1. Genes and Genomic Entities
  2. ZNF599

ZNF599

zinc finger protein 599
Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
No list ZNF599 in DDG2P


Version 8.1
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Removed
    • DD-Gene2Phenotype
    Phenotypes
    • NOT IN OMIM
    Tags
    • curated_removed
    Red ZNF599 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.9
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    Phenotypes
    • ?Chromosome 19q13.11 deletion syndrome, distal, 613026 (includes intellectual disability and developmental delay)