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TNNT1 - troponin T1, slow skeletal type
- Synonym(s) : ANM, FLJ98147, MGC104241, NEM5, nemaline myopathy type 5, slow skeletal muscle troponin T, STNT, TNT, TNTS, troponin T1, skeletal, slow
- Previous symbols and names : troponin T type 1 (skeletal, slow)
- Type : gene with protein product
- Chromosomal location : 19q13.42
- OMIM: 191041
- HGNC: 11948
- UniProtKB: P13805
- Genatlas: TNNT1
- GenCC: TNNT1
- Ensembl: ENSG00000105048
- IUPHAR-DB: -
- Reactome: P13805
- LOVD: TNNT1
Diseases list
- Disease-causing germline mutation(s) in Amish nemaline myopathy
ORPHA:98902

Additional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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