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COG5

COG5

Protein-coding gene in the species Homo sapiens

oligomeric Golgi complex subunit 5 is a protein that in humans is encoded by the COG5 gene. Multiprotein complexes are key determinants of Golgi apparatus structure

COG5

Conserved oligomeric Golgi complex

complex contains subunits Cog1-Cog4 and the second lobe contains subunits Cog5-Cog8 . The lobes are connected by thin, rod-like complexes . The two lobes

Conserved oligomeric Golgi complex

Conserved_oligomeric_Golgi_complex

Intracellular transport

Directed movement of vesicles and substances within a cell

MCOLN2 KIF6, KIF5A, involved in intracellular organelle transport COG2, COG4, COG5, COG7 Sterol carrier protein Barlan K, Gelfand VI (May 2017). "Microtubule-Based

Intracellular transport

Intracellular_transport

Congenital disorder of glycosylation

Medical condition

(COG1-CDG) 611209 COG1 17q25.1 IIh (COG8-CDG) 611182 COG8 16q22.1 IIi (COG5-CDG) 613612 COG5 7q31 IIj (COG4-CDG) 613489 COG4 16q22.1 IIL (COG6-CDG) n/a COG6

Congenital disorder of glycosylation

Congenital_disorder_of_glycosylation

Coventry Corporation Transport

Operator of trams and buses in Coventry, Warwickshire

vehicles have been saved from the scrapyard. EVC 244 is single deck Daimler COG5, new in 1940, with 38 seat body by Park Royal. It passed to Derby Corporation

Coventry Corporation Transport

Coventry_Corporation_Transport

COG7

Protein-coding gene in the species Homo sapiens

2002).[supplied by OMIM] COG7 has been shown to interact with COG4 and COG5. GRCh38: Ensembl release 89: ENSG00000168434 – Ensembl, May 2017 GRCm38:

COG7

List of human protein-coding genes 2

HGNC:6546; Q14746 3325 COG3 HGNC:18619; Q96JB2 3326 COG4 HGNC:18620; Q9H9E3 3327 COG5 HGNC:14857; Q9UP83 3328 COG6 HGNC:18621; Q9Y2V7 3329 COG7 HGNC:18622; P83436

List of human protein-coding genes 2

List_of_human_protein-coding_genes_2

COG4

Protein-coding gene in the species Homo sapiens

[supplied by OMIM] COG4 has been shown to interact with COG7, COG2, COG1 and COG5. Mutations in this gene have been associated with Saul-Wilson syndrome. GRCh38:

COG4