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Conserved oligomeric Golgi complex subunit 6
Summary
- UniProt ID
- Q9Y2V7
- Gene Symbol
-
- COG6
- KIAA1134
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Congenital disorder of glycosylation
- Disease variant
- Golgi apparatus
- Intellectual disability
- 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 |
Sequence
MAEGSGEVVAVSATGAANGLNNGAGGTSATTCNPLSRKLHKILETRLDNDKEMLEALKALSTFFVENSLRTRRNLRGDIERKSLAINEEFVSIFKEVKEELESISEDVQAMSNCCQDMTSRLQAAKEQTQDLIVKTTKLQSESQKLEIRAQVADAFLSKFQLTSDEMSLLRGTREGPITEDFFKALGRVKQIHNDVKVLLRTNQQTAGLEIMEQMALLQETAYERLYRWAQSECRTLTQESCDVSPVLTQAMEALQDRPVLYKYTLDEFGTARRSTVVRGFIDALTRGGPGGTPRPIEMHSHDPLRYVGDMLAWLHQATASEKEHLEALLKHVTTQGVEENIQEVVGHITEGVCRPLKVRIEQVIVAEPGAVLLYKISNLLKFYHHTISGIVGNSATALLTTIEEMHLLSKKIFFNSLSLHASKLMDKVELPPPDLGPSSALNQTLMLLREVLASHDSSVVPLDARQADFVQVLSCVLDPLLQMCTVSASNLGTADMATFMVNSLYMMKTTLALFEFTDRRLEMLQFQIEAHLDTLINEQASYVLTRVGLSYIYNTVQQHKPEQGSLANMPNLDSVTLKAAMVQFDRYLSAPDNLLIPQLNFLLSATVKEQIVKQSTELVCRAYGEVYAAVMNPINEYKDPENILHRSPQQVQTLLS
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 168 |
|
|||
| 173 |
|
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 |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:3393 | coronary artery disease | |
| DOID:3891 | placental insufficiency | |
| DOID:4386 | myofibroma | |
| DOID:4398 | pustulosis of palm and sole | |
| DOID:5212 | congenital disorder of glycosylation | |
| DOID:5295 | intestinal disease | |
| DOID:612 | primary immunodeficiency disease | |
| DOID:676 | juvenile rheumatoid arthritis | |
| DOID:693 | dental enamel hypoplasia | |
| DOID:7148 | rheumatoid arthritis |
