Protein Name: Conserved oligomeric Golgi complex subunit 7
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UniprotKB/SwissProt ID: COG7_HUMAN (P83436)
Gene Name: COG7
Organism: Homo sapiens (Human).
Function: Required for normal Golgi function (By similarity).
Other Modifications: View all modification sites in dbPTM
Protein Subcellular Localization: Golgi apparatus membrane; Peripheral membrane protein.
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Protein disease:
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| Disease database |
Database Entry |
Disease information | | KEGG | H00119 | Congenital disorders of glycosylation (CDG) type II | | OMIM | 606978 | COMPONENT OF OLIGOMERIC GOLGI COMPLEX 7; COG7 | | OMIM | 608779 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E ;;CDG IIe; CDGIIe | | HPRD | 07373 | Congenital disorder of glycosylation, type IIe |
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Graphical Visualization of S-nitrosylation Sites:
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| Overview of Protein S-nitrosylation Sites with Functional and Structural Information |  |
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