Protein-coding gene in the species Homo sapiens
| COG7 |
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| Identifiers |
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| Aliases | COG7, CDG2E, component of oligomeric golgi complex 7 |
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| External IDs | OMIM: 606978 MGI: 2685013 HomoloGene: 33431 GeneCards: COG7 |
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| Gene location (Human) |
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 | | Chr. | Chromosome 16 (human)[1] |
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| | Band | 16p12.2 | Start | 23,388,493 bp[1] |
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| End | 23,453,189 bp[1] |
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| Gene location (Mouse) |
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 | | Chr. | Chromosome 7 (mouse)[2] |
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| | Band | 7|7 F2 | Start | 121,478,586 bp[2] |
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| End | 121,580,934 bp[2] |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - right uterine tube
- anterior pituitary
- canal of the cervix
- right lobe of thyroid gland
- left lobe of thyroid gland
- bronchial epithelial cell
- trachea
- minor salivary glands
- body of stomach
- skin of abdomen
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| | Top expressed in | - otolith organ
- utricle
- supraoptic nucleus
- retinal pigment epithelium
- arcuate nucleus
- paraventricular nucleus of hypothalamus
- median eminence
- seminal vesicula
- sciatic nerve
- medial vestibular nucleus
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| | More reference expression data |
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| BioGPS |  | | More reference expression data |
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| Gene ontology |
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| Molecular function | | | Cellular component | - nucleolus
- membrane
- Golgi apparatus
- Golgi transport complex
- trans-Golgi network membrane
- Golgi membrane
| | Biological process | - protein localization to organelle
- protein glycosylation
- endoplasmic reticulum to Golgi vesicle-mediated transport
- protein transport
- protein stabilization
- intracellular protein transport
- retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum
- Golgi organization
- protein localization to Golgi apparatus
| | Sources:Amigo / QuickGO |
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| Orthologs |
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| Species | Human | Mouse |
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| Entrez | | |
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| Ensembl | | |
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| UniProt | | |
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| RefSeq (mRNA) | | |
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| RefSeq (protein) | | |
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| Location (UCSC) | Chr 16: 23.39 – 23.45 Mb | Chr 7: 121.48 – 121.58 Mb |
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| PubMed search | [3] | [4] |
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| Wikidata |
| View/Edit Human | View/Edit Mouse |
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Conserved oligomeric Golgi complex subunit 7 is a protein that in humans is encoded by the COG7 gene.[5][6]
Multiprotein complexes are key determinants of Golgi apparatus structure and its capacity for intracellular transport and glycoprotein modification. Several complexes have been identified, including the Golgi transport complex (GTC), the LDLC complex, which is involved in glycosylation reactions, and the SEC34 complex, which is involved in vesicular transport. These 3 complexes are identical and have been termed the conserved oligomeric Golgi (COG) complex, which includes COG7 (Ungar et al., 2002).[supplied by OMIM][6]
Interactions
COG7 has been shown to interact with COG4[7] and COG5.[7]
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000168434 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000034951 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Ungar D, Oka T, Brittle EE, Vasile E, Lupashin VV, Chatterton JE, Heuser JE, Krieger M, Waters MG (Apr 2002). "Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function". J Cell Biol. 157 (3): 405–15. doi:10.1083/jcb.200202016. PMC 2173297. PMID 11980916.
- ^ a b "Entrez Gene: COG7 component of oligomeric golgi complex 7".
- ^ a b Loh, Eva; Hong Wanjin (Jun 2004). "The binary interacting network of the conserved oligomeric Golgi tethering complex". J. Biol. Chem. 279 (23): 24640–8. doi:10.1074/jbc.M400662200. ISSN 0021-9258. PMID 15047703.
Further reading
- Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction". Anal. Biochem. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474.
- Yu W, Andersson B, Worley KC, et al. (1997). "Large-scale concatenation cDNA sequencing". Genome Res. 7 (4): 353–8. doi:10.1101/gr.7.4.353. PMC 139146. PMID 9110174.
- Loh E, Hong W (2002). "Sec34 is implicated in traffic from the endoplasmic reticulum to the Golgi and exists in a complex with GTC-90 and ldlBp". J. Biol. Chem. 277 (24): 21955–61. doi:10.1074/jbc.M202326200. PMID 11929878.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Loh E, Hong W (2004). "The binary interacting network of the conserved oligomeric Golgi tethering complex". J. Biol. Chem. 279 (23): 24640–8. doi:10.1074/jbc.M400662200. PMID 15047703.
- Wu X, Steet RA, Bohorov O, et al. (2004). "Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder". Nat. Med. 10 (5): 518–23. doi:10.1038/nm1041. PMID 15107842. S2CID 29322859.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Oka T, Vasile E, Penman M, et al. (2005). "Genetic analysis of the subunit organization and function of the conserved oligomeric golgi (COG) complex: studies of COG5- and COG7-deficient mammalian cells". J. Biol. Chem. 280 (38): 32736–45. doi:10.1074/jbc.M505558200. PMID 16051600.
- Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.
- Steet R, Kornfeld S (2006). "COG-7-deficient Human Fibroblasts Exhibit Altered Recycling of Golgi Proteins". Mol. Biol. Cell. 17 (5): 2312–21. doi:10.1091/mbc.E05-08-0822. PMC 1446086. PMID 16510524.
- Morava E, Zeevaert R, Korsch E, et al. (2007). "A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia". Eur. J. Hum. Genet. 15 (6): 638–45. doi:10.1038/sj.ejhg.5201813. PMID 17356545.
External links
- GeneReviews/NCBI/NIH/UW entry on Congenital Disorders of Glycosylation Overview
- Human COG7 genome location and COG7 gene details page in the UCSC Genome Browser.
