glycogen storage disease IXd

Summary
Synonym
  • GSD IXd
  • GSD due to muscle phosphorylase kinase deficiency
  • GSD type 9D
  • GSD type 9E
  • GSD type IXd
  • GSD type IXe
  • GSD9D
  • X-linked muscke glycogenosis
  • glycogen storage disease due to muscle phosphorylase kinase deficiency
  • glycogen storage disease type 9D
  • glycogen storage disease type 9E
  • glycogen storage disease type IXd
  • glycogen storage disease type IXe
  • glycogenosis due to muscle phosphorylase kinase deficiency
  • glycogenosis type 9D
  • glycogenosis type 9E
  • glycogenosis type IXd
  • glycogenosis type IXe
  • muscle phosphorylase kinase deficiency
Definition
A glycogen storage disease IX that is characterized by X-linked inheritance of variable exercise-induced muscle weakness or stiffness that has_material_basis_in mutation in the PHKA1 gene on chromosome Xq13.
Super Class
X-linked recessive disease glycogen storage disease IX
External Links
Disease Ontology
DOID:0111040
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 30 in total
Gene ID Gene Symbol Description Source
2632 GBE1 1,4-alpha-glucan branching enzyme 1
2717 GLA galactosidase alpha
2992 GYG1 glycogenin 1
2998 GYS2 glycogen synthase 2
3030 HADHA hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
3939 LDHA lactate dehydrogenase A
5211 PFKL phosphofructokinase, liver type
5213 PFKM phosphofructokinase, muscle
5224 PGAM2 phosphoglycerate mutase 2
5230 PGK1 phosphoglycerate kinase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
18679 Phka1 phosphorylase kinase alpha 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
31839 CG7766 uncharacterized protein
Displaying 1 entry
Gene ID Gene Symbol Description Source
176149 C14B9.8 Phosphorylase b kinase regulatory subunit;putative phosphorylase b kinase regulatory subunit alpha

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024