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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:0110508 | autosomal recessive nonsyndromic deafness 51 | |
| DOID:0110509 | autosomal recessive nonsyndromic deafness 53 | |
| DOID:0110510 | autosomal recessive nonsyndromic deafness 55 | |
| DOID:0110511 | autosomal recessive nonsyndromic deafness 59 | |
| DOID:0110512 | autosomal recessive nonsyndromic deafness 6 | |
| DOID:0110513 | autosomal recessive nonsyndromic deafness 61 | |
| DOID:0110514 | autosomal recessive nonsyndromic deafness 62 | |
| DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | |
| DOID:0110516 | autosomal recessive nonsyndromic deafness 65 | |
| DOID:0110517 | autosomal recessive nonsyndromic deafness 66 |
- 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 |
|---|---|---|---|
| 101135282 | GORGO11451 | ||
| 100982384 | PANPA15573 | ||
| 100173259 | PONAB10677 | ||
| 489716 | CANLF15966 | ||
| 112929502 | VULVU24638 | ||
| 123800543 | URSAM02926 | ||
| 100482101 | AILME11017 | ||
| 101676503 | MUSPF12963 | ||
| 101086615 | FELCA32991 | ||
| 122208050 | PANLE29961 |
