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WNT4 - Wnt family member 4
- Synonym(s) : WNT-4
- Previous symbols and names : wingless-type MMTV integration site family, member 4
- Type : gene with protein product
- Chromosomal location : 1p36.12
- OMIM: 603490
- HGNC: 12783
- UniProtKB: P56705
- Genatlas: WNT4
- GenCC: WNT4
- Ensembl: ENSG00000162552
- IUPHAR-DB: -
- Reactome: P56705
- LOVD: WNT4
Diseases list
- Disease-causing germline mutation(s) (loss of function) in Müllerian aplasia and hyperandrogenism
ORPHA:247768 
- Disease-causing germline mutation(s) (loss of function) in SERKAL syndrome
ORPHA:139466
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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