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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 4
Summary
- Gene Symbol
-
- COG4
- Aliases
-
- COD1
- DKFZP586E1519
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Coiled coil
- Congenital disorder of glycosylation
- Cytoplasm
- Disease variant
- Dwarfism
- Golgi apparatus
- Membrane
- Phosphoprotein
- Protein transport
- Proteomics identification
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9H9E3 |
|
| J3KNI1 |
|
| Q8N8L9 |
|
| A0A0A0MS45 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| retrograde transport, vesicle recycling within Golgi | ||
| retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | ||
| retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | ||
| Golgi organization | ||
| Golgi organization |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| Golgi membrane | ||
| Golgi membrane | ||
| cytosol | ||
| Golgi transport complex | ||
| Golgi transport complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| identical protein binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- xylosidase
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- P: Inorganic ion transport and metabolism
| Gene Ontology |
|---|
| hydrolase activity, acting on glycosyl bonds |
| hydrolase activity |
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:0070262 | congenital disorder of glycosylation type IIj | |
| DOID:0111673 | Saul-Wilson syndrome |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000252 | Microcephaly |
| HP:0000260 | Wide anterior fontanel |
| HP:0000272 | Malar flattening |
| HP:0000340 | Sloping forehead |
| HP:0000347 | Micrognathia |
| HP:0000365 | Hearing impairment |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000444 | Convex nasal ridge |
| Disease ID | Disease Name |
|---|---|
| ORPHA:85172 |
|
| OMIM:613489 |
|
| ORPHA:263501 |
|
| OMIM:618150 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 25839 | Xenbase:XB-GENE-6085196 | ||
| 102339 | MOUSE58222 | ||
| 361407 | RATNO15074 | ||
| 489716 | CANLF15966 | ||
| 533007 | BOVIN10112 | ||
| 569049 | DANRE40655 | ||
| 712103 | MACMU27340 | ||
| 856220 | Xenbase:XB-GENE-6085196 | ||
| 100024504 | MONDO07881 | ||
| 100054801 | HORSE31407 |
