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RPGR

—Retinitis Pigmentosa GTPase Regulator

Chromosome: X

Location: X:38269115-38327573

OMIM: 312610

Ensembl: ENSG00000156313

Official·OMIM:312610 Official·ENSG00000156313

Encodes retinitis pigmentosa GTPase regulator. Mutations cause X-linked RP.

Treatment Roadmap — RPGR

Preclinical

Phase 1

Phase 2

4 trial

Phase 3

4 trial

Approved

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

Associated Diseases

Retinitis Pigmentosa

X-Linked RecessivePrevalence: 1/4000ophthalmologic

Official·OMIM:268000 Official·ORPHA791

Summary

Clinical Trial

Approved Therapy

Registered Variant