Ryanodine receptor 2

Preferred Label : Ryanodine receptor 2;

Symbol : RYR2;

CISMeF acronym : RYR2;

Type : Gene;

Alternative titles and symbols : Ryanodine receptor, cardiac;

Ensembl ID : ENSG00000198626;

Prefixed ID : *180902;

Details

Origin ID

180902;

UMLS CUI

C1419779;

Automatic exact mappings (from CISMeF team)
- ryanodine receptor 2 [ORDO Gene]
- ryanodine receptor 2 [MeSH concept]
- ryanodine receptor 2 [HGNC gene]
- ryanodine receptor calcium release channel [MeSH Descriptor]
HGNC gene
- ryanodine receptor 2 [HGNC gene]
NCIt concept(s)
- RYR2 Gene [NCIt concept]
- RYR2 wt Allele [NCIt concept]
- Ryanodine Receptor 2 [NCIt concept]
ORDO concept(s)
- ryanodine receptor 2 [ORDO Gene]
Phenotypes related
- Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome [OMIM Phenotype]
- Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ryanodine receptor 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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