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STK11

—Serine/Threonine Kinase 11

Chromosome: 19

Location: 19:1177558-1228431

OMIM: 602216

Ensembl: ENSG00000118046

Official·OMIM:602216 Official·ENSG00000118046

Encodes serine/threonine kinase. Mutations cause Peutz-Jeghers syndrome.

Treatment Roadmap — STK11

Preclinical

Phase 1

Phase 2

6 trial

Phase 3

2 trial

Approved

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

Associated Diseases

Peutz-Jeghers Syndrome

Autosomal DominantPrevalence: 1/200000oncologic

Official·OMIM:175200 Official·ORPHA2869

Summary

Clinical Trial

Approved Therapy

Registered Variant