Search for a gene
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
- GenCC: 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
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.