PRDM15

PR/SET domain 15
OMIM: 617692, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red PRDM15 in DDG2P


Version 3.88
Latest signed off version: v3.1 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • PRDM15-related renal and neurodevelopmental disorder
    Amber PRDM15 in Proteinuric renal disease

    Level 3: Syndromes with prominent renal abnormalities
    Level 2: Renal and urinary tract disorders
    Version 4.12
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Renal superpanel - broad
  • Renal superpanel - narrow
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • steroid-resistant nephrotic syndrome, MONDO:0044765
    Tags
    • Q2_24_promote_green