Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0050534 | congenital stationary night blindness | |
| DOID:0050564 | autosomal dominant nonsyndromic deafness | |
| DOID:0050565 | autosomal recessive nonsyndromic deafness | |
| DOID:0050566 | X-linked nonsyndromic deafness | |
| DOID:0050570 | congenital disorder of glycosylation type I | |
| DOID:0050571 | congenital disorder of glycosylation type II | |
| DOID:0050572 | cone-rod dystrophy | |
| DOID:0050590 | severe congenital neutropenia | |
| DOID:0060135 | apraxia | |
| DOID:0060690 | autosomal dominant auditory neuropathy 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002673 | Coxa valga |
| HP:0002788 | Recurrent upper respiratory tract infections |
| HP:0002910 | Elevated circulating hepatic transaminase concentration |
| HP:0003015 | Flared metaphysis |
| HP:0003067 | Madelung deformity |
| HP:0003124 | Hypercholesterolemia |
| HP:0003155 | Elevated circulating alkaline phosphatase concentration |
| HP:0003256 | Abnormality of the coagulation cascade |
| HP:0003301 | Irregular vertebral endplates |
| HP:0003311 | Hypoplasia of the odontoid process |
| 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 |
|---|---|---|---|
| 103265656 | CARSF15455 | ||
| 115619586 | STRHB07581 |
