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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 |
|---|---|---|---|
| 5836 | PYGL | glycogen phosphorylase L | |
| 5837 | PYGM | glycogen phosphorylase, muscle associated | |
| 6476 | SI | sucrase-isomaltase | |
| 6514 | SLC2A2 | solute carrier family 2 member 2 | |
| 6517 | SLC2A4 | solute carrier family 2 member 4 | |
| 6519 | SLC3A1 | solute carrier family 3 member 1 | |
| 7086 | TKT | transketolase | |
| 7355 | SLC35A2 | solute carrier family 35 member A2 | |
| 7360 | UGP2 | UDP-glucose pyrophosphorylase 2 | |
| 7368 | UGT8 | UDP glycosyltransferase 8 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9H6U8 | Alpha-1,2-mannosyltransferase ALG9 | |
| Q9HAW7 | UDP-glucuronosyltransferase 1A7 | |
| Q9HAW8 | UDP-glucuronosyltransferase 1A10 | |
| Q9HAW9 | UDP-glucuronosyltransferase 1A8 | |
| Q9NQR9 | Glucose-6-phosphatase 2 |
- 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 |
