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SLC5A5

—Solute Carrier Family 5 Member 5

Chromosome: 19

Location: 19:17871939-17895174

OMIM: 601843

Ensembl: ENSG00000105641

Official·OMIM:601843 Official·ENSG00000105641

Encodes sodium/iodide symporter. Mutations cause iodide transport defect.

Treatment Roadmap — SLC5A5

Preclinical

Phase 1

7 trial

Phase 2

1 trial

Phase 3

Approved

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

Associated Diseases

SLC5A5 No associated disease records found for this gene.

Summary

Clinical Trial

Approved Therapy

Registered Variant