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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
phosphoglucomutase 1
Summary
- Gene Symbol
-
- PGM1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Congenital disorder of glycosylation
- Cytoplasm
- Disease variant
- Glucose metabolism
- Glycogen storage disease
- Isomerase
- Magnesium
- Metal-binding
- Phosphoprotein
- Reference proteome
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| carbohydrate metabolic process | ||
| galactose catabolic process via UDP-galactose | ||
| glucose metabolic process | ||
| glycolytic process | ||
| gluconeogenesis |
GO Hierarchy
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
catabolic process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound catabolic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
cellular catabolic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle catabolic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
organophosphate metabolic process [inference]
organic cyclic compound metabolic process [inference]
organonitrogen compound metabolic process [inference]
organic substance catabolic process [inference]
cellular process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound catabolic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
cellular catabolic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle catabolic process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol | ||
| extracellular region | ||
| cytoplasm | ||
| tertiary granule lumen | ||
| ficolin-1-rich granule lumen |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| phosphoglucomutase activity | ||
| magnesium ion binding | ||
| protein binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism | |
| DOID:0050539 | Charcot-Marie-Tooth disease type 2 | |
| DOID:0050570 | congenital disorder of glycosylation type I | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0060600 | obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum | |
| DOID:0060728 | NGLY1-deficiency | |
| DOID:0060843 | hereditary neuropathy with liability to pressure palsies | |
| DOID:0070161 | hereditary sensory and autonomic neuropathy type 2 | |
| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | |
| DOID:0070219 | familial hyperinsulinemic hypoglycemia 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001263 | Global developmental delay |
| HP:0001270 | Motor delay |
| HP:0001324 | Muscle weakness |
| HP:0001397 | Hepatic steatosis |
| HP:0001406 | Intrahepatic cholestasis |
| HP:0001510 | Growth delay |
| HP:0001629 | Ventricular septal defect |
| HP:0001640 | Cardiomegaly |
| HP:0001644 | Dilated cardiomyopathy |
| HP:0001645 | Sudden cardiac death |
| Disease ID | Disease Name |
|---|---|
| OMIM:614921 |
|
PubChem Disease
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 173843 | WB:WBGene00019890 | ||
| 44010 | FB:FBgn0003076 | ||
| 102358793 | LATCH06641 | ||
| 394000 | ZFIN:ZDB-GENE-040426-1245 | ||
| 379864 | Xenbase:XB-GENE-948534 | ||
| 414455 | Xenbase:XB-GENE-17334071 | ||
| 407960 | Xenbase:XB-GENE-948527 | ||
| 101947993 | CHRPI04276 | ||
| 109307555 | CROPO13566 | ||
| 113447947 | PSETE21506 |
