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RYR2

—Ryanodine Receptor 2

Chromosome: 1

Location: 1:237042184-237833988

OMIM: 180902

Ensembl: ENSG00000198626

Official·OMIM:180902 Official·ENSG00000198626

Encodes cardiac ryanodine receptor. Mutations cause catecholaminergic polymorphic VT.

Treatment Roadmap — RYR2

Preclinical

Phase 1

1 trial

Phase 2

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Catecholaminergic Polymorphic Ventricular Tachycardia

Autosomal DominantPrevalence: 1/10000cardiac

Official·OMIM:604772 Official·ORPHA3286

Summary

Clinical Trial

Approved Therapy

Registered Variant