Wnt2 Gene Search Result

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5 records found for search term Wnt2

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
736431	WNT2	Wnt family member 2	This gene is a member of the WNT gene family. The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryo ... (more) genesis. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]	7	117275451	117323058	Human	180	symbol , COSMIC , Human Proteome Map	gene, protein-coding, REVIEWED [RefSeq]
733303	WNT2B	Wnt family member 2B	This gene encodes a member of the wingless-type MMTV integration site (WNT) family of highly conserved, secreted signaling factors. WNT family members function in a variety of developmental processes including regulation of cell growth and differentiation and are characterized by a WNT-core domain. ... (more) This gene may play a role in human development as well as carcinogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]	1	112466541	112530165	Human	152	symbol , old_gene_name , COSMIC , Human Proteome Map , old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
733867	WNT4	Wnt family member 4	The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene ... (more) family, and is the first signaling molecule shown to influence the sex-determination cascade. It encodes a protein which shows 98% amino acid identity to the Wnt4 protein of mouse and rat. This gene and a nuclear receptor known to antagonize the testis-determining factor play a concerted role in both the control of female development and the prevention of testes formation. This gene and another two family members, WNT2 and WNT7B, may be associated with abnormal proliferation in breast tissue. Mutations in this gene can result in Rokitansky-Kuster-Hauser syndrome and in SERKAL syndrome. [provided by RefSeq, Jul 2008]	1	22117313	22143097	Human	441	description	gene, protein-coding, REVIEWED [RefSeq]
16566873	AL354760.1	novel transcript, antisense to WNT2B					Human		name	gene, lncrna
1342887	ST7L	suppression of tumorigenicity 7 like	This gene was identified by its similarity to the ST7 tumor suppressor gene found in the chromosome 7q31 region. This gene is clustered in a tail-to-tail manner with the WNT2B gene in a chromosomal region known to be deleted and rearranged in a variety of cancer ... (more) s. Several transcript variants encoding many different isoforms have been described, but some have not been fully characterized. [provided by RefSeq, Feb 2011]	1	112517803	112619684	Human	66	description	gene, protein-coding, REVIEWED [RefSeq]