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ATP7B

—ATPase Copper Transporting Beta

Chromosome: 13

Location: 13:51930436-52012198

OMIM: 606882

Ensembl: ENSG00000123191

Official·OMIM:606882 Official·ENSG00000123191

Encodes copper-transporting ATPase enzyme. Mutations cause Wilson disease.

Treatment Roadmap — ATP7B

Preclinical

Phase 1

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

Wilson Disease

Autosomal RecessivePrevalence: 1/30000hepatic

Official·OMIM:277900 Official·ORPHA905

Summary

Clinical Trial

Approved Therapy

Registered Variant