troponin T1, slow skeletal type

Preferred Label : troponin T1, slow skeletal type;

Approved symbol HGNC : TNNT1;

Name synonyms HGNC : troponin T1; skeletal; slow; slow skeletal muscle troponin T; nemaline myopathy type 5;

Alias symbols HGNC : ANM; STNT; MGC104241; TNT; NEM5; TNTS; FLJ98147;

Chromosome HGNC : 19q13.42;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000105048;

Details

Origin ID

HGNC:11948;

UMLS CUI

C1420827;

Automatic exact mappings (from CISMeF team)
- Nemaline myopathy 5a, autosomal recessive, severe infantile [OMIM Phenotype]
- Skeletal System [NCIt concept]
- Slow [NCIt concept]
- Slow (qualifier value) [SNOMED CT concept]
- Troponin t1, skeletal, slow [OMIM gene]
- slow [Radlex concept]
- troponin T1 [MeSH concept]
- troponin T1, slow skeletal type [ORDO Gene]
- troponin t [MeSH Descriptor]
OMIM gene
- Troponin t1, skeletal, slow [OMIM gene]
Orphanet gene
- troponin T1, slow skeletal type [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Troponin t1, skeletal, slow [OMIM gene]

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