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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 N-linked glycosylation | ||
| oligosaccharide metabolic process | ||
| viral protein processing | ||
| protein folding |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| membrane | ||
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| Glc3Man9GlcNAc2 oligosaccharide glucosidase activity | ||
| glucosidase activity |
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:0050458 | juvenile myelomonocytic leukemia | |
| DOID:0050570 | congenital disorder of glycosylation type I | |
| DOID:0050571 | congenital disorder of glycosylation type II | |
| DOID:0050894 | ameloblastoma | |
| DOID:0060478 | Zika fever | |
| DOID:0070254 | congenital disorder of glycosylation type IIb | |
| DOID:0080147 | lymphoblastic lymphoma | |
| DOID:0080188 | chronic myelomonocytic leukemia | |
| DOID:0080566 | congenital disorder of glycosylation In | |
| DOID:0080568 | congenital disorder of glycosylation Iq |
- 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 |
|---|---|---|---|
| 177998 | WB:WBGene00008775 | ||
| 32073 | FB:FBgn0030289 | ||
| 100183132 | CIOIN12045 | ||
| 102359377 | LATCH02522 | ||
| 567913 | ZFIN:ZDB-GENE-070112-412 | DANRE17993 | |
| 103032841 | ASTMX21752 | ||
| 108260492 | ICTPU24137 | ||
| 108260493 | ICTPU24136 | ||
| 113578999 | ELEEL23225 | ||
| 106602766 | SALSA25137 |
