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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 membrane |
| nucleolus |
| Golgi apparatus |
| intracellular membrane-bounded organelle |
| Golgi transport complex |
| 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:0060717 | autosomal recessive congenital ichthyosis 8 | |
| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | |
| DOID:0060719 | autosomal recessive congenital ichthyosis 10 | |
| DOID:0070257 | congenital disorder of glycosylation type IIe | |
| DOID:0080326 | familial hypertrophic cardiomyopathy | |
| DOID:0111338 | isolated elevated serum creatine phosphokinase levels | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:10907 | microcephaly | |
| DOID:11111 | hydronephrosis | |
| DOID:11577 | Cauda equina syndrome |
