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PARK3 Parkinson disease 3 (autosomal dominant, Lewy body) [ Homo sapiens (human) ]

Gene ID: 5072, updated on 2-Oct-2019

Summary

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Gene symbol
PARK3
Gene description
Parkinson disease 3 (autosomal dominant, Lewy body)
Primary source
MIM:602404
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
2p13

Bibliography

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Related articles in PubMed

  1. PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study. DeStefano AL, et al. Am J Hum Genet, 2002 May. PMID 11920285, Free PMC Article
  2. A susceptibility locus for Parkinson's disease maps to chromosome 2p13. Gasser T, et al. Nat Genet, 1998 Mar. PMID 9500549
  3. The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations. Sharma M, et al. J Med Genet, 2006 Jul. PMID 16443856, Free PMC Article

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study
    Title: PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study.
  2. a haplotype across the sepiapterin reductase (SPR) gene, which is located in the PARK3 linkage region, modulates age of onset of Parkinson's disease in sibships.
    Title: The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations.
Submit: New GeneRIF Correction

Phenotypes

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Parkinson disease 3 (autosomal dominant, Lewy body)

General gene information

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Markers

Other Names

  • Parkinson disease (autosomal dominant, Lewy body) 3
  • Parkinson disease, dominant Lewy-body, 3

Property

  • phenotype only

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