Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.300 Biomarker group BEFREE Leucine rich repeat kinase 2 (LRRK2) is a key molecule in the pathogenesis of many neurodegenerative disorders. 29408508 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.300 GeneticVariation group BEFREE Several mutations in leucine rich repeat kinase 2 (LRRK2) gene have been associated with pathogenesis of Parkinson's disease (PD), a neurodegenerative disorder marked by resting tremors, and rigidity, leading to Postural instability. 29482628 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.300 GeneticVariation group BEFREE Interestingly, Rab10 is a key substrate of leucine-rich repeat kinase 2 (LRRK2), a serine/threonine protein kinase genetically associated with the second most common neurodegenerative disease Parkinson's disease. 29562525 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.300 Biomarker group BEFREE The aim of this study was to identify new potentially active compounds for three protein targets, tropomyosin receptor kinase A (TrkA), <i>N</i>-methyl-d-aspartate (NMDA) receptor, and leucine-rich repeat kinase 2 (LRRK2), that are related to various neurodegenerative diseases such as Alzheimer's, Parkinson's, and neuropathic pain. 30044400 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.300 GeneticVariation group BEFREE We believe that these findings provide important supplementary information about the regulatory mechanisms by which both variants influence PILRB and LRRK2 gene expression and neurodegenerative disease risk. 30619483 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.300 Biomarker group BEFREE Collectively, these results suggest that LRRK2 could be a potential molecular target for developing therapeutics to treat Mn-related neurodegenerative disorders. 30645642 2019
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.300 GeneticVariation group BEFREE Mechanisms involving deregulated processing of proteins such as amyloid beta (Aβ) oligomerization; tau hyperphosphorylation, prion misfolding; α-synuclein accumulation/lewy body formation, chaperone deregulation, acetylcholine depletion, adenosine 2A (A2A) receptor hyperactivation, secretase deregulation, leucine-rich repeat kinase 2 (LRRK2) mutation and mitochondrial proteinopathies have deeper implications in neurodegenerative disorders. 31584139 2020