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KRT5

—Keratin 5

Chromosome: 12

Location: 12:52514575-52520530

OMIM: 148040

Ensembl: ENSG00000186081

Official·OMIM:148040 Official·ENSG00000186081

Encodes keratin 5 protein. Mutations cause epidermolysis bullosa simplex.

Treatment Roadmap — KRT5

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

Epidermolysis Bullosa Simplex

Autosomal DominantPrevalence: 1/50000dermatologic

Official·OMIM:131900 Official·ORPHA304

Summary

Clinical Trial

Approved Therapy

Registered Variant