WNT10A

WNT10A
Identifiers
AliasesWNT10A, OODD, SSPS, STHAG4, Wnt family member 10A
External IDsOMIM: 606268; MGI: 108071; HomoloGene: 22525; GeneCards: WNT10A; OMA:WNT10A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_025216

NM_009518

RefSeq (protein)

NP_079492

NP_033544

Location (UCSC)Chr 2: 218.88 – 218.9 MbChr 1: 74.83 – 74.84 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Wnt-10a is a protein that in humans is encoded by the WNT10A gene.[5][6][7]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000135925Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000026167Ensembl, 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. ^ "Entrez Gene: wingless-type MMTV integration site family".
  6. ^ Kirikoshi H, Sekihara H, Katoh M (May 2001). "WNT10A and WNT6, clustered in human chromosome 2q35 region with head-to-tail manner, are strongly coexpressed in SW480 cells". Biochem. Biophys. Res. Commun. 283 (4): 798–805. doi:10.1006/bbrc.2001.4855. PMID 11350055.
  7. ^ Adaimy L, Chouery E, Megarbane H, Mroueh S, Delague V, Nicolas E, Belguith H, de Mazancourt P, Megarbane A (October 2007). "Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia". Am. J. Hum. Genet. 81 (4): 821–8. doi:10.1086/520064. PMC 1973944. PMID 17847007.