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 1 - 10 of 30 in total
Gene ID Gene Symbol Description Source
34 ACADM acyl-CoA dehydrogenase medium chain
178 AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
226 ALDOA aldolase, fructose-bisphosphate A
353 APRT adenine phosphoribosyltransferase
1962 EHHADH enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
2027 ENO3 enolase 3
2203 FBP1 fructose-bisphosphatase 1
2538 G6PC1 glucose-6-phosphatase catalytic subunit 1
2542 SLC37A4 solute carrier family 37 member 4
2548 GAA alpha glucosidase
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

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024