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Overview of included studies for PARK-LRRK2:
Click here for summary of patients' characteristics
Click here for summary of in vitro effect of mutations on LRRK2 kinase pathway activity
Click here to show world map of all countries
Filter for
all included patients
index patients only
AAO < 50 (adjustable)
AAO >= 50 (adjustable)
females only
males only
homozygous only
heterozygous only
compound heterozygous only
homozygous and compound heterozygous
carrying
pathogenic variant
likely pathogenic variant
variant of uncertain significance
c.1004A>G
c.1132C>T
c.1163T>C
c.1240G>A
c.1256C>T
c.1310T>C
c.1312T>C
c.1375G>T
c.1382G>T
c.1421A>G
c.158A>G
c.1630A>G
c.1735A>G
c.1829T>C
c.1847A>G
c.1898C>T
c.1982C>T
c.2025A>G
c.2165G>A
c.2170A>G
c.2200G>A
c.2216A>G
c.2291G>A
c.2299C>T
c.2300G>A
c.2314C>T
c.2327C>T
c.2352C>A
c.2356A>T
c.2375G>A
c.2378G>T
c.2480C>T
c.2500+5delGTAA
c.2531T>A
c.2653A>T
c.2697A>C
c.2769G>C
c.2789A>G
c.2821G>T
c.2831A>T
c.2843G>A
c.2873C>T
c.28G>A
c.2915A>G
c.2917A>G
c.2918G>A
c.2942G>A
c.299T>C
c.3020G>C
c.3056A>G
c.3200G>A
c.3287C>G
c.3342A>G
c.3364A>G
c.3382C>A
c.3451G>A
c.3455G>T
c.3477T>G
c.3494T>C
c.3542C>A
c.3574A>G
c.3576T>G
c.3643G>A
c.3647A>G
c.3683G>C
c.3812C>T
c.3960G>T
c.3974G>A
c.4001G>A
c.4017T>G
c.4018G>A
c.4057C>A
c.4106T>C
c.4117G>A
c.4165G>A
c.4192C>T
c.4194T>G
c.4205A>G
c.4215T>A
c.4280A>G
c.4306T>C
c.4309A>C
c.4309A>G
c.4310A>G
c.4317+1G>C
c.4318G>C
c.4321C>A
c.4321C>G
c.4321C>T
c.4322G>A
c.4324G>C
c.4334C>G
c.4337C>T
c.4339G>A
c.4348G>A
c.4351G>A
c.4391C>G
c.4402A>G
c.4439C>T
c.4441G>A
c.4448G>A
c.4471_4473delACC
c.4474G>A
c.4501C>T
c.4536+3A>G
c.4559G>C
c.458T>G
c.4621G>A
c.4642A>G
c.4654C>T
c.4765G>T
c.4827+6T>A
c.4827+78T>C
c.4827+79T>C
c.4838T>C
c.4859A>G
c.4862A>G
c.4863C>A
c.4864C>A
c.4865C>T
c.4867A>G
c.4876A>G
c.4879T>A
c.4880C>T
c.4882C>T
c.4934A>C
c.4943A>G
c.4946A>C
c.5031G>C
c.5096A>G
c.5098T>C
c.5136A>T
c.5174G>A
c.518A>G
c.5255C>G
c.5266G>T
c.5267A>G
c.5273A>C
c.5281A>C
c.5318-29G>T
c.5321G>A
c.5385G>C
c.5385G>T
c.5417C>T
c.5467C>A
c.5605A>G
c.5606T>C
c.5620G>T
c.5659G>A
c.5672G>C
c.5740C>A
c.574T>G
c.577G>A
c.5822G>A
c.5882A>G
c.5949-28A>T
c.5971A>G
c.6016T>C
c.6028G>A
c.6035T>C
c.6055G>A
c.6058A>C
c.6059T>C
c.6059T>G
c.6091A>T
c.6187_6191delCTCTA
c.632C>T
c.6398A>G
c.6415T>A
c.6503G>T
c.6523G>C
c.6566A>G
c.6707A>G
c.6752A>C
c.6880G>A
c.689A>G
c.6922A>G
c.6929C>T
c.6938A>G
c.6967A>T
c.7006A>G
c.7049G>T
c.7067C>T
c.713A>T
c.7153G>A
c.7168G>A
c.7169T>C
c.7224G>A
c.7267A>T
c.7300A>G
c.7315C>A
c.7388T>C
c.7390+178A>G
c.7481C>T
c.749A>G
c.7570A>G
c.763G>A
c.774A>T
c.856C>G
c.872T>C
c.917C>T
c.922T>A
c.935C>T
c.958A>T
Country
Algeria
Argentina
Australia
Austria
Belarus
Belgium
Brazil
Canada
Chile
China
Colombia
Costa Rica
Cuba
Czech Republic
Denmark
Ecuador
Egypt
Estonia
Faroe Islands
Finland
France
Germany
Greece
Guatemala
Hungary
India
Iran
Ireland
Israel
Italy
Japan
Kazakhstan
Libya
Lithuania
Malaysia
Malta
Mexico
Mixed/Other
Morocco
Netherlands
Norway
Peru
Poland
Portugal
Puerto Rico
Russia
Serbia
Singapore
Slovakia
South Africa
South Korea
Spain
Sweden
Taiwan
Tunisia
Turkey
United Kingdom
United States
Uruguay
Zambia
Study
Study design
N cases
Ethnicities
Sex
(%
♂
)
Mean AAO (+/- SD)
Reported mutations
Fernández-Santiago, 2021
Case report/Case series
5
n.a.
40%
49(+/-10)
Gly2019Ser
: het
Sakuwa, 2021
Case report/Case series
1
n.a.
100%
n.a.
Gly2019Ser
: het
Torrealba-Acosta, 2021
Mutational screen
9
n.a.
n.a.
n.a.
His1621Gln
: het
His1621Arg
: het
c.4827+78T>C
: het
c.4827+79T>C
: het
c.5318-29G>T
: het
Lys1620Arg
: het
Lys1623Glu
: het
Pro1622Leu
: het
Pro1622Thr
: het
Show more (+6)
Abrahams, 2021
Other/Mixed
3
n.a.
33%
55(+/-11)
Gly2019Ser
: het
Arg1441Cys
: het
Isonaka, 2021
Associated study
5
n.a.
80%
51(+/-7)
Arg1441Gly
+
Gly2019Ser
: comp. het.
Gly2019Ser
: het
Ogata, 2021
Case report/Case series
1
n.a.
0%
67
Gly2294Arg
: het
Bright, 2021
Other/Mixed
7
n.a.
71%
n.a.
Gly2019Ser
: het
Gly2019Ser
: hom
Kaiyrzhanov, 2021
Mutational screen
12
n.a.
n.a.
43(+/-5)
Ala419Val
: het
Arg1334Gln
: het
Arg1441Cys
: het
Thr1271Ile
: het
Show more (+1)
Kanaya, 2021
Mutational screen
6
n.a.
n.a.
63(+/-13)
Ile2323Phe
: het
Leu1128Met
: het
Met724Val
: het
Asn238Ile
: het
Ser438Pro
: het
Ser973Gly
: het
Show more (+3)
Unknown, 2021
Mutational screen
1
n.a.
0%
n.a.
Gly2019Ser
: het
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