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COG6
Required for normal Golgi function. Belongs to the COG6 family. 3 alternatively spliced human isoforms have been reported. Note: This description may include information from UniProtKB.
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| Protein type: Vesicle |
| Chromosomal Location of human Ortholog: 13q14.11 |
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Cellular Component:
Golgi membrane; Golgi transport complex; trans-Golgi network membrane
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Molecular Function:
protein binding
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Biological Process:
glycosylation; Golgi organization; intra-Golgi vesicle-mediated transport; protein transport; retrograde transport, vesicle recycling within Golgi
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Disease: Congenital Disorder Of Glycosylation, Type Iil; Shaheen Syndrome
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Reference #:
Q9Y2V7
(UniProtKB)
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Alt. Names/Synonyms: CDG2L; COD2; COG complex subunit 6; COG6; complexed with Dor1p 2; Component of oligomeric Golgi complex 6; conserved oligomeric Golgi complex protein 6; Conserved oligomeric Golgi complex subunit 6; DKFZp313D191; KIAA1134; SHNS; testicular tissue protein Li 41
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Gene Symbols: COG6
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Molecular weight:
73,279 Da
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Basal Isoelectric point:
5.51
Predict pI for various phosphorylation states
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