Myosin, light chain 3, alkali, ventricular, skeletal, slow

Preferred Label : Myosin, light chain 3, alkali, ventricular, skeletal, slow;

Symbol : MYL3;

CISMeF acronym : MYL3;

Type : Gene;

Alternative titles and symbols : Essential light chain of myosin; Elc of myosin; Myosin, light chain 1, slow, b; Myosin, light chain 1, ventricular; MLC1SB; MLC1V;

Ensembl ID : ENSG00000160808;

Prefixed ID : *160790;

Détails

Origin ID

160790;

UMLS CUI

C1417548;

Automatic exact mappings (from CISMeF team)
- 'Myosin, light chain 3, alkali; ventricular, skeletal, slow' [ORDO Gene]
- Myosin Light Chain 3 Measurement [NCIt concept]
- myosin essential light chains [MeSH concept]
- myosin light chain 3 [HGNC gene]
- myosin light chains [MeSH Descriptor]
HGNC gene
- myosin light chain 3 [HGNC gene]
Phenotypes related
- Cardiomyopathy, familial hypertrophic, 8 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- myosin light chain 3 [HGNC gene]

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