rs74315351, PARK7

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.050 GeneticVariation BEFREE A PD-associated mutant of DJ-1 (M26I) lacked activity. 27556455 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.050 GeneticVariation BEFREE Consequently, the peripheral cysteine mutants retained cytoprotective activity, whereas the PD-associated mutant [M26I]DJ-1 failed to suppress ASK1 activity and nuclear export of the death domain-associated protein Daxx and did not promote cytoprotection. 19293155 2009
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.050 GeneticVariation BEFREE Molecular dynamics calculations suggest that: (i) the structure of DJ-1 wild type (WT) in aqueous solution, in both oxidized and reduced forms, is similar to the crystal structure of the reduced form; (ii) the Parkinson disease-causing M26I variant is structurally similar to the WT, consistent with the experimental evidence showing the protein is a dimer as WT; (iii) R98Q is structurally similar to the WT, consistent with the fact that this is a physiological variant; and (iv) the L166P monomer rapidly evolves toward a conformation significantly different from WT, suggesting a change in its ability to oligomerize. 17504761 2007
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.050 GeneticVariation BEFREE Both homozygous (L166P, M26I, deletion) and heterozygous mutations (D149A, A104T) in the DJ-1 gene have been identified in Parkinson's disease (PD) patients. 15944198 2005
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.050 GeneticVariation BEFREE A homozygous M26I missense mutation was also recently reported in an Ashkenazi Jewish patient with early onset PD. 14713311 2003