MCF2

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

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red MCF2 in Polymicrogyria and Schizencephaly


Level 2: Neurology and neurodevelopmental disorders
Version 0.189

Component of the following Super Panels:

  • Malformations of cortical development_Superpanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Perisylvian polymicrogyria

    Red MCF2 in Mendeliome


    Version 1.1902

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Perisylvian polymicrogyria

    Red MCF2 in Fetal anomalies


    Version 1.255

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Perisylvian polymicrogyria