1. Genes and Genomic Entities
  2. ZNF81

ZNF81

zinc finger protein 81
OMIM: 314998, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red ZNF81 in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Red
    • Radboud University Medical Center, Nijmegen
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • Mental Retardation, X-linked
    • Mental retardation, X-linked 45, 300498