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SLC26A2

—Solute Carrier Family 26 Member 2

Chromosome: 5

Location: 5:149960748-149993455

OMIM: 606718

Ensembl: ENSG00000155850

Official·OMIM:606718 Official·ENSG00000155850

Encodes sulfate transporter. Mutations cause diastrophic dysplasia and achondrogenesis.

Treatment Roadmap — SLC26A2

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

Diastrophic Dysplasia

Autosomal RecessivePrevalence: 1/100000skeletal

Official·OMIM:222600 Official·ORPHA628

Summary

Clinical Trial

Approved Therapy

Registered Variant