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ANK1

—Ankyrin 1

Chromosome: 8

Location: 8:41653220-41896812

OMIM: 612641

Ensembl: ENSG00000029534

Official·OMIM:612641 Official·ENSG00000029534

Encodes erythrocyte membrane skeleton protein. Mutations cause hereditary spherocytosis.

Treatment Roadmap — ANK1

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

Hereditary Spherocytosis

Autosomal DominantPrevalence: 1/2000hematologic

Official·OMIM:182900 Official·ORPHA822

Summary

Clinical Trial

Approved Therapy

Registered Variant