1. Genes and Genomic Entities
  2. SLC25A32

SLC25A32

solute carrier family 25 member 32
OMIM: 610815, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green SLC25A32 in Likely inborn error of metabolism


Level 2: Metabolic
Version 8.91
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

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

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert list
    • Expert Review Green
    Phenotypes
    • ?Exercise intolerance, riboflavin-responsive
    Tags
    • gene-checked
    Green SLC25A32 in Possible mitochondrial disorder - nuclear genes


    Level 2: Mitochondrial
    Version 4.20
    Latest signed off version: v4.0 (30 Apr 2025)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • ?Exercise intolerance, riboflavin-responsive, 616839
    Tags
    • treatable
    • gene-checked
    Green SLC25A32 in Mitochondrial disorders


    Level 2: Mitochondrial
    Version 9.41
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • ?Exercise intolerance, riboflavin-responsive 616839
    Tags
    • treatable
    • gene-checked
    Red SLC25A32 in Hereditary ataxia with onset in adulthood


    Level 2: Neurology
    Version 8.23
    Latest signed off version: v8.0 (30 Apr 2025)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Wessex and West Midlands GLH
    Phenotypes
    • Riboflavin-responsive exericise intolerance, 616839