1. Genes and Genomic Entities
  2. KIRREL3

KIRREL3

kirre like nephrin family adhesion molecule 3
OMIM: 607761, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red KIRREL3 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Red KIRREL3 in DDG2P


Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • MENTAL RETARDATION AUTOSOMAL DOMINANT TYPE 4 612581
    Amber KIRREL3 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 6.12
    Latest signed off version: v6.0 (1 May 2024)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • Intellectual developmental disorder, autosomal dominant 4, OMIM:612581
    • intellectual disability, autosomal dominant 4, MONDO:0012947
    Tags
    • Q1_24_promote_green
    Red KIRREL3 in Severe Paediatric Disorders


    Version 1.184

    		review Unknown
    Sources
    • Next Generation Children Project
    • Expert Review Red
    • Expert list
    Phenotypes
    • Systemic lupus erythematous, suscpetibility to