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PMP22

—Peripheral Myelin Protein 22

Chromosome: 17

Location: 17:15176316-15272292

OMIM: 601097

Ensembl: ENSG00000109099

Official·OMIM:601097 Official·ENSG00000109099

Encodes peripheral myelin protein 22. Duplication causes CMT1A, deletion causes HNPP.

Treatment Roadmap — PMP22

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

Charcot-Marie-Tooth Disease Type 1A

Autosomal DominantPrevalence: 1/5000neurological

Official·OMIM:118220 Official·ORPHA101081

Summary

Clinical Trial

Approved Therapy

Registered Variant