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. 2011 Jun 23;4:81–92. doi: 10.2147/TACG.S7333

Table 3.

Summary of monogenic forms of Parkinson’s disease (PD)

Name Disease Inheritance Chromosome Protein Function
PARK1 Familial PD Autosomal dominant 4q21-q22 α-synuclein Synaptic protein
PARK2 Young-onset PD Autosomal recessive 6q25.2-q27 Parkin Ubiquitin-protein ligase
PARK4 Familial PD Autosomal dominant 4q region α-synuclein duplication or triplications Synaptic protein
PARK5 Familial PD Autosomal recessive 4p15 Ubiquitin carboxy-terminal hydrolase Hydrolase of ubiquitin
PARK6 Young-onset PD Autosomal recessive 1p35-p36 PINK-1 Mitochondrial anti-stress-induced degeneration
PARK7 Young-onset PD Autosomal recessive 1p36 DJ-1 Sumolyation pathway
PARK8 Familial PD Autosomal dominant 12p11.2-q13.1 LRRK2 Protein phosphorylation
GBA Familial PD Autosomal dominant 1q21 Gluco-cerebrosidase Membrane lipid