WNT2

WNT2
Identifiers
Aliases WNT2, INT1L1, IRP, Wnt family member 2
External IDs MGI: 98954 HomoloGene: 20719 GeneCards: WNT2
Genetically Related Diseases
plantar fascial fibromatosis[1]
Orthologs
Species Human Mouse
Entrez

7472

22413

Ensembl

ENSG00000105989

ENSMUSG00000010797

UniProt

P09544

P21552

RefSeq (mRNA)

NM_003391

NM_023653

RefSeq (protein)

NP_003382.1

NP_076142.3

Location (UCSC) Chr 7: 117.28 – 117.32 Mb Chr 6: 17.99 – 18.03 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

Wingless-type MMTV integration site family, member 2, also known as WNT2, is a human gene.[4][5]

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.[4]

References

Further reading

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


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