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:0110498 | autosomal recessive nonsyndromic deafness 4 | |
| DOID:0110499 | autosomal recessive nonsyndromic deafness 40 | |
| DOID:0110500 | autosomal recessive nonsyndromic deafness 42 | |
| DOID:0110501 | autosomal recessive nonsyndromic deafness 44 | |
| DOID:0110502 | autosomal recessive nonsyndromic deafness 45 | |
| DOID:0110503 | autosomal recessive nonsyndromic deafness 46 | |
| DOID:0110504 | autosomal recessive nonsyndromic deafness 47 | |
| DOID:0110505 | autosomal recessive nonsyndromic deafness 48 | |
| DOID:0110506 | autosomal recessive nonsyndromic deafness 49 | |
| DOID:0110507 | autosomal recessive nonsyndromic deafness 5 |
- 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 |
|---|---|---|---|
| 116833720 | CHEAB14245 | ||
| 105305830 | PTEVA10474 | ||
| 115040837 | ECHNA23491 | ||
| 115390790 | SALFA56003 | ||
| 113484327 | ATHCN15065 | ||
| 105808000 | PROCO17991 | ||
| 856220 | SGD:S000006309 | ||
| 109065042 | CYPCA09398 | ||
| 103735636 | NANGA10876 | ||
| 116450144 | CORMO02091 |
