PanelApp (test)
  1. Genes and Genomic Entities
  2. GRIA2

GRIA2

glutamate ionotropic receptor AMPA type subunit 2
OMIM: 138247, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green GRIA2 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Intellectual disability
  • autism
  • Rett-like features
  • epileptic encephalopathy
  • Neurodevelopmental disorder with language impairment and behavioral abnormalities, MIM# 618917

Green GRIA2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Intellectual disability
    • autism
    • Rett-like features
    • epileptic encephalopathy
    • Neurodevelopmental disorder with language impairment and behavioral abnormalities, MIM# 618917

    Green GRIA2 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with language impairment and behavioral abnormalities, MIM# 618917