Wingless-type mmtv integration site family, member 5a

Preferred Label : Wingless-type mmtv integration site family, member 5a;

Symbol : WNT5A;

CISMeF acronym : WNT5A;

Type : Gene;

Alternative titles and symbols : Oncogene wnt5a;

Ensembl ID : ENSG00000114251;

Prefixed ID : *164975;

Details

Origin ID

164975;

UMLS CUI

C0812229;

Automatic exact mappings (from CISMeF team)
- Protein Wnt-5a [NCIt concept]
- WNT5A Gene [NCIt concept]
- WNT5A wt Allele [NCIt concept]
- Wnt family member 5A [ORDO Gene]
- Wnt family member 5A [HGNC gene]
- Wnt-5a Protein [MeSH Descriptor]
HGNC gene
- Wnt family member 5A [HGNC gene]
NCIt concept(s)
- Protein Wnt-5a [NCIt concept]
- WNT5A Gene [NCIt concept]
- WNT5A wt Allele [NCIt concept]
ORDO concept(s)
- Wnt family member 5A [ORDO Gene]
Phenotypes related
- Robinow syndrome, autosomal dominant 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WNT5A Gene [NCIt concept]
- Wnt family member 5A [HGNC gene]

Keyword's position in hierarchy(ies) :

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