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PPARD, peroxisome proliferator activated receptor delta

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PPARD, peroxisome proliferator activated receptor delta

  • This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) family. The encoded protein is thought to function as an integrator of transcriptional repression and nuclear receptor signaling. It may inhibit the ligand-induced transcriptional activity of peroxisome proliferator activated receptors alpha and gamma, though evidence for this effect is inconsistent. Expression of this gene in colorectal cancer cells may be variable but is typically relatively low. Knockout studies in mice suggested a role for this protein in myelination of the corpus callosum, lipid metabolism, differentiation, and epidermal cell proliferation. Alternative splicing results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Aug 2017]

  • Gene Synonyms (peroxisome proliferator-activated receptor delta, PPAR-beta, PPAR-delta, PPARD/MYO1D fusion, nuclear hormone receptor 1, nuclear receptor subfamily 1 group C member 2, peroxisome proliferator-activated receptor beta, FAAR, NR1C2, NUC1, NUCI, NUCII, PPARB,)
  • NCBI Gene ID: 5467
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A024RCW6
    UNIPROT ID#>>F1D8S7
    UNIPROT ID#>>Q03181
  • 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.

peroxisome proliferator activated receptor delta 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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