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COG4, component of oligomeric golgi complex 4

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COG4, component of oligomeric golgi complex 4

  • The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2010]

  • Gene Synonyms (conserved oligomeric Golgi complex subunit 4, COG complex subunit 4, complexed with Dor1p, conserved oligomeric Golgi complex protein 4, CDG2J, COD1, SWILS,)
  • NCBI Gene ID: 25839
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9H9E3
    UNIPROT ID#>>A0A0A0MS45
    UNIPROT ID#>>J3KNI1
    UNIPROT ID#>>Q8N8L9
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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