MAPK10

mitogen-activated protein kinase 10
OMIM: 602897, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red MAPK10 in Familial Hirschsprung Disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.11

review Unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • association with HSCR
Tags
  • cnv
Red MAPK10 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
    • EPILEPTIC ENCEPHALOPATHY LENNOX-GASTAUT TYPE 606369
    Red MAPK10 in Early onset or syndromic epilepsy


    Level 2: Neurology
    Version 8.125
    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
    • Wessex and West Midlands GLH
    • NHS GMS
    • Expert Review Red
    • Illumina TruGenome Clinical Sequencing Services
    • Expert
    Phenotypes
    • Epileptic Encephalopathy
    • EPILEPTIC ENCEPHALOPATHY LENNOX-GASTAUT TYPE
    Amber MAPK10 in Intellectual disability


    Level 2: Developmental disorders
    Version 9.285
    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, imprinted status unknown
    Sources
    • Expert Review Amber
    • Expert Review Amber
    Phenotypes
    • Lennox-Gastaut syndrome
    • LGS
    • Epileptic Encephalopathy
    • Epileptic Encephalopathy Lennox-Gastaut type
    Tags
    • watchlist