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SLC6A1

—Solute Carrier Family 6 Member 1

Chromosome: 3

Location: 3:10992177-11039247

OMIM: 137165

Ensembl: ENSG00000157103

Official·OMIM:137165 Official·ENSG00000157103

Encodes GABA transporter. Mutations cause myoclonic-atonic epilepsy.

Treatment Roadmap — SLC6A1

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

SLC6A1 No associated disease records found for this gene.

Summary

Clinical Trial

Approved Therapy

Registered Variant