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TNC - tenascin C
- Synonym(s) : hexabrachion (tenascin), MGC167029, TN
- Previous symbols and names : DFNA56, HXB, deafness, autosomal dominant 56, hexabrachion (tenascin C, cytotactin)
- Type : gene with protein product
- Chromosomal location : 9q33.1
- OMIM: 187380
- HGNC: 5318
- UniProtKB: P24821
- Genatlas: TNC
- GenCC: TNC
- Ensembl: ENSG00000041982
- IUPHAR-DB: -
- Reactome: P24821
- LOVD: TNC
Diseases list
- Disease-causing germline mutation(s) in Autosomal dominant non-syndromic sensorineural deafness type DFNA
ORPHA:90635 
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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