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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
mannosyl-oligosaccharide glucosidase
Summary
- Gene Symbol
-
- MOGS
- Aliases
-
- CWH41
- DER7
- GCS1
- glucosidase I
- processing A-glucosidase I
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Disease variant
- Endoplasmic reticulum
- Glycoprotein
- Glycosidase
- Reference proteome
- Signal-anchor
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A384MDR6 |
|
| Q58F09 |
|
| Q13724 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein folding | ||
| protein N-linked glycosylation | ||
| oligosaccharide metabolic process | ||
| viral protein processing |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| endoplasmic reticulum membrane | ||
| membrane | ||
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| Glc3Man9GlcNAc2 oligosaccharide glucosidase activity | ||
| Glc3Man9GlcNAc2 oligosaccharide glucosidase activity | ||
| glucosidase activity |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Glucosidase I
- Functional Category
-
- G: Carbohydrate transport and metabolism
- H: Coenzyme transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
| Gene Ontology |
|---|
| Glc3Man9GlcNAc2 oligosaccharide glucosidase activity |
| hydrolase activity, acting on glycosyl bonds |
| hydrolase activity |
| protein N-linked glycosylation |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
G57930PW
G18948TG
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070254 | congenital disorder of glycosylation type IIb |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000034 | Hydrocele testis |
| HP:0000218 | High palate |
| HP:0000269 | Prominent occiput |
| HP:0000278 | Retrognathia |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000445 | Wide nose |
| HP:0000527 | Long eyelashes |
| HP:0000581 | Blepharophimosis |
| HP:0000648 | Optic atrophy |
| Disease ID | Disease Name |
|---|---|
| OMIM:606056 |
|
| ORPHA:79330 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 7841 | Xenbase:XB-GENE-5911793 | ||
| 57377 | Xenbase:XB-GENE-5911793 | MOUSE50894 | |
| 78947 | Xenbase:XB-GENE-5911793 | RATNO29484 | |
| 177998 | Xenbase:XB-GENE-5911793 | ||
| 483104 | CANLF05217 | ||
| 516155 | BOVIN02092 | ||
| 567913 | DANRE17993 | ||
| 708913 | MACMU08150 | ||
| 740472 | PANTR27967 | ||
| 852857 | Xenbase:XB-GENE-5911793 |
