | CDS | 469670 | 831 | + | 0.345367 | |
g852 | DLA_00932 | F4PJNLW01A00V1 | CDS | 470736 | 10092 | + | 0.339279 | |
g853 | DLA_00933 | catalyzes the reaction Nsub2sub-acetyl-L-ornithine 2-oxoglutarate N-acetyl-L-glutamate 5-semialdehyde L-glutamate | F4PJNLW01A00V1 | CDS | 481206 | 1332 | - | 0.354354 |
g854 | DLA_00934 | F4PJNLW01A00V1 | CDS | 482667 | 663 | - | 0.374057 | |
g855 | DLA_00935 | F4PJNLW01A00V1 | CDS | 483602 | 570 | + | 0.308772 | |
g856 | DLA_00936 | F4PJNLW01A00V1 | CDS | 484234 | 2835 | - | 0.31358 | |
g857 | DLA_00937 | F4PJNLW01A00V1 | CDS | 487333 | 2793 | + | 0.368779 | |
g858 | DLA_00938 | F4PJNLW01A00V1 | CDS | 490212 | 684 | - | 0.282164 | |
g859 | DLA_00940 | F4PJNLW01A00V1 | CDS | 491788 | 6873 | + | 0.295941 | |
g860 | DLA_00941 | F4PJNLW01A00V1 | CDS | 500057 | 6390 | + | 0.291549 | |
g861 | DLA_00942 | F4PJNLW01A00V1 | CDS | 506676 | 2997 | - | 0.331999 | |
g862 | DLA_00943 | F4PJNLW01A00V1 | CDS | 510412 | 966 | + | 0.350932 | |
g863 | DLA_00945 | F4PJNLW01A00V1 | CDS | 512443 | 837 | + | 0.297491 | |
g864 | DLA_00947 | F4PJNLW01A00V1 | CDS | 513891 | 819 | + | 0.285714 | |
g865 | DLA_00948 | F4PJNLW01A00V1 | CDS | 515333 | 1656 | + | 0.347826 | |
g866 | DLA_00950 | F4PJNLW01A00V1 | CDS | 517473 | 261 | - | 0.302682 | |
g867 | DLA_00951 | F4PJNLW01A00V1 | CDS | 518095 | 1188 | - | 0.361111 | |
g868 | DLA_00952 | component of the RNA polymerase III complex has similarity to H. sapiens RPC5 and S. cerevisiae RPC37 | F4PJNLW01A00V1 | CDS | 519855 | 1971 | - | 0.369863 |
g869 | DLA_00954 | F4PJNLW01A00V1 | CDS | 522511 | 3792 | + | 0.336234 | |
g870 | DLA_00955 | F4PJNLW01A00V1 | CDS | 526863 | 3900 | + | 0.317949 | |
g871 | DLA_11457 | F4PJNLW01A00V1 | CDS | 531095 | 1464 | + | 0.29918 | |
g872 | DLA_00956 | F4PJNLW01A00V1 | CDS | 532952 | 3276 | + | 0.330891 | |
g873 | DLA_00957 | ortholog of MYH which removes misincorporated adenine residues opposite template 8-oxoguanine during DNA replication | F4PJNLW01A00V1 | CDS | 536344 | 1554 | - | 0.301158 |
g874 | DLA_00958 | F4PJNLW01A00V1 | CDS | 538081 | 1455 | - | 0.386942 | |
g875 | DLA_00959 | F4PJNLW01A00V1 | CDS | 539707 | 5337 | - | 0.34214 | |
g876 | DLA_00960 | F4PJNLW01A00V1 | CDS | 545252 | 1101 | + | 0.347866 | |
g877 | DLA_00961 | F4PJNLW01A00V1 | CDS | 546414 | 765 | - | 0.351634 | |
g878 | DLA_00962 | F4PJNLW01A00V1 | CDS | 547571 | 732 | + | 0.289617 | |
g879 | DLA_00963 | F4PJNLW01A00V1 | CDS | 548403 | 1671 | - | 0.348294 | |
g880 | DLA_00964 | F4PJNLW01A00V1 | CDS | 550332 | 1758 | - | 0.344141 | |
g881 | DLA_00965 | similar to H. sapiens SWISNF subunit SMARCC1 and the yeast subunit SWI3 of the chromatin remodeling complex | F4PJNLW01A00V1 | CDS | 552489 | 3174 | + | 0.331758 |
g882 | DLA_00969 | F4PJNLW01A00V1 | CDS | 557087 | 288 | + | 0.28125 | |
g883 | DLA_00972 | belongs to the costars family similar to the C terminal region of mammalian striated muscle activator of Rho signaling | F4PJNLW01A00V1 | CDS | 558983 | 252 | + | 0.281746 |
g884 | DLA_00974 | contains two selenocysteine residues at positions 20 and 88 conserved in the green algae such as Chlamydomonas Ostreococcus and Volvox contains 4 transmembrane domains | F4PJNLW01A00V1 | CDS | 559580 | 660 | + | 0.371212 |
g885 | DLA_00976 | F4PJNLW01A00V1 | CDS | 561707 | 996 | + | 0.35743 | |
g886 | DLA_00977 | F4PJNLW01A00V1 | CDS | 562847 | 1089 | - | 0.311295 | |
g887 | DLA_00979 | F4PJNLW01A00V1 | CDS | 564254 | 1008 | + | 0.28373 | |
g888 | DLA_11458 | F4PJNLW01A00V1 | CDS | 565346 | 681 | + | 0.331865 | |
g889 | DLA_00980 | F4PJNLW01A00V1 | CDS | 566096 | 345 | + | 0.33913 | |
g890 | DLA_00982 | F4PJNLW01A00V1 | CDS | 566858 | 1032 | - | 0.312016 | |
g891 | DLA_00983 | F4PJNLW01A00V1 | CDS | 569380 | 1380 | - | 0.301449 | |
g892 | DLA_00985 | putative ortholog of H. sapiens POMP similar to S. cerevisiae UMP1 involved in maturation of the 20S proteasome | F4PJNLW01A00V1 | CDS | 571149 | 375 | - | 0.288 |
g893 | DLA_00986 | F4PJNLW01A00V1 | CDS | 572060 | 1311 | + | 0.293669 | |
g894 | DLA_00987 | F4PJNLW01A00V1 | CDS | 573450 | 2103 | - | 0.320495 | |
g895 | DLA_00988 | F4PJNLW01A00V1 | CDS | 575860 | 2082 | - | 0.303554 | |
g896 | DLA_00989 | F4PJNLW01A00V1 | CDS | 578251 | 2115 | - | 0.334279 | |
g897 | DLA_00990 | F4PJNLW01A00V1 | CDS | 580658 | 1035 | - | 0.264734 | |
g898 | DLA_00991 | conserved protein alpha-galactosidase (melibiase) catalyses the hydrolysis of melibiose into galactose and glucose | F4PJNLW01A00V1 | CDS | 582053 | 1026 | - | 0.395712 |
g899 | DLA_00992 | F4PJNLW01A00V1 | CDS | 583527 | 1824 | - | 0.305921 | |
g900 | DLA_00994 | F4PJNLW01A00V1 | CDS | 585872 | 1056 | - | 0.354167 | |
g901 | DLA_00995 | F4PJNLW01A00V1 | CDS | 587482 | 636 | + | 0.356918 | |
g902 | DLA_00996 | F4PJNLW01A00V1 | CDS | 588650 | 1767 | - | 0.259196 | |
g903 | DLA_00997 | F4PJNLW01A00V1 | CDS | 590940 | 2199 | - | 0.35789 | |
g904 | DLA_00998 | F4PJNLW01A00V1 | CDS | 594349 | 1296 | + | 0.323302 | |
g905 | DLA_00999 | F4PJNLW01A00V1 | CDS | 595915 | 1293 | + | 0.302398 | |
g906 | DLA_01000 | F4PJNLW01A00V1 | CDS | 597281 | 2322 | - | 0.270026 | |
g907 | DLA_01002 | F4PJNLW01A00V1 | CDS | 600317 | 3663 | + | 0.340977 | |
g908 | DLA_01003 | F4PJNLW01A00V1 | CDS | 604634 | 726 | + | 0.272727 | |
g909 | DLA_01004 | F4PJNLW01A00V1 | CDS | 605631 | 1041 | + | 0.254563 | |
g910 | DLA_01005 | F4PJNLW01A00V1 | CDS | 606787 | 522 | - | 0.316092 | |
g911 | DLA_01006 | F4PJNLW01A00V1 | CDS | 607514 | 3234 | + | 0.325603 | |
g912 | DLA_01008 | F4PJNLW01A00V1 | CDS | 611271 | 201 | + | 0.328358 | |
g913 | DLA_01009 | F4PJNLW01A00V1 | CDS | 611778 | 2223 | + | 0.332434 | |
g914 | DLA_01010 | F4PJNLW01A00V1 | CDS | 614964 | 1410 | + | 0.236879 | |
g915 | DLA_01011 | F4PJNLW01A00V1 | CDS | 616468 | 4905 | - | 0.355759 | |
g916 | DLA_01012 | F4PJNLW01A00V1 | CDS | 621709 | 1854 | - | 0.330636 | |
g917 | DLA_01013 | F4PJNLW01A00V1 | CDS | 623958 | 3978 | + | 0.302162 | |
g918 | DLA_01014 | F4PJNLW01A00V1 | CDS | 628231 | 690 | + | 0.294203 | |
g919 | DLA_01016 | F4PJNLW01A00V1 | CDS | 630388 | 348 | - | 0.29023 | |
g920 | DLA_01018 | F4PJNLW01A00V1 | CDS | 632223 | 8535 | + | 0.320211 | |
g921 | DLA_01019 | F4PJNLW01A00V1 | CDS | 641138 | 1953 | + | 0.293907 | |
g922 | DLA_01020 | F4PJNLW01A00V1 | CDS | 643466 | 2934 | + | 0.308453 | |
g923 | DLA_01021 | F4PJNLW01A00V1 | CDS | 646744 | 1170 | - | 0.331624 | |
g924 | DLA_01023 | F4PJNLW01A00V1 | CDS | 649237 | 2628 | + | 0.285008 | |
g925 | DLA_01024 | F4PJNLW01A00V1 | CDS | 652057 | 360 | - | 0.333333 | |
g926 | DLA_01025 | F4PJNLW01A00V1 | CDS | 652828 | 2121 | + | 0.311645 | |
g927 | DLA_01026 | F4PJNLW01A00V1 | CDS | 655383 | 900 | - | 0.258889 | |
g928 | DLA_01027 | F4PJNLW01A00V1 | CDS | 656534 | 405 | + | 0.306173 | |
g929 | DLA_01028 | F4PJNLW01A00V1 | CDS | 657204 | 945 | + | 0.307937 | |
g930 | DLA_01029 | F4PJNLW01A00V1 | CDS | 658432 | 2052 | - | 0.298733 | |
g931 | DLA_01031 | F4PJNLW01A00V1 | CDS | 661501 | 4101 | + | 0.333821 | |
g932 | DLA_01032 | F4PJNLW01A00V1 | CDS | 665942 | 846 | + | 0.336879 | |
g933 | DLA_01033 | F4PJNLW01A00V1 | CDS | 667032 | 873 | + | 0.342497 | |
g934 | DLA_01034 | F4PJNLW01A00V1 | CDS | 668187 | 690 | - | 0.347826 | |
g935 | DLA_11459 | F4PJNLW01A00V1 | CDS | 669504 | 240 | - | 0.279167 | |
g936 | DLA_01035 | F4PJNLW01A00V1 | CDS | 670163 | 411 | + | 0.304136 | |
g937 | DLA_01036 | F4PJNLW01A00V1 | CDS | 670824 | 549 | - | 0.391621 | |
g938 | DLA_01037 | F4PJNLW01A00V1 | CDS | 673562 | 1203 | - | 0.412303 | |
g939 | DLA_01038 | F4PJNLW01A00V1 | CDS | 675097 | 1035 | - | 0.256039 | |
g940 | DLA_01039 | F4PJNLW01A00V1 | CDS | 676275 | 627 | - | 0.266348 | |
g941 | DLA_01040 | F4PJNLW01A00V1 | CDS | 677007 | 867 | - | 0.342561 | |
g942 | DLA_01041 | F4PJNLW01A00V1 | CDS | 678385 | 510 | - | 0.288235 | |
g943 | DLA_01042 | F4PJNLW01A00V1 | CDS | 678951 | 1272 | - | 0.275157 | |
g944 | DLA_01043 | fatty acid synthases catalyze the formation of long-chain fatty acids from acetyl-CoA malonyl-CoA and NADPH multifunctional protein with several catalytic activities and an acyl carrier protein enriched in gametes | F4PJNLW01A00V1 | CDS | 681151 | 7635 | + | 0.339358 |
g945 | DLA_01044 | F4PJNLW01A00V1 | CDS | 689006 | 3144 | - | 0.310433 | |
g946 | DLA_01045 | F4PJNLW01A00V1 | CDS | 692544 | 3042 | - | 0.323143 | |
g947 | DLA_01046 | F4PJNLW01A00V1 | CDS | 696119 | 843 | - | 0.329775 | |
g949 | DLA_01048 | F4PJNLW01A00V1 | CDS | 701075 | 1980 | + | 0.283333 | |
g950 | DLA_01049 | F4PJNLW01A00V1 | CDS | 703367 | 771 | - | 0.302205 | |
g951 | DLA_01050 | F4PJNLW01A00V1 | CDS | 704291 | 1440 | + | 0.311111 | |
g952 | DLA_01051 | F4PJNLW01A00V1 | CDS | 706016 | 1749 | + | 0.317324 | |
g953 | DLA_01052 | F4PJNLW01A00V1 | CDS | 707902 | 3888 | - | 0.273663 | |
g954 | DLA_01057 | F4PJNLW01A00V1 | CDS | 715689 | 1680 | - | 0.289881 | |
g955 | DLA_01058 | F4PJNLW01A00V1 | CDS | 717747 | 477 | + | 0.377358 | |
g956 | DLA_01059 | F4PJNLW01A00V1 | CDS | 718550 | 678 | + | 0.353982 | |
g957 | DLA_01060 | F4PJNLW01A00V1 | CDS | 720039 | 5316 | + | 0.357976 | |
g958 | DLA_01061 | F4PJNLW01A00V1 | CDS | 726071 | 399 | - | 0.278196 | |
g959 | DLA_01062 | F4PJNLW01A00V1 | CDS | 726650 | 957 | + | 0.289446 | |
g960 | DLA_01063 | F4PJNLW01A00V1 | CDS | 727967 | 435 | + | 0.312644 | |
g961 | DLA_01064 | F4PJNLW01A00V1 | CDS | 729224 | 540 | - | 0.298148 | |
g962 | DLA_01065 | F4PJNLW01A00V1 | CDS | 733365 | 2331 | - | 0.324324 | |
g963 | DLA_01066 | F4PJNLW01A00V1 | CDS | 736130 | 7947 | - | 0.317227 | |
g964 | DLA_01067 | F4PJNLW01A00V1 | CDS | 746101 | 276 | + | 0.358696 | |
g965 | DLA_01070 | F4PJNLW01A00V1 | CDS | 747836 | 2991 | - | 0.348378 | |
g966 | DLA_01072 | 40S ribosomal protein SA (p40) homolog belongs to the ribosomal protein S2P family contains ribosomal protein S2 domain | F4PJNLW01A00V1 | CDS | 751133 | 1494 | - | 0.349398 |
g967 | DLA_01073 | F4PJNLW01A00V1 | CDS | 753088 | 2076 | - | 0.315029 | |
g968 | DLA_01076 | F4PJNLW01A00V1 | CDS | 755516 | 921 | - | 0.30836 | |
g969 | DLA_01078 | F4PJNLW01A00V1 | CDS | 758688 | 597 | - | 0.370184 | |
g970 | DLA_01079 | F4PJNLW01A00V1 | CDS | 759689 | 1269 | + | 0.332545 | |
g971 | DLA_01080 | F4PJNLW01A00V1 | CDS | 761769 | 591 | + | 0.324873 | |
g972 | DLA_01081 | belongs to the band 7 proteins integral membrane proteins that ares thought to regulate cation conductance stomatin is an erythrocyte membrane protein contains one predicted transmembrane domain | F4PJNLW01A00V1 | CDS | 762954 | 1002 | + | 0.352295 |
g973 | DLA_01082 | full transporter consisting of two ABC domains and two transmembrane domains | F4PJNLW01A00V1 | CDS | 764221 | 4836 | - | 0.341605 |
g974 | DLA_01083 | F4PJNLW01A00V1 | CDS | 770184 | 1392 | + | 0.280172 | |
g975 | DLA_01084 | F4PJNLW01A00V1 | CDS | 771802 | 2058 | - | 0.322157 | |
g976 | DLA_01085 | F4PJNLW01A00V1 | CDS | 774402 | 1425 | + | 0.29614 | |
g977 | DLA_01087 | F4PJNLW01A00V1 | CDS | 776180 | 2457 | - | 0.293447 | |
g978 | DLA_01088 | F4PJNLW01A00V1 | CDS | 779353 | 1389 | + | 0.264939 | |
g979 | DLA_01089 | ortholog of mammalian ubxn7 (UBX domain-containing protein 7) contains a UBX domain found in ubiquitin-regulatory proteins | F4PJNLW01A00V1 | CDS | 781092 | 1422 | - | 0.291139 |
g980 | DLA_01090 | F4PJNLW01A00V1 | CDS | 782778 | 2493 | - | 0.347774 | |
g981 | DLA_01091 | F4PJNLW01A00V1 | CDS | 785704 | 2373 | + | 0.337969 | |
g982 | DLA_01092 | F4PJNLW01A00V1 | CDS | 788419 | 816 | + | 0.300245 | |
g983 | DLA_01093 | F4PJNLW01A00V1 | CDS | 790191 | 747 | + | 0.368139 | |
g984 | DLA_01094 | F4PJNLW01A00V1 | CDS | 792035 | 897 | + | 0.294314 | |
g985 | DLA_01095 | F4PJNLW01A00V1 | CDS | 793082 | 369 | + | 0.311653 | |
g986 | DLA_01096 | F4PJNLW01A00V1 | CDS | 794819 | 3531 | + | 0.353724 | |
g987 | DLA_11460 | F4PJNLW01A00V1 | CDS | 798527 | 3270 | + | 0.355352 | |
g988 | DLA_01097 | F4PJNLW01A00V1 | CDS | 802039 | 576 | - | 0.369792 | |
g989 | DLA_01098 | F4PJNLW01A00V1 | CDS | 803485 | 516 | - | 0.286822 | |
g990 | DLA_01099 | F4PJNLW01A00V1 | CDS | 804435 | 1251 | - | 0.311751 | |
g991 | DLA_01100 | F4PJNLW01A00V1 | CDS | 805807 | 1434 | - | 0.35007 | |
g992 | DLA_01101 | F4PJNLW01A00V1 | CDS | 807902 | 7191 | + | 0.329996 | |
g993 | DLA_01103 | similar to UPF0451 family proteins contains 3 predicted transmembrane domains there is an almost identical gene | F4PJNLW01A00V1 | CDS | 816787 | 357 | - | 0.358543 |
g994 | DLA_01104 | F4PJNLW01A00V1 | CDS | 817343 | 3006 | - | 0.311045 | |
g995 | DLA_01105 | F4PJNLW01A00V1 | CDS | 820466 | 2223 | + | 0.332883 | |
g996 | DLA_01106 | F4PJNLW01A00V1 | CDS | 823363 | 1206 | + | 0.35738 | |
g997 | DLA_01108 | F4PJNLW01A00V1 | CDS | 825611 | 1149 | + | 0.302872 | |
g998 | DLA_11461 | F4PJNLW01A00V1 | CDS | 826790 | 339 | - | 0.230089 | |
g999 | DLA_01109 | F4PJNLW01A00V1 | CDS | 827257 | 1368 | - | 0.33845 |