WNT10B

Wingless-type MMTV integration site family, member 10B
Identifiers
SymbolsWNT10B ; SHFM6; WNT-12
External IDsOMIM: 601906 MGI: 108061 HomoloGene: 20721 GeneCards: WNT10B Gene
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez748022410
EnsemblENSG00000169884ENSMUSG00000022996
UniProtO00744P48614
RefSeq (mRNA)NM_003394NM_011718
RefSeq (protein)NP_003385NP_035848
Location (UCSC)Chr 12:
49.36 – 49.37 Mb
Chr 15:
98.77 – 98.78 Mb
PubMed search

Protein Wnt-10b is a protein that in humans is encoded by the WNT10B gene.[1][2][3][4]

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. 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.[4]

References

  1. Bui TD, Rankin J, Smith K, Huguet EL, Ruben S, Strachan T, Harris AL, Lindsay S (Apr 1997). "A novel human Wnt gene, WNT10B, maps to 12q13 and is expressed in human breast carcinomas". Oncogene 14 (10): 1249–53. doi:10.1038/sj.onc.1200936. PMID 9121776.
  2. Hardiman G, Kastelein RA, Bazan JF (Sep 1997). "Isolation, characterization and chromosomal localization of human WNT10B". Cytogenet Cell Genet 77 (3–4): 278–82. doi:10.1159/000134597. PMID 9284937.
  3. Ugur SA, Tolun A (Aug 2008). "Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation". Hum Mol Genet 17 (17): 2644–53. doi:10.1093/hmg/ddn164. PMID 18515319.
  4. 4.0 4.1 "Entrez Gene: WNT10B wingless-type MMTV integration site family, member 10B".

Further reading