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WNT7A - Wnt family member 7A
- Synonym(s) : proto-oncogene Wnt7a protein, Wnt-7a
- Previous symbols and names : wingless-type MMTV integration site family, member 7A
- Type : gene with protein product
- Chromosomal location : 3p25.1
- OMIM: 601570
- HGNC: 12786
- UniProtKB: O00755
- Genatlas: WNT7A
- GenCC: WNT7A
- Ensembl: ENSG00000154764
- IUPHAR-DB: -
- Reactome: O00755
- LOVD: WNT7A
Diseases list
- Disease-causing germline mutation(s) (loss of function) in Fuhrmann syndrome
ORPHA:2854 
- Disease-causing germline mutation(s) (loss of function) in Phocomelia, Schinzel type
ORPHA:2879
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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