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Overview of included studies for PxMD-CACNA1A:
Click here for summary of patients' characteristics
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
definitely pathogenic mutations
probably pathogenic mutations
possibly pathogenic mutations
c.(3092+1_3093-1)_(5634+1_5635-1)del
c.(4253+1_4254-1)_(4391+1_4392-1)del
c.(4962+1_4963-1)_(871_?)del
c.(539+1_540-1)_(1604_?)del
c.(539+1_540-1)_(631+1_632-1)del
c.(5634+1_5635-1)_(1604_?)del
c.(5734+1_5735-1)_(5943+1_5944-1)del
c.(784+1_785-1)_(978+1_979-1)del
c.1063dupG
c.1088T>C
c.1213G>A
c.1360G>A
c.1363C>T
c.1364G>A
c.1502C>T
c.1597G>A
c.1618G>A
c.165dupA
c.1741G>C
c.1747C>T
c.1748G>A
c.1799_1800delTC
c.1849C>G
c.1872_1875delCATT
c.1913G>A
c.1997C>T
c.2003A>C
c.2042_2043delAG
c.2134A>G
c.2137G>A
c.2206C>T
c.2393T>C
c.2407C>A
c.2464dupC
c.2691dupC
c.2736G>C
c.2816delG
c.2816dupG
c.2852_2861delGCGCGGACGG
c.3092+2T>C
c.3207_3208insG
c.3396_3404dupATCCAATCC
c.3414dupC
c.3460C>T
c.3492delC
c.3695 + 1G>A
c.3695+1G>A
c.37G>A
c.3832C>T
c.3846C>G
c.3992+1G>A
c.4009A>T
c.4013T>C
c.4025T>C
c.4036C>T
c.4037G>A
c.4046G>A
c.4048G>T
c.4055G>A
c.4075C>T
c.4101T>G
c.4106G>A
c.4107T>A
c.410A>G
c.4118C>T
c.4151A>G
c.4160A>G
c.4173delC
c.4186G>A
c.4249_4253+2delTGTCGGT
c.4301G>A
c.4306T>A
c.4344G>A
c.4392-1G>C
c.4503_4505delCTT
c.4517T>C
c.4601G>C
c.4681C>T
c.4759-1545_4869+2385del
c.4845delG
c.4982G>A
c.4990C>T
c.4991G>A
c.4999C>T
c.5018G>C
c.5020C>T
c.504delC
c.5126T>C
c.5137-10_2delAATTCCACA
c.5251C>T
c.5267A>G
c.5315A>G
c.5396C>T
c.5455C>T
c.5532-2A>G
c.5605T>C
c.5629-1151_5943+452del
c.5629-2A>G
c.5776G>T
c.5838C>G
c.5871C>A
c.6053+4delAGTG
c.6269G>A
c.653C>T
c.6657_6659dupCCA
c.6975_6976insCAG
c.743A>G
c.757C>T
c.766T>C
c.785-2645_978+14740del
c.815G>A
c.835C>T
c.877G>A
c.889G>A
c.904G>A
c.978+1G>A
c.979-1G>A
c.979-2453_1348+3157del
Country
Australia
Austria
China
Estonia
Finland
France
Italy
Japan
Morocco
Netherlands
Portugal
Slovakia
South Korea
Spain
Sweden
Switzerland
United Kingdom
United States
Study
Study design
N cases
Ethnicities
Sex
(%
♂
)
Mean AAO (+/- SD)
Reported mutations
Mantuano, 2010
Mutational screen
12
C
60%
12(+/-9)
p.Ala56Serfs*20
: n.a.
p.Trp169Glyfs*10
: n.a.
c.979-1G>A
: n.a.
p.Thr501Met
: n.a.
p.Gln681Argfs*100
: n.a.
p.Met798Thr
: n.a.
p.Arg822Profs*246
: n.a.
p.Ala952Serfs*115
: n.a.
c.3695+1G>A
: n.a.
p.Arg1664*
: n.a.
p.Cys1869Arg
: n.a.
p.Glu1926*
: n.a.
Show more (+9)
Blumkin, 2010
Case report/Case series
1
n.a.
100%
0
p.Arg1349Gln
: het
Zangaladze, 2010
Case report/Case series
1
n.a.
0%
n.a.
p.Ser218Leu
: het
Riant, 2010
Mutational screen
5
n.a.
80%
19(+/-21)
c.5629-1151_5943+452del
: het
c.979-2453_1348+3157del
: het
c.4759-1545_4869+2385del
: het
c.785-2645_978+14740del
: het
Show more (+1)
Cleves, 2010
Family study
1
n.a.
100%
14
p.Arg583Gln
: het
Bertholon, 2009
Other/Mixed
5
n.a.
60%
9(+/-9)
p.Gly939Alafs*131
: het
p.Gln1154*
: het
p.Arg1751Trp
: het
Labrum, 2009
Mutational screen
7
n.a.
17%
11(+/-14)
c.(539+1_540-1)_(631+1_632-1)del
: het
c.(784+1_785-1)_(978+1_979-1)del
: het
c.(4253+1_4254-1)_(4391+1_4392-1)del
: het
c.(3092+1_3093-1)_(5634+1_5635-1)del
: het
c.(5634+1_5635-1)_(*1604_?)del
: het
Show more (+2)
Stam, 2009
Mutational screen
1
n.a.
0%
n.a.
p.Ser218Leu
: het
Robbins, 2009
Case report/Case series
1
H
100%
8
p.Arg583*
: het
Cuenca-León, 2009
Case report/Case series
1
n.a.
100%
58
p.Gly638Asp
: het
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