Wnt family member 10B

Preferred Label : Wnt family member 10B;

Approved symbol HGNC : WNT10B;

Alias symbols HGNC : WNT-12; SHFM6;

Chromosome HGNC : 12q13.12;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000169884;

Details

Origin ID

HGNC:12775;

UMLS CUI

C1421511;

Automatic exact mappings (from CISMeF team)
- Split-hand/foot malformation 6 [OMIM Phenotype]
- Wingless-type mmtv integration site family, member 10b [OMIM gene]
- Wnt family member 10B [ORDO Gene]
NCIt concept
- WNT10B Gene [NCIt concept]
OMIM gene
- Wingless-type mmtv integration site family, member 10b [OMIM gene]
Orphanet gene
- Wnt family member 10B [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WNT10B Gene [NCIt concept]
- Wingless-type mmtv integration site family, member 10b [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients