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WNT10B - Wnt family member 10B
- Synonym(s) : SHFM6, WNT-12
- Previous symbols and names : wingless-type MMTV integration site family, member 10B
- Type : gene with protein product
- Chromosomal location : 12q13.12
- OMIM: 601906
- HGNC: 12775
- UniProtKB: O00744
- Genatlas: WNT10B
- Ensembl: ENSG00000169884
- IUPHAR-DB: -
- Reactome: O00744
- LOVD: WNT10B
Diseases list
- Disease-causing germline mutation(s) in Isolated split hand-split foot malformation
ORPHA:2440 
- Disease-causing germline mutation(s) in Oligodontia
ORPHA:99798
: AssessedGene included in a panel of genes performed as part of a diagnostic test
Additional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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