Skip to main content
. 2022 Jun 20;14:885500. doi: 10.3389/fnagi.2022.885500

TABLE 1.

Mitochondrial dysfunction-related genes in Parkinson’s disease.

Mode Gene Protein name PARK locus Gene locus Age at onset
Autosomal dominant SNCA (Polymeropoulos et al., 1996) Alpha-synuclein PARK 1/4 4q21-23 Early or late
LRRK2 (Funayama et al., 2002) Leucine-rich repeat kinase 2 PARK 8 12p11.2-q13.1 Early or late
VPS35 (Paravicini et al., 1992) Vacuolar protein sorting 35 PARK 17 16q11.2 Late
CHCHD2 (Funayama et al., 2015) Coiled-helix-coiled-helix domain containing 2 PARK 22 7q11.2 Early
Autosomal recessive PRNK (Matsumine et al., 1997) Parkin PARK 2 6q25.2-27 Juvenile (>20 years)
Early (20–40 years)
PINK1 (Valente et al., 2001) PTEN-induced putative kinase 1 PARK 6 1p35-p36 Juvenile (>20 years)
Early (20–40 years)
DJ-1 (van Duijn et al., 2001) DJ-1 (parkinsonism associated deglycase) PARK 7 1p36 Early
ATP13A2 (Ramirez et al., 2006) ATPase 13A2 PARK 9 1p36 Early
PLA2G6 (Kinghorn et al., 2015) Calcium-independent phospholipase A2β (iPLA2β) PARK 14 22q13.1 Early (Juvenile dystonia-parkinsonism)
FBXO7 (Burchell et al., 2013) F-box domain of protein 7 PARK 15 22q12-13 Early