Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Clinical features of LRRK2-associated Parkinson's disease in central Norway. 15852371

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT G2019S LRRK2 mutation in French and North African families with Parkinson's disease. 16240353

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT LRRK2 mutations in Parkinson disease. 16157908

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Lrrk2 pathogenic substitutions in Parkinson's disease. 16172858

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity. 16269541

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. 15732108

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT LRRK2 mutations and Parkinsonism. 15811454

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data. 16272164

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor. 16272257

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Analysis of LRRK2 functional domains in nondominant Parkinson disease. 16247070

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations. 16157909

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT LRRK2 gene in Parkinson disease: mutation analysis and case control association study. 16157901

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD. 16102999

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation. 15929036

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. 15726496

2005
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. 15541309

2004
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0.930 GeneticVariation UNIPROT Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. 15541308

2004