Genomics England
GMS Panels
Panels
Genes and Entities

PHKG2

phosphorylase kinase catalytic subunit gamma 2
OMIM: 172471
PanelMode of inheritanceDetails
2 panels
Green
in Glycogen storage disease
R-numbers: R274
Signed-off version 2.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Glycogen storage disease IXc 613027
Green
in Likely inborn error of metabolism
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 6.14
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
hepatomegaly and variable myopathy, Glycogen Storage Disorders- Liver, Glycogen Storage Disease, Glycogen storage disease IXc, 613027, Glycogen storage disease type IX Hepatic phosphorylase kinase deficiency with cirrhosis (Glycogen storage disorders), Cirrhosis due to liver phosphorylase kinase deficiency