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SLC25A13

—Solute Carrier Family 25 Member 13

Chromosome: 7

Location: 7:96120218-96322181

OMIM: 603859

Ensembl: ENSG00000004864

Official·OMIM:603859 Official·ENSG00000004864

Encodes citrin mitochondrial aspartate/glutamate carrier. Mutations cause citrullinemia type 2.

Treatment Roadmap — SLC25A13

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

Citrullinemia Type 2

Autosomal RecessivePrevalence: 1/100000hepatic

Official·OMIM:605814 Official·ORPHA247585

Summary

Clinical Trial

Approved Therapy

Registered Variant