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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:0000007 | Autosomal recessive inheritance |
| HP:0000023 | Inguinal hernia |
| HP:0000053 | Macroorchidism |
| HP:0000154 | Wide mouth |
| HP:0000158 | Macroglossia |
| HP:0000164 | Abnormality of the dentition |
| HP:0000179 | Thick lower lip vermilion |
| HP:0000212 | Gingival overgrowth |
| HP:0000248 | Brachycephaly |
| HP:0000252 | Microcephaly |
| 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 |
