1. Genes and Genomic Entities
  2. SLC25A36

SLC25A36

solute carrier family 25 member 36
OMIM: 616149, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber SLC25A36 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 Review Amber
    • Literature
    • NHS GMS
    Phenotypes
    • Hyperinsulinemic hypoglycemia, familial, 8, OMIM:620211
    Tags
    • Q2_25_ promote_green
    Green SLC25A36 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
    • Literature
    Phenotypes
    • Hyperinsulinemic hypoglycemia, familial, 8, OMIM:620211