PanelApp
  1. Genes and Genomic Entities
  2. NRXN1

NRXN1

neurexin 1
OMIM: 600565, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green NRXN1 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 0.224

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Pitt-Hopkins-like syndrome 2 - MIM#614325

Green NRXN1 in Mendeliome


Version 1.3512

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Pitt-Hopkins-like syndrome 2 - MIM#614325

Green NRXN1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.267

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Pitt-Hopkins-like syndrome 2 - MIM#614325

    Green NRXN1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.410

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Pitt-Hopkins-like syndrome 2 - MIM#614325

    Red NRXN1 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		0 reviews Unknown
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Autism

    Red NRXN1 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		0 reviews Unknown
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Autism