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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      


aggcagaacggtcgccgcgtcgcctcagcacggacctccagggagctcctcagcaagatcctgccagggcgcccctcagcgcgattctgccggggtgcctctcagcgtggtcctccccggggctcctcagcacgattctcccggtgcgcccctcagcgcggtcctcctcggtgcgtcagtcatcgtggttctccccggcgcgcccctcggcgcggttctcctcggggctcctcagcgcggcgctcttctgggggctcctcggcgcagttctccccggggactcctcggcgccgttctcctcggggcacccggggcttttcggcgcggttctccccgggggttcttcggcgcggttgtccccgggggttcttcggcgcggttctctccgggggcctctcgccgcggttctgttctccccgggggctcctcagcatggttctcctccgcgcggtcctccctgggcctcctcagcgcggcactctcctgggggctcctcagcgcggcactctccccgggggctcctcagcgcggcactctcccggcggctcctcagtgcggttctcccagactctcctcagcgcggccctccccatctctctgggagggtttgaacacggtcagcacggacctgggcggacggcgcgggacgggtgatcactggcgttgctgaggtgagctgtgtgccccgcggccgtcccagatcacaggcgtcagcagtgcagcctggcctgggcagtgcgctcccatctgcaccttatggacagcgtggccagggtcgaggtccgagttcctggccgcgtcccaaggatcggattccgggtctatagttctcatggtggttcagagtgggctgaattgggattggagtctggaatccgcatcgtggttctgagtccgcgctattgggatggaagttgggaatccatgttgtggttttgagtcaaagcccgaattgggaccggagtcggaaatccacttagtggttctgagtcagggcccgaattaggatcggaggtgggaatccccgttgtggttctgagttaggtatcctagttgggatcagaattcgggtctagggtccacatcctggctgggagtttgcctgagttgggatctgagtagttggggtcccagtcagtccgggtctggagtccgcatggtggttttaggtagggcctcattagggacagaggatcgggagtctgagttggggacctgaatcccggtctggagtctgcatcatggctctgagttgagatccaagggaggtccgagttggcgactggagtcagggtctggagtctgtctttgggtagaggttctgaatggggggctctgagttaagagattgggattggggttagaggtctcagtggggtatgggagtcaggaattgaagtcgaagttctgcctctaggtggggattctgagtcaggaattagggggcgaagtaaaggttgcagtctgagttgggggtggtgatcacctgccaggtgagaggtagtggtagaagtctcttggtcatattggagatgagagttgatcagatgcaggtctcagtctgggtagtaggcttgaagggccaccactatgttcagatcccagtaccccactgtggtccctgagcaggtcaaatagccttttatataaaattgagagtaagagtgccttcccacagcactgttctggttatgaaagagaataattcatccaggtagaatagttctgtcttagattatcacaaagtataaaaactttcctgataatatccacatttgatgtgcatttaccagttctttctttactgtggtgccccttttgctagaccaaaagctcccaacgaggaactctgttttgttttctgctgcctgctctgtacccagccaagagcctgatacacagccttactcagtcagtacttgaaggaaagcaggcaggcaggattaaccagatttctatggtgtctcaaatgatccatttctgcacctgttttccagatactcagtaggagaaaaatttaaggattgagttgcttgattatgggtgtattttaatgtgtttcctaacatgctgaggagaaaagtgggtctgtttcaggatttatgctccagctagagggattttttaaaattgcgaatcagagcatgtccaaattcagatagaaagcacaagaaaactataaagaatttcccttatgaatgtagatgcagaagttccttgtacaatgctagctaactgaatccaataatatgtattaaacaacaattcttaaacaagtgggattgctcttaggaatgcaaagatgatccaatatcagaaactttatccatgtaattcacattaagaggctacaggagaaaaaccatatggttccctcaatagaggcagaaaaaaatgatgtgataaagtttaacgcctatgtgtgattttggggtagtggagtacaccacttagcaagccaggactagagaggaacttcttcaacttgatacaagttataaaccaaaacttaacttttcagtaaacttgatagagaaattaaaagtgtatcattctctttaagataaggagtaggccaaggatgtcatcctggccataccctaatacaagaaaaagaaatggggatgtgaggatcaggtaggaagtgataaaacttagtgtagctcatagggttgatggtctccataaagattctcaaacattttggtgttacgacttgttgtattcttaaaagttattgaaacccccaaagggcttttcttgatagagattctatctgttgatagttaccatcttagaagttaaaactaagaaatgtttaaagcagaactatacaagcacatattccactggggtcatggtgtgctgcctctggaaaactctttatctttgtgagaatgaaagaaaaggcaaataatgtcgagtattattatgaaaatgtttttgacctttcctgaaagggtctggggggctctctggaatccccagactacactttgaaaattactgggctacatggaaaaaaaaaattaaggaacttaacaactaaagagagatttcagatttcagagaggttttggatataagatcagtgtactcaaaacaaaaaacaaaaacaaaccacatttctttatgccaatagcaactgactaaaaaaaagcataatagagattaggacagcaatcagaatagcagcaaaatttataccagtctaggaattaacaaagacgacgacttttatggaaaaaattttaaaactctattggaggatatagagggagatctttccatatgcagagacattttattttcttgaacagggcaacttggcattagaatgacgtcaggattttccaaatctgttaagttcaacaggactccactcaaacttccagttggagggcttgagtaatttaacaaacatattctaaaatgtatgtggaagaaaaatatttgtaaatgccaactgaacttttgaaaaggagagcagaggacttctgctggcagataccagggcacacgccaacttcagcaatcagagcggtgtggtgacagaggcccagaagagagctcagaggtaactccaagtctagaggaaggggacatgtgataaaggtggcaccacatatcagtggggactgttcagaagatgatgttggaaagccagccctaaaatggaggaataggaatatggattcctaactgagcccctaggaaaagtagactccaaatggactaaatatttgaaagcaaaaggtagttgccatttgtttaataggagaaaaaatgaataatctccagggccagggtggccgtggggttcttaaacaggatccagaaagcacaaacctcaagactaaaatgtatgaacttgaatgcattaatgattatggattaaggatttctgttaaataaatccatcatggcaagggtcaagactgttttcataataatactaaggaaacaatttgcgtttttcacttttacactcatgaatgtaactttgccatgactcattacaagatatttgaaacaattaaagctgaggagggaacaacagctaaaatataccagaaagcaccacaaatcattaagaaaaaggtaggaagattgccagtttgcaggagggttaacaaacagatgaaaatttgcccaagctaatcagttatcagagaaatgtaaatgaaagcaacagctattcttcataggagaagcattagaaagtaggataaggccaagtgttggcagaaggcaaggaacaagcctccctgtgtgctgcaggtggggacggagacaggcacagacgttctgaagagctggccaacacttcttcctcaaataaaatattttatacctgtggcccagcagtttccctcctaagtaaacatgctggagcagttctcacccagaacaacgagaggctgtgtgtgtgcatgctcagggcagcatggcccataggggtgggcagttggagctggtcactgtggttaggagcaggggactagatgtacacttcacaagatagagacgcgtggaaacacagtgctgagtgacacaaatgccaaacagaaagagggcctcagtacatgactgtgtatttaaattaaaattacacaccacccagacacgcagtactagggagtgctcgtgagtgcacacacacacacacaatgatataaataaattaccctggagaagctgtttgtgtagggaggagagcaaggatagaggctagagatgaagtggaaaagcatggagaggaagagagcggtgactttatgcagacccttacagggtgacagtgtttcataggctgagggctgtgatcaactctgtgcagagtcccaaaagccaagaaccaacgaatgaatgtgcctccatgactctcctgccagataccctctagtggcttctatttctaggaaataaaattcaaattccatcaggtttttacaagatctgccctgcttacctctctgaccactgtcctccctcactga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