Protein Name parkin RBR E3 ubiquitin protein ligase
Organism Homo sapiens
Gene ID 5071
Gene Symbol

PRKN

UniProt O60260 (PRKN_HUMAN), X5DR79 (X5DR79_HUMAN)
Relationships Total Number of functionally related compound(s) : 92
Total Number of Articles : 116
Description

parkin RBR E3 ubiquitin protein ligase

Gene Summary

The precise function of this gene is unknown; however, the encoded protein is a component of a multiprotein E3 ubiquitin ligase complex that mediates the targeting of substrate proteins for proteasomal degradation. Mutations in this gene are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease. Alternative splicing of this gene produces multiple transcript variants encoding distinct isoforms. Additional splice variants of this gene have been described but currently lack transcript support. [provided by RefSeq, Jul 2008]

synonyms
  • E3 ubiquitin-protein ligase parkin
  • Parkinson disease (autosomal recessive, juvenile) 2, parkin
  • parkinson juvenile disease protein 2
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Properties