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KCNH2

—Potassium Voltage-Gated Channel Subfamily H Member 2

Chromosome: 7

Location: 7:150944064-150978394

OMIM: 152427

Ensembl: ENSG00000055118

Official·OMIM:152427 Official·ENSG00000055118

Encodes HERG potassium channel. Mutations cause long QT syndrome type 2.

Treatment Roadmap — KCNH2

Preclinical

Phase 1

Phase 2

1 trial

Phase 3

Approved

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

Associated Diseases

Long QT Syndrome Type 2

Autosomal DominantPrevalence: 1/5000cardiac

Official·OMIM:613688 Official·ORPHA768

Summary

Clinical Trial

Approved Therapy

Registered Variant