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Gene : WNT2B Homo sapiens

Name  ? Wnt family member 2B Cytological Location  1p13.2
Brief Description  Wnt family member 2B
Description  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. 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]
  • synonyms:
  • XWNT2, Xenopus, homolog of,
  • WNT13,
  • WNT2B,
  • uc001ecb.4,
  • HGNC:12781,
  • AB045116,
  • XWNT2,
  • wingless-type MMTV integration site family, member 2B,
  • NM_004185,
  • OTTHUMG00000011157,
  • WNT13,
  • wingless-type MMTV integration site family, member 13
  • identifiers:
  • 7482,
  • ENSG00000134245,
  • WNT2B

Genome feature

Region: gene ? Length: 63625  
Location: 1:112466541-112530165 Cyto location: 1p13.2


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

3753 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results