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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:0070262 | congenital disorder of glycosylation type IIj | |
| DOID:0080561 | congenital disorder of glycosylation Ii | |
| DOID:0110255 | cataract 5 multiple types | |
| DOID:0110414 | retinitis pigmentosa 3 | |
| DOID:0110462 | autosomal recessive nonsyndromic deafness 101 | |
| DOID:0110463 | autosomal recessive nonsyndromic deafness 102 | |
| DOID:0110464 | autosomal recessive nonsyndromic deafness 103 | |
| DOID:0110465 | autosomal recessive nonsyndromic deafness 104 | |
| DOID:0110466 | obsolete autosomal recessive nonsyndromic deafness 105 | |
| DOID:0110467 | autosomal recessive nonsyndromic deafness 12 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003396 | Syringomyelia |
| HP:0003577 | Congenital onset |
| HP:0003593 | Infantile onset |
| HP:0004279 | Short palm |
| HP:0004322 | Short stature |
| HP:0004582 | Irregularity of vertebral bodies |
| HP:0004798 | Recurrent infection of the gastrointestinal tract |
| HP:0005328 | Progeroid facial appearance |
| HP:0006391 | Overtubulated long bones |
| HP:0006442 | Hypoplasia of proximal fibula |
| 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 |
|---|---|---|---|
| 114039971 | VOMUR28859 | ||
| 105875428 | MICMU10863 | ||
| 100940943 | OTOGA10734 | ||
| 101075831 | TAKRU07481 | ||
| 102029633 | CHILA18684 | ||
| 105706826 | AOTNA15693 | ||
| 101049645 | SAIBB32486 | ||
| 101956809 | ICTTR11918 | ||
| 101615068 | JACJA10740 | ||
| 102422188 | MYOLU06660 |
