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Glycomics MS raw data Repository
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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
component of oligomeric golgi complex 5
Summary
- Gene Symbol
-
- COG5
- Aliases
-
- GTC90
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative initiation
- Alternative splicing
- Congenital disorder of glycosylation
- Cytoplasm
- Golgi apparatus
- Membrane
- Phosphoprotein
- Protein transport
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9UP83 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| retrograde transport, vesicle recycling within Golgi | ||
| intra-Golgi vesicle-mediated transport | ||
| intra-Golgi vesicle-mediated transport | ||
| Golgi organization | ||
| protein transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| Golgi membrane | ||
| Golgi membrane | ||
| nucleoplasm | ||
| Golgi apparatus | ||
| cytosol |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Conserved oligomeric Golgi complex, subunit 5
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| intra-Golgi vesicle-mediated transport |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070261 | congenital disorder of glycosylation type IIi |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000011 | Neurogenic bladder |
| HP:0000020 | Urinary incontinence |
| HP:0000028 | Cryptorchidism |
| HP:0000054 | Micropenis |
| HP:0000218 | High palate |
| HP:0000252 | Microcephaly |
| HP:0000278 | Retrognathia |
| HP:0000358 | Posteriorly rotated ears |
| HP:0000365 | Hearing impairment |
| Disease ID | Disease Name |
|---|---|
| ORPHA:263487 |
|
| OMIM:613612 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 10466 | Xenbase:XB-GENE-6485792 | ||
| 238123 | MOUSE08612 | ||
| 314030 | RATNO35503 | ||
| 463651 | PANTR41149 | ||
| 567886 | DANRE33968 | ||
| 699108 | MACMU32757 | ||
| 855676 | ZFIN:ZDB-GENE-041210-47 | ||
| 100010261 | MONDO33643 | ||
| 100060129 | HORSE33507 | ||
| 100078156 | ORNAN05284 |
