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FERMT1

—FERM Domain Containing Kindlin 1

Chromosome: 20

Location: 20:6070288-6123644

OMIM: 607900

Ensembl: ENSG00000101311

Official·OMIM:607900 Official·ENSG00000101311

Encodes kindlin-1 protein. Mutations cause Kindler syndrome.

Treatment Roadmap — FERMT1

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

Kindler Syndrome

Autosomal RecessivePrevalence: 1/1000000dermatologic

Official·OMIM:173650 Official·ORPHA2908

Summary

Clinical Trial

Approved Therapy

Registered Variant