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component of oligomeric golgi complex 5
Summary
- Gene Symbol
-
- COG5
- Aliases
-
- GTC90
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative initiation
- Alternative splicing
- Congenital disorder of glycosylation
- Cytoplasm
- Golgi apparatus
- Membrane
- Phosphoprotein
- Protein transport
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9UP83 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| Golgi organization | ||
| inter-Golgi cisterna vesicle-mediated transport | ||
| protein transport | ||
| retrograde transport, vesicle recycling within Golgi | ||
| intra-Golgi vesicle-mediated transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol | ||
| trans-Golgi network membrane |
|
|
| membrane | ||
| Golgi apparatus | ||
| Golgi membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| molecular_function |
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:0050571 | congenital disorder of glycosylation type II | |
| DOID:0060224 | atrial fibrillation | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0070261 | congenital disorder of glycosylation type IIi | |
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 | |
| DOID:0110038 | Alzheimer's disease 6 | |
| DOID:0110039 | Alzheimer's disease 7 | |
| DOID:0110041 | Alzheimer's disease 8 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000011 | Neurogenic bladder |
| HP:0000020 | Urinary incontinence |
| HP:0000028 | Cryptorchidism |
| HP:0000054 | Micropenis |
| HP:0000218 | High palate |
| HP:0000252 | Microcephaly |
| HP:0000278 | Retrognathia |
| HP:0000358 | Posteriorly rotated ears |
| HP:0000365 | Hearing impairment |
| Disease ID | Disease Name |
|---|---|
| ORPHA:263487 |
|
| OMIM:613612 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 172025 | WB:WBGene00016608 | ||
| 35054 | FB:FBgn0024689 | ||
| 103189354 | CALMI41266 | ||
| 102694295 | LEPOC16479 | ||
| 567886 | ZFIN:ZDB-GENE-041210-47 | DANRE33968 | |
| 103045199 | ASTMX19320 | ||
| 108279731 | ICTPU12256 | ||
| 105020138 | ESOLU66587 | ||
| 115180419 | SALTR55819 | ||
| 115198758 | SALTR65444 |
