MARK2

microtubule affinity regulating kinase 2
OMIM: 600526, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green MARK2 in Early onset or syndromic epilepsy


Level 2: Neurology
Version 8.167
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    • NHS GMS
    Phenotypes
    • Intellectual developmental disorder, autosomal dominant 76, OMIM:621285
    • intellectual developmental disorder, autosomal dominant 76, MONDO:0979575
    Green MARK2 in Intellectual disability


    Level 2: Developmental disorders
    Version 9.345
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Intellectual developmental disorder, autosomal dominant 76, OMIM:621285
    • intellectual developmental disorder, autosomal dominant 76, MONDO:0979575