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 2: Developmental disorders
Version 9.279
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

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