Gene Name	H19
Gene ID	283120
Gene Full Name	H19 imprinted maternally expressed transcript
Gene Alias	ASM|ASM1|BWS|D11S813E|GMRSP|LINC00008|MIR675HG|NCRNA00008|WT2
Transcripts	ENSG00000130600
Virus	XMRV
Gene Type	ncRNA
HGNC ID	HGNC:4713
OMIM ID	103280
lncRNASNP2 ID	H19
Summary	This gene is located in an imprinted region of chromosome 11 near the insulin-like growth factor 2 (IGF2) gene. This gene is only expressed from the maternally-inherited chromosome, whereas IGF2 is only expressed from the paternally-inherited chromosome. The product of this gene is a long non-coding RNA which functions as a tumor suppressor. Mutations in this gene have been associated with Beckwith-Wiedemann Syndrome and Wilms tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]

Integration Table: if previous studies reported that target gene was altered by virus integration events, the overlap between VISs in this literature and Cistrome factors was listed in this section

DVID	Chromosome	HM	TFBS	CA	Sum of Overlapped Records	Detail
8000048	chr11	1411	493	531	2435	View