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KCNQ2

—Potassium Voltage-Gated Channel Subfamily Q Member 2

Chromosome: 20

Location: 20:63400208-63472689

OMIM: 602235

Ensembl: ENSG00000075043

Official·OMIM:602235 Official·ENSG00000075043

Encodes potassium channel subunit. Mutations cause neonatal epilepsy.

Treatment Roadmap — KCNQ2

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

KCNQ2 Neonatal Epilepsy

Autosomal DominantPrevalence: 1/100000neurological

Official·OMIM:121200 Official·ORPHA1949

Summary

Clinical Trial

Approved Therapy

Registered Variant