glycogen storage disease Ia

Summary
Definition
A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PC gene, which encodes glucose-6-phosphatase (G6Pase), on chromosome 17q21.
Super Class
autosomal recessive disease glycogen storage disease I
External Links
Disease Ontology
DOID:2749
Mondo Disease Ontology
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 31 - 40 of 65 in total
Gene ID Gene Symbol Description Source
4023 LPL lipoprotein lipase
4051 CYP4F3 cytochrome P450 family 4 subfamily F member 3
4245 MGAT1 alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
4534 MTM1 myotubularin 1
4706 NDUFAB1 NADH:ubiquinone oxidoreductase subunit AB1
5211 PFKL phosphofructokinase, liver type
5213 PFKM phosphofructokinase, muscle
5224 PGAM2 phosphoglycerate mutase 2
5230 PGK1 phosphoglycerate kinase 1
5236 PGM1 phosphoglucomutase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14377 G6pc1 glucose-6-phosphatase catalytic subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
25634 G6pc1 glucose-6-phosphatase catalytic subunit 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 31 in total
HPO ID HPO Term
HP:0001733 Pancreatitis
HP:0000822 Hypertension
HP:0003077 Hyperlipidemia
HP:0000105 Enlarged kidney
HP:0002149 Hyperuricemia
HP:0003593 Infantile onset
HP:0001114 Xanthelasma
HP:0000093 Proteinuria
HP:0001943 Hypoglycemia
HP:0003162 Fasting hypoglycemia
Displaying 1 entry
Gene ID Gene Symbol Description
2538 G6PC1 glucose-6-phosphatase catalytic subunit 1

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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