2024-03-29 08:21:41, GGRNA : RefSeq release 60 (20130726)
LOCUS NR_002728 91671 bp RNA linear PRI 17-JUL-2013 DEFINITION Homo sapiens KCNQ1 opposite strand/antisense transcript 1 (non-protein coding) (KCNQ1OT1), non-coding RNA. ACCESSION NR_002728 VERSION NR_002728.3 GI:381342489 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 91671) AUTHORS Peng,H.H., Chang,S.D., Chao,A.S., Wang,C.N., Cheng,P.J., Hwang,S.M. and Wang,T.H. TITLE DNA methylation patterns of imprinting centers for H19, SNRPN, and KCNQ1OT1 in single-cell clones of human amniotic fluid mesenchymal stem cell JOURNAL Taiwan J Obstet Gynecol 51 (3), 342-349 (2012) PUBMED 23040914 REMARK GeneRIF: Human amniotic fluid mesenchymal stem cells contain a unique epigenetic signature during in vitro cell culture. H19 and KCNQ1OT1 possessed a substantial degree of hypermethylation status, and variable DNA methylation patterns of SNRPN was observed. REFERENCE 2 (bases 1 to 91671) AUTHORS Wijnen,M., Alders,M., Zwaan,C.M., Wagner,A. and van den Heuvel-Eibrink,M.M. TITLE KCNQ1OT1 hypomethylation: a novel disguised genetic predisposition in sporadic pediatric adrenocortical tumors? JOURNAL Pediatr Blood Cancer 59 (3), 565-566 (2012) PUBMED 22610651 REMARK GeneRIF: findings show that hypomethylation of the KCNQ1OT1 gene contributes to the occurrence of adrenocortical carcinoma and adenoma in patients without clear phenotypic features of the Beckwith-Wiedemann syndrome REFERENCE 3 (bases 1 to 91671) AUTHORS Pauler,F.M., Barlow,D.P. and Hudson,Q.J. TITLE Mechanisms of long range silencing by imprinted macro non-coding RNAs JOURNAL Curr. Opin. Genet. Dev. 22 (3), 283-289 (2012) PUBMED 22386265 REMARK Review article REFERENCE 4 (bases 1 to 91671) AUTHORS Robbins,K.M., Chen,Z., Wells,K.D. and Rivera,R.M. TITLE Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine JOURNAL J. Biomed. Sci. 19, 95 (2012) PUBMED 23153226 REMARK GeneRIF: Based on these findings we conclude that the imprinted gene expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 are conserved between human and bovine Publication Status: Online-Only REFERENCE 5 (bases 1 to 91671) AUTHORS Mohammad,F., Mondal,T. and Kanduri,C. TITLE Epigenetics of imprinted long noncoding RNAs JOURNAL Epigenetics 4 (5), 277-286 (2009) PUBMED 19617707 REMARK Review article REFERENCE 6 (bases 1 to 91671) AUTHORS DeBaun,M.R., Niemitz,E.L., McNeil,D.E., Brandenburg,S.A., Lee,M.P. and Feinberg,A.P. TITLE Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects JOURNAL Am. J. Hum. Genet. 70 (3), 604-611 (2002) PUBMED 11813134 REMARK GeneRIF: epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects REFERENCE 7 (bases 1 to 91671) AUTHORS Smilinich,N.J., Day,C.D., Fitzpatrick,G.V., Caldwell,G.M., Lossie,A.C., Cooper,P.R., Smallwood,A.C., Joyce,J.A., Schofield,P.N., Reik,W., Nicholls,R.D., Weksberg,R., Driscoll,D.J., Maher,E.R., Shows,T.B. and Higgins,M.J. TITLE A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome JOURNAL Proc. Natl. Acad. Sci. U.S.A. 96 (14), 8064-8069 (1999) PUBMED 10393948 REFERENCE 8 (bases 1 to 91671) AUTHORS Mitsuya,K., Meguro,M., Lee,M.P., Katoh,M., Schulz,T.C., Kugoh,H., Yoshida,M.A., Niikawa,N., Feinberg,A.P. and Oshimura,M. TITLE LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids JOURNAL Hum. Mol. Genet. 8 (7), 1209-1217 (1999) PUBMED 10369866 REMARK GeneRIF: KCNQ1OT1 gene encodes a non-protein coding, antisense RNA that is preferentially expressed from the paternal allele. REFERENCE 9 (bases 1 to 91671) AUTHORS Lee,M.P., DeBaun,M.R., Mitsuya,K., Galonek,H.L., Brandenburg,S., Oshimura,M. and Feinberg,A.P. TITLE Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting JOURNAL Proc. Natl. Acad. Sci. U.S.A. 96 (9), 5203-5208 (1999) PUBMED 10220444 REFERENCE 10 (bases 1 to 91671) AUTHORS Adams,M.D., Kerlavage,A.R., Fleischmann,R.D., Fuldner,R.A., Bult,C.J., Lee,N.H., Kirkness,E.F., Weinstock,K.G., Gocayne,J.D., White,O. et al. TITLE Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence JOURNAL Nature 377 (6547 SUPPL), 3-174 (1995) PUBMED 7566098 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC021424.6 and AC124055.6. This sequence is a reference standard in the RefSeqGene project. On Mar 28, 2012 this sequence version replaced gi:166091427. Summary: Human chromosomal region 11p15.5 contains two clusters of epigenetically-regulated genes that are expressed from only one chromosome in a parent-of-origin manner. Each cluster, or imprinted domain, is regulated by a functionally independent imprinting control region (ICR). The human CDKN1C/KCNQ1OT1 domain is regulated by an ICR located in an intron of KCNQ1, and contains at least eight genes that are expressed exclusively or preferentially from the maternally-inherited allele. The DNA of the ICR is specifically methylated on the maternally-inherited chromosome, and unmethylated on the paternally-inherited chromosome. The ICR contains the promoter of the KCNQ1OT1 gene that is exclusively expressed from the paternal allele. The KCNQ1OT1 transcript is the antisense to the KCNQ1 gene and is a unspliced long non-coding RNA. It interacts with chromatin and regulates transcription of multiple target genes through epigenetic modifications. The transcript is abnormally expressed from both chromosomes in most patients with Beckwith-Wiedemann syndrome, and the transcript also plays an important role in colorectal carcinogenesis. [provided by RefSeq, Apr 2012]. Sequence Note: The RefSeq transcript was derived from the reference genome assembly. The genomic coordinates were determined from shorter mRNA and EST alignments, and literature report (PubMed ID: 18951091). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##RefSeq-Attributes-START## imprinted gene :: PMID: 10369866, 19617707 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 5' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-53139 AC021424.6 127887-181025 53140-91671 AC124055.6 52014-90545 FEATURES Location/Qualifiers source 1..91671 /organism="Homo sapiens" /mol_type="transcribed RNA" /db_xref="taxon:9606" /chromosome="11" /map="11p15" gene 1..91671 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /note="KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)" /db_xref="GeneID:10984" /db_xref="HGNC:6295" /db_xref="MIM:604115" misc_RNA 1..91671 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /product="KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)" /db_xref="GeneID:10984" /db_xref="HGNC:6295" /db_xref="MIM:604115" exon 1..91671 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /inference="alignment:Splign:1.39.8" variation 209 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:449357" variation 261 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:443572" variation 274 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:429298" variation 292 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:424834" variation 394 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:364930" variation 424 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:422946" variation 2691 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:624471" variation 3549 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:463924" variation 3936 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:462402" variation 4255 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:457704" variation 8071 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:3948803" variation 9065 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:2214065" variation 12689 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:2188448" variation 12859 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:151209" variation 13841 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:151210" variation 23828 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:179510" variation 23841 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:179511" variation 23958 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:179512" variation 24164 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:2073953" variation 24200 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:2073954" variation 24340 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:2073955" variation 24350 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:179513" variation 24397 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:179514" variation 24569 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:1052175" variation 24832 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:2073956" variation 25050 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:179515" variation 25648 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="g" /replace="t" /db_xref="dbSNP:179516" variation 25713 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:404101" variation 25715 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:413736" variation 25722 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="g" /db_xref="dbSNP:179517" variation 26623 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="g" /replace="t" /db_xref="dbSNP:231359" variation 26862 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:151211" variation 27497 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="g" /db_xref="dbSNP:415020" variation 27500 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:423540" variation 27527 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:149538" variation 28980 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:231360" variation 29729 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:231361" variation 29758 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:231362" variation 30936 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="g" /replace="t" /db_xref="dbSNP:151212" variation 31103 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:151213" variation 31160 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="t" /db_xref="dbSNP:2611695" variation 31683 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:1459825" variation 36567 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:2073957" variation 37777 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="g" /replace="t" /db_xref="dbSNP:231363" variation 38553 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:231364" variation 39790 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:151214" variation 40157 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:151215" variation 40414 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:151216" variation 40675 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:151217" variation 41919 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:189137" variation 42179 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:231341" variation 42362 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:231342" variation 42576 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="g" /replace="t" /db_xref="dbSNP:231343" variation 43584 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="g" /db_xref="dbSNP:41517049" variation 43863 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:179518" variation 43868 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:231344" variation 48992 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:170762" variation 50364 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:466597" variation 50850 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:463337" variation 50995..50996 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="" /replace="aa" /db_xref="dbSNP:71029154" variation 51011 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:410244" variation 53566 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:2412055" variation 57338 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:756852" variation 58418 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:77174864" variation 71705 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:2106462" variation 73436 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:2412056" variation 78306 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:2157899" variation 79438 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:74915644" variation 79899 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:2412057" variation 80035 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="" /replace="t" /db_xref="dbSNP:71029152" variation 80100 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:2412058" variation 81937 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:2106463" variation 81996 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:2106464" variation 83911 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="t" /db_xref="dbSNP:2106465" variation 84103 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:2106466" variation 85432 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="c" /db_xref="dbSNP:2106467" variation 88676 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="g" /db_xref="dbSNP:1965606" variation 88988 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="c" /replace="t" /db_xref="dbSNP:2412059" variation 89858 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="a" /replace="g" /db_xref="dbSNP:1465196" variation 90409..90425 /gene="KCNQ1OT1" /gene_synonym="KCNQ1-AS2; KCNQ10T1; KvDMR1; KvLQT1-AS; LIT1; NCRNA00012" /replace="" /replace="gaaagaagatcaataag" /db_xref="dbSNP:71029150" ORIGIN
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