PanelApp
  1. Genes and Genomic Entities
  2. SLC25A26

SLC25A26

solute carrier family 25 member 26
OMIM: 611037, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green SLC25A26 in Mendeliome


Version 1.3512

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Combined oxidative phosphorylation deficiency 28, MIM# 616794

Green SLC25A26 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.1085

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Mitochondrial Flagship
    Phenotypes
    • Combined oxidative phosphorylation deficiency 28, MIM# 616794

    Amber SLC25A26 in Fetal anomalies


    Version 1.465

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Genomics England PanelApp
    Phenotypes
    • Combined oxidative phosphorylation deficiency 28 (MIM#616794)