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ATRX

—ATRX Chromatin Remodeler

Chromosome: X

Location: X:77504862-77786233

OMIM: 300032

Ensembl: ENSG00000085224

Official·OMIM:300032 Official·ENSG00000085224

Encodes chromatin remodeling protein. Mutations cause alpha-thalassemia/intellectual disability syndrome.

Treatment Roadmap — ATRX

Preclinical

Phase 1

Phase 2

3 trial

Phase 3

Approved

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

Associated Diseases

ATRX No associated disease records found for this gene.

Summary

Clinical Trial

Approved Therapy

Registered Variant