GRIA1

glutamate ionotropic receptor AMPA type subunit 1
OMIM: 138248, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green GRIA1 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 67, MIM# 619927
  • Intellectual developmental disorder, autosomal recessive 76, MIM# 619931

Red GRIA1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Intellectual developmental disorder, autosomal dominant 67, MIM# 619927
    • Intellectual developmental disorder, autosomal recessive 76, MIM# 619931

    Green GRIA1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Intellectual developmental disorder, autosomal dominant 67, MIM# 619927
    • Intellectual developmental disorder, autosomal recessive 76, MIM# 619931