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KCNQ1

—Potassium Voltage-Gated Channel Subfamily Q Member 1

Chromosome: 11

Location: 11:2444654-2849105

OMIM: 607542

Ensembl: ENSG00000053918

Official·OMIM:607542 Official·ENSG00000053918

Encodes potassium channel subunit. Mutations cause long QT syndrome type 1.

Treatment Roadmap — KCNQ1

Preclinical

Phase 1

Phase 2

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 1

Autosomal DominantPrevalence: 1/2500cardiac

Official·OMIM:192500 Official·ORPHA768

Summary

Clinical Trial

Approved Therapy

Registered Variant