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KCNJ11

—Potassium Inwardly Rectifying Channel Subfamily J Member 11

Chromosome: 11

Location: 11:17364082-17389364

OMIM: 600937

Ensembl: ENSG00000187486

Official·OMIM:600937 Official·ENSG00000187486

Encodes Kir6.2 potassium channel. Mutations cause neonatal diabetes and DEND syndrome.

Treatment Roadmap — KCNJ11

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

Neonatal Diabetes

Autosomal DominantPrevalence: 1/100000endocrine

Official·OMIM:606176 Official·ORPHA224

Summary

Clinical Trial

Approved Therapy

Registered Variant