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SCO2

—SCO2 Assembly Factor

Chromosome: 22

Location: 22:50523564-50526461

OMIM: 604272

Ensembl: ENSG00000284194

Official·OMIM:604272 Official·ENSG00000284194

Encodes cytochrome c oxidase assembly factor. Mutations cause fatal infantile cardioencephalomyopathy.

Treatment Roadmap — SCO2

Preclinical

Phase 1

Phase 2

Phase 3

Approved

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

Associated Diseases

SCO2 No associated disease records found for this gene.

Summary

Clinical Trial

Approved Therapy

Registered Variant