MARK4

microtubule affinity regulating kinase 4
OMIM: 606495, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red MARK4 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
    • MONDO:0700092
    • MARK4-related neurodevelopmental disorder