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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
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 54657 | UGT1A4 | UDP glucuronosyltransferase family 1 member A4 | |
| 54658 | UGT1A1 | UDP glucuronosyltransferase family 1 member A1 | |
| 57818 | G6PC2 | glucose-6-phosphatase catalytic subunit 2 | |
| 79796 | ALG9 | ALG9 alpha-1,2-mannosyltransferase | |
| 92579 | G6PC3 | glucose-6-phosphatase catalytic subunit 3 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O14561 | Acyl carrier protein, mitochondrial | |
| O15488 | Glycogenin-2 | |
| O43451 | Maltase-glucoamylase | |
| O60760 | Hematopoietic prostaglandin D synthase | |
| O75352 | Mannose-P-dolichol utilization defect 1 protein | |
| P00338 | L-lactate dehydrogenase A chain | |
| P00558 | Phosphoglycerate kinase 1 | |
| P04075 | Fructose-bisphosphate aldolase A | |
| P05362 | Intercellular adhesion molecule 1 | |
| P06280 | Alpha-galactosidase A |
- The Human Phenotype Ontology
| 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 |
