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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
aspartylglucosaminidase
Summary
- Gene Symbol
-
- AGA
- Aliases
-
- ASRG
- N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase
- glycosylasparaginase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Autocatalytic cleavage
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Lysosome
- Protease
- Reference proteome
- Signal
- Proteins
| UniProt | Protein Name |
|---|---|
| P20933 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein deglycosylation | ||
| proteolysis |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| extracellular region |
|
|
| cytoplasm | ||
| extracellular space | ||
| lysosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| N4-(beta-N-acetylglucosaminyl)-L-asparaginase activity | ||
| peptidase activity | ||
| protein binding |
GO Hierarchy
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:1639 | skeletal tuberculosis | |
| DOID:1826 | epilepsy | |
| DOID:1837 | diabetic ketoacidosis | |
| DOID:1883 | hepatitis C | |
| DOID:1949 | cholecystitis | |
| DOID:216 | dental caries | |
| DOID:2300 | spondylolysis | |
| DOID:2321 | obsolete dyspepsia | |
| DOID:2340 | craniosynostosis | |
| DOID:2377 | multiple sclerosis |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003304 | Spondylolysis |
| HP:0003468 | Abnormal vertebral morphology |
| HP:0004322 | Short stature |
| HP:0004337 | Abnormality of amino acid metabolism |
| HP:0004568 | Beaking of vertebral bodies |
| HP:0005280 | Depressed nasal bridge |
| HP:0008430 | Anterior beaking of lumbar vertebrae |
| HP:0008551 | Microtia |
| HP:0011276 | Vascular skin abnormality |
| HP:0011463 | Childhood onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:208400 |
|
| ORPHA:93 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115569151 | SPAAU63742 | ||
| 496249 | Xenbase:XB-GENE-1001623 | ||
| 100485379 | Xenbase:XB-GENE-1001622 | ||
| 101936557 | CHRPI15764 | ||
| 109309774 | CROPO18499 | ||
| 113435702 | PSETE06666 | ||
| 103826212 | SERCA03507 | ||
| 100087946 | ORNAN04319 | ||
| 100930206 | SARHA11673 | ||
| 103128055 | ERIEU09314 |
