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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:11328 | schizophreniform disorder | |
| DOID:11371 | functional diarrhea | |
| DOID:11502 | mitral valve insufficiency | |
| DOID:11569 | neurocirculatory asthenia | |
| DOID:11701 | selective IgA deficiency disease | |
| DOID:11714 | gestational diabetes | |
| DOID:11832 | visual epilepsy | |
| DOID:11836 | clubfoot | |
| DOID:12176 | goiter | |
| DOID:1227 | neutropenia |
- 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 |
|---|---|---|---|
| 105874671 | MICMU11312 | ||
| 100966470 | OTOGA09535 | ||
| 101062413 | TAKRU10451 | ||
| 102014731 | CHILA00617 | ||
| 110215973 | PHACI09726 | ||
| 101955969 | ICTTR06374 | ||
| 101607435 | JACJA08518 | ||
| 118319483 | SCOMX05148 | ||
| 102435560 | MYOLU12756 | ||
| 117021813 | RHIFE04621 |
