Gene: ATP13A2 ×
Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2 		0.600 Biomarker disease GENOMICS_ENGLAND Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78). 28137957 2017
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2 		0.600 Biomarker disease CTD_human Correlation between the biochemical pathways altered by mutated parkinson-related genes and chronic exposure to manganese. 25149416 2014
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2 		0.600 Biomarker disease CTD_human Down-regulation of LRRK2 in control and DAT transfected HEK cells increases manganese-induced oxidative stress and cell toxicity. 23628791 2013
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2 		0.600 Biomarker disease GENOMICS_ENGLAND Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. 21060012 2010