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DYNC1H1

—Dynein Cytoplasmic 1 Heavy Chain 1

Chromosome: 14

Location: 14:101964519-102056443

OMIM: 600112

Ensembl: ENSG00000197102

Official·OMIM:600112 Official·ENSG00000197102

Encodes cytoplasmic dynein heavy chain. Mutations cause SMA-LED and cortical malformations.

Treatment Roadmap — DYNC1H1

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

DYNC1H1 No associated disease records found for this gene.

Summary

Clinical Trial

Approved Therapy

Registered Variant