Actin, alpha-1, skeletal muscle

Preferred Label : Actin, alpha-1, skeletal muscle;

Symbol : ACTA1;

CISMeF acronym : ACTA1;

Type : Gene;

Alternative titles and symbols : ASMA;

Ensembl ID : ENSG00000143632;

Prefixed ID : *102610;

Details

Origin ID

102610;

UMLS CUI

C1412136;

Automatic exact mappings (from CISMeF team)
- ACTA1 gene [LOINC component]
- actin alpha 1, skeletal muscle [ORDO Gene]
- actin alpha 1, skeletal muscle [HGNC gene]
- myasthenia gravis anti-skeletal muscle antibody [MeSH Supplementary Concept]
HGNC gene
- actin alpha 1, skeletal muscle [HGNC gene]
NCIt concept(s)
- ACTA1 Gene [NCIt concept]
- ACTA1 wt Allele [NCIt concept]
- Actin, Alpha Skeletal Muscle [NCIt concept]
ORDO concept(s)
- actin alpha 1, skeletal muscle [ORDO Gene]
Phenotypes related
- Congenital myopathy 2a, typical, autosomal dominant [OMIM Phenotype]
- Congenital myopathy 2b, severe infantile, autosomal recessive [OMIM Phenotype]
- Congenital myopathy 2c, severe infantile, autosomal dominant [OMIM Phenotype]
- Myopathy, scapulohumeroperoneal [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ACTA1 Gene [NCIt concept]
- ACTA1 gene [LOINC component]
- actin alpha 1, skeletal muscle [HGNC gene]

Keyword's position in hierarchy(ies) :

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