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SLC4A1

—Solute Carrier Family 4 Member 1

Chromosome: 17

Location: 17:44248390-44268162

OMIM: 109270

Ensembl: ENSG00000004939

Official·OMIM:109270 Official·ENSG00000004939

Encodes band 3 protein. Mutations cause hereditary spherocytosis and distal RTA.

Treatment Roadmap — SLC4A1

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