NLGN3

neuroligin 3
OMIM: 300336, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Amber NLGN3 in Autism


Version 0.22

review Not set
Sources
  • Expert Review Amber
  • SFARI

No list NLGN3 in Fetal anomalies


Version 1.732
Latest signed off version: v1.92 (21 Aug 2020)

review Not set
Sources
  • Expert Review Removed

Amber NLGN3 in DDG2P


Version 2.49
Latest signed off version: v2.2 (13 Feb 2020)

Component of the following Super Panels:

  • Paediatric disorders
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • DD-Gene2Phenotype
    • Expert Review Amber
    Phenotypes
    • AUTISM SPECTRUM DISORDERS 198890

    Green NLGN3 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 3.1371
    Latest signed off version: v3.2 (13 Feb 2020)

    Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green
    • Emory Genetics Laboratory
    Phenotypes
    • AUTISM SPECTRUM DISORDERS

    Green NLGN3 in Severe Paediatric Disorders


    Version 1.84

    review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • {Autism susceptibility, X-linked 1}, 300425
    • {Asperger syndrome susceptibility, X-linked 1}, 300494