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Gene overview of all published PD-association studies for ATP13A2
Gene:
ATP13A2
(KRPPD; PARK9; HSA9947; FLJ26510)
Protein:
ATPase type 13A2
(putative ATPase; OTTHUMP00000002399)
Chromosome:
1
(View:
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
X
Y
MT
)
Status:
Updated 22 June 2010
1. Case-Control Studies (by ethnic group)
PD Cases
Normal Controls
Study
Population
Source
# Polys
# Subjects
(% women)
DX
Onset Age
(range)
Age
(range)
# Subjects
(% women)
Age
(range)
Result
Comment
Caucasian
Fung, 2006
Overlaps with
Simon-Sanchez, 2009 (USA)
CL
5
(detail)
267
(-)
C
-
-
270
(-)
68
(55-88)
Negative
Submit comment
Pankratz, 2008
USA (PROGENI, GenePD)
CL
4
(detail)
857
(41%)
C
61.9 + 10.8
(-)
-
867
(60%)
54.8 + 13.1
(-)
Negative
Submit comment
Rakovic, 2009
Germany
CL
2
(detail)
220
(30%)
C
60.1 + 9
(41-85)
-
232
(55%)
69.6 + 11.7
(41-99)
Negative
Submit comment
Rakovic, 2009
Germany, Serbia
CL
2
(detail)
161
(22%)
C
51.7 + 10.3
(40-80)
-
150
(35%)
53.9 + 10.8
(40-90)
Negative
Submit comment
Simon-Sanchez, 2009
USA, Germany (GWAS)
CL,PO
3
(detail)
1745
(45%)
C
55.8
(7-98)
-
4047
(50%)
-
Negative
Sutherland, 2009
Australia
CL
3
(detail)
331
(51%)
C
60.1 + 10.6
(-)
70.3 + 8.7
(-)
296
(51%)
70.5 + 8.9
(-)
Negative
Submit comment
Other/Mixed
Vilarino-Guell, 2008
Tunisia
CL
23
(detail)
240
(53%)
C
-
64 + 11
(25-85)
372
(50%)
56 + 11
(29-90)
Negative
Submit comment
Contact us
if you are an author of an association study regarding this gene and do not find your study in this table or find errors in the representation of your study details.
Source:
Source of case population -> “CL” (clinic-based), “PO” (population-based), or “CO” (community-based).
# Polys:
Number of polymorphisms tested per gene and per sample.
Onset Age and Age:
Mean or median age at onset or examination, respectively.
DX:
Criteria used to determine PD diagnosis -> "C" (clinical PD diagnosis), "N" (neuropathological PD diagnosis), "M" (mixed, i.e. PD sample contains both clinical and neuropathological cases), "U" (unknown).
Result:
Overall conclusion reached by authors of the original publication (“positive” usually indicates significant (P<0.05) association in at least one of the performed analyses, and “negative” indicates no evidence for significant association, while “trend” indicates results in between).
(-)
: Either no data provided or in case of overlap, data included in original study.
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PDGene Top Results
*New*
Top Results Details
1.
SNCA
2.
MAPT/STH
3.
NUCKS1
4.
PM20D1
5.
SLC41A1
6.
BST1
7.
LRRK2
8.
USP24
9.
SLC6A3
10.
GBA
[see more]
[close]
11.
SLC45A3
12.
SOD2
13.
MTHFR
14.
BDNF
15.
PDXK
16.
GWA_7p14.2
17.
DRD3
18.
APOE
19.
UCHL1
20.
GWA_2q36.3
21.
GSTM1
22.
PINK1
23.
FGF20
24.
CYP2D6
25.
PARK2
26.
GLIS1
27.
HLA-DRA
28.
MAOB
29.
CALB1
30.
FARP1
31.
LRP8
32.
DRD2
PDGene Stats
Studies: 764
Genes: 547
Polymorphisms: 2407
Meta-analyses: 224
GEO-PD Meeting 2010
PDmutDB
Curated by the VIB Department of Molecular Genetics of the University of Antwerp
Parkinson's disease Mutation Database
Curated by Parkinson's Institute from Leiden University Medical Center
Mutation Database for Parkinson's Disease
Curated by the Institute for Infocomm Research in Singapore
The PDGene database
is supported by a grant from
The Michael J. Fox Foundation
in partnership with the
Alzheimer Research Forum
.
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An up-to-date collection of all published genetic association studies.
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