Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Conserved oligomeric Golgi complex subunit 7
Summary
- UniProt ID
- P83436
- Gene Symbol
-
- COG7
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Congenital disorder of glycosylation
- Golgi apparatus
- Membrane
- Protein transport
- Reference proteome
- Gene Ontology (GO)
| GO Term |
|---|
| Golgi transport complex |
| Golgi membrane |
| nucleolus |
| Golgi apparatus |
| intracellular membrane-bounded organelle |
| trans-Golgi network membrane |
Sequence
MDFSKFLADDFDVKEWINAAFRAGSKEAASGKADGHAATLVMKLQLFIQEVNHAVEETSHQALQNMPKVLRDVEALKQEASFLKEQMILVKEDIKKFEQDTSQSMQVLVEIDQVKSRMQLAAESLQEADKWSTLSADIEETFKTQDIAVISAKLTGMQNSLMMLVDTPDYSEKCVHLEALKNRLEALASPQIVAAFTSQAVDQSKVFVKVFTEIDRMPQLLAYYYKCHKVQLLAAWQELCQSDLSLDRQLTGLYDALLGAWHTQIQWATQVFQKPHEVVMVLLIQTLGALMPSLPSCLSNGVERAGPEQELTRLLEFYDATAHFAKGLEMALLPHLHEHNLVKVTELVDAVYDPYKPYQLKYGDMEESNLLIQMSAVPLEHGEVIDCVQELSHSVNKLFGLASAAVDRCVRFTNGLGTCGLLSALKSLFAKYVSDFTSTLQSIRKKCKLDHIPPNSLFQEDWTAFQNSIRIIATCGELLRHCGDFEQQLANRILSTAGKYLSDSCSPRSLAGFQESILTDKKNSAKNPWQEYNYLQKDNPAEYASLMEILYTLKEKGSSNHNLLAAPRAALTRLNQQAHQLAFDSVFLRIKQQLLLISKMDSWNTAGIGETLTDELPAFSLTPLEYISNIGQYIMSLPLNLEPFVTQEDSALELALHAGKLPFPPEQGDELPELDNMADNWLGSIARATMQTYCDAILQIPELSPHSAKQLATDIDYLINVMDALGLQPSRTLQHIVTLLKTRPEDYRQVSKGLPRRLATTVATMRSVNY
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 516 |
|
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:0050571 | congenital disorder of glycosylation type II | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0060655 | autosomal recessive congenital ichthyosis | |
| DOID:0060656 | autosomal recessive congenital ichthyosis 1 | |
| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | |
| DOID:0060711 | autosomal recessive congenital ichthyosis 3 | |
| DOID:0060712 | autosomal recessive congenital ichthyosis 4A | |
| DOID:0060714 | autosomal recessive congenital ichthyosis 5 | |
| DOID:0060715 | autosomal recessive congenital ichthyosis 6 | |
| DOID:0060716 | autosomal recessive congenital ichthyosis 7 |
