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Previous release (v1)
2024-04-28 11:11:49, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_046622 564 bp RNA linear PRI 03-SEP-2020
DEFINITION Homo sapiens LNX1 antisense RNA 1 (LNX1-AS1), long non-coding RNA.
ACCESSION NR_046622
VERSION NR_046622.1
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AA405946.1 and BX103714.1.
##Evidence-Data-START##
Transcript exon combination :: BX103714.1, AA496074.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968968, SAMEA2148874
[ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-1 AA405946.1 1-1
2-564 BX103714.1 1-563
FEATURES Location/Qualifiers
source 1..564
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="4"
/map="4q12"
gene 1..564
/gene="LNX1-AS1"
/note="LNX1 antisense RNA 1"
/db_xref="GeneID:100873939"
/db_xref="HGNC:HGNC:40345"
ncRNA 1..564
/ncRNA_class="lncRNA"
/gene="LNX1-AS1"
/product="LNX1 antisense RNA 1"
/db_xref="GeneID:100873939"
/db_xref="HGNC:HGNC:40345"
exon 1..51
/gene="LNX1-AS1"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1445955462"
variation 4
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1725365235"
variation 6
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1725365459"
variation 8
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408932471"
variation 11
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2109484306"
variation 18
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725365830"
variation 22
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725366007"
variation 26
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725366207"
variation 28
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1368149522"
variation 29
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:535643322"
variation 30
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175454642"
variation 35
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2109484399"
variation 40
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286402644"
variation 45
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725367180"
variation 47
/gene="LNX1-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1725367386"
exon 52..137
/gene="LNX1-AS1"
/inference="alignment:Splign:2.1.0"
variation 52
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725388222"
variation 54
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1725388601"
variation 56
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725388904"
variation 57
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725389101"
variation 71
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725389394"
variation 75
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1725389717"
variation 76
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725390305"
variation 77
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725390622"
variation 80
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1725390825"
variation 83
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:958663175"
variation 84..86
/gene="LNX1-AS1"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1725391331"
variation 87
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:565778221"
variation 88
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:770597167"
variation 89..90
/gene="LNX1-AS1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1725392300"
variation 92
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470079951"
variation 95
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:571510738"
variation 96
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1725393108"
variation 98
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1725393389"
variation 101
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2109485909"
variation 105
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1725393680"
variation 115
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725393898"
variation 117
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725394110"
variation 121
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274733297"
variation 133
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1579418804"
variation 137
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:774392825"
exon 138..266
/gene="LNX1-AS1"
/inference="alignment:Splign:2.1.0"
variation 138
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2109492625"
variation 141
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176378880"
variation 146
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432190072"
variation 149
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1422598304"
variation 151
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1032361652"
variation 152
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725529480"
variation 161
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1202632464"
variation 165..170
/gene="LNX1-AS1"
/replace="tctc"
/replace="tctctc"
/db_xref="dbSNP:2109492690"
variation 173
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1579421831"
variation 175
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725530207"
variation 182
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472631103"
variation 183
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:957603527"
variation 184
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1725530880"
variation 187
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368611299"
variation 188
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:571193975"
variation 189
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1725531564"
variation 192
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:537380059"
variation 199
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725532100"
variation 201
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:990340837"
variation 205..210
/gene="LNX1-AS1"
/replace="ctatct"
/replace="ctatctatct"
/db_xref="dbSNP:2109492817"
variation 205
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1579421928"
variation 207
/gene="LNX1-AS1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1725532992"
variation 207
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1579421940"
variation 218
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1725533210"
variation 219
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725533427"
variation 225
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:182746263"
variation 227
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:954178737"
variation 228
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148371553"
variation 229
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725534399"
variation 230
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1725534600"
variation 233
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254238005"
variation 236
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1725535013"
variation 245
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1725535208"
variation 248
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:912312799"
variation 249
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398233283"
variation 250
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1403386490"
variation 251
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302686327"
variation 252
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1579422031"
variation 253
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:939707243"
variation 254
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1725537635"
variation 257
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1725537838"
variation 262
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1357141499"
variation 263
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160909049"
exon 267..551
/gene="LNX1-AS1"
/inference="alignment:Splign:2.1.0"
variation 267
/gene="LNX1-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1727344284"
variation 268
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1727344577"
variation 274
/gene="LNX1-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:770716676"
variation 277
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:532609411"
variation 278
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311794313"
variation 284
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727345769"
variation 286
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219261645"
variation 288
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1727346456"
variation 289
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2109582983"
variation 291
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2109582998"
variation 296
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:184428217"
variation 297
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:75492489"
variation 299
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1361856221"
variation 302..304
/gene="LNX1-AS1"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1727347561"
variation 305
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1189357059"
variation 313
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424675877"
variation 314
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1257037213"
variation 320
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:796791812"
variation 322
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2109583132"
variation 323
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217820839"
variation 326
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1286756329"
variation 329..332
/gene="LNX1-AS1"
/replace="ga"
/replace="gaga"
/db_xref="dbSNP:1205060810"
variation 329
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1248638918"
variation 332
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2109583188"
variation 335
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1267663095"
variation 336
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1245955620"
variation 337
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:904676208"
variation 338
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292333136"
variation 344..345
/gene="LNX1-AS1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2109583231"
variation 345
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1412488796"
variation 348
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1341853691"
variation 349
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1727351343"
variation 351
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298202922"
variation 352
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381645239"
variation 354
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377032985"
variation 357
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164834771"
variation 362
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458247751"
variation 368
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1727352974"
variation 370
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2109583335"
variation 374
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1727353300"
variation 380
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727353646"
variation 381..387
/gene="LNX1-AS1"
/replace="aca"
/replace="acagaca"
/db_xref="dbSNP:1727353961"
variation 384
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416833302"
variation 386
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1727354474"
variation 390
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727354699"
variation 394
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163068620"
variation 395
/gene="LNX1-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017997451"
variation 396
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727355186"
variation 397
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264074537"
variation 400
/gene="LNX1-AS1"
/replace=""
/replace="g"
/db_xref="dbSNP:1727355779"
variation 400
/gene="LNX1-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1192540723"
variation 403
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:965059060"
variation 405..406
/gene="LNX1-AS1"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1727356194"
variation 412
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1727356415"
variation 414
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270054453"
variation 415
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:57276714"
variation 422
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:147377797"
variation 424
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1025303181"
variation 425
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1727357626"
variation 433
/gene="LNX1-AS1"
/replace=""
/replace="a"
/db_xref="dbSNP:1727357838"
variation 436
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:951415868"
variation 438
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1727358285"
variation 451
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158020254"
variation 453
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1727358768"
variation 459
/gene="LNX1-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:984039382"
variation 460
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1577657484"
variation 462
/gene="LNX1-AS1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270327906"
variation 468
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:565191277"
variation 473
/gene="LNX1-AS1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1324129671"
variation 476
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:909738211"
variation 482
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1387219937"
variation 484..488
/gene="LNX1-AS1"
/replace="aa"
/replace="aagaa"
/db_xref="dbSNP:776513621"
variation 487
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1393464323"
variation 490
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323636387"
variation 491
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/db_xref="dbSNP:140956191"
variation 492
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:969265114"
variation 493
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1577657569"
variation 495
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727362132"
variation 500
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1727362350"
variation 501
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727362565"
variation 509
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424575728"
variation 514
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:190449864"
variation 517
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727363432"
variation 519
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2109583948"
variation 522
/gene="LNX1-AS1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1727363634"
variation 526
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560644537"
variation 530
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1727364083"
variation 543
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1727364291"
variation 544
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727364492"
variation 545
/gene="LNX1-AS1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167447717"
variation 549
/gene="LNX1-AS1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1727364864"
variation 551
/gene="LNX1-AS1"
/replace="a"
/replace="g"
/db_xref="dbSNP:563208257"
ORIGIN
gagtgaagtaactgactggacatcccaaagttaggtggtcctgagagccaggtgctgacagctgcctcaccttaagagtctcctttcgttatggcatctggaaagatctcacatggcaggcctgcttctagttccttcttcctagtgtgtctgaggaaatccaatctctcccactccagcccgcctactcattgaacatggctgctatctctgtcttctggaaacacggctccaatcctgcaacaactctatacaagagctcccagtggttcttaaccttggctgagcaacagacccatttgggaagatttttaaaaatctagcttatgagatacctcagatcaatcaatccctggcagtgggtctgctaaacatcagatacagacaaacaactgcatagatctccaactagattgaagaacaggaccctccagagagcttccaagaagacaccaacctaggcatgggtttatgttcctgacaaagaataaggattgttatgaagaatgttctattttgaattgtgaaaataattatttaaagctgtacaaaaaaaaaaaaaaa
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]