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PARK7, Parkinsonism associated deglycase

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PARK7, Parkinsonism associated deglycase

  • The product of this gene belongs to the peptidase C56 family of proteins. It acts as a positive regulator of androgen receptor-dependent transcription. It may also function as a redox-sensitive chaperone, as a sensor for oxidative stress, and it apparently protects neurons against oxidative stress and cell death. Defects in this gene are the cause of autosomal recessive early-onset Parkinson disease 7. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (Parkinson disease protein 7, Parkinson disease (autosomal recessive, early onset) 7, epididymis secretory sperm binding protein Li 67p, maillard deglycase, oncogene DJ1, parkinson protein 7, protein DJ-1, protein deglycase DJ-1, protein/nucleic acid deglycase DJ-1, DJ-1, DJ1, GATD2, HEL-S-67p,)
  • NCBI Gene ID: 11315
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q99497
    UNIPROT ID#>>V9HWC2
  • 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.

Parkinsonism associated deglycase 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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