1. Genes and Genomic Entities
  2. ZNF668

ZNF668

zinc finger protein 668
OMIM: 617103, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber ZNF668 in Severe microcephaly


Level 2: Neurology
Version 8.31
Latest signed off version: v8.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Amber
Phenotypes
  • DNA damage repair defect
  • microcephaly
  • growth deficiency
  • severe global developmental delay
  • brain malformation
  • facial dysmorphism
Tags
  • watchlist
Amber ZNF668 in Intellectual disability


Level 2: Developmental disorders
Version 9.279
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • DNA damage repair defect
    • microcephaly
    • growth deficiency
    • severe global developmental delay
    • brain malformation
    • facial dysmorphism
    Tags
    • watchlist
    Amber ZNF668 in Monogenic short stature


    Level 2: Endocrinology
    Version 1.31
    Latest signed off version: v1.0 (7 Aug 2024)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Expert Review Amber
    Phenotypes
    • Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies, OMIM:620194
    Tags
    • watchlist