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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:0040099 | livedoid vasculitis | |
| DOID:0050461 | aspartylglucosaminuria | |
| DOID:0050589 | inflammatory bowel disease | |
| DOID:0050590 | severe congenital neutropenia | |
| DOID:0050801 | androgenic alopecia | |
| DOID:0060025 | immunoglobulin alpha deficiency | |
| DOID:0060185 | Clostridium difficile colitis | |
| DOID:0060249 | scoliosis | |
| DOID:0060320 | inguinal hernia | |
| DOID:0060321 | umbilical hernia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002376 | Developmental regression |
| HP:0002650 | Scoliosis |
| HP:0002684 | Thickened calvaria |
| HP:0002738 | Hypoplastic frontal sinuses |
| HP:0002750 | Delayed skeletal maturation |
| HP:0002756 | Pathologic fracture |
| HP:0002808 | Kyphosis |
| HP:0003103 | Abnormal cortical bone morphology |
| HP:0003196 | Short nose |
| HP:0003302 | Spondylolisthesis |
| 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 |
