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. Author manuscript; available in PMC: 2019 Apr 23.
Published in final edited form as: Prog Neurobiol. 2015 Jun 11;131:21–64. doi: 10.1016/j.pneurobio.2015.05.002

Table 5.

Epigenetic dysregulation in Parkinson’s disease: DNA (de)methylation.

Gene Regulation Epigenetic modification Observed in Sample size Approach Methods Reference

SNCA Methylation sPD patients (SN,
Putamen, Cortex)
6, 14 Targeted
(1 locus)
BS Jowaed et al., 2010
11 Targeted
(1 locus)
BS Matsumoto et al., 2010
PARK16 Methylation PD patients 12.386 Genome-wide methQTL Plagnol et al., 2011
GPNMB Methylation PD patients
STX1B Methylation PD patients
FANCC Methylation PD patients 30 Genome-wide Infinium Moore et al., 2014
TNKS2

indicates decreased expression levels and

indicates altered expression, not further specified.

Abbreviations: FANCC, fanconi anemia group C; GPNMB, glycoprotein (transmembrane) nmb; PARK16, Parkinson disease 16; (s)PD, (sporadic) Parkinson’s disease; SN, substantia nigra; SNCA, synuclein alpha; sPD, sporadic PD; STX1B, syntaxin 1B; TNKS2, tankyrase 2; BS, bisulfite sequencing; GWA: genome-wide association; methQTL, methylation quantitative trait locusc.