Gene list
Applied filters:
Genomic element: F4PJNLW01EE5MJ
Number of genes found: 541
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_11852 | tRNA-Leu | F4PJNLW01EE5MJ | tRNA | 138096 | 81 | + | 0.493827 |
NA | DLA_11853 | tRNA-Met | F4PJNLW01EE5MJ | tRNA | 784643 | 73 | - | 0.479452 |
g2206 | DLA_02429 | F4PJNLW01EE5MJ | CDS | 154 | 1812 | + | 0.312362 | |
g2207 | DLA_02432 | F4PJNLW01EE5MJ | CDS | 5435 | 1047 | - | 0.30277 | |
g2208 | DLA_02433 | F4PJNLW01EE5MJ | CDS | 7786 | 3030 | + | 0.29934 | |
g2209 | DLA_02434 | F4PJNLW01EE5MJ | CDS | 11521 | 4248 | - | 0.305085 | |
g2210 | DLA_02435 | F4PJNLW01EE5MJ | CDS | 15976 | 4845 | - | 0.31806 | |
g2211 | DLA_02436 | F4PJNLW01EE5MJ | CDS | 21053 | 4320 | - | 0.290509 | |
g2212 | DLA_02437 | F4PJNLW01EE5MJ | CDS | 25737 | 4242 | - | 0.303866 | |
g2213 | DLA_02438 | F4PJNLW01EE5MJ | CDS | 30323 | 546 | - | 0.31685 | |
g2214 | DLA_02439 | F4PJNLW01EE5MJ | CDS | 31062 | 2133 | - | 0.311299 | |
g2215 | DLA_02440 | F4PJNLW01EE5MJ | CDS | 33600 | 810 | + | 0.328395 | |
g2216 | DLA_02442 | F4PJNLW01EE5MJ | CDS | 37107 | 2034 | + | 0.345133 | |
g2217 | DLA_02443 | F4PJNLW01EE5MJ | CDS | 39460 | 954 | + | 0.316562 | |
g2218 | DLA_02444 | F4PJNLW01EE5MJ | CDS | 40852 | 1836 | - | 0.328431 | |
g2219 | DLA_02446 | very similar to the mammalian glucosidase II subunit beta also known as protein kinase C substrate 80K-H which catalyzes the sequential removal of two alpha-13-linked glucose residues in the second step of N-linked oligosaccharide processing also similar to yeast GTB1 defects in human PRKCSH are a cause of polycystic liver disease (PCLD) | F4PJNLW01EE5MJ | CDS | 44405 | 1395 | + | 0.326882 |
g2220 | DLA_02447 | F4PJNLW01EE5MJ | CDS | 46366 | 828 | - | 0.373188 | |
g2221 | DLA_02448 | F4PJNLW01EE5MJ | CDS | 48223 | 651 | + | 0.298003 | |
g2222 | DLA_02449 | F4PJNLW01EE5MJ | CDS | 49018 | 1320 | - | 0.368182 | |
g2223 | DLA_02450 | F4PJNLW01EE5MJ | CDS | 50619 | 546 | - | 0.300366 | |
g2224 | DLA_02451 | F4PJNLW01EE5MJ | CDS | 51431 | 1824 | + | 0.302632 | |
g2225 | DLA_02452 | F4PJNLW01EE5MJ | CDS | 53523 | 2505 | - | 0.295409 | |
g2226 | DLA_02456 | F4PJNLW01EE5MJ | CDS | 57774 | 1611 | - | 0.371819 | |
g2227 | DLA_02457 | F4PJNLW01EE5MJ | CDS | 59569 | 825 | + | 0.321212 | |
g2228 | DLA_02458 | in S. cerevisiae essential for the fidelity of chromosome transmission and component of the RFC complexbrbr bCommunity annotation:b CTF18 ( | F4PJNLW01EE5MJ | CDS | 60463 | 2562 | - | 0.323575 |
g2229 | DLA_02460 | F4PJNLW01EE5MJ | CDS | 64137 | 1395 | + | 0.32043 | |
g2230 | DLA_02462 | F4PJNLW01EE5MJ | CDS | 66467 | 2622 | - | 0.31312 | |
g2231 | DLA_02463 | F4PJNLW01EE5MJ | CDS | 69546 | 1530 | + | 0.347712 | |
g2232 | DLA_02464 | F4PJNLW01EE5MJ | CDS | 71463 | 1431 | + | 0.415793 | |
g2233 | DLA_02465 | F4PJNLW01EE5MJ | CDS | 73342 | 2217 | + | 0.28507 | |
g2234 | DLA_02466 | F4PJNLW01EE5MJ | CDS | 76241 | 747 | - | 0.344043 | |
g2235 | DLA_02469 | F4PJNLW01EE5MJ | CDS | 78419 | 2289 | - | 0.351682 | |
g2236 | DLA_02470 | F4PJNLW01EE5MJ | CDS | 81014 | 1212 | + | 0.285479 | |
g2237 | DLA_02471 | F4PJNLW01EE5MJ | CDS | 82403 | 3486 | - | 0.335341 | |
g2238 | DLA_02472 | F4PJNLW01EE5MJ | CDS | 86819 | 1212 | - | 0.306931 | |
g2239 | DLA_02473 | dual specificity phosphatases remove phosphate groups from tyrosine and serinethreonine residues | F4PJNLW01EE5MJ | CDS | 89204 | 498 | + | 0.359438 |
g2240 | DLA_02474 | F4PJNLW01EE5MJ | CDS | 90599 | 333 | + | 0.375375 | |
g2241 | DLA_02475 | F4PJNLW01EE5MJ | CDS | 91269 | 729 | - | 0.322359 | |
g2242 | DLA_02476 | F4PJNLW01EE5MJ | CDS | 92490 | 585 | + | 0.305983 | |
g2243 | DLA_02477 | F4PJNLW01EE5MJ | CDS | 93131 | 2730 | - | 0.335897 | |
g2244 | DLA_02481 | F4PJNLW01EE5MJ | CDS | 99352 | 2415 | - | 0.342443 | |
g2245 | DLA_02482 | F4PJNLW01EE5MJ | CDS | 102051 | 534 | - | 0.397004 | |
g2246 | DLA_02483 | F4PJNLW01EE5MJ | CDS | 103357 | 627 | + | 0.414673 | |
g2247 | DLA_02484 | catalyzes the reaction alpha-D-mannose 1-phosphate D-mannose 6-phosphate | F4PJNLW01EE5MJ | CDS | 104560 | 741 | + | 0.306343 |
g2248 | DLA_02485 | F4PJNLW01EE5MJ | CDS | 105506 | 1389 | - | 0.362131 | |
g2249 | DLA_02486 | F4PJNLW01EE5MJ | CDS | 107128 | 1710 | - | 0.380702 | |
g2250 | DLA_02487 | F4PJNLW01EE5MJ | CDS | 109186 | 201 | - | 0.238806 | |
g2251 | DLA_02488 | F4PJNLW01EE5MJ | CDS | 109636 | 4569 | + | 0.33968 | |
g2252 | DLA_02489 | F4PJNLW01EE5MJ | CDS | 115007 | 2484 | - | 0.293076 | |
g2253 | DLA_11522 | F4PJNLW01EE5MJ | CDS | 117818 | 1245 | + | 0.324498 | |
g2254 | DLA_02490 | F4PJNLW01EE5MJ | CDS | 120402 | 1422 | + | 0.291842 | |
g2255 | DLA_02491 | F4PJNLW01EE5MJ | CDS | 122005 | 1104 | - | 0.320652 | |
g2256 | DLA_11523 | F4PJNLW01EE5MJ | CDS | 123438 | 1152 | - | 0.333333 | |
g2257 | DLA_02492 | F4PJNLW01EE5MJ | CDS | 124939 | 1149 | - | 0.37772 | |
g2258 | DLA_02493 | F4PJNLW01EE5MJ | CDS | 127130 | 4536 | + | 0.309965 | |
g2259 | DLA_02494 | F4PJNLW01EE5MJ | CDS | 131950 | 5448 | - | 0.324706 | |
g2260 | DLA_02495 | F4PJNLW01EE5MJ | CDS | 138880 | 2247 | - | 0.365821 | |
g2261 | DLA_02496 | F4PJNLW01EE5MJ | CDS | 141455 | 6441 | - | 0.334886 | |
g2262 | DLA_02497 | F4PJNLW01EE5MJ | CDS | 148989 | 6384 | + | 0.350877 | |
g2263 | DLA_02499 | F4PJNLW01EE5MJ | CDS | 157099 | 1092 | + | 0.311355 | |
g2264 | DLA_02500 | F4PJNLW01EE5MJ | CDS | 158741 | 1872 | - | 0.313034 | |
g2265 | DLA_02501 | F4PJNLW01EE5MJ | CDS | 161286 | 4029 | + | 0.315215 | |
g2266 | DLA_02502 | F4PJNLW01EE5MJ | CDS | 165514 | 1254 | - | 0.389952 | |
g2267 | DLA_02503 | F4PJNLW01EE5MJ | CDS | 167375 | 2418 | - | 0.330438 | |
g2268 | DLA_02504 | CLC chloride channels are conserved from prokaryotes to mammals where they play broad physiological roles they assemble to form homo-dimers | F4PJNLW01EE5MJ | CDS | 170057 | 2556 | - | 0.330595 |
g2269 | DLA_02508 | F4PJNLW01EE5MJ | CDS | 174693 | 1038 | + | 0.266859 | |
g2270 | DLA_02509 | F4PJNLW01EE5MJ | CDS | 176088 | 1011 | - | 0.292779 | |
g2271 | DLA_02510 | catalyzes the reaction succinate ubiquinone fumarate ubiquinol cytochrome b560 subunit contains 2 transmembrane domains | F4PJNLW01EE5MJ | CDS | 177446 | 597 | + | 0.351759 |
g2272 | DLA_02511 | F4PJNLW01EE5MJ | CDS | 178455 | 1602 | - | 0.314607 | |
g2273 | DLA_02513 | F4PJNLW01EE5MJ | CDS | 181437 | 918 | - | 0.339869 | |
g2274 | DLA_02514 | similar to ubiquitin in the N-terminal region contains one von Willebrand factor (vWF) type A domain | F4PJNLW01EE5MJ | CDS | 182810 | 1980 | - | 0.322222 |
g2275 | DLA_02515 | F4PJNLW01EE5MJ | CDS | 184989 | 2679 | - | 0.329601 | |
g2276 | DLA_02517 | F4PJNLW01EE5MJ | CDS | 187796 | 369 | + | 0.289973 | |
g2277 | DLA_02519 | F4PJNLW01EE5MJ | CDS | 188812 | 960 | + | 0.309375 | |
g2278 | DLA_02520 | F4PJNLW01EE5MJ | CDS | 190279 | 1485 | + | 0.297643 | |
g2279 | DLA_02521 | F4PJNLW01EE5MJ | CDS | 192285 | 1467 | + | 0.306748 | |
g2280 | DLA_02522 | F4PJNLW01EE5MJ | CDS | 194409 | 1344 | + | 0.306548 | |
g2281 | DLA_02523 | F4PJNLW01EE5MJ | CDS | 195831 | 1731 | + | 0.302137 | |
g2282 | DLA_02524 | F4PJNLW01EE5MJ | CDS | 198242 | 2193 | - | 0.336981 | |
g2283 | DLA_02525 | catalyzes the hydrolysis of the terminal 12-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 some members of this family are responsible for protein N-linked glycosylation while other participate in the degradation of misfolded glycoproteins in the endoplasmic reticulum | F4PJNLW01EE5MJ | CDS | 200780 | 1800 | + | 0.306667 |
g2284 | DLA_02526 | F4PJNLW01EE5MJ | CDS | 202874 | 3267 | - | 0.373125 | |
g2285 | DLA_02527 | F4PJNLW01EE5MJ | CDS | 207745 | 1950 | - | 0.38359 | |
g2286 | DLA_02528 | F4PJNLW01EE5MJ | CDS | 210161 | 1857 | - | 0.283791 | |
g2287 | DLA_11524 | F4PJNLW01EE5MJ | CDS | 212292 | 267 | + | 0.307116 | |
g2288 | DLA_02529 | F4PJNLW01EE5MJ | CDS | 212854 | 930 | - | 0.337634 | |
g2289 | DLA_02531 | F4PJNLW01EE5MJ | CDS | 214852 | 5394 | + | 0.342047 | |
g2290 | DLA_02532 | F4PJNLW01EE5MJ | CDS | 220604 | 456 | + | 0.342105 | |
g2291 | DLA_02533 | F4PJNLW01EE5MJ | CDS | 221235 | 4041 | + | 0.309329 | |
g2292 | DLA_02534 | F4PJNLW01EE5MJ | CDS | 225419 | 1422 | - | 0.362166 | |
g2293 | DLA_02535 | F4PJNLW01EE5MJ | CDS | 227311 | 2112 | + | 0.309186 | |
g2294 | DLA_02536 | F4PJNLW01EE5MJ | CDS | 229541 | 363 | - | 0.272727 | |
g2295 | DLA_02537 | F4PJNLW01EE5MJ | CDS | 230488 | 1137 | + | 0.282322 | |
g2296 | DLA_02538 | F4PJNLW01EE5MJ | CDS | 231917 | 831 | - | 0.305656 | |
g2297 | DLA_02539 | homolog of human SLC35B4 S. cerevisiae YEA4 contains 9 putative transmembrane domains | F4PJNLW01EE5MJ | CDS | 233195 | 1620 | + | 0.271605 |
g2298 | DLA_02541 | F4PJNLW01EE5MJ | CDS | 235127 | 4590 | - | 0.325272 | |
g2299 | DLA_02542 | F4PJNLW01EE5MJ | CDS | 240220 | 2424 | + | 0.304043 | |
g2300 | DLA_02543 | F4PJNLW01EE5MJ | CDS | 242888 | 2571 | + | 0.317775 | |
g2301 | DLA_02544 | F4PJNLW01EE5MJ | CDS | 245689 | 2445 | + | 0.345603 | |
g2302 | DLA_02545 | F4PJNLW01EE5MJ | CDS | 248576 | 1083 | - | 0.322253 | |
g2303 | DLA_02546 | F4PJNLW01EE5MJ | CDS | 250911 | 1335 | + | 0.322097 | |
g2304 | DLA_02547 | F4PJNLW01EE5MJ | CDS | 252570 | 3954 | + | 0.262013 | |
g2305 | DLA_02548 | F4PJNLW01EE5MJ | CDS | 256752 | 3549 | - | 0.31051 | |
g2306 | DLA_02550 | F4PJNLW01EE5MJ | CDS | 260902 | 897 | - | 0.338907 | |
g2307 | DLA_11525 | F4PJNLW01EE5MJ | CDS | 262147 | 885 | - | 0.310734 | |
g2308 | DLA_02551 | F4PJNLW01EE5MJ | CDS | 263249 | 1152 | + | 0.305556 | |
g2309 | DLA_02552 | F4PJNLW01EE5MJ | CDS | 264490 | 1134 | - | 0.29806 | |
g2310 | DLA_02553 | F4PJNLW01EE5MJ | CDS | 265738 | 1455 | - | 0.287285 | |
g2311 | DLA_02555 | F4PJNLW01EE5MJ | CDS | 267824 | 2103 | + | 0.309082 | |
g2312 | DLA_02556 | F4PJNLW01EE5MJ | CDS | 270520 | 1629 | - | 0.304481 | |
g2313 | DLA_02557 | F4PJNLW01EE5MJ | CDS | 273651 | 1254 | + | 0.358852 | |
g2314 | DLA_02558 | F4PJNLW01EE5MJ | CDS | 275444 | 555 | - | 0.245045 | |
g2315 | DLA_02559 | F4PJNLW01EE5MJ | CDS | 276235 | 741 | + | 0.300945 | |
g2316 | DLA_02561 | F4PJNLW01EE5MJ | CDS | 277899 | 348 | - | 0.241379 | |
g2317 | DLA_02562 | F4PJNLW01EE5MJ | CDS | 278398 | 1965 | - | 0.354198 | |
g2318 | DLA_02563 | F4PJNLW01EE5MJ | CDS | 280458 | 603 | + | 0.268657 | |
g2319 | DLA_02564 | bifunctional enzyme that catalyzes the reactions Nsup10sup-formyl-Hsub4subF AICAR tetrahydrofolate phosphoribosyl-formamido-carboxamide and phosphoribosyl-formamido-carboxamide IMP Hsub2subO expressed in prespore cells | F4PJNLW01EE5MJ | CDS | 281676 | 1587 | + | 0.361689 |
g2320 | DLA_02566 | F4PJNLW01EE5MJ | CDS | 284500 | 1374 | - | 0.36754 | |
g2321 | DLA_02567 | F4PJNLW01EE5MJ | CDS | 286080 | 1269 | - | 0.287628 | |
g2322 | DLA_02568 | F4PJNLW01EE5MJ | CDS | 287875 | 1101 | + | 0.369664 | |
g2323 | DLA_02569 | F4PJNLW01EE5MJ | CDS | 289151 | 3285 | - | 0.327549 | |
g2324 | DLA_02570 | F4PJNLW01EE5MJ | CDS | 292896 | 543 | - | 0.360958 | |
g2325 | DLA_02571 | F4PJNLW01EE5MJ | CDS | 294226 | 1146 | + | 0.399651 | |
g2326 | DLA_02573 | F4PJNLW01EE5MJ | CDS | 296326 | 2718 | - | 0.336277 | |
g2327 | DLA_02574 | F4PJNLW01EE5MJ | CDS | 299310 | 1146 | + | 0.356021 | |
g2328 | DLA_02575 | similar to human TMEM144 contains 10 predicted transmembrane domains | F4PJNLW01EE5MJ | CDS | 300819 | 1098 | - | 0.351548 |
g2329 | DLA_02576 | F4PJNLW01EE5MJ | CDS | 302604 | 1479 | + | 0.369844 | |
g2330 | DLA_02577 | F4PJNLW01EE5MJ | CDS | 304268 | 1359 | + | 0.292862 | |
g2331 | DLA_02578 | F4PJNLW01EE5MJ | CDS | 306650 | 234 | + | 0.324786 | |
g2332 | DLA_02579 | F4PJNLW01EE5MJ | CDS | 308501 | 2493 | + | 0.30365 | |
g2333 | DLA_02580 | F4PJNLW01EE5MJ | CDS | 311170 | 1512 | - | 0.39418 | |
g2334 | DLA_02581 | F4PJNLW01EE5MJ | CDS | 313047 | 876 | + | 0.284247 | |
g2335 | DLA_02583 | F4PJNLW01EE5MJ | CDS | 315011 | 810 | - | 0.311111 | |
g2336 | DLA_02584 | F4PJNLW01EE5MJ | CDS | 316180 | 1230 | - | 0.321138 | |
g2337 | DLA_02585 | F4PJNLW01EE5MJ | CDS | 317569 | 1173 | - | 0.384484 | |
g2338 | DLA_02588 | F4PJNLW01EE5MJ | CDS | 321261 | 813 | - | 0.367774 | |
g2339 | DLA_02589 | F4PJNLW01EE5MJ | CDS | 322533 | 963 | + | 0.330218 | |
g2340 | DLA_02590 | ZIP family zinc transporter LZT subfamily member contains 8 transmembrane domains expressed in pstAB cells | F4PJNLW01EE5MJ | CDS | 323676 | 885 | + | 0.281356 |
g2341 | DLA_02591 | F4PJNLW01EE5MJ | CDS | 324958 | 2022 | - | 0.300198 | |
g2342 | DLA_02594 | F4PJNLW01EE5MJ | CDS | 327477 | 2202 | + | 0.343778 | |
g2343 | DLA_11526 | F4PJNLW01EE5MJ | CDS | 329858 | 801 | - | 0.324594 | |
g2344 | DLA_02595 | F4PJNLW01EE5MJ | CDS | 330963 | 870 | - | 0.344828 | |
g2345 | DLA_02596 | F4PJNLW01EE5MJ | CDS | 332082 | 2229 | + | 0.32795 | |
g2346 | DLA_11527 | F4PJNLW01EE5MJ | CDS | 334523 | 477 | - | 0.408805 | |
g2347 | DLA_02597 | F4PJNLW01EE5MJ | CDS | 335037 | 1137 | - | 0.310466 | |
g2348 | DLA_02598 | F4PJNLW01EE5MJ | CDS | 336903 | 2295 | - | 0.342484 | |
g2349 | DLA_02599 | F4PJNLW01EE5MJ | CDS | 339679 | 1890 | + | 0.356614 | |
g2350 | DLA_02600 | F4PJNLW01EE5MJ | CDS | 341646 | 693 | - | 0.290043 | |
g2351 | DLA_02601 | F4PJNLW01EE5MJ | CDS | 343120 | 753 | + | 0.318725 | |
g2352 | DLA_02602 | F4PJNLW01EE5MJ | CDS | 343941 | 1917 | - | 0.34168 | |
g2353 | DLA_02603 | F4PJNLW01EE5MJ | CDS | 346036 | 1038 | - | 0.330443 | |
g2354 | DLA_02604 | F4PJNLW01EE5MJ | CDS | 347562 | 1611 | + | 0.359404 | |
g2355 | DLA_02605 | F4PJNLW01EE5MJ | CDS | 349403 | 1944 | + | 0.297839 | |
g2356 | DLA_02606 | F4PJNLW01EE5MJ | CDS | 351662 | 2148 | - | 0.3473 | |
g2357 | DLA_02607 | F4PJNLW01EE5MJ | CDS | 354640 | 645 | - | 0.339535 | |
g2358 | DLA_02608 | F4PJNLW01EE5MJ | CDS | 356045 | 1539 | + | 0.359324 | |
g2359 | DLA_02609 | F4PJNLW01EE5MJ | CDS | 357944 | 339 | - | 0.312684 | |
g2360 | DLA_02610 | F4PJNLW01EE5MJ | CDS | 358341 | 906 | + | 0.307947 | |
g2361 | DLA_02611 | F4PJNLW01EE5MJ | CDS | 359488 | 1440 | + | 0.297917 | |
g2362 | DLA_02612 | F4PJNLW01EE5MJ | CDS | 361585 | 2547 | + | 0.299176 | |
g2363 | DLA_02613 | F4PJNLW01EE5MJ | CDS | 364580 | 621 | - | 0.289855 | |
g2364 | DLA_02614 | F4PJNLW01EE5MJ | CDS | 365601 | 5229 | - | 0.347676 | |
g2365 | DLA_02615 | catalyzes the reaction ATP ethanolamine ADP O-phosphoethanolamine | F4PJNLW01EE5MJ | CDS | 371747 | 1074 | + | 0.290503 |
g2366 | DLA_02616 | F4PJNLW01EE5MJ | CDS | 373247 | 591 | + | 0.279188 | |
g2367 | DLA_02618 | F4PJNLW01EE5MJ | CDS | 373941 | 1221 | - | 0.328419 | |
g2368 | DLA_02619 | F4PJNLW01EE5MJ | CDS | 375408 | 1371 | - | 0.408461 | |
g2369 | DLA_02621 | F4PJNLW01EE5MJ | CDS | 377325 | 1002 | - | 0.291417 | |
g2370 | DLA_02622 | F4PJNLW01EE5MJ | CDS | 378817 | 768 | + | 0.291667 | |
g2371 | DLA_02623 | F4PJNLW01EE5MJ | CDS | 379741 | 2967 | - | 0.296933 | |
g2372 | DLA_02625 | F4PJNLW01EE5MJ | CDS | 383687 | 2985 | - | 0.307873 | |
g2373 | DLA_02627 | F4PJNLW01EE5MJ | CDS | 387997 | 471 | + | 0.292994 | |
g2374 | DLA_02628 | F4PJNLW01EE5MJ | CDS | 390127 | 1431 | + | 0.297694 | |
g2375 | DLA_02629 | F4PJNLW01EE5MJ | CDS | 392072 | 1374 | - | 0.315138 | |
g2376 | DLA_02630 | F4PJNLW01EE5MJ | CDS | 394228 | 465 | + | 0.288172 | |
g2377 | DLA_02631 | member of the alpha-actininspectrin superfamily dimerizes with cortexillin I involved in cytokinesis and development and associates with the actin cytoskeleton | F4PJNLW01EE5MJ | CDS | 395523 | 1353 | - | 0.36881 |
g2378 | DLA_02632 | F4PJNLW01EE5MJ | CDS | 397210 | 1104 | - | 0.274457 | |
g2379 | DLA_02633 | F4PJNLW01EE5MJ | CDS | 398493 | 1431 | - | 0.360587 | |
g2380 | DLA_02635 | F4PJNLW01EE5MJ | CDS | 401669 | 4497 | + | 0.381143 | |
g2381 | DLA_02636 | F4PJNLW01EE5MJ | CDS | 406795 | 3672 | + | 0.353214 | |
g2382 | DLA_02637 | F4PJNLW01EE5MJ | CDS | 410668 | 450 | - | 0.313333 | |
g2383 | DLA_02638 | F4PJNLW01EE5MJ | CDS | 411622 | 3039 | + | 0.348799 | |
g2384 | DLA_02639 | F4PJNLW01EE5MJ | CDS | 415069 | 1365 | - | 0.315751 | |
g2385 | DLA_02640 | catalytic subunit of the Casup2supcalmodulin-dependent serinethreonine protein phosphatase | F4PJNLW01EE5MJ | CDS | 416797 | 1710 | + | 0.330994 |
g2386 | DLA_02641 | F4PJNLW01EE5MJ | CDS | 419950 | 1467 | + | 0.408316 | |
g2387 | DLA_02642 | F4PJNLW01EE5MJ | CDS | 421773 | 1086 | - | 0.316759 | |
g2388 | DLA_02643 | F4PJNLW01EE5MJ | CDS | 423201 | 1062 | + | 0.339925 | |
g2389 | DLA_02644 | F4PJNLW01EE5MJ | CDS | 424427 | 822 | - | 0.343066 | |
g2390 | DLA_02645 | 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 | F4PJNLW01EE5MJ | CDS | 425446 | 1080 | - | 0.308333 |
g2391 | DLA_02646 | F4PJNLW01EE5MJ | CDS | 427191 | 471 | + | 0.392781 | |
g2392 | DLA_02647 | F4PJNLW01EE5MJ | CDS | 427686 | 870 | - | 0.293103 | |
g2393 | DLA_02648 | subunit of the splicing factor SF3B required for spliceosome assembly belongs to the SF3b10 (splicing factor 3B 10 kDa subunit) family | F4PJNLW01EE5MJ | CDS | 428837 | 285 | + | 0.34386 |
g2394 | DLA_02649 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages | F4PJNLW01EE5MJ | CDS | 429301 | 1893 | - | 0.364501 |
g2395 | DLA_02650 | F4PJNLW01EE5MJ | CDS | 432099 | 2643 | - | 0.331063 | |
g2396 | DLA_02652 | F4PJNLW01EE5MJ | CDS | 436038 | 390 | - | 0.294872 | |
g2397 | DLA_02654 | F4PJNLW01EE5MJ | CDS | 437395 | 1938 | - | 0.325593 | |
g2398 | DLA_02657 | F4PJNLW01EE5MJ | CDS | 440849 | 750 | + | 0.293333 | |
g2399 | DLA_02658 | F4PJNLW01EE5MJ | CDS | 441816 | 1785 | - | 0.347339 | |
g2400 | DLA_11528 | F4PJNLW01EE5MJ | CDS | 443870 | 609 | - | 0.326765 | |
g2401 | DLA_02659 | F4PJNLW01EE5MJ | CDS | 445106 | 1449 | - | 0.434783 | |
g2402 | DLA_02660 | F4PJNLW01EE5MJ | CDS | 446810 | 2196 | - | 0.32969 | |
g2403 | DLA_02661 | F4PJNLW01EE5MJ | CDS | 449307 | 336 | + | 0.25 | |
g2404 | DLA_02662 | F4PJNLW01EE5MJ | CDS | 450030 | 423 | - | 0.394799 | |
g2405 | DLA_02663 | F4PJNLW01EE5MJ | CDS | 450963 | 1677 | + | 0.294574 | |
g2406 | DLA_02664 | F4PJNLW01EE5MJ | CDS | 452756 | 450 | - | 0.306667 | |
g2407 | DLA_02665 | F4PJNLW01EE5MJ | CDS | 453401 | 4122 | - | 0.34983 | |
g2408 | DLA_02668 | F4PJNLW01EE5MJ | CDS | 458284 | 3003 | + | 0.330003 | |
g2409 | DLA_02669 | F4PJNLW01EE5MJ | CDS | 462028 | 5133 | + | 0.337619 | |
g2410 | DLA_02670 | TFIID subunit involved in RNA polymerase II transcription initiation | F4PJNLW01EE5MJ | CDS | 467525 | 1728 | + | 0.311343 |
g2411 | DLA_02671 | F4PJNLW01EE5MJ | CDS | 469324 | 723 | - | 0.290456 | |
g2412 | DLA_02672 | full transporter consisting of two ABC domains and two transmembrane domains there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 470340 | 4365 | - | 0.376174 |
g2413 | DLA_02674 | catalyzes the reaction acyl-CoA Osub2sub trans-23-dehydroacyl-CoA Hsub2subOsub2sub expressed in pstAB cells and in upper cup during culmination | F4PJNLW01EE5MJ | CDS | 475903 | 1905 | - | 0.342782 |
g2414 | DLA_02675 | catalyzes the reaction: acyl-CoA 12-diacylglycerol CoA triacylglycerol similar to mammalian DGAT1 contains 9 predicted transmembrane domains | F4PJNLW01EE5MJ | CDS | 478140 | 1689 | + | 0.328005 |
g2415 | DLA_02676 | contains 3 zinc-binding LIM domains LIM domains are found in proteins with differing functions including gene expression and cytoskeleton organisation and development | F4PJNLW01EE5MJ | CDS | 480213 | 552 | - | 0.342391 |
g2416 | DLA_02677 | contains a N-terminal uridine kinase domaine domain and a C-terminal adenylate cyclase domain like the UdkC protein and other plant proteins | F4PJNLW01EE5MJ | CDS | 480988 | 1494 | + | 0.323963 |
g2417 | DLA_02678 | catalyzes the reaction isocitrate NAD 2-oxoglutarate CO2 NADH | F4PJNLW01EE5MJ | CDS | 482810 | 1047 | - | 0.372493 |
g2418 | DLA_02679 | F4PJNLW01EE5MJ | CDS | 484352 | 1005 | + | 0.342289 | |
g2419 | DLA_02680 | F4PJNLW01EE5MJ | CDS | 485473 | 1023 | - | 0.309873 | |
g2420 | DLA_02681 | CAZy family GH9 catalyzes the hydrolysis of glucosidic linkages induced by Legionella pneumophila infection | F4PJNLW01EE5MJ | CDS | 486833 | 1524 | + | 0.370735 |
g2421 | DLA_02682 | F4PJNLW01EE5MJ | CDS | 488927 | 750 | - | 0.325333 | |
g2422 | DLA_02683 | F4PJNLW01EE5MJ | CDS | 490169 | 492 | - | 0.284553 | |
g2423 | DLA_02684 | F4PJNLW01EE5MJ | CDS | 490736 | 3402 | + | 0.289242 | |
g2424 | DLA_02685 | F4PJNLW01EE5MJ | CDS | 494455 | 1422 | - | 0.415612 | |
g2425 | DLA_02686 | F4PJNLW01EE5MJ | CDS | 497320 | 1461 | + | 0.381246 | |
g2426 | DLA_02687 | F4PJNLW01EE5MJ | CDS | 499115 | 4104 | + | 0.34308 | |
g2427 | DLA_02690 | F4PJNLW01EE5MJ | CDS | 506870 | 1776 | + | 0.310248 | |
g2428 | DLA_02691 | F4PJNLW01EE5MJ | CDS | 508852 | 2733 | + | 0.320161 | |
g2429 | DLA_02692 | F4PJNLW01EE5MJ | CDS | 512012 | 333 | - | 0.324324 | |
g2430 | DLA_02693 | F4PJNLW01EE5MJ | CDS | 512515 | 1812 | + | 0.351545 | |
g2431 | DLA_02694 | F4PJNLW01EE5MJ | CDS | 514560 | 2319 | - | 0.351013 | |
g2432 | DLA_02697 | F4PJNLW01EE5MJ | CDS | 519322 | 3981 | + | 0.373524 | |
g2433 | DLA_02698 | F4PJNLW01EE5MJ | CDS | 523589 | 1584 | + | 0.275884 | |
g2434 | DLA_02699 | F4PJNLW01EE5MJ | CDS | 525262 | 972 | + | 0.337449 | |
g2435 | DLA_02700 | F4PJNLW01EE5MJ | CDS | 526323 | 1653 | - | 0.304295 | |
g2436 | DLA_02701 | F4PJNLW01EE5MJ | CDS | 528190 | 2787 | - | 0.311446 | |
g2437 | DLA_02702 | F4PJNLW01EE5MJ | CDS | 531535 | 972 | - | 0.269547 | |
g2438 | DLA_02703 | F4PJNLW01EE5MJ | CDS | 532795 | 498 | + | 0.25502 | |
g2439 | DLA_02704 | F4PJNLW01EE5MJ | CDS | 533451 | 2232 | - | 0.338262 | |
g2440 | DLA_02705 | F4PJNLW01EE5MJ | CDS | 535762 | 1254 | - | 0.313397 | |
g2441 | DLA_02706 | F4PJNLW01EE5MJ | CDS | 538396 | 1752 | - | 0.376142 | |
g2442 | DLA_02708 | F4PJNLW01EE5MJ | CDS | 540537 | 732 | + | 0.331967 | |
g2443 | DLA_02710 | F4PJNLW01EE5MJ | CDS | 542134 | 1761 | - | 0.329358 | |
g2444 | DLA_02712 | F4PJNLW01EE5MJ | CDS | 544525 | 2784 | + | 0.336566 | |
g2445 | DLA_02715 | F4PJNLW01EE5MJ | CDS | 549691 | 1638 | - | 0.263126 | |
g2446 | DLA_02716 | F4PJNLW01EE5MJ | CDS | 551853 | 2004 | + | 0.271956 | |
g2447 | DLA_02717 | F4PJNLW01EE5MJ | CDS | 554514 | 1056 | + | 0.316288 | |
g2448 | DLA_02718 | F4PJNLW01EE5MJ | CDS | 555757 | 1047 | - | 0.321872 | |
g2449 | DLA_02719 | F4PJNLW01EE5MJ | CDS | 557376 | 7473 | + | 0.372006 | |
g2450 | DLA_02720 | F4PJNLW01EE5MJ | CDS | 565066 | 2763 | + | 0.338762 | |
g2451 | DLA_02721 | F4PJNLW01EE5MJ | CDS | 568245 | 2721 | - | 0.334803 | |
g2452 | DLA_02722 | F4PJNLW01EE5MJ | CDS | 572857 | 1359 | - | 0.296542 | |
g2453 | DLA_02723 | F4PJNLW01EE5MJ | CDS | 574428 | 1848 | - | 0.350649 | |
g2454 | DLA_02724 | F4PJNLW01EE5MJ | CDS | 576949 | 1017 | - | 0.311701 | |
g2455 | DLA_02725 | F4PJNLW01EE5MJ | CDS | 579082 | 2658 | - | 0.322047 | |
g2456 | DLA_11529 | F4PJNLW01EE5MJ | CDS | 582034 | 387 | - | 0.374677 | |
g2457 | DLA_02726 | F4PJNLW01EE5MJ | CDS | 582875 | 5502 | - | 0.321156 | |
g2458 | DLA_02727 | F4PJNLW01EE5MJ | CDS | 588955 | 3414 | - | 0.347393 | |
g2459 | DLA_02728 | F4PJNLW01EE5MJ | CDS | 593887 | 2484 | + | 0.324477 | |
g2460 | DLA_02729 | F4PJNLW01EE5MJ | CDS | 597268 | 1272 | - | 0.316824 | |
g2461 | DLA_02730 | F4PJNLW01EE5MJ | CDS | 598939 | 1338 | + | 0.289985 | |
g2462 | DLA_02731 | 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 | F4PJNLW01EE5MJ | CDS | 600513 | 1497 | - | 0.370073 |
g2463 | DLA_02732 | F4PJNLW01EE5MJ | CDS | 602542 | 888 | + | 0.275901 | |
g2464 | DLA_02733 | F4PJNLW01EE5MJ | CDS | 603644 | 5577 | - | 0.337637 | |
g2465 | DLA_02735 | F4PJNLW01EE5MJ | CDS | 610087 | 1056 | - | 0.356061 | |
g2466 | DLA_02736 | F4PJNLW01EE5MJ | CDS | 611396 | 2547 | + | 0.328229 | |
g2467 | DLA_02737 | F4PJNLW01EE5MJ | CDS | 614224 | 2649 | + | 0.348056 | |
g2468 | DLA_02738 | F4PJNLW01EE5MJ | CDS | 617381 | 840 | - | 0.264286 | |
g2469 | DLA_02740 | F4PJNLW01EE5MJ | CDS | 619141 | 1839 | + | 0.353453 | |
g2470 | DLA_02741 | subunit 4 of the conserved replication complex GINS which is essential for initiation of DNA replication in X. laevis | F4PJNLW01EE5MJ | CDS | 621318 | 597 | - | 0.247906 |
g2471 | DLA_02742 | F4PJNLW01EE5MJ | CDS | 622198 | 1227 | + | 0.277099 | |
g2472 | DLA_02743 | F4PJNLW01EE5MJ | CDS | 623570 | 633 | + | 0.257504 | |
g2473 | DLA_02744 | F4PJNLW01EE5MJ | CDS | 624351 | 3513 | + | 0.317108 | |
g2474 | DLA_02745 | F4PJNLW01EE5MJ | CDS | 627998 | 1914 | - | 0.323929 | |
g2475 | DLA_02746 | F4PJNLW01EE5MJ | CDS | 630181 | 2235 | + | 0.332438 | |
g2476 | DLA_02747 | F4PJNLW01EE5MJ | CDS | 633838 | 2796 | + | 0.311516 | |
g2477 | DLA_02748 | F4PJNLW01EE5MJ | CDS | 637138 | 1848 | - | 0.33171 | |
g2478 | DLA_02749 | F4PJNLW01EE5MJ | CDS | 639638 | 564 | - | 0.319149 | |
g2479 | DLA_02750 | F4PJNLW01EE5MJ | CDS | 640671 | 258 | - | 0.27907 | |
g2480 | DLA_02751 | F4PJNLW01EE5MJ | CDS | 641186 | 1014 | + | 0.324458 | |
g2481 | DLA_02752 | weakly similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | F4PJNLW01EE5MJ | CDS | 642626 | 11559 | + | 0.33541 |
g2482 | DLA_02753 | F4PJNLW01EE5MJ | CDS | 654387 | 5724 | - | 0.332809 | |
g2483 | DLA_02754 | F4PJNLW01EE5MJ | CDS | 660861 | 1974 | - | 0.295339 | |
g2484 | DLA_02755 | F4PJNLW01EE5MJ | CDS | 663291 | 963 | + | 0.266874 | |
g2485 | DLA_02756 | F4PJNLW01EE5MJ | CDS | 664548 | 966 | + | 0.442029 | |
g2486 | DLA_02757 | F4PJNLW01EE5MJ | CDS | 665749 | 648 | + | 0.376543 | |
g2487 | DLA_02758 | F4PJNLW01EE5MJ | CDS | 666600 | 420 | - | 0.330952 | |
g2488 | DLA_02759 | F4PJNLW01EE5MJ | CDS | 667342 | 6816 | + | 0.359008 | |
g2489 | DLA_02760 | F4PJNLW01EE5MJ | CDS | 674351 | 555 | - | 0.263063 | |
g2490 | DLA_02761 | F4PJNLW01EE5MJ | CDS | 675292 | 3822 | + | 0.343799 | |
g2491 | DLA_02762 | F4PJNLW01EE5MJ | CDS | 680144 | 1761 | + | 0.334469 | |
g2492 | DLA_02763 | F4PJNLW01EE5MJ | CDS | 681946 | 621 | - | 0.275362 | |
g2493 | DLA_02764 | F4PJNLW01EE5MJ | CDS | 682829 | 612 | - | 0.263072 | |
g2494 | DLA_02766 | F4PJNLW01EE5MJ | CDS | 683815 | 1683 | - | 0.314914 | |
g2495 | DLA_02767 | F4PJNLW01EE5MJ | CDS | 685824 | 1446 | + | 0.375519 | |
g2496 | DLA_02768 | subunit of the exocyst complex which targets secretory vesicles to active sites of exocytosis | F4PJNLW01EE5MJ | CDS | 687331 | 2985 | - | 0.344389 |
g2497 | DLA_02769 | F4PJNLW01EE5MJ | CDS | 690595 | 297 | + | 0.296296 | |
g2498 | DLA_02770 | F4PJNLW01EE5MJ | CDS | 691045 | 969 | - | 0.298246 | |
g2499 | DLA_02771 | F4PJNLW01EE5MJ | CDS | 692274 | 1284 | + | 0.332555 | |
g2500 | DLA_02772 | F4PJNLW01EE5MJ | CDS | 693787 | 798 | - | 0.303258 | |
g2501 | DLA_02773 | F4PJNLW01EE5MJ | CDS | 695125 | 1632 | - | 0.315564 | |
g2502 | DLA_02774 | F4PJNLW01EE5MJ | CDS | 697422 | 1587 | + | 0.293006 | |
g2503 | DLA_02776 | F4PJNLW01EE5MJ | CDS | 699156 | 999 | - | 0.286286 | |
g2504 | DLA_02777 | F4PJNLW01EE5MJ | CDS | 700257 | 1089 | + | 0.315886 | |
g2505 | DLA_02778 | F4PJNLW01EE5MJ | CDS | 701735 | 1137 | + | 0.326297 | |
g2506 | DLA_02779 | F4PJNLW01EE5MJ | CDS | 703198 | 1284 | - | 0.358255 | |
g2507 | DLA_02780 | F4PJNLW01EE5MJ | CDS | 704784 | 1113 | - | 0.322552 | |
g2508 | DLA_02781 | F4PJNLW01EE5MJ | CDS | 706288 | 2118 | + | 0.352691 | |
g2509 | DLA_02782 | F4PJNLW01EE5MJ | CDS | 708861 | 1593 | - | 0.29818 | |
g2510 | DLA_02783 | F4PJNLW01EE5MJ | CDS | 710638 | 1659 | - | 0.283303 | |
g2511 | DLA_02785 | F4PJNLW01EE5MJ | CDS | 713149 | 4359 | + | 0.332416 | |
g2512 | DLA_02786 | F4PJNLW01EE5MJ | CDS | 717933 | 1389 | + | 0.349892 | |
g2513 | DLA_02787 | F4PJNLW01EE5MJ | CDS | 719586 | 828 | - | 0.345411 | |
g2514 | DLA_02788 | F4PJNLW01EE5MJ | CDS | 721035 | 2421 | + | 0.327551 | |
g2515 | DLA_02789 | F4PJNLW01EE5MJ | CDS | 724167 | 387 | + | 0.268734 | |
g2516 | DLA_02790 | F4PJNLW01EE5MJ | CDS | 724995 | 1611 | + | 0.340161 | |
g2517 | DLA_02791 | F4PJNLW01EE5MJ | CDS | 726759 | 1041 | + | 0.295869 | |
g2518 | DLA_02792 | F4PJNLW01EE5MJ | CDS | 727968 | 2568 | - | 0.315031 | |
g2519 | DLA_02793 | F4PJNLW01EE5MJ | CDS | 730885 | 1683 | + | 0.289958 | |
g2520 | DLA_02794 | F4PJNLW01EE5MJ | CDS | 732818 | 813 | - | 0.341943 | |
g2521 | DLA_02795 | F4PJNLW01EE5MJ | CDS | 734003 | 3651 | - | 0.326212 | |
g2522 | DLA_02796 | F4PJNLW01EE5MJ | CDS | 737876 | 1452 | - | 0.302342 | |
g2523 | DLA_02797 | F4PJNLW01EE5MJ | CDS | 739700 | 3531 | - | 0.323138 | |
g2524 | DLA_02798 | F4PJNLW01EE5MJ | CDS | 743917 | 831 | - | 0.320096 | |
g2525 | DLA_02799 | F4PJNLW01EE5MJ | CDS | 745500 | 744 | + | 0.349462 | |
g2526 | DLA_02800 | F4PJNLW01EE5MJ | CDS | 746832 | 1137 | + | 0.307828 | |
g2527 | DLA_02801 | F4PJNLW01EE5MJ | CDS | 748256 | 2673 | + | 0.354284 | |
g2528 | DLA_02802 | ortholog of the human DHX9 that unwinds double-stranded DNA and RNA in a 3' to 5' direction | F4PJNLW01EE5MJ | CDS | 751371 | 4032 | - | 0.312252 |
g2529 | DLA_02803 | F4PJNLW01EE5MJ | CDS | 755693 | 927 | - | 0.283711 | |
g2530 | DLA_02804 | F4PJNLW01EE5MJ | CDS | 756724 | 1689 | + | 0.28656 | |
g2531 | DLA_02805 | F4PJNLW01EE5MJ | CDS | 758432 | 1533 | - | 0.306588 | |
g2532 | DLA_02806 | F4PJNLW01EE5MJ | CDS | 760271 | 447 | - | 0.261745 | |
g2533 | DLA_02807 | F4PJNLW01EE5MJ | CDS | 760964 | 339 | + | 0.227139 | |
g2534 | DLA_02808 | F4PJNLW01EE5MJ | CDS | 761715 | 4392 | - | 0.346084 | |
g2535 | DLA_02809 | F4PJNLW01EE5MJ | CDS | 767285 | 1239 | + | 0.274415 | |
g2536 | DLA_02810 | F4PJNLW01EE5MJ | CDS | 768921 | 1665 | - | 0.332132 | |
g2537 | DLA_02811 | F4PJNLW01EE5MJ | CDS | 770710 | 1575 | + | 0.363175 | |
g2538 | DLA_02812 | F4PJNLW01EE5MJ | CDS | 772707 | 996 | + | 0.331325 | |
g2539 | DLA_02813 | F4PJNLW01EE5MJ | CDS | 774560 | 1326 | - | 0.273002 | |
g2540 | DLA_02814 | F4PJNLW01EE5MJ | CDS | 776978 | 2097 | + | 0.304244 | |
g2541 | DLA_02815 | F4PJNLW01EE5MJ | CDS | 779152 | 1344 | - | 0.338542 | |
g2542 | DLA_02816 | F4PJNLW01EE5MJ | CDS | 781075 | 2442 | + | 0.285831 | |
g2543 | DLA_02817 | F4PJNLW01EE5MJ | CDS | 784926 | 1428 | + | 0.362045 | |
g2544 | DLA_02821 | highly conserved protein interacts with TATA binding protein (TBP) and with the SCF (Skp1-Cul1-F-box) ubiquitin ligase complex | F4PJNLW01EE5MJ | CDS | 788159 | 3693 | - | 0.315732 |
g2545 | DLA_02822 | catalyzes the reaction ATP L-histidine tRNAHis AMP diphosphate L-histidyl-tRNAHis | F4PJNLW01EE5MJ | CDS | 792242 | 1569 | - | 0.312938 |
g2546 | DLA_02823 | F4PJNLW01EE5MJ | CDS | 794069 | 3654 | - | 0.315545 | |
g2547 | DLA_02824 | F4PJNLW01EE5MJ | CDS | 798262 | 1302 | - | 0.300307 | |
g2548 | DLA_02825 | F4PJNLW01EE5MJ | CDS | 803547 | 1668 | + | 0.395084 | |
g2549 | DLA_02826 | F4PJNLW01EE5MJ | CDS | 806057 | 1491 | + | 0.327968 | |
g2550 | DLA_02827 | F4PJNLW01EE5MJ | CDS | 807819 | 1671 | - | 0.308797 | |
g2551 | DLA_02829 | F4PJNLW01EE5MJ | CDS | 810255 | 2385 | - | 0.307338 | |
g2552 | DLA_02830 | F4PJNLW01EE5MJ | CDS | 813504 | 555 | - | 0.295496 | |
g2553 | DLA_02831 | F4PJNLW01EE5MJ | CDS | 815035 | 1290 | - | 0.347287 | |
g2554 | DLA_02832 | F4PJNLW01EE5MJ | CDS | 816913 | 1428 | - | 0.334734 | |
g2555 | DLA_02833 | F4PJNLW01EE5MJ | CDS | 819149 | 828 | + | 0.365942 | |
g2556 | DLA_02834 | F4PJNLW01EE5MJ | CDS | 820222 | 621 | + | 0.294686 | |
g2557 | DLA_02835 | F4PJNLW01EE5MJ | CDS | 821312 | 303 | - | 0.313531 | |
g2558 | DLA_02836 | F4PJNLW01EE5MJ | CDS | 821803 | 708 | - | 0.303672 | |
g2559 | DLA_02840 | F4PJNLW01EE5MJ | CDS | 823472 | 318 | - | 0.305031 | |
g2560 | DLA_02841 | F4PJNLW01EE5MJ | CDS | 824531 | 777 | - | 0.311454 | |
g2561 | DLA_02843 | F4PJNLW01EE5MJ | CDS | 827504 | 351 | + | 0.270655 | |
g2562 | DLA_02844 | F4PJNLW01EE5MJ | CDS | 827942 | 3414 | - | 0.345636 | |
g2563 | DLA_02846 | F4PJNLW01EE5MJ | CDS | 831991 | 3546 | - | 0.295262 | |
g2564 | DLA_02847 | F4PJNLW01EE5MJ | CDS | 836147 | 1173 | - | 0.310315 | |
g2565 | DLA_02848 | F4PJNLW01EE5MJ | CDS | 837770 | 2082 | - | 0.306436 | |
g2566 | DLA_02849 | F4PJNLW01EE5MJ | CDS | 840278 | 3147 | - | 0.31109 | |
g2567 | DLA_02851 | F4PJNLW01EE5MJ | CDS | 843820 | 2844 | - | 0.300281 | |
g2568 | DLA_02852 | F4PJNLW01EE5MJ | CDS | 846859 | 660 | + | 0.321212 | |
g2569 | DLA_02853 | F4PJNLW01EE5MJ | CDS | 847624 | 3453 | - | 0.32812 | |
g2570 | DLA_02854 | contains one putative transmembrane domain similar to D. purpureum protein | F4PJNLW01EE5MJ | CDS | 851806 | 2226 | + | 0.320305 |
g2571 | DLA_02855 | F4PJNLW01EE5MJ | CDS | 854469 | 1170 | + | 0.323932 | |
g2572 | DLA_02856 | F4PJNLW01EE5MJ | CDS | 855747 | 1704 | + | 0.316901 | |
g2573 | DLA_02857 | contains a putative Like-Sm (Lsm) domain possible homolog of LSM12 | F4PJNLW01EE5MJ | CDS | 857550 | 537 | - | 0.3054 |
g2574 | DLA_02858 | catalyzes the reaction GDP-L-fucose NADP GDP-4-dehydro-6-deoxy-D-mannose NADPH H | F4PJNLW01EE5MJ | CDS | 858491 | 948 | + | 0.341772 |
g2575 | DLA_02859 | F4PJNLW01EE5MJ | CDS | 859900 | 1149 | - | 0.326371 | |
g2576 | DLA_02860 | F4PJNLW01EE5MJ | CDS | 861531 | 1191 | + | 0.313182 | |
g2577 | DLA_11530 | F4PJNLW01EE5MJ | CDS | 863338 | 726 | + | 0.330579 | |
g2578 | DLA_02861 | F4PJNLW01EE5MJ | CDS | 864104 | 2604 | - | 0.320276 | |
g2579 | DLA_02862 | catalyzes the reaction NADPH n oxidized hemoprotein NADP() n reduced hemoprotein similar to the H. sapiens POR protein that is defect in adrenal hyperplasia variant type (AHV) a syndrome with disordered steroidogenesis | F4PJNLW01EE5MJ | CDS | 866908 | 1932 | - | 0.371636 |
g2580 | DLA_02863 | ortholog of CLN2TPP1 contains a predicted signal peptide enriched in prespore cells | F4PJNLW01EE5MJ | CDS | 869289 | 1596 | - | 0.390977 |
g2581 | DLA_02864 | F4PJNLW01EE5MJ | CDS | 871672 | 1962 | + | 0.392457 | |
g2582 | DLA_02865 | belongs to the acyltransferase superfamily contains 2 predicted transmembrane domains | F4PJNLW01EE5MJ | CDS | 874026 | 1086 | - | 0.331492 |
g2583 | DLA_02866 | F4PJNLW01EE5MJ | CDS | 875987 | 948 | - | 0.295359 | |
g2584 | DLA_02867 | F4PJNLW01EE5MJ | CDS | 877359 | 1086 | - | 0.298343 | |
g2585 | DLA_02868 | F4PJNLW01EE5MJ | CDS | 878837 | 1809 | - | 0.328911 | |
g2586 | DLA_02869 | F4PJNLW01EE5MJ | CDS | 880997 | 1695 | + | 0.315634 | |
g2587 | DLA_11531 | F4PJNLW01EE5MJ | CDS | 882745 | 3390 | - | 0.314159 | |
g2588 | DLA_02870 | F4PJNLW01EE5MJ | CDS | 886645 | 5736 | - | 0.339435 | |
g2589 | DLA_02871 | F4PJNLW01EE5MJ | CDS | 893127 | 1461 | + | 0.27447 | |
g2590 | DLA_02873 | F4PJNLW01EE5MJ | CDS | 896635 | 1440 | + | 0.272917 | |
g2591 | DLA_02874 | similar to S. cerevisiae VPS13 involved in vacuolar protein sorting and protein-Golgi retention | F4PJNLW01EE5MJ | CDS | 898216 | 14703 | - | 0.327484 |
g2592 | DLA_02875 | F4PJNLW01EE5MJ | CDS | 913386 | 1989 | + | 0.293615 | |
g2593 | DLA_02876 | F4PJNLW01EE5MJ | CDS | 915521 | 2775 | - | 0.338378 | |
g2594 | DLA_02877 | F4PJNLW01EE5MJ | CDS | 918769 | 3492 | + | 0.340779 | |
g2595 | DLA_02878 | F4PJNLW01EE5MJ | CDS | 922352 | 609 | - | 0.321839 | |
g2596 | DLA_02879 | F4PJNLW01EE5MJ | CDS | 923135 | 2952 | + | 0.315041 | |
g2597 | DLA_02880 | F4PJNLW01EE5MJ | CDS | 926238 | 558 | + | 0.317204 | |
g2598 | DLA_02883 | F4PJNLW01EE5MJ | CDS | 929105 | 1083 | + | 0.351801 | |
g2599 | DLA_02884 | F4PJNLW01EE5MJ | CDS | 930398 | 1143 | + | 0.31671 | |
g2600 | DLA_02885 | catalyzes the reaction AMP pyrophosphate PRPP adenine in nucleoside salvage pathways | F4PJNLW01EE5MJ | CDS | 932083 | 597 | - | 0.341709 |
g2601 | DLA_02886 | F4PJNLW01EE5MJ | CDS | 933002 | 534 | + | 0.28839 | |
g2602 | DLA_02887 | F4PJNLW01EE5MJ | CDS | 934016 | 3438 | - | 0.357475 | |
g2603 | DLA_02888 | F4PJNLW01EE5MJ | CDS | 938672 | 708 | - | 0.351695 | |
g2604 | DLA_02889 | ortholog of the mammalian GTPBP3 and S. cerevisiae MSS1 GTPases responsible for the 5-carboxymethylaminomethyl modification of the wobble uridine base in mitochondrial tRNAs | F4PJNLW01EE5MJ | CDS | 939609 | 1605 | - | 0.321495 |
g2605 | DLA_02890 | contains six kelch repeats which are known to be involved in various biological processes | F4PJNLW01EE5MJ | CDS | 941357 | 1224 | - | 0.343954 |
g2606 | DLA_02891 | contains Sec23Sec24 zinc finger trunk and helical domains yeast Sec23Sec24 is a component of COPII (coat protein complex II) involved in ER to Golgi transport | F4PJNLW01EE5MJ | CDS | 943766 | 2277 | + | 0.317523 |
g2607 | DLA_02893 | F4PJNLW01EE5MJ | CDS | 946211 | 1323 | + | 0.357521 | |
g2608 | DLA_02894 | F4PJNLW01EE5MJ | CDS | 947771 | 1821 | - | 0.319055 | |
g2609 | DLA_02895 | F4PJNLW01EE5MJ | CDS | 949884 | 711 | + | 0.309423 | |
g2610 | DLA_02896 | F4PJNLW01EE5MJ | CDS | 951271 | 549 | - | 0.315118 | |
g2611 | DLA_02897 | F4PJNLW01EE5MJ | CDS | 952213 | 2286 | + | 0.306649 | |
g2612 | DLA_02898 | F4PJNLW01EE5MJ | CDS | 954839 | 1068 | - | 0.308989 | |
g2613 | DLA_11532 | F4PJNLW01EE5MJ | CDS | 956438 | 558 | - | 0.299283 | |
g2614 | DLA_02899 | conserved from bacteria to plants to alveolata contains 10 predicted transmembrane domains | F4PJNLW01EE5MJ | CDS | 957651 | 1221 | - | 0.325143 |
g2615 | DLA_02902 | similar to bacterial endo-14-beta-glucanase expressed in pstAO cells | F4PJNLW01EE5MJ | CDS | 960317 | 1725 | + | 0.361739 |
g2616 | DLA_02903 | F4PJNLW01EE5MJ | CDS | 962934 | 1245 | + | 0.330924 | |
g2617 | DLA_02905 | F4PJNLW01EE5MJ | CDS | 964648 | 1923 | - | 0.368175 | |
g2618 | DLA_02906 | F4PJNLW01EE5MJ | CDS | 967215 | 1188 | + | 0.285354 | |
g2619 | DLA_02907 | F4PJNLW01EE5MJ | CDS | 968642 | 354 | + | 0.276836 | |
g2620 | DLA_02908 | F4PJNLW01EE5MJ | CDS | 969208 | 3174 | - | 0.333018 | |
g2621 | DLA_02909 | F4PJNLW01EE5MJ | CDS | 973377 | 288 | + | 0.315972 | |
g2622 | DLA_02910 | F4PJNLW01EE5MJ | CDS | 973891 | 2289 | - | 0.328965 | |
g2623 | DLA_02911 | F4PJNLW01EE5MJ | CDS | 976541 | 699 | + | 0.32475 | |
g2624 | DLA_02912 | F4PJNLW01EE5MJ | CDS | 977594 | 636 | + | 0.34434 | |
g2625 | DLA_02913 | F4PJNLW01EE5MJ | CDS | 978386 | 1458 | + | 0.391632 | |
g2626 | DLA_02914 | F4PJNLW01EE5MJ | CDS | 980007 | 2058 | + | 0.3207 | |
g2627 | DLA_02915 | F4PJNLW01EE5MJ | CDS | 982387 | 687 | - | 0.326055 | |
g2628 | DLA_02916 | F4PJNLW01EE5MJ | CDS | 983803 | 1734 | + | 0.318916 | |
g2629 | DLA_02917 | F4PJNLW01EE5MJ | CDS | 985681 | 558 | - | 0.290323 | |
g2630 | DLA_02918 | F4PJNLW01EE5MJ | CDS | 986682 | 1068 | + | 0.425094 | |
g2631 | DLA_02920 | F4PJNLW01EE5MJ | CDS | 987952 | 834 | + | 0.303357 | |
g2632 | DLA_02921 | F4PJNLW01EE5MJ | CDS | 989364 | 1104 | + | 0.336957 | |
g2633 | DLA_02923 | F4PJNLW01EE5MJ | CDS | 993468 | 3117 | + | 0.336221 | |
g2634 | DLA_02924 | F4PJNLW01EE5MJ | CDS | 997192 | 1437 | - | 0.268615 | |
g2635 | DLA_02925 | F4PJNLW01EE5MJ | CDS | 998892 | 1449 | + | 0.348516 | |
g2636 | DLA_02926 | F4PJNLW01EE5MJ | CDS | 1000811 | 2118 | - | 0.344193 | |
g2637 | DLA_11533 | F4PJNLW01EE5MJ | CDS | 1004492 | 969 | + | 0.302374 | |
g2638 | DLA_02927 | F4PJNLW01EE5MJ | CDS | 1005629 | 1932 | - | 0.321429 | |
g2639 | DLA_02928 | F4PJNLW01EE5MJ | CDS | 1007985 | 1662 | + | 0.299639 | |
g2640 | DLA_02929 | F4PJNLW01EE5MJ | CDS | 1009683 | 1953 | - | 0.303635 | |
g2641 | DLA_02930 | F4PJNLW01EE5MJ | CDS | 1013205 | 1566 | + | 0.298851 | |
g2642 | DLA_02933 | colocalizes with clathrin spots suggesting involvement in endocytosis does not localize to pseudopods in wild type in SCAR depleted mutants WASP replaces the functions of SCAR and localizes to pseudopods | F4PJNLW01EE5MJ | CDS | 1015460 | 1269 | + | 0.405831 |
g2643 | DLA_02934 | F4PJNLW01EE5MJ | CDS | 1016942 | 1704 | + | 0.2723 | |
g2644 | DLA_02935 | F4PJNLW01EE5MJ | CDS | 1019362 | 948 | + | 0.280591 | |
g2645 | DLA_02936 | ortholog of the H. sapiens L2HGDH which when defective causes L-2-hydroxyglutaric aciduria-a rare autosomal recessive disorder | F4PJNLW01EE5MJ | CDS | 1020371 | 1296 | - | 0.330247 |
g2646 | DLA_02937 | F4PJNLW01EE5MJ | CDS | 1022156 | 1284 | + | 0.35514 | |
g2647 | DLA_02938 | F4PJNLW01EE5MJ | CDS | 1023584 | 2526 | - | 0.300871 | |
g2648 | DLA_02939 | wealky similar to acid ceramidase which catalyzes the reaction N-acylsphingoside Hsub2subO a carboxylate sphingosine | F4PJNLW01EE5MJ | CDS | 1026651 | 1278 | + | 0.356025 |
g2649 | DLA_02940 | F4PJNLW01EE5MJ | CDS | 1028129 | 6285 | + | 0.322832 | |
g2650 | DLA_02941 | F4PJNLW01EE5MJ | CDS | 1034745 | 1086 | - | 0.347145 | |
g2651 | DLA_02942 | F4PJNLW01EE5MJ | CDS | 1035977 | 888 | - | 0.414414 | |
g2652 | DLA_02944 | F4PJNLW01EE5MJ | CDS | 1037367 | 2694 | - | 0.308463 | |
g2653 | DLA_02945 | F4PJNLW01EE5MJ | CDS | 1040175 | 618 | - | 0.326861 | |
g2654 | DLA_02946 | F4PJNLW01EE5MJ | CDS | 1041294 | 681 | + | 0.309838 | |
g2655 | DLA_02947 | similar to human HSBP1 HSBP1 is a negative regulator of the heat shock response there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 1042211 | 306 | + | 0.281046 |
g2656 | DLA_02948 | F4PJNLW01EE5MJ | CDS | 1042739 | 1278 | - | 0.311424 | |
g2657 | DLA_02949 | F4PJNLW01EE5MJ | CDS | 1044784 | 1410 | - | 0.338298 | |
g2658 | DLA_02950 | similar to human PDAP1 (PDGFA-associated protein 1) there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 1046830 | 597 | + | 0.356784 |
g2659 | DLA_02951 | similar to the mammalian Hypoxia up-regulated protein 1 (HYOU1) a protein that plays a role in cytoprotective cellular mechanisms triggered by oxygen deprivation there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 1047513 | 2721 | - | 0.336641 |
g2660 | DLA_02952 | F4PJNLW01EE5MJ | CDS | 1050672 | 2481 | - | 0.310762 | |
g2661 | DLA_02954 | 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 | F4PJNLW01EE5MJ | CDS | 1053508 | 780 | + | 0.384615 |
g2662 | DLA_02955 | F4PJNLW01EE5MJ | CDS | 1054406 | 618 | - | 0.313916 | |
g2663 | DLA_02956 | F4PJNLW01EE5MJ | CDS | 1055224 | 1890 | - | 0.325397 | |
g2664 | DLA_02957 | F4PJNLW01EE5MJ | CDS | 1057419 | 3426 | - | 0.345593 | |
g2665 | DLA_02958 | F4PJNLW01EE5MJ | CDS | 1061283 | 4632 | + | 0.360751 | |
g2666 | DLA_02959 | F4PJNLW01EE5MJ | CDS | 1066576 | 1845 | + | 0.339295 | |
g2667 | DLA_02960 | catalyzes the reduction of sphinganine to 3-dehydrosphinganine in glycosphingolipid metabolism there is a second copy of this gene | F4PJNLW01EE5MJ | CDS | 1068664 | 1044 | - | 0.319923 |
g2668 | DLA_02961 | F4PJNLW01EE5MJ | CDS | 1070320 | 777 | + | 0.328185 | |
g2669 | DLA_02962 | F4PJNLW01EE5MJ | CDS | 1071253 | 3879 | - | 0.364527 | |
g2670 | DLA_02963 | F4PJNLW01EE5MJ | CDS | 1076247 | 225 | + | 0.324444 | |
g2671 | DLA_02964 | F4PJNLW01EE5MJ | CDS | 1076687 | 1122 | - | 0.34492 | |
g2672 | DLA_02965 | F4PJNLW01EE5MJ | CDS | 1078535 | 3300 | + | 0.35697 | |
g2673 | DLA_02966 | F4PJNLW01EE5MJ | CDS | 1082165 | 1071 | - | 0.3324 | |
g2674 | DLA_02967 | F4PJNLW01EE5MJ | CDS | 1083851 | 354 | + | 0.285311 | |
g2675 | DLA_02968 | F4PJNLW01EE5MJ | CDS | 1084369 | 1584 | - | 0.315025 | |
g2676 | DLA_02970 | F4PJNLW01EE5MJ | CDS | 1086402 | 1746 | - | 0.256586 | |
g2677 | DLA_02972 | F4PJNLW01EE5MJ | CDS | 1089833 | 405 | + | 0.34321 | |
g2678 | DLA_02974 | F4PJNLW01EE5MJ | CDS | 1090682 | 1731 | - | 0.257077 | |
g2679 | DLA_02975 | F4PJNLW01EE5MJ | CDS | 1094434 | 1740 | + | 0.256897 | |
g2680 | DLA_02976 | belongs to the MCAKKif2 subfamily contains 1 SAM domain predicted to play a role in mitosis | F4PJNLW01EE5MJ | CDS | 1096365 | 3057 | + | 0.342493 |
g2681 | DLA_02977 | F4PJNLW01EE5MJ | CDS | 1100171 | 1548 | - | 0.289406 | |
g2682 | DLA_02978 | F4PJNLW01EE5MJ | CDS | 1101852 | 648 | - | 0.322531 | |
g2683 | DLA_02979 | F4PJNLW01EE5MJ | CDS | 1102678 | 996 | - | 0.341365 | |
g2684 | DLA_02980 | F4PJNLW01EE5MJ | CDS | 1104230 | 873 | + | 0.315006 | |
g2685 | DLA_11534 | F4PJNLW01EE5MJ | CDS | 1105164 | 399 | - | 0.305764 | |
g2686 | DLA_02981 | F4PJNLW01EE5MJ | CDS | 1106577 | 735 | - | 0.315646 | |
g2687 | DLA_02982 | F4PJNLW01EE5MJ | CDS | 1107434 | 2595 | - | 0.322158 | |
g2688 | DLA_02983 | F4PJNLW01EE5MJ | CDS | 1110499 | 987 | + | 0.256332 | |
g2689 | DLA_02984 | F4PJNLW01EE5MJ | CDS | 1111560 | 1422 | - | 0.274262 | |
g2690 | DLA_02985 | F4PJNLW01EE5MJ | CDS | 1113660 | 1383 | + | 0.326103 | |
g2691 | DLA_02986 | F4PJNLW01EE5MJ | CDS | 1115334 | 1575 | - | 0.335238 | |
g2692 | DLA_02987 | F4PJNLW01EE5MJ | CDS | 1117694 | 1050 | + | 0.345714 | |
g2693 | DLA_02988 | F4PJNLW01EE5MJ | CDS | 1119035 | 1752 | - | 0.311073 | |
g2694 | DLA_11535 | F4PJNLW01EE5MJ | CDS | 1121026 | 1623 | - | 0.316081 | |
g2695 | DLA_02989 | F4PJNLW01EE5MJ | CDS | 1123189 | 1227 | + | 0.308883 | |
g2696 | DLA_02990 | F4PJNLW01EE5MJ | CDS | 1124736 | 1419 | + | 0.275546 | |
g2697 | DLA_02991 | F4PJNLW01EE5MJ | CDS | 1127162 | 1287 | + | 0.34965 | |
g2698 | DLA_02992 | F4PJNLW01EE5MJ | CDS | 1128734 | 1071 | + | 0.286648 | |
g2699 | DLA_02993 | regulatory subunit 2 of the protein serinethreonine phosphatase 4 PPC4 ( | F4PJNLW01EE5MJ | CDS | 1129951 | 798 | + | 0.302005 |
g2700 | DLA_02994 | F4PJNLW01EE5MJ | CDS | 1131119 | 945 | + | 0.277249 | |
g2701 | DLA_02995 | F4PJNLW01EE5MJ | CDS | 1132168 | 750 | - | 0.357333 | |
g2702 | DLA_02996 | F4PJNLW01EE5MJ | CDS | 1133112 | 1554 | + | 0.29408 | |
g2703 | DLA_02997 | F4PJNLW01EE5MJ | CDS | 1135019 | 1623 | + | 0.340727 | |
g2704 | DLA_02998 | F4PJNLW01EE5MJ | CDS | 1136943 | 1596 | + | 0.282581 | |
g2705 | DLA_02999 | F4PJNLW01EE5MJ | CDS | 1138608 | 2625 | - | 0.299429 | |
g2706 | DLA_03000 | F4PJNLW01EE5MJ | CDS | 1141772 | 873 | + | 0.317297 | |
g2707 | DLA_03001 | F4PJNLW01EE5MJ | CDS | 1142690 | 738 | - | 0.319783 | |
g2708 | DLA_03003 | endoplasmic reticulum receptor for the KDEL signal sequence of proteins resident in the endoplasmic reticulum believed to cycle between the cis side of the Golgi apparatus and the ER | F4PJNLW01EE5MJ | CDS | 1143920 | 663 | + | 0.266968 |
g2709 | DLA_03004 | F4PJNLW01EE5MJ | CDS | 1144961 | 318 | - | 0.289308 | |
g2710 | DLA_03006 | F4PJNLW01EE5MJ | CDS | 1146469 | 1509 | - | 0.348575 | |
g2711 | DLA_03007 | F4PJNLW01EE5MJ | CDS | 1148480 | 1926 | + | 0.286085 | |
g2712 | DLA_03008 | F4PJNLW01EE5MJ | CDS | 1150620 | 1479 | - | 0.338742 | |
g2713 | DLA_03009 | F4PJNLW01EE5MJ | CDS | 1152979 | 1371 | + | 0.28884 | |
g2714 | DLA_03010 | F4PJNLW01EE5MJ | CDS | 1154444 | 4911 | - | 0.321116 | |
g2715 | DLA_03011 | F4PJNLW01EE5MJ | CDS | 1160692 | 624 | - | 0.299679 | |
g2716 | DLA_03012 | F4PJNLW01EE5MJ | CDS | 1161711 | 456 | - | 0.333333 | |
g2717 | DLA_03013 | F4PJNLW01EE5MJ | CDS | 1162905 | 4197 | + | 0.340481 | |
g2718 | DLA_03014 | F4PJNLW01EE5MJ | CDS | 1167232 | 900 | - | 0.27 | |
g2719 | DLA_03015 | F4PJNLW01EE5MJ | CDS | 1168470 | 1383 | + | 0.361533 | |
g2720 | DLA_03016 | F4PJNLW01EE5MJ | CDS | 1170267 | 1944 | + | 0.314815 | |
g2721 | DLA_03017 | F4PJNLW01EE5MJ | CDS | 1172536 | 321 | - | 0.29595 | |
g2722 | DLA_03018 | F4PJNLW01EE5MJ | CDS | 1173334 | 7125 | + | 0.278456 | |
g2723 | DLA_03019 | F4PJNLW01EE5MJ | CDS | 1180703 | 774 | - | 0.276486 | |
g2724 | DLA_03020 | component of the signal recognition particle (SRP) which ensures correct targeting of nascent secretory proteins to the endoplasmic reticulum | F4PJNLW01EE5MJ | CDS | 1181808 | 477 | + | 0.333333 |
g2725 | DLA_11536 | F4PJNLW01EE5MJ | CDS | 1182673 | 393 | + | 0.348601 | |
g2726 | DLA_03021 | F4PJNLW01EE5MJ | CDS | 1183360 | 573 | + | 0.209424 | |
g2727 | DLA_03022 | F4PJNLW01EE5MJ | CDS | 1183977 | 1803 | - | 0.298392 | |
g2728 | DLA_03023 | F4PJNLW01EE5MJ | CDS | 1186112 | 7353 | - | 0.300286 | |
g2729 | DLA_03024 | F4PJNLW01EE5MJ | CDS | 1194441 | 1767 | + | 0.348048 | |
g2730 | DLA_03025 | F4PJNLW01EE5MJ | CDS | 1196433 | 2709 | + | 0.287929 | |
g2731 | DLA_03026 | F4PJNLW01EE5MJ | CDS | 1199446 | 831 | + | 0.262335 | |
g2732 | DLA_03027 | F4PJNLW01EE5MJ | CDS | 1200415 | 2052 | - | 0.263158 | |
g2733 | DLA_03028 | F4PJNLW01EE5MJ | CDS | 1203141 | 2085 | - | 0.267146 | |
g2734 | DLA_03029 | F4PJNLW01EE5MJ | CDS | 1205355 | 546 | + | 0.305861 | |
g2735 | DLA_03030 | F4PJNLW01EE5MJ | CDS | 1206039 | 4062 | - | 0.28582 | |
g2736 | DLA_03032 | F4PJNLW01EE5MJ | CDS | 1210577 | 453 | - | 0.293598 | |
g2737 | DLA_03033 | F4PJNLW01EE5MJ | CDS | 1211230 | 1098 | + | 0.295082 | |
g2738 | DLA_03034 | F4PJNLW01EE5MJ | CDS | 1212538 | 609 | - | 0.341544 | |
g2739 | DLA_03035 | F4PJNLW01EE5MJ | CDS | 1213710 | 1593 | + | 0.338983 | |
g2740 | DLA_03036 | F4PJNLW01EE5MJ | CDS | 1215730 | 2028 | + | 0.354537 | |
g2741 | DLA_03037 | F4PJNLW01EE5MJ | CDS | 1218082 | 477 | + | 0.264151 | |
g2742 | DLA_03038 | F4PJNLW01EE5MJ | CDS | 1218792 | 1533 | + | 0.296151 | |
g2743 | DLA_03039 | F4PJNLW01EE5MJ | CDS | 1220955 | 1596 | + | 0.323308 | |
g2744 | DLA_03040 | F4PJNLW01EE5MJ | CDS | 1222843 | 381 | - | 0.272966 |