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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:0110588 | autosomal dominant nonsyndromic deafness 67 | |
| DOID:0110589 | autosomal dominant nonsyndromic deafness 68 | |
| DOID:0110590 | autosomal dominant nonsyndromic deafness 69 | |
| DOID:0110591 | autosomal dominant nonsyndromic deafness 7 | |
| DOID:0110592 | autosomal dominant nonsyndromic deafness 70 | |
| DOID:0110593 | autosomal dominant nonsyndromic deafness 9 | |
| DOID:0110870 | congenital stationary night blindness 1A | |
| DOID:0111673 | Saul-Wilson syndrome | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:10584 | retinitis pigmentosa |
- 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 |
|---|---|---|---|
| 103816669 | SERCA09827 | ||
| 100075069 | ORNAN02776 | ||
| 100916777 | SARHA18260 | ||
| 100414252 | CALJA21696 | ||
| 105589455 | CERAT00997 | ||
| 101925621 | MACFA25329 | ||
| 712103 | MACMU27340 | ||
| 105491545 | MACNE07627 | ||
| 101006069 | PAPAN15334 | ||
| 105537217 | MANLE05506 |
