Obscurin - CISMeF

Preferred Label : Obscurin;

Symbol : OBSCN;

CISMeF acronym : OBSCN;

Type : Gene;

Alternative titles and symbols : KIAA1556; KIAA1639;

Included titles and symbols : Obscurin-rhogef; Obscurin-mlck;

Ensembl ID : ENSG00000154358;

Prefixed ID : *608616;

Details

Origin ID

608616;

UMLS CUI

C1423682;

Automatic exact mappings (from CISMeF team)
- OBSCN Gene [NCIt concept]
- OBSCN wt Allele [NCIt concept]
- Obscurin [NCIt concept]
- obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF [HGNC gene]
- obscurin-MLCK [MeSH Supplementary Concept]
- obscurin-MLCK [MeSH concept]
- obscurine [MeSH Supplementary Concept]
- obscurine [MeSH concept]
HGNC gene
- obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF [HGNC gene]
NCIt concept(s)
- OBSCN Gene [NCIt concept]
- OBSCN wt Allele [NCIt concept]
- Obscurin [NCIt concept]
Phenotypes related
- Rhabdomyolysis, susceptibility to, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- OBSCN Gene [NCIt concept]
- obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF [HGNC gene]

Keyword's position in hierarchy(ies) :

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