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MIRAGE
glucose-6-phosphate dehydrogenase
Summary
- Gene Symbol
-
- G6PD
- Aliases
-
- G6PD1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Cytoplasm
- Direct protein sequencing
- Disease variant
- Glucose metabolism
- Hereditary hemolytic anemia
- Hydroxylation
- Membrane
- NADP
- Oxidoreductase
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| P11413 |
|
| A0A384NL00 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucose metabolic process |
|
|
| glucose metabolic process |
|
|
| pentose-phosphate shunt |
|
|
| pentose-phosphate shunt |
|
|
| lipid metabolic process |
|
GO Hierarchy
biological process
cellular process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of localization [inference]
regulation of growth [inference]
positive regulation of biological process [inference]
negative regulation of biological process [inference]
regulation of developmental process [inference]
regulation of cellular process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucose-6-phosphate dehydrogenase activity |
|
|
| glucose-6-phosphate dehydrogenase activity |
|
|
| glucose-6-phosphate dehydrogenase activity |
|
|
| glucose-6-phosphate dehydrogenase activity |
|
|
| glucose-6-phosphate dehydrogenase activity |
|
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Glucose-6-phosphate
- Functional Category
-
- G: Carbohydrate transport and metabolism
- K: Transcription
- T: Signal transduction mechanisms
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:13628 | favism | |
| DOID:6713 | cerebrovascular disease | |
| DOID:14067 | Plasmodium falciparum malaria | |
| DOID:2383 | neonatal jaundice | |
| DOID:2861 | congenital nonspherocytic hemolytic anemia | |
| DOID:2355 | anemia | |
| DOID:9351 | diabetes mellitus | |
| DOID:12365 | malaria |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000952 | Jaundice |
| HP:0000980 | Pallor |
| HP:0001423 | X-linked dominant inheritance |
| HP:0001744 | Splenomegaly |
| HP:0001923 | Reticulocytosis |
| HP:0001945 | Fever |
| HP:0001974 | Leukocytosis |
| HP:0002027 | Abdominal pain |
| HP:0003577 | Congenital onset |
| HP:0003593 | Infantile onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:300908 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 14381 | MGI:105979 | |
| 14380 | MGI:105977 | |
| 24377 | RGD:2645 | |
| 178046 | WB:WBGene00007108 | |
| 32974 | FB:FBgn0004057 | |
| 855480 | SGD:S000005185 |
