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MPZ

—Myelin Protein Zero

Chromosome: 1

Location: 1:161304735-161309974

OMIM: 159440

Ensembl: ENSG00000158887

Official·OMIM:159440 Official·ENSG00000158887

Encodes myelin protein zero. Mutations cause CMT1B, CMT2I, and Dejerine-Sottas syndrome.

Treatment Roadmap — MPZ

Preclinical

Phase 1

Phase 2

Phase 3

2 trial

Approved

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

Associated Diseases

MPZ No associated disease records found for this gene.

Summary

Clinical Trial

Approved Therapy

Registered Variant