WNT2

WNT2

WNT2

Protein-coding gene in the species Homo sapiens


Wingless-type MMTV integration site family, member 2, also known as WNT2, is a human gene.[5][6]

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This gene is a member of the WNT gene family. The WNT gene family consists of structurally related genes that encode secreted signaling proteins involved in the Wnt signaling pathway. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. Alternatively spliced transcript variants have been identified for this gene.[5]


References

  1. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Wainwright BJ, Scambler PJ, Stanier P, Watson EK, Bell G, Wicking C, Estivill X, Courtney M, Boue A, Pedersen PS (June 1988). "Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless". EMBO J. 7 (6): 1743–8. doi:10.1002/j.1460-2075.1988.tb03003.x. PMC 457162. PMID 2971536.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.



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