The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.

KRT14

—Keratin 14

Chromosome: 17

Location: 17:41582279-41586896

OMIM: 148066

Ensembl: ENSG00000186847

Official·OMIM:148066 Official·ENSG00000186847

Encodes keratin 14 protein. Mutations cause epidermolysis bullosa simplex.

Treatment Roadmap — KRT14

Preclinical

Phase 1

1 trial

Phase 2

Phase 3

Approved

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

Associated Diseases

Epidermolysis Bullosa Simplex

Autosomal DominantPrevalence: 1/50000dermatologic

Official·OMIM:131900 Official·ORPHA304

Summary

Clinical Trial

Approved Therapy

Registered Variant