KCNQ1OT1 Gene

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1		Dean Liu	+ 530 word(s)	530	2020-12-15 07:58:15

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Liu, D. KCNQ1OT1 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4300 (accessed on 29 September 2026).

Liu D. KCNQ1OT1 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4300. Accessed September 29, 2026.

Liu, Dean. "KCNQ1OT1 Gene" Encyclopedia, https://encyclopedia.pub/entry/4300 (accessed September 29, 2026).

Liu, D. (2020, December 23). KCNQ1OT1 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4300

Liu, Dean. "KCNQ1OT1 Gene." Encyclopedia. Web. 23 December, 2020.

KCNQ1OT1 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/kcnq1ot1

KCNQ1 opposite strand/antisense transcript 1

genes

References

Bliek J, Maas SM, Ruijter JM, Hennekam RC, Alders M, Westerveld A, Mannens MM.Increased tumour risk for BWS patients correlates with aberrant H19 and notKCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases ofBWS. Hum Mol Genet. 2001 Mar 1;10(5):467-76.
Chiesa N, De Crescenzo A, Mishra K, Perone L, Carella M, Palumbo O, Mussa A,Sparago A, Cerrato F, Russo S, Lapi E, Cubellis MV, Kanduri C, Cirillo Silengo M,Riccio A, Ferrero GB. The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome andSilver-Russell syndrome cases. Hum Mol Genet. 2012 Jan 1;21(1):10-25. doi:10.1093/hmg/ddr419.
Du M, Zhou W, Beatty LG, Weksberg R, Sadowski PD. The KCNQ1OT1 promoter, a keyregulator of genomic imprinting in human chromosome 11p15.5. Genomics. 2004Aug;84(2):288-300.
Kanduri C. Functional insights into long antisense noncoding RNA Kcnq1ot1mediated bidirectional silencing. RNA Biol. 2008 Oct-Dec;5(4):208-11.
Kanduri C. Kcnq1ot1: a chromatin regulatory RNA. Semin Cell Dev Biol. 2011Jun;22(4):343-50. doi: 10.1016/j.semcdb.2011.02.020.
Pandey RR, Mondal T, Mohammad F, Enroth S, Redrup L, Komorowski J, Nagano T,Mancini-Dinardo D, Kanduri C. Kcnq1ot1 antisense noncoding RNA mediateslineage-specific transcriptional silencing through chromatin-level regulation.Mol Cell. 2008 Oct 24;32(2):232-46. doi: 10.1016/j.molcel.2008.08.022.
Thakur N, Tiwari VK, Thomassin H, Pandey RR, Kanduri M, Göndör A, Grange T,Ohlsson R, Kanduri C. An antisense RNA regulates the bidirectional silencingproperty of the Kcnq1 imprinting control region. Mol Cell Biol. 2004Sep;24(18):7855-62.
Weksberg R, Nishikawa J, Caluseriu O, Fei YL, Shuman C, Wei C, Steele L,Cameron J, Smith A, Ambus I, Li M, Ray PN, Sadowski P, Squire J. Tumordevelopment in the Beckwith-Wiedemann syndrome is associated with a variety ofconstitutional molecular 11p15 alterations including imprinting defects ofKCNQ1OT1. Hum Mol Genet. 2001 Dec 15;10(26):2989-3000.

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Subjects: Genetics & Heredity

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Entry Collection: MedlinePlus

Update Date: 23 Dec 2020

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