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RYR2

Gene

ryanodine receptor 2

HGNCHGNC:10484EnsemblENSG00000198626NCBI Gene6262
Locus: gene with protein productLocation: 1q43

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asARVD2 · ARVC2 · VTSIP
View full nomenclature history (5)
Previous symbolsARVD2
Alias symbolsARVC2, VTSIP
Previous namesarrhythmogenic right ventricular dysplasia 2, ryanodine receptor 2 (cardiac)

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Arrhythmogenic Right Ventricular Dysplasia
Cardiomyopathies

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Ryanodine receptorsEF-hand domain containingArmadillo like helical domain containingMicroRNA protein coding host genes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.