1. Genes and Genomic Entities
  2. KIRREL3

KIRREL3

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

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red KIRREL3 in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

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
    Red KIRREL3 in Intellectual disability


    Level 2: Developmental disorders
    Version 10.18
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • NHS GMS
    • Victorian Clinical Genetics Services
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • complex neurodevelopmental disorder, MONDO:0100038
    Tags
    • gene-checked
    • disputed