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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:10461 | dentin caries | |
| DOID:10534 | stomach cancer | |
| DOID:1059 | intellectual disability | |
| DOID:10607 | tropical sprue | |
| DOID:10608 | celiac disease | |
| DOID:10754 | otitis media | |
| DOID:10907 | microcephaly | |
| DOID:1094 | attention deficit hyperactivity disorder | |
| DOID:11165 | common wart | |
| DOID:11199 | hypoparathyroidism |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000280 | Coarse facial features |
| HP:0000283 | Broad face |
| HP:0000303 | Mandibular prognathia |
| HP:0000316 | Hypertelorism |
| HP:0000389 | Chronic otitis media |
| HP:0000431 | Wide nasal bridge |
| HP:0000463 | Anteverted nares |
| HP:0000518 | Cataract |
| HP:0000670 | Carious teeth |
| HP:0000708 | Atypical behavior |
| 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 |
|---|---|---|---|
| 100472378 | AILME07070 | ||
| 101086138 | FELCA08465 | ||
| 118887954 | BALMU31027 | ||
| 100658416 | LOXAF08739 | ||
| 100060636 | HORSE25058 | ||
| 100152203 | PIGXX09049 | ||
| 511345 | BOVIN21892 | ||
| 102190099 | CAPHI18380 | ||
| 101106396 | SHEEP13045 | ||
| 100338965 | RABIT08160 |
