1. Genes and Genomic Entities
  2. SLC25A2

SLC25A2

solute carrier family 25 member 2
OMIM: 608157, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red SLC25A2 in Undiagnosed metabolic disorders

Level 3: Specific metabolic abnormalities
Level 2: Metabolic disorders
Version 1.617

review Unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Riboflavin transporter deficiency (Disorders of riboflavin transport and metabolism)
Red SLC25A2 in Likely inborn error of metabolism - targeted testing not possible


Version 4.137
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review Unknown
    Sources
    • London North GLH
    • NHS GMS
    • Expert Review Red
    Phenotypes
    • Riboflavin transporter deficiency (Disorders of riboflavin transport and metabolism)