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WNT10B

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This is an old revision of this page, as edited by Rjwilmsi (talk | contribs) at 22:45, 17 December 2016 (Further reading: Journal cites, added 1 PMC using AWB (12130)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

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
View/Edit HumanView/Edit Mouse

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

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References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000169884Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022996Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Schubert M, Holland LZ, Holland ND, Jacobs DK (2000). "A phylogenetic tree of the Wnt genes based on all available full-length sequences, including five from the cephalochordate amphioxus". Molecular Biology and Evolution. 17 (12): 1896–903. doi:10.1093/oxfordjournals.molbev.a026291. PMID 11110906.
  6. ^ 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.
  7. ^ 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.
  8. ^ 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.
  9. ^ Cite error: The named reference entrez was invoked but never defined (see the help page).

Further reading

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