NCKAP1

NCK associated protein 1
OMIM: 604891, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber NCKAP1 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Amber
  • SFARI
Red NCKAP1 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
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • NCKAP1-related Neurodevelopmental Disorder
    Green NCKAP1 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 6.11
    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 Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Intellectual disability
    • Autism
    Tags
    • gene-checked