MYH1 wt Allele

Preferred Label : MYH1 wt Allele;

NCIt synonyms : MYHC IIx/d; MYH2X/D; Myosin, Heavy Polypeptide 1, Skeletal Muscle, Adult Gene; MYHC2X/D; MYHa; MYHSA1; MyHC-2x; Myosin, Heavy Chain 1, Skeletal Muscle, Adult wt Allele; MHC IIx/d; MyHC-2X/D; MGC133384;

NCIt definition : Human MYH1 wild-type allele is located in the vicinity of 17p13.1 and is approximately 26 kb in length. This allele, which encodes myosin-1 protein, is involved in the contraction of skeletal muscles.;

GenBank Accession Number : NM_005963;

Détails

Origin ID

C112131;

UMLS CUI

C3813588;

Automatic exact mappings (from CISMeF team)
- Myosin, heavy chain 1, skeletal muscle, adult [OMIM gene]
OMIM relation
- Myosin, heavy chain 1, skeletal muscle, adult [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 17p13.1 [NCIt concept]
gene_is_element_in_pathway
- Tight Junction Assembly Pathway [NCIt concept]
- Viral Myocarditis Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Movement Process [NCIt concept]
- Cytoskeletal Process [NCIt concept]
- Muscle Contraction [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Regulation of Cell Shape [NCIt concept]

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