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RS1

—Retinoschisin 1

Chromosome: X

Location: X:18639688-18672108

OMIM: 300839

Ensembl: ENSG00000102104

Official·OMIM:300839 Official·ENSG00000102104

Encodes retinoschisin protein. Mutations cause X-linked retinoschisis.

Treatment Roadmap — RS1

Preclinical

Phase 1

2 trial

Phase 2

1 trial

Phase 3

1 trial

Approved

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

Associated Diseases

X-linked Retinoschisis

X-Linked RecessivePrevalence: 1/15000ophthalmologic

Official·OMIM:312700 Official·ORPHA792

Summary

Clinical Trial

Approved Therapy

Registered Variant