WNT2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

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

AliasesWNT2, INT1L1, IRP, Wnt family member 2
End117,323,152 bp[1]
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WNT2
Identifiers
AliasesWNT2, INT1L1, IRP, Wnt family member 2
External IDsOMIM: 147870; MGI: 98954; HomoloGene: 20719; GeneCards: WNT2; OMA:WNT2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003391

NM_023653

RefSeq (protein)

NP_003382

NP_076142

Location (UCSC)Chr 7: 117.28 – 117.32 MbChr 6: 17.99 – 18.03 Mb
PubMed search[3][4]
Wikidata
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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

Further reading

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