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component of oligomeric golgi complex 1
Summary
- Gene Symbol
-
- COG1
- Aliases
-
- KIAA1381
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Congenital disorder of glycosylation
- Golgi apparatus
- Membrane
- Phosphoprotein
- Protein transport
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| Q8WTW3 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| Golgi organization | ||
| protein transport | ||
| retrograde transport, vesicle recycling within Golgi | ||
| intra-Golgi vesicle-mediated transport |
|
|
| glycosylation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| trans-Golgi network membrane |
|
|
| Golgi apparatus | ||
| 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:0050570 | congenital disorder of glycosylation type I | |
| DOID:0050571 | congenital disorder of glycosylation type II | |
| DOID:0060229 | Baraitser-Winter syndrome | |
| DOID:0060232 | branchiootic syndrome | |
| DOID:0060249 | scoliosis | |
| DOID:0060316 | orofaciodigital syndrome I | |
| DOID:0060359 | Sakati-Nyhan syndrome | |
| DOID:0060380 | orofaciodigital syndrome X | |
| DOID:0060599 | Nance-Horan syndrome | |
| DOID:0060703 | Muenke Syndrome |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000028 | Cryptorchidism |
| HP:0000047 | Hypospadias |
| HP:0000083 | Renal insufficiency |
| HP:0000126 | Hydronephrosis |
| HP:0000160 | Narrow mouth |
| HP:0000162 | Glossoptosis |
| HP:0000175 | Cleft palate |
| HP:0000201 | Pierre-Robin sequence |
| HP:0000218 | High palate |
| Disease ID | Disease Name |
|---|---|
| ORPHA:263508 |
|
| OMIM:611209 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 3565555 | WB:WBGene00003258 | ||
| 41479 | FB:FBgn0037998 | ||
| 103175546 | CALMI08232 | ||
| 102350501 | LATCH19014 | ||
| 100334475 | ZFIN:ZDB-GENE-050302-128 | DANRE32218 | |
| 103045070 | ASTMX16394 | ||
| 108278688 | ICTPU25560 | ||
| 113580245 | ELEEL26307 | ||
| 115171923 | SALTR93480 | ||
| 101155201 | ORYLA17203 |
