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MECP2

—Methyl-CpG Binding Protein 2

Chromosome: X

Location: X:154021573-154137103

OMIM: 300005

Ensembl: ENSG00000169057

Official·OMIM:300005 Official·ENSG00000169057

Encodes methyl-CpG binding protein. Mutations cause Rett syndrome.

Treatment Roadmap — MECP2

Preclinical

Phase 1

2 trial

Phase 2

3 trial

Phase 3

3 trial

Approved

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

Associated Diseases

Rett Syndrome

X-Linked DominantPrevalence: ~50Kneurological

Official·OMIM:312750 Official·ORPHA778

Summary

Clinical Trial

Approved Therapy

Registered Variant