NRXN3

neurexin 3
OMIM: 600567, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red NRXN3 in Autism


Version 0.15

review Not set
Sources
  • Expert Review Red
  • SFARI

Red NRXN3 in DDG2P


Version 2.3
Signed off v.2.2 on 13 Feb 2020

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • AUTISM 209850

    Red NRXN3 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 3.3
    Signed off v.3.2 on 13 Feb 2020

    Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    Phenotypes
    • Autism spectrum disorder
    Tags
    • microdeletion