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Overview of included studies for HSP-SPAST:
Click here for summary of patients' characteristics
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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.(1098+1+1099-1)_(1493+1_1494-1)del
c.(1098+1_1099-1)_(3149_?)del
c.(1098+1_1099-1)_(1173+1_1174-1)del
c.(1098+1_1099-1)_(1245+1_1246-1)del
c.(1173+1_1174-1)_(3149_?)del
c.(1173+1_1174-1)_(1245+1_1246-1)del
c.(1173+1_1174-1)_(1493+1_1494-1)del
c.(1245+1_1246-1)_(3149_?)del
c.(1245+1_1246-1)_(1321+1_1322-1)del
c.(1245+1_1246-1)_(1493+1_1494-1)del
c.(1245+1_1246-1)_(1728+1_1729-1)del
c.(1245+1_1246-1)_(1728+1_1729-1)dup
c.(1493+1_1494-1)_(1536+1_1537-1)del
c.(1493+1_1494-1)_(1728+1_1729-1)del
c.(1536+1_1537-1)_(1687+1_1688-1)dup
c.(1536+1_1537-1)_(1728+1_1729-1)del
c.(1687+1_1688-1)_(3149_?)del
c.(1687+1_1688-1)_(1728+1_1729-1)del
c.(1687+1_1688-1)_(1728+1_1729-1)dup
c.(1728+1_1729-1)_(3149_?)del
c.(415+1_416-1)_(3149_?)del
c.(415+1_416-1)_(1245+1_1246-1)del
c.(415+1_416-1)_(1493+1_1494-1)dup
c.(415+1_416-1)_(1728+1_1729-1)del
c.(586+1_587-1)_(3149_?)del
c.(586+1_587-1)_(1098+1_1099-1)del
c.(586+1_587-1)_(1245+1_1246-1)del
c.(682+1_683-1)_(3149_?)del
c.(682+1_683-1)_(1004+1_1005-1)del
c.(682+1_683-1)_(1098+1_1099-1)del
c.(682+1_683-1)_(870+1_871-1)del
c.(870+1_871-1)_(1004+1_1005-1)del
c.(870+1_871-1)_(1098+1_1099-1)del
c.(?_-221)_(3149_?)del
c.(?_-221)_(1245+1_1246-1)del
c.(?_-221)_(415+1_416-1)del
c.(?_-221)_(415+1_416-1)dup
c.(?_-221)_(502+1_503-1)del
c.(?_-221)_(586+1_587-1)del
c.(?_-221)_(682+1_683-1)del
c.1-763_c.683-650del
c.1004+1G>T
c.1004+2T>A
c.1004+2T>G
c.1004+3A>C
c.1004+5G>C
c.1005-1G>A
c.1005-1G>C
c.1005-2A>G
c.1014delT
c.1024G>C
c.1031T>A
c.1036G>T
c.1039C>A
c.1039C>T
c.1040A>C
c.1048G>C
c.1054C>T
c.1055A>C
c.1067A>G
c.1070T>A
c.1072G>C
c.1078C>G
c.1079T>C
c.1081C>A
c.1081C>T
c.1082C>G
c.1082C>T
c.1088T>C
c.1091G>C
c.1092_1098+1delGCCTGAGG
c.1096G>A
c.1098+1G>A
c.1098+1G>C
c.1098+1_1098+2delinsCTCAGA
c.1099-1G>A
c.1099-2_1099delAGT
c.1100T>C
c.1101_1103delGTT
c.1103T>C
c.1105A>C
c.1105dupA
c.1108G>A
c.1111C>T
c.1114A>G
c.1120C>A
c.1121C>G
c.1128A>C
c.1133T>A
c.1133T>C
c.1136dupT
c.1137_1142delACTCTT
c.1137dupA
c.1139T>A
c.1141T>C
c.1151C>G
c.1153G>T
c.1154G>A
c.1158T>G
c.1160_1170del11
c.1163A>G
c.1165A>G
c.1167_1168delAA
c.1168A>G
c.1172T>C
c.1173+1G>A
c.1174-1G>A
c.1174-1G>C
c.1174-1G>T
c.1174-1_1174delinsCT
c.1174_1180delGCTAAAG
c.1174delG
c.1176dupT
c.1177_1188del12
c.1180delG
c.1185delA
c.1192_1193delinsT
c.1196C>T
c.1209C>A
c.1209C>G
c.1209_1211delCTT
c.1210_1212delTTT
c.1215_1219delTATAA
c.1215dupT
c.1216A>G
c.1217T>G
c.1225G>A
c.1226C>A
c.1238C>T
c.1242A>G
c.1243_1244insA
c.1244dupA
c.1245+1G>A
c.1245+1G>T
c.1245+3insT
c.1245+4A>G
c.1245+5G>A
c.1245delC
c.1246-1G>C
c.1246-2896_1493+523dup
c.1246-4_1246-2delinsCT
c.1250G>A
c.1251_1253delAGA
c.1253_1255delAAG
c.1255G>T
c.1267G>T
c.1270A>G
c.1270_1271dupAG
c.1276C>G
c.1276C>T
c.1276_1277delCT
c.127G>T
c.1280T>G
c.1281delT
c.1281dupT
c.1282G>C
c.1282delG
c.1291C>T
c.1300C>T
c.1304C>T
c.1306T>C
c.1307C>T
c.1317delT
c.131C>A
c.131C>T
c.1321+2T>A
c.1321G>A
c.1322-2A>C
c.1322-2A>G
c.1322A>G
c.1322A>T
c.1322_31del29
c.1324G>A
c.1324G>T
c.1325A>C
c.1326_1331delAGTTGA
c.1330G>A
c.1331A>G
c.1332T>G
c.1334G>C
c.1339T>G
c.1340delT
c.1341_1342insTC
c.134C>A
c.1350_1351delAA
c.1352_1356delGAGAA
c.1353_1357delAGAAG
c.1355_1357delAAG
c.1356delA
c.1358_1360dupGGG
c.1360G>A
c.1361A>G
c.1375A>G
c.1376G>C
c.1378C>A
c.1378C>T
c.1379G>A
c.1379G>T
c.1379delG
c.1382T>C
c.1384A>G
c.1385A>G
c.1387A>G
c.1392A>T
c.139A>T
c.1402G>T
c.1408G>T
c.1409A>T
c.1412G>A
c.1413+1G>A
c.1413+2T>A
c.1413+2T>G
c.1413+3A>C
c.1413+3_1413+6delAAGT
c.1413+4A>G
c.1413+5G>A
c.1413+6T>C
c.1413dupT
c.1414-1G>A
c.1414-1G>C
c.1414-2A>C
c.1414-2A>G
c.1414G>A
c.1417C>T
c.1418_1431del14
c.1426_1427delGG
c.1435_1441delAGAGTAC
c.1437_1438delAG
c.1439_1445delinsC
c.1442_1443insA
c.1447_1448delAT
c.1450G>C
c.1450_1458delGGTGCAACT
c.1454C>T
c.1459A>C
c.1459A>G
c.1461_1462dupTA
c.1466C>G
c.1466C>T
c.1468C>T
c.1474C>T
c.1478A>G
c.1492A>G
c.1492_1493+2delAGGT
c.1493+1G>A
c.1493+1_1493+2insATGG
c.1493+2T>C
c.1493+2_1493+5delTAGG
c.1493G>C
c.1494-2A>G
c.1494G>T
c.1495C>T
c.1496G>A
c.1504A>T
c.1507C>T
c.1507_1509dupCGG
c.1511dupT
c.1512_1514dupATA
c.1517T>A
c.1517T>G
c.1520_1521dupCT
c.1529A>T
c.1535delA
c.1536+1G>A
c.1536+1G>T
c.1540A>G
c.1543_1545delCTA
c.1555A>T
c.155A>G
c.1560_1563delTCTG
c.1573C>T
c.1597G>T
c.1601T>C
c.1601_1608delins30
c.1608_1615delACTTGCTA
c.1610T>C
c.1610T>G
c.1616+1G>A
c.1617-1G>A
c.1617-1G>T
c.1617-2A>G
c.1625A>G
c.1630_1643del14
c.1634C>T
c.1635_1636insAA
c.1636G>A
c.1642G>A
c.1644_1649dupCCTAAC
c.1646T>C
c.1646dupT
c.1649C>T
c.1650_1651delAG
c.1651G>C
c.1656_1664delinsTGACCT
c.1664A>G
c.1666G>A
c.1667C>T
c.1667_1668delCA
c.1670C>T
c.1673T>G
c.1675G>C
c.1676G>A
c.1676insG
c.1684C>T
c.1685G>A
c.1687+1G>A
c.1687+1G>T
c.1687+2T>G
c.1687+2_1687+6delTAGGT
c.1687G>A
c.1688-2A>G
c.1688-3C>G
c.1688–1G>C
c.1689_1698del10
c.1691delT
c.1702C>T
c.1708_1716delAAGAATATG
c.1714_1715delAT
c.1724G>T
c.1728+1G>A
c.1728+1G>C
c.1728+1G>T
c.1728+2T>C
c.1728+2T>G
c.1729-1G>C
c.1729-2A>G
c.1729-2A>T
c.1732A>T
c.1735A>C
c.1738_1740delinsGA
c.1739T>C
c.1741C>T
c.1750G>C
c.1751A>T
c.1771A>G
c.1774delA
c.1776_1780delAAAAC
c.1779dupA
c.1783A>C
c.1789A>G
c.1805_1808dupAAGC
c.1812dupC
c.1815dupA
c.1821G>A
c.1821G>C
c.1837G>C
c.1838A>C
c.1838A>G
c.1840dupA
c.1841C>T
c.1841_1842delCC
c.1849T>G
c.194G>A
c.283G>A
c.283_323del41
c.286delG
c.289C>A
c.313_320delCCGGCGCC
c.334G>A
c.334G>T
c.343_352del10
c.343_352dup10
c.349C>T
c.373G>T
c.382delT
c.403G>T
c.412A>T
c.415+1G>A
c.415+1G>T
c.421C>T
c.422_425delAGAA
c.427dupG
c.439G>T
c.443G>A
c.444G>A
c.448_451delAAGA
c.450_451delGA
c.451_454delAAAG
c.458delT
c.469delG
c.484G>A
c.486dupT
c.499C>T
c.513_514delTG
c.524_525dupGA
c.532C>T
c.549dupT
c.562delG
c.571delC
c.577C>T
c.583C>G
c.584_585delTA
c.586+9_586+12delTAAT
c.602T>A
c.629_682+22003delinsAGT
c.67_85dup19
c.683-1G>A
c.683-1G>T
c.703dupA
c.706_710delAAAGA
c.712C>A
c.727_737del11
c.730_731insT
c.732_733insCA
c.734C>G
c.746C>G
c.751dupA
c.781dupT
c.782C>G
c.807C>A
c.807C>G
c.80_98dup19
c.838C>T
c.839_840delAG
c.843_846dupATCT
c.857_859delCTA
c.85dupC
c.867_868delTA
c.868A>T
c.870+1G>A
c.870+1delG
c.870+3A>G
c.871-2A>G
c.871delG
c.872_875delinsCCA
c.878C>T
c.879delG
c.906delT
c.90_91insAGCC
c.913_923delins11
c.926G>A
c.932_938delAAAAAGA
c.936_937insA
c.936dupA
c.937delG
c.941T>C
c.945delG
c.961dupG
c.96C>G
c.977dupA
c.983_984dupTA
c.990_993delTGAA
Country
Armenia
Australia
Austria
Brazil
Bulgaria
Canada
China
Czech Republic
Denmark
Estonia
France
Germany
Greece
Hungary
Ireland
Italy
Japan
Netherlands
Norway
Poland
Portugal
Russia
South Korea
Spain
Taiwan
Tunisia
Turkey
United Kingdom
United States
Study
Study design
N cases
Ethnicities
Sex
(%
♂
)
Mean AAO (+/- SD)
Reported mutations
Molon, 2003
Case report/Case series
3
C
n.a.
n.a.
p.Phe439Leufs*2
: het
p.Leu534Pro
: het
Tallaksen, 2003
Other/Mixed
25
n.a.
n.a.
28(+/-16)
p.Leu521Tyrfs*8
: het
p.Ala556Val
: het
p.Asn405Lysfs*36
: het
p.Arg431*
: het
p.Arg499Cys
: het
c.1687+1G>A
: het
c.1004+2T>G
: het
c.1413+5G>A
: het
p.Leu426Val
: het
Show more (+6)
Bönsch, 2003
Family study
10
C
90%
22(+/-13)
p.Ala392Leufs*4
: het
c.(1493+1_1494-1)_(1728+1_1729-1)del
: het
Namekawa, 2002
Family study
3
A
67%
32(+/-16)
p.Ala485Val
: het
Ki, 2002
Family study
7
A
57%
28(+/-11)
p.Ile344Lys
: het
Proukakis, 2002
Mutational screen
12
n.a.
n.a.
31(+/-13)
p.Phe404del
: het
p.Arg235Lysfs*9
: het
p.Lys236Profs*6
: het
Yabe, 2002
Case report/Case series
5
A
n.a.
n.a.
p.Arg499Cys
: het
c.1617-1G>T
: het
p.Gln347Lys
: het
p.Lys388Arg
: het
c.1245+1G>T
: het
Show more (+2)
Sauter, 2002
Mutational screen
3
C
100%
33(+/-17)
c.1601_1608delins30
: het
p.Asn316Ilefs*13
: het
p.Arg562*
: het
Morita, 2002
Family study
9
n.a.
67%
31(+/-21)
c.1005-1G>A
: het
Meijer, 2002
Mutational screen
13
C
n.a.
47(+/-15)
p.Arg562*
: het
c.1729-1G>C
: het
p.Arg562Gln
: het
p.Leu426Val
: het
p.Lys414Lys
: het
p.Pro489Leu
: het
p.Gly559Asp
: het
p.Ala188Profs*8
: het
c.1173+1G>A
: het
p.Ser399Leu
: het
p.Gln434*
: het
c.1414-2A>G
: het
Show more (+9)
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