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

Papers overview

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Highly Cited
2010
Highly Cited
2010
A long noncoding RNA, Kcnq1ot1, regulates the expression of both ubiquitously and tissue-specific imprinted genes within the… (More)
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2009
2009
Beckwith–Wiedemann syndrome (BWS) and Silver–Russell syndrome (SRS) are caused by imprinting defects on chromosome 11p15.5… (More)
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Highly Cited
2008
Highly Cited
2008
Genomic imprinting regulates parental-specific expression of particular genes and is required for normal mammalian development… (More)
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2008
2008
BACKGROUND Imprinted genes, many of which are involved in development, are marked during gametogenesis to allow their parent-of… (More)
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Highly Cited
2008
Highly Cited
2008
Imprinting control regions (ICRs) are known to repress genes by utilizing one of two mechanisms, CTCF-mediated insulation or the… (More)
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Highly Cited
2004
Highly Cited
2004
Beckwith-Wiedemann syndrome (BWS) is a fetal overgrowth disorder involving the deregulation of a number of genes, including IGF2… (More)
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Highly Cited
2002
Highly Cited
2002
Beckwith-Wiedemann syndrome (BWS) presents with visceromegaly, macroglossia, tumor predisposition and other congenital… (More)
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Highly Cited
2002
Highly Cited
2002
Genomic imprinting is an epigenetic modification that results in expression from only one of the two parental copies of a gene… (More)
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Highly Cited
2001
Highly Cited
2001
Beckwith-Wiedemann syndrome (BWS) is an overgrowth malformation syndrome that maps to human chromosome 11p15.5, a region that… (More)
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Highly Cited
1999
Highly Cited
1999
Loss of imprinting at IGF2, generally through an H19-independent mechanism, is associated with a large percentage of patients… (More)
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