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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Conserved oligomeric Golgi complex subunit 8
Summary
- UniProt ID
- Q96MW5
- Gene Symbol
-
- COG8
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Congenital disorder of glycosylation
- Golgi apparatus
- Membrane
- Protein transport
- Reference proteome
- Gene Ontology (GO)
| GO Term |
|---|
| glycosylation |
| retrograde transport, vesicle recycling within Golgi |
| intra-Golgi vesicle-mediated transport |
| Golgi organization |
| protein transport |
| GO Term |
|---|
| Golgi transport complex |
| trans-Golgi network membrane |
| Golgi membrane |
| Golgi apparatus |
| membrane |
Sequence
MATAATIPSVATATAAALGEVEDEGLLASLFRDRFPEAQWRERPDVGRYLRELSGSGLERLRREPERLAEERAQLLQQTRDLAFANYKTFIRGAECTERIHRLFGDVEASLGRLLDRLPSFQQSCRNFVKEAEEISSNRRMNSLTLNRHTEILEILEIPQLMDTCVRNSYYEEALELAAYVRRLERKYSSIPVIQGIVNEVRQSMQLMLSQLIQQLRTNIQLPACLRVIGYLRRMDVFTEAELRVKFLQARDAWLRSILTAIPNDDPYFHITKTIEASRVHLFDIITQYRAIFSDEDPLLPPAMGEHTVNESAIFHGWVLQKVSQFLQVLETDLYRGIGGHLDSLLGQCMYFGLSFSRVGADFRGQLAPVFQRVAISTFQKAIQETVEKFQEEMNSYMLISAPAILGTSNMPAAVPATQPGTLQPPMVLLDFPPLACFLNNILVAFNDLRLCCPVALAQDVTGALEDALAKVTKIILAFHRAEEAAFSSGEQELFVQFCTVFLEDLVPYLNRCLQVLFPPAQIAQTLGIPPTQLSKYGNLGHVNIGAIQEPLAFILPKRETLFTLDDQALGPELTAPAPEPPAEEPRLEPAGPACPEGGRAETQAEPPSVGP
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 239 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| COPI-mediated anterograde transport | Homo sapiens |
| Intra-Golgi traffic | Homo sapiens |
| Retrograde transport at the Trans-Golgi-Network | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050570 | congenital disorder of glycosylation type I | |
| DOID:0050571 | congenital disorder of glycosylation type II | |
| DOID:0050841 | focal hand dystonia | |
| DOID:0060249 | scoliosis | |
| DOID:0070260 | congenital disorder of glycosylation type IIh | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0080470 | developmental and epileptic encephalopathy 36 | |
| DOID:0080561 | congenital disorder of glycosylation Ii | |
| DOID:0111338 | isolated elevated serum creatine phosphokinase levels | |
| DOID:10534 | stomach cancer |
