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NOG - noggin
- Synonym(s) :
- Previous symbols and names : SYM1, SYNS1, symphalangism 1 (proximal), synostoses (multiple) syndrome 1
- Type : gene with protein product
- Chromosomal location : 17q22
- OMIM: 602991
- HGNC: 7866
- UniProtKB: Q13253
- Genatlas: NOG
- GenCC: NOG
- Ensembl: ENSG00000183691
- IUPHAR-DB: -
- Reactome: Q13253
- LOVD: NOG
Diseases list
- Disease-causing germline mutation(s) in Brachydactyly type B2
ORPHA:140908 
- Disease-causing germline mutation(s) in Multiple synostoses syndrome
ORPHA:3237 - Disease-causing germline mutation(s) in Proximal symphalangism
ORPHA:3250 - Disease-causing germline mutation(s) in Stapes ankylosis with broad thumbs and toes
ORPHA:140917 - Disease-causing germline mutation(s) in Tarsal-carpal coalition syndrome
ORPHA:1412
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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