Gene |
Chromosome |
Location |
Syndrome |
ADH1C | 4 | q23 | Parkinson disease susceptability |
ATP13A2 | 1 | p36.13 | Parkinson disease type 9 |
ATXN2 | 12 | q24.12 | Parkinson disease susceptability |
ATXN8OS | 13 | q21.33 | Parkinson disease susceptability |
CHCHD2 | 7 | p11.2 | Parkinson disease autosomal dominant |
DNAJC6 | 1 | p31.3 | Parkinson disease early onset |
EIF4G1 | 3 | q27.1 | Parkinson disease 18 |
FBXO7 | 22 | q12.3 | Parkinson disease autosomal recessive |
GBA | 1 | q22 | Parkinson disease - other |
GIGYF2 | 2 | q37.1 | Parkinson disease type 11 |
GLUD2 | 23 | q24 | Parkinson disease susceptability |
HTRA2 | 2 | p13.1 | Parkinson disease 13 |
LRRK2 | 12 | q12 | Parkinson disease - other |
MAPT | 17 | q21.31 | Parkinson-dementia syndrome |
PARK10 | 1 | p32 | Parkinson disease age at onset |
PARK12 | 23/td> | q21-25 | Parkinson disease x-linked |
PARK3 | 2 | p13 | Parkinson disease autosomal dominant |
PARK7 | 1 | p36.23 | Parkinson disease - other |
PINK1 | 1 | p36.12 | Parkinson disease - other |
PRKN | 6 | q26 | Parkinson disease - other |
PLA2G6 | 22 | q13.1 | Parkinson disease autosomal recessive |
SLC6A3 | 5 | p15.33 | Infantile Parkinsonism dystonia |
SNCA | 4 | q22.1 | Parkinson disease - other |
SYNJ1 | 21 | q22.11 | Parkinson disease early onset |
TBP | 6 | q27 | Parkinson disease susceptability |
UCHL1 | 4 | p13 | Parkinson disease - other |
VPS13C | 15 | q22.2 | Parkinson disease autosomal recessive |
VPS35 | 16 | q11.2 | Parkinson disease type 17 |