PanelApp (test)
  1. Genes and Genomic Entities
  2. PRDM8

PRDM8

PR/SET domain 8
OMIM: 616639, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red PRDM8 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Epilepsy, progressive myoclonic, 10 MIM#616640

Red PRDM8 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • ?Epilepsy, progressive myoclonic, 10 MIM#616640

    Red PRDM8 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genetic Health Queensland
    Phenotypes
    • Epilepsy, progressive myoclonic, 10, MIM#616640