SLC25A10

solute carrier family 25 member 10
OMIM: 606794, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SLC25A10 in Mitochondrial disorders


Level 2: Mitochondrial
Version 10.19
Latest signed off version: v10.18 (12 Aug 2026)

Component of the following Super Panels:

  • Leukodystrophy, childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert list
    Phenotypes
    • ?Mitochondrial DNA depletion syndrome 19, OMIM:618972