ZNF335

zinc finger protein 335
OMIM: 610827, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ZNF335 in Arthrogryposis

Level 3: Neuromuscular disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.11
Signed off v.3.2 on 13 Feb 2020

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Microcephaly 10, primary, autosomal recessive

Amber ZNF335 in Severe microcephaly

Level 3: DNA repair disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.8
Signed off v.2.2 on 2 Mar 2020

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Amber
  • Other
  • Literature
Phenotypes
  • Autosomal recessive primary microcephaly (MCPH)
  • ?Microcephaly 10, primary, autosomal recessive, 615095

Amber ZNF335 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.130
Signed off v.3.2 on 13 Feb 2020

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review Unknown
    Sources
    • Expert Review Amber
    • Expert Review Red
    • Other
    Phenotypes
    • ?Microcephaly 10, primary, autosomal recessive, 615095
    • developmental delay
    • intellectual disability
    Tags
    • watchlist