COG4

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Conserved oligomeric Golgi complex subunit 4 is a protein that in humans is encoded by the COG4 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesCOG4, CDG2J, COD1, component of oligomeric golgi complex 4, SWILS
Quick facts Available structures, PDB ...
COG4
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCOG4, CDG2J, COD1, component of oligomeric golgi complex 4, SWILS
External IDsOMIM: 606976; MGI: 2142808; HomoloGene: 7155; GeneCards: COG4; OMA:COG4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001195139
NM_015386
NM_001365426
NM_145818

NM_133973
NM_001310607

RefSeq (protein)

NP_001182068
NP_056201
NP_001352355

NP_001297536
NP_598734

Location (UCSC)Chr 16: 70.48 – 70.52 MbChr 8: 111.57 – 111.61 Mb
PubMed search[3][4]
Wikidata
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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 COG4 (Ungar et al., 2002).[supplied by OMIM][6]

Interactions

COG4 has been shown to interact with COG7,[7] COG2,[7] COG1[7] and COG5.[7]

Clinical

Mutations in this gene have been associated with Saul-Wilson syndrome.[8]

References

Further reading

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