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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 |
|---|---|---|
| Golgi organization | ||
| retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | ||
| protein transport | ||
| retrograde transport, vesicle recycling within Golgi | ||
| glycosylation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol | ||
| trans-Golgi network membrane |
|
|
| Golgi membrane | ||
| Golgi transport complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| 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
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110528 | autosomal recessive nonsyndromic deafness 83 | |
| DOID:0110529 | autosomal recessive nonsyndromic deafness 84A | |
| DOID:0110530 | autosomal recessive nonsyndromic deafness 84B | |
| DOID:0110531 | autosomal recessive nonsyndromic deafness 85 | |
| DOID:0110532 | autosomal recessive nonsyndromic deafness 86 | |
| DOID:0110533 | autosomal recessive nonsyndromic deafness 88 | |
| DOID:0110534 | autosomal recessive nonsyndromic deafness 89 | |
| DOID:0110535 | autosomal recessive nonsyndromic deafness 9 | |
| DOID:0110536 | autosomal recessive nonsyndromic deafness 91 | |
| DOID:0110537 | autosomal recessive nonsyndromic deafness 93 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000926 | Platyspondyly |
| HP:0001015 | Prominent superficial veins |
| HP:0001250 | Seizure |
| HP:0001251 | Ataxia |
| HP:0001263 | Global developmental delay |
| HP:0001270 | Motor delay |
| HP:0001344 | Absent speech |
| HP:0001347 | Hyperreflexia |
| HP:0001394 | Cirrhosis |
| HP:0001399 | Hepatic failure |
| 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 |
|---|---|---|---|
| 115558333 | GADMO12885 | ||
| 101166702 | ORYLA12435 | ||
| 100707434 | ORENI33281 | ||
| 115580098 | SPAAU24772 | ||
| 108714149 | Xenbase:XB-GENE-6486341 | ||
| 100145689 | Xenbase:XB-GENE-6085196 | ||
| 101940703 | CHRPI23892 | ||
| 109310454 | CROPO16261 | ||
| 113445251 | PSETE18216 | ||
| 100543631 | MELGA03353 |
