CRKL

CRK like proto-oncogene, adaptor protein
OMIM: 602007, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CRKL in Familial non syndromic congenital heart disease

Level 3: Congenital heart disease
Level 2: Cardiovascular disorders
Version 1.90

review Not set
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Tetralogy of Fallot (Tomita-Mitchell (2012) Physiol Genomics 44,518)
Red CRKL in DDG2P


Version 6.424
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • Bladder exstrophy plus