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KCNQ1OT1 gene

Known as: KCNQ1 antisense RNA 2 (non-protein coding), NCRNA00012, KCNQ1 overlapping transcript 1 (non-protein coding) 
This gene plays a role in the epigenetic regulation of gene transcription.
National Institutes of Health

Related topics

Related topics

3 relations
Epigenetic ProcessKCNQ1OT1 protein, humanTranscriptional Regulation

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Stanovení metylace H19 a KCNQ1OT1 u nefrobastů, feochromocytomů a paragangliomů pomocí MLPA techniky
2015
2015
Characterization of a rare analphoid supernumerary marker chromosome in mosaic
ties, which are responsible for recognizable syndromes create phenotypic effects that more or less reflect and combine the… 
Review
2014
Review
2014
Isolated hypermethylation of GRB 10 ( 7 p 12 . 2 ) in a Silver – Russell syndrome patient carrying a 20 p 13 microdeletion
  • 2014
  • Corpus ID: 40833032
To the Editor : Silver–Russell syndrome (SRS; OMIM 180860) is an imprinting disorder characterized by primordial growth… 
2008
2008
Determination of KCNQ 1 OT 1 and H 19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis
Beckwith–Wiedemann syndrome (BWS) and Silver–Russell syndrome (SRS) are caused by imprinting defects on chromosome 11p15.5… 
2007
2007
Domain on Distal Mouse Chromosome 7 of a Truncation Disrupting the Imprinted Epigenetic and Phenotypic Consequences Supplemental Material
2005
2005
Analysis of both the H19 and KCNQ1OT1 DMRs in Beckwith-Wiedemann Syndrome using two newly developed methylation specific PCRs
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