cofilin 2 - CISMeF

Preferred Label : cofilin 2;

Approved symbol HGNC : CFL2;

Name synonyms HGNC : nemaline myopathy type 7;

Alias symbols HGNC : NEM7;

Chromosome HGNC : 14q13.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000165410;

Details

Origin ID

HGNC:1875;

UMLS CUI

C1413356;

Automatic exact mappings (from CISMeF team)
- Cofilin 2 [OMIM gene]
- Nemaline myopathy 7 [OMIM Phenotype]
- cofilin 2 [ORDO Gene]
- cofilin 2 [MeSH Descriptor]
- cofilin 2 [MeSH concept]
OMIM gene
- Cofilin 2 [OMIM gene]
Orphanet gene
- cofilin 2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Cofilin 2 [OMIM gene]

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