SLC25A6

solute carrier family 25 member 6
OMIM: 300151, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SLC25A6 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.1
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review Unknown
    Sources
    • Expert Review Red
    Tags
    • Pseudoautosomal region 1