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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:10907 | microcephaly | |
| DOID:11105 | fundus albipunctatus | |
| DOID:11175 | enophthalmos | |
| DOID:11771 | spontaneous ocular nystagmus | |
| DOID:11836 | clubfoot | |
| DOID:1227 | neutropenia | |
| DOID:1247 | blood coagulation disease | |
| DOID:12987 | agranulocytosis | |
| DOID:13174 | dissociated nystagmus | |
| DOID:1443 | cerebral degeneration |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001433 | Hepatosplenomegaly |
| HP:0001508 | Failure to thrive |
| HP:0001510 | Growth delay |
| HP:0001511 | Intrauterine growth retardation |
| HP:0001531 | Failure to thrive in infancy |
| HP:0001744 | Splenomegaly |
| HP:0001762 | Talipes equinovarus |
| HP:0001873 | Thrombocytopenia |
| HP:0001875 | Neutropenia |
| HP:0001999 | Abnormal facial shape |
| 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 |
|---|---|---|---|
| 116833720 | CHEAB14245 | ||
| 105305830 | PTEVA10474 | ||
| 115040837 | ECHNA23491 | ||
| 115390790 | SALFA56003 | ||
| 113484327 | ATHCN15065 | ||
| 105808000 | PROCO17991 | ||
| 856220 | SGD:S000006309 | ||
| 109065042 | CYPCA09398 | ||
| 103735636 | NANGA10876 | ||
| 116450144 | CORMO02091 |
