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APOO, apolipoprotein O

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APOO, apolipoprotein O

  • This gene is a member of the apolipoprotein family. Members of this protein family are involved in the transport and metabolism of lipids. The encoded protein associates with HDL, LDL and VLDL lipoproteins and is characterized by chondroitin-sulfate glycosylation. This protein may be involved in preventing lipid accumulation in the myocardium in obese and diabetic patients. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 4, 5, 12 and 16.[provided by RefSeq, Sep 2009]

  • Gene Synonyms (MICOS complex subunit MIC26, MICOS complex subunit MIC23, brain my025, family with sequence similarity 121B, mitochondrial contact site and cristae organizing system subunit 26, FAM121B, MIC26, MICOS26, Mic23, My025,)
  • NCBI Gene ID: 79135
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9BUR5
  • 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.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

apolipoprotein O interacts with:

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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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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