MCF2

MCF.2 cell line derived transforming sequence
OMIM: 311030, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red MCF2 in Malformations of cortical development

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.4
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Cerebral malformation
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Perisylvian polymicrogyria
    • bilateral perisylvian polymicrogyria, MONDO:0020340