MAP3K15

mitogen-activated protein kinase kinase kinase 15
OMIM: 300820, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red MAP3K15 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.66
Signed off v.3.2 on 13 Feb 2020

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Red