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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:0110548 | autosomal dominant nonsyndromic deafness 17 | |
| DOID:0110549 | autosomal dominant nonsyndromic deafness 18 | |
| DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | |
| DOID:0110551 | autosomal dominant nonsyndromic deafness 21 | |
| DOID:0110552 | autosomal dominant nonsyndromic deafness 22 | |
| DOID:0110553 | autosomal dominant nonsyndromic deafness 23 | |
| DOID:0110554 | autosomal dominant nonsyndromic deafness 24 | |
| DOID:0110555 | autosomal dominant nonsyndromic deafness 25 | |
| DOID:0110556 | autosomal dominant nonsyndromic deafness 27 | |
| DOID:0110557 | autosomal dominant nonsyndromic deafness 28 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0006583 | Fatal liver failure in infancy |
| HP:0006892 | Frontotemporal cerebral atrophy |
| HP:0008897 | Postnatal growth retardation |
| HP:0008935 | Generalized neonatal hypotonia |
| HP:0008936 | Axial hypotonia |
| HP:0009193 | Pseudoepiphyses of the metacarpals |
| HP:0009882 | Short distal phalanx of finger |
| HP:0010049 | Short metacarpal |
| HP:0010230 | Cone-shaped epiphyses of the phalanges of the hand |
| HP:0010580 | Enlarged epiphyses |
| 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 |
