ZNF142

zinc finger protein 142
OMIM: 604083
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ZNF142-related neurodevelopmental disorder, OMIM:618425
Component of the following Super Panels:
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R59
Signed-off version 5.10
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Seizures, Dystonia, Intellectual disability, Global developmental delay, Tremor, Neurodevelopmental disorder with impaired speech and hyperkinetic movements, 618425
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.13
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Seizures, Dystonia, Intellectual disability, Global developmental delay, Tremor, Neurodevelopmental disorder with impaired speech and hyperkinetic movements, 618425