WNT10B

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

Protein Wnt-10b (formerly Wnt12[5]) is a protein that in humans is encoded by the WNT10B gene.[6][7][8][9]

AliasesWNT10B, SHFM6, WNT-12, Wnt family member 10B, STHAG8
End48,971,735 bp[1]
Quick facts Identifiers, Aliases ...
WNT10B
Identifiers
AliasesWNT10B, SHFM6, WNT-12, Wnt family member 10B, STHAG8
External IDsOMIM: 601906; MGI: 108061; HomoloGene: 20721; GeneCards: WNT10B; OMA:WNT10B - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003394

NM_011718

RefSeq (protein)

NP_003385

NP_035848

Location (UCSC)Chr 12: 48.97 – 48.97 MbChr 15: 98.67 – 98.68 Mb
PubMed search[3][4]
Wikidata
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The WNT gene family consists of structurally related genes that 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 family. It may be involved in breast cancer, and its protein signaling is, it is presumed, a molecular switch that governs adipogenesis. Gain-of-function of Wnt10b in mouse hearts has shown to improve cardiac tissue repair after myocardial injury, by promoting coronary vessel formation and attenuating pathological fibrosis.[10] This protein is 96% identical to the mouse Wnt10b protein at the amino acid level. This gene is clustered with another family member, WNT1, in the chromosome 12q13 region.[9]

References

Further reading

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