2025-09-16 17:35:49, GGRNA.v2 : RefSeq release 231 (Jul, 2025)
LOCUS NR_135038 686 bp RNA linear PRI 05-MAR-2024 DEFINITION Homo sapiens long intergenic non-protein coding RNA 2609 (LINC02609), transcript variant 1, long non-coding RNA. ACCESSION NR_135038 VERSION NR_135038.1 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 686) AUTHORS Xiao,H., Qu,Y., Li,H., Zhang,Y., Fei,M., Liang,C., Yang,H. and Zhang,X. TITLE HIF-2alpha/LINC02609/APOL1-mediated lipid storage promotes endoplasmic reticulum homeostasis and regulates tumor progression in clear-cell renal cell carcinoma JOURNAL J Exp Clin Cancer Res 43 (1), 29 (2024) PUBMED 38263248 REMARK GeneRIF: HIF-2alpha/LINC02609/APOL1-mediated lipid storage promotes endoplasmic reticulum homeostasis and regulates tumor progression in clear-cell renal cell carcinoma. Publication Status: Online-Only REFERENCE 2 (bases 1 to 686) AUTHORS Wang,A.G., Yoon,S.Y., Oh,J.H., Jeon,Y.J., Kim,M., Kim,J.M., Byun,S.S., Yang,J.O., Kim,J.H., Kim,D.G., Yeom,Y.I., Yoo,H.S., Kim,Y.S. and Kim,N.S. TITLE Identification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags JOURNAL Biochem Biophys Res Commun 345 (3), 1022-1032 (2006) PUBMED 16712791 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BJ993392.1, BJ993393.1 and CB164346.1. ##Evidence-Data-START## Transcript exon combination :: BJ993392.1, SRR1803612.98491.1 [ECO:0000332] RNAseq introns :: partial sample support SAMEA1966682, SAMEA1968832 [ECO:0000350] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-432 BJ993392.1 1-432 433-660 BJ993393.1 1-228 c 661-686 CB164346.1 495-520 FEATURES Location/Qualifiers source 1..686 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="1" /map="1p22.2" gene 1..686 /gene="LINC02609" /note="long intergenic non-protein coding RNA 2609" /db_xref="GeneID:105378853" /db_xref="HGNC:HGNC:27140" ncRNA 1..686 /ncRNA_class="lncRNA" /gene="LINC02609" /product="long intergenic non-protein coding RNA 2609, transcript variant 1" /db_xref="GeneID:105378853" /db_xref="HGNC:HGNC:27140" exon 1..156 /gene="LINC02609" /inference="alignment:Splign:2.1.0" variation 1 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1647233093" variation 2 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1647233064" variation 4..35 /gene="LINC02609" /replace="gctggggc" /replace="gctggggcgggcgcaggactgcaggctggggc" /db_xref="dbSNP:1647231052" variation 4 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1469367532" variation 5 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:2523947330" variation 7 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:2523947328" variation 8 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1647233002" variation 10 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1647232978" variation 11 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:2523947322" variation 12..14 /gene="LINC02609" /replace="g" /replace="ggg" /db_xref="dbSNP:2523947313" variation 12 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1570664795" variation 15 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1647232907" variation 16 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1647232878" variation 17 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1028697787" variation 18 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1194183167" variation 19 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1374610813" variation 22 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:999851200" variation 23 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1647232705" variation 25 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:904296736" variation 28 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:2523947267" variation 29 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1041486335" variation 32 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1436731509" variation 33 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1647231105" variation 34 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1041767505" variation 35 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1010371985" variation 36 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1400864004" variation 37 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:895658383" variation 39 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1647230962" variation 41 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:895736256" variation 42 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1262166453" variation 43 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:2523947227" variation 46 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1241278925" variation 48 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:376600850" variation 52 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:576659150" variation 54 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:937170532" variation 56 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:937297605" variation 58 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1276023946" variation 59 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1647230727" variation 60 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:909703461" variation 61 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1647230633" variation 65 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:2523947164" variation 68 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1647230595" variation 70 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:927203129" variation 72 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1647230540" variation 73 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1647230519" variation 75 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1647230490" variation 78 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1045072283" variation 79 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1647230445" variation 81 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1468488760" variation 83 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:930625082" variation 87 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1647230371" variation 88 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:930044766" variation 90 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:920570555" variation 91 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:867962766" variation 93 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1647230171" variation 94 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1647230152" variation 95 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1192191251" variation 98 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:555183195" variation 99 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1647227640" variation 101 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1647227599" variation 104 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:977161387" variation 106 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:1647227527" variation 109 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1570664729" variation 113 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:912104068" variation 114 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1374958638" variation 115 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1387374953" variation 116 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1647225420" variation 119 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1383057525" variation 121 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:965326962" variation 122 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1647225343" variation 124 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:911489986" variation 126 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:985666297" variation 127 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:988039956" variation 128 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1420030477" variation 136..137 /gene="LINC02609" /replace="g" /replace="gg" /db_xref="dbSNP:34957521" variation 142 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1647225195" variation 143 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1647225174" variation 144 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1346530152" variation 147 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:2523947045" variation 148 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:2523947041" variation 151 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1240219342" variation 156 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1394258684" exon 157..246 /gene="LINC02609" /inference="alignment:Splign:2.1.0" variation 158 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1242977590" variation 159 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:912840029" variation 161 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659473991" variation 164 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659473940" variation 165 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:187405513" variation 169 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:183803285" variation 170 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659473775" variation 171 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:2523833597" variation 173 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:1434479372" variation 176 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1289763289" variation 179..180 /gene="LINC02609" /replace="" /replace="a" /db_xref="dbSNP:1659473567" variation 179 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:545503891" variation 180 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:953750837" variation 181..186 /gene="LINC02609" /replace="c" /replace="ccttcc" /db_xref="dbSNP:1659473314" variation 185 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1659473454" variation 187..188 /gene="LINC02609" /replace="" /replace="at" /db_xref="dbSNP:2523833517" variation 190 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1236657797" variation 196..197 /gene="LINC02609" /replace="" /replace="t" /db_xref="dbSNP:2523833515" variation 199 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659473220" variation 210 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1659473172" variation 212 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1659473121" variation 213 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1031959758" variation 215 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:771507155" variation 224 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:2523833487" variation 226 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1177607007" variation 229 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:7515293" variation 233 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:369503849" variation 236 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:1659472757" variation 240 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1412487069" variation 242 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659472644" variation 244 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:1659472609" variation 245 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:191095649" variation 246 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659472515" exon 247..686 /gene="LINC02609" /inference="alignment:Splign:2.1.0" variation 249 /gene="LINC02609" /replace="" /replace="c" /db_xref="dbSNP:1570633095" variation 249 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:949585102" variation 250 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:572411926" variation 256 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659354731" variation 257 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:541956017" variation 258 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1433507456" variation 260 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659354560" variation 261 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659354520" variation 263 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1659354465" variation 266 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659354421" variation 272 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659354376" variation 275 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1201318505" variation 278 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659354265" variation 279 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:1427386526" variation 287 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:749363441" variation 296 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:2523824965" variation 299 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1659354075" variation 302 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:57896054" variation 303 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1347077126" variation 310 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:972398143" variation 311 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:1659353765" variation 314 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:964994967" variation 316 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1659353631" variation 318 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:983488915" variation 319 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:190359174" variation 322 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1019360184" variation 323 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:923377995" variation 324 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1484618295" variation 327 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1222596489" variation 328 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659353106" variation 329 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1659353049" variation 332 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1570633055" variation 334 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:2100673579" variation 336 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1268176140" variation 337 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:2100673574" variation 343 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:971564537" variation 357 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:1024085434" variation 361 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659352348" variation 364 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1659352302" variation 365 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:2100673568" variation 369 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:976563290" variation 371 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1659352189" variation 372 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1005102926" variation 375 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1262080016" variation 376 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:78549189" variation 382 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1266588640" variation 388..390 /gene="LINC02609" /replace="" /replace="act" /db_xref="dbSNP:1659351787" variation 388 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659351830" variation 389 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:2523824862" variation 390 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:953789118" variation 391..396 /gene="LINC02609" /replace="gaga" /replace="gagaga" /db_xref="dbSNP:1659351576" variation 393 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:756631616" variation 398 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659351520" variation 403 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659351459" variation 409 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659351418" variation 413 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1557488146" variation 416 /gene="LINC02609" /replace="" /replace="g" /db_xref="dbSNP:1225812791" variation 416 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1417353952" variation 417 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1158481178" variation 420..428 /gene="LINC02609" /replace="aagaag" /replace="aagaagaag" /db_xref="dbSNP:1659351163" variation 420 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659351233" variation 422 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:2523824822" variation 424 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1000683850" variation 428 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1332117446" variation 434 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:985402233" variation 435 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659351004" variation 437 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:902445358" variation 440 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1301674145" variation 448 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:753240175" variation 451 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1403932362" variation 461 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1570632989" variation 462 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:78590428" variation 463 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1419456615" variation 466 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1659349713" variation 467 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:1375118528" variation 470 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1221513660" variation 471 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1305740825" variation 472 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659349539" variation 473 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:999183126" variation 478 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1322247274" variation 479 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:867495053" variation 481 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659349337" variation 482 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1659349288" variation 487 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:895818389" variation 488 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:569508208" variation 490 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:1289294987" variation 494 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:1364211286" variation 495 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:902259481" variation 498 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659348770" variation 508 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659348721" variation 510 /gene="LINC02609" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1205648399" variation 511 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659348295" variation 513 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:1234749909" variation 514 /gene="LINC02609" /replace="c" /replace="g" /db_xref="dbSNP:1479788764" variation 516 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1024705708" variation 524 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:2100673480" variation 532 /gene="LINC02609" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:554255507" variation 537 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1162278680" variation 538 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1385184882" variation 539 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1430763604" variation 540..543 /gene="LINC02609" /replace="a" /replace="aata" /db_xref="dbSNP:1404269314" variation 542 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:76473235" variation 546 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:574105847" variation 554 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:371848508" variation 555 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:533482872" variation 557 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:1382944143" variation 559 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:2523824465" variation 560 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1570632937" variation 566 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659347464" variation 567 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1378082170" variation 568 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659347366" variation 574 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:2100673443" variation 579 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1055743107" variation 580 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659347280" variation 581 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:139795038" variation 582 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:931483939" variation 588 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659347120" variation 589 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659347072" variation 590 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:918861024" variation 593 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659346977" variation 594 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659346941" variation 603 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1274926425" variation 604 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659346854" variation 609 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:77100997" variation 613 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:146156135" variation 614 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:1659346660" variation 615 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1238105411" variation 620 /gene="LINC02609" /replace="a" /replace="c" /db_xref="dbSNP:1659346580" variation 625 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:550492355" variation 629 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:2523824145" variation 633 /gene="LINC02609" /replace="" /replace="c" /db_xref="dbSNP:1659346510" variation 634..635 /gene="LINC02609" /replace="t" /replace="tt" /db_xref="dbSNP:1659346474" variation 635 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:929315501" variation 638 /gene="LINC02609" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:923327184" variation 639..644 /gene="LINC02609" /replace="ctt" /replace="cttctt" /db_xref="dbSNP:1205909056" variation 639 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1659346355" variation 640..645 /gene="LINC02609" /replace="tt" /replace="ttcttt" /db_xref="dbSNP:1169999868" variation 651 /gene="LINC02609" /replace="a" /replace="t" /db_xref="dbSNP:1417862521" variation 652 /gene="LINC02609" /replace="g" /replace="t" /db_xref="dbSNP:1346179947" variation 653 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1407833262" variation 660 /gene="LINC02609" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:943738932" variation 661 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:1454053933" variation 664 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659345902" variation 671 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:1659345847" variation 674 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:912238698" variation 678 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:976179021" variation 681 /gene="LINC02609" /replace="c" /replace="t" /db_xref="dbSNP:2100673394" variation 685 /gene="LINC02609" /replace="a" /replace="g" /db_xref="dbSNP:943835340" ORIGIN
ggtgctggggcgggcgcaggactgcaggctggggctccgctccccggcgggagcccgcgcgtggttcccagcgaagtccccgcgcggctgggcccagcgtgagtattctccgcccgctgtcctccccctggaggcggcagcgcccgtttatttgagccgtgtgaagatgtgcctgcttcgccttccatcatgactgaagtttcctgaggcctccccagctatgctccctatacagcctgcagaacggtcggctgcctccaatcctgaggtcatcactcatcaagaggggataatcccagggacagcaggatctgcttcgttacttggatttaggagccagaaacccatcaggcaactaaacagtaacaatgacccgccattaaacacactgagagaagagcatgatgaagagtttgtacaagaagaagccaggagcacttgctgacaatgcttacagagacgcaggcttctatgagctctgcctgttgaactgcagtaaaaatagatctccttccccagagaggcttggatgtgggcacaatatcagttcagacgatggtcaatgcatgtacttaatagagtgaaaagactttggactgtgaagtcagattacctgggtctgaattgttattcttctacttctttgtagtatgctttcaccacattaaaaattgtctgagcctcaa
//
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.
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