Wingless-type mmtv integration site family, member 4

Preferred Label : Wingless-type mmtv integration site family, member 4;

Symbol : WNT4;

CISMeF acronym : WNT4;

Type : Gene;

Ensembl ID : ENSG00000162552;

Prefixed ID : *603490;

Details

Origin ID

603490;

UMLS CUI

C1337002;

Automatic exact mappings (from CISMeF team)
- Protein Wnt-4 [NCIt concept]
- WNT4 Gene [NCIt concept]
- WNT4 wt Allele [NCIt concept]
- Wnt family member 4 [ORDO Gene]
- Wnt family member 4 [HGNC gene]
HGNC gene
- Wnt family member 4 [HGNC gene]
NCIt concept(s)
- Protein Wnt-4 [NCIt concept]
- WNT4 Gene [NCIt concept]
- WNT4 wt Allele [NCIt concept]
ORDO concept(s)
- Wnt family member 4 [ORDO Gene]
Phenotypes related
- 46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs [OMIM Phenotype]
- Mullerian aplasia and hyperandrogenism [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WNT4 Gene [NCIt concept]
- Wnt family member 4 [HGNC gene]

Keyword's position in hierarchy(ies) :

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