PCK1

phosphoenolpyruvate carboxykinase 1
OMIM: 614168
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Phosphoenolpyruvate carboxykinase deficiency, cytosolic 261680