1. Genes and Genomic Entities
  2. SLC9A9

SLC9A9

solute carrier family 9 member A9
OMIM: 608396, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red SLC9A9 in DDG2P


Version 8.1
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • SUSCEPTIBILITY TO AUTISM TYPE 16 613410
    Red SLC9A9 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.1
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Red
    Phenotypes
    • {?Autism susceptibility 16}, 613410