Tropomyosin 3 - CISMeF

Preferred Label : Tropomyosin 3;

Symbol : TPM3;

CISMeF acronym : TPM3;

Type : Gene;

Alternative titles and symbols : Alpha-tropomyosin 3; Alpha-tropomyosin, slow skeletal;

Included titles and symbols : Trk oncogene; Tpm3/ntrk1 fusion gene;

Ensembl ID : ENSG00000143549;

Prefixed ID : *191030;

Details

Origin ID

191030;

UMLS CUI

C1420874;

Automatic exact mappings (from CISMeF team)
- NTRK1/TPM3 Fusion Gene [NCIt concept]
- TPM3/NTRK1 Fusion Gene [NCIt concept]
- Tropomyosin Alpha-3 Chain [NCIt concept]
Currated CISMeF NLP mapping
- TPM3 Gene [NCIt concept]
- tropomyosin 3 [ORDO Gene]
- tropomyosin 3 [HGNC gene]
False automatic mappings
- Oncogene TRK [NCIt concept]
HGNC gene
- tropomyosin 3 [HGNC gene]
NCIt concept(s)
- TPM3 Gene [NCIt concept]
- TPM3 wt Allele [NCIt concept]
- Tropomyosin Alpha-3 Chain [NCIt concept]
- Tropomyosin Alpha-3 Chain Isoform 2 [NCIt concept]
- Tropomyosin Alpha-3 Chain Isoform 3 [NCIt concept]
- hTM5 Allele [NCIt concept]
ORDO concept(s)
- tropomyosin 3 [ORDO Gene]
Phenotypes related
- Congenital myopathy 4a, autosomal dominant [OMIM Phenotype]
- Congenital myopathy 4b, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TPM3 Gene [NCIt concept]
- tropomyosin 3 [HGNC gene]
Validated automatic mappings to BTNT
- TPM3 wt Allele [NCIt concept]
- hTM5 Allele [NCIt concept]

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