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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:0110204 | Charcot-Marie-Tooth disease recessive intermediate B | |
| DOID:0110205 | Charcot-Marie-Tooth disease dominant intermediate E | |
| DOID:0110206 | Charcot-Marie-Tooth disease dominant intermediate F | |
| DOID:0110207 | Charcot-Marie-Tooth disease X-linked dominant 6 | |
| DOID:0110208 | Charcot-Marie-Tooth disease X-linked recessive 2 | |
| DOID:0110209 | Charcot-Marie-Tooth disease X-linked dominant 1 | |
| DOID:0110210 | Charcot-Marie-Tooth disease X-linked recessive 5 | |
| DOID:0110211 | Charcot-Marie-Tooth disease X-linked recessive 3 | |
| DOID:0110212 | Charcot-Marie-Tooth disease X-linked recessive 4 | |
| DOID:0110213 | isolated cleft palate |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002910 | Elevated circulating hepatic transaminase concentration |
| HP:0003160 | Abnormal isoelectric focusing of serum transferrin |
| HP:0003201 | Rhabdomyolysis |
| HP:0003236 | Elevated circulating creatine kinase concentration |
| HP:0003546 | Exercise intolerance |
| HP:0003645 | Prolonged partial thromboplastin time |
| HP:0004322 | Short stature |
| HP:0005305 | Cerebral venous thrombosis |
| HP:0006568 | Increased hepatic glycogen content |
| HP:0008151 | Prolonged prothrombin time |
| Disease ID | Disease Name |
|---|---|
| OMIM:614921 |
|
PubChem Disease
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 100753184 | CRIGR03574 | ||
| 72157 | MGI:97565 | MOUSE42258 | |
| 24645 | RGD:3316 | RATNO33408 | |
| 100721478 | CAVPO01788 | ||
| 101569468 | OCTDE11271 | ||
| 101879196 | MELUD04859 | ||
| 102456218 | PELSI10424 | ||
| 100562877 | ANOCA06060 | ||
| 103663061 | URSMA05657 | ||
| 114036293 | VOMUR22231 |
