PanelApp
  1. Genes and Genomic Entities
  2. GRIA4

GRIA4

glutamate ionotropic receptor AMPA type subunit 4
OMIM: 138246, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green GRIA4 in Mendeliome


Version 1.3520

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864

Green GRIA4 in Neurotransmitter Defects


Level 2: Neurology and neurodevelopmental disorders
Version 1.7

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    Phenotypes
    • Glutamate neurotransmitter disorders
    • Neurodevelopmental disorder with or without seizures and gait abnormalities MONDO:0060641

    Green GRIA4 in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.267

    Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864

    Green GRIA4 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.411

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864