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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:50 | thyroid gland disease | |
| DOID:5082 | liver cirrhosis | |
| DOID:5212 | congenital disorder of glycosylation | |
| DOID:5338 | gingival hypertrophy | |
| DOID:5418 | schizoaffective disorder | |
| DOID:5419 | schizophrenia | |
| DOID:543 | dystonia | |
| DOID:5517 | stomach carcinoma | |
| DOID:6050 | esophageal disease | |
| DOID:640 | encephalomyelitis |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001290 | Generalized hypotonia |
| HP:0001369 | Arthritis |
| HP:0001382 | Joint hypermobility |
| HP:0001387 | Joint stiffness |
| HP:0001537 | Umbilical hernia |
| HP:0001609 | Hoarse voice |
| HP:0001653 | Mitral regurgitation |
| HP:0001744 | Splenomegaly |
| HP:0001763 | Pes planus |
| HP:0001875 | Neutropenia |
| 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 |
|---|---|---|---|
| 105992880 | DIPOR00864 | ||
| 100754017 | CRIGR10815 | ||
| 11593 | MGI:104873 | MOUSE58215 | |
| 290923 | RGD:1309646 | RATNO11876 | |
| 101581743 | OCTDE20728 | ||
| 101721618 | HETGA20583 | ||
| 100017534 | MONDO26305 | ||
| 100565704 | ANOCA07621 | ||
| 114024578 | VOMUR06561 | ||
| 113884868 | BOBOX26500 |
