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RP1

—RP1 Axonemal Microtubule Associated

Chromosome: 8

Location: 8:54509422-54871720

OMIM: 603937

Ensembl: ENSG00000104237

Official·OMIM:603937 Official·ENSG00000104237

Encodes axonemal microtubule-associated protein. Mutations cause retinitis pigmentosa.

Treatment Roadmap — RP1

Preclinical

Phase 1

1 trial

Phase 2

1 trial

Phase 3

Approved

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

Associated Diseases

Retinitis Pigmentosa

Autosomal DominantPrevalence: 1/4000ophthalmologic

Official·OMIM:268000 Official·ORPHA791

Summary

Clinical Trial

Approved Therapy

Registered Variant