SLC1A1

solute carrier family 1 member 1
OMIM: 133550, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red SLC1A1 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Green SLC1A1 in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.453
Latest signed off version: v5.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Dicarboxylic aminoaciduria 222730