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WNT1 - Wnt family member 1
- Synonym(s) :
- Previous symbols and names : INT1, wingless-type MMTV integration site family, member 1
- Type : gene with protein product
- Chromosomal location : 12q13.12
- OMIM: 164820
- HGNC: 12774
- UniProtKB: P04628
- Genatlas: WNT1
- GenCC: WNT1
- Ensembl: ENSG00000125084
- IUPHAR-DB: -
- Reactome: P04628
- LOVD: WNT1
Diseases list
- Disease-causing germline mutation(s) (loss of function) in Osteogenesis imperfecta type 3
ORPHA:216812 
- Disease-causing germline mutation(s) (loss of function) in Osteogenesis imperfecta type 4
ORPHA:216820 - Major susceptibility factor in Idiopathic juvenile osteoporosis
ORPHA:85193
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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