Total number of Results for G10U are 25
Search:
ASPsiRNA ID Pairing of target region (top) and ASP-siRNA (bottom) Efficacy (mut)(%) Efficacy (wt) (%) Diff Gene Disease Mutation RefSNP Analysis Pubmed ID
aspsirna2010 UUUAUGAGGCUCUCUCUGA
AAAUACUCCGAGAGAGACU
45 30 15 P. luciferase NA NA NA
US2005/0176045A1
aspsirna2067 CUCUCCUGUCGCUAAGGCC
GAGAGGACAGCGAUUCCGG
30 45 -15 PPIB/Cyclophilin B NA NA NA
US2005/0176045A1
aspsirna2949 CACUAGUAGCAAGUAUAAU
GUGAUCAUCGUUCAUAUUA
50 20 30 SNCA Parkinsons disease (PD) SNCA locus triplication NA
25965551
aspsirna2975 CACUAGUAGCAAGUAUAAU
GUGAUCAUCGUUCAUAUUA
24 20 4 SNCA Parkinsons disease (PD) SNCA locus triplication NA
25965551
aspsirna3005 CACUAGUAGCAAGUAUAAU
GUGAUCAUCGUUCAUAUUA
70 20 50 SNCA Parkinsons disease (PD) SNCA locus triplication NA
25965551
aspsirna2173 GGGACAGUACUUCAACGCUU
CCCUGUCAUGAAGUUGCGAA
80 5 75 HTT Huntington disease (HD) c.52CAG(36_39) rs19392295
24926995
aspsirna2178 GGAAGUCUGCGCCCUUGUG
CCUUCAGACGCGGGAACAC
85 55 30 HTT Huntington disease (HD) c.52CAG(36_39) rs19392295
24926995
aspsirna3438 GGGACAGUACUUCAACGCUU
CCCUGUCAUGAAGUUGCGAA
80 5 75 HTT Huntington disease (HD) NM_002111.7:c.5165C>A rs363125
24926995
aspsirna3443 GGAAGUCUGCGCCCUUGUG
CCUUCAGACGCGGGAACAC
85 55 30 HTT Huntington disease (HD) NM_002111.6:c.9810C>T rs362307
24926995
aspsirna3448 GGGACAGUACUUCAACGCUU
CCCUGUCAUGAAGUUGCGAA
80 5 75 HTT Huntington disease (HD) NM_002111.7:c.5165C>A rs363125
24926995
aspsirna3453 GGAAGUCUGCGCCCUUGUG
CCUUCAGACGCGGGAACAC
85 55 30 HTT Huntington disease (HD) NM_002111.6:c.9810C>T rs362307
24926995
aspsirna3458 GGGACAGUACUUCAACGCUU
CCCUGUCAUGAAGUUGCGAA
97 67 30 HTT Huntington disease (HD) NM_002111.7:c.5165C>A rs363125
24926995
aspsirna3463 GGAAGUCUGCGCCCUUGUG
CCUUCAGACGCGGGAACAC
85 55 30 HTT Huntington disease (HD) NM_002111.6:c.9810C>T rs362307
24926995
aspsirna3468 GGGACAGUACUUCAACGCUU
CCCUGUCAUGAAGUUGCGAA
97 67 30 HTT Huntington disease (HD) NM_002111.7:c.5165C>A rs363125
24926995
aspsirna3473 GGAAGUCUGCGCCCUUGUG
CCUUCAGACGCGGGAACAC
85 55 30 HTT Huntington disease (HD) NM_002111.6:c.9810C>T rs362307
24926995
aspsirna3478 GGGACAGUACUUCAACGCUU
CCCUGUCAUGAAGUUGCGAA
97 30 67 HTT Huntington disease (HD) NM_002111.7:c.5165C>A rs363125
24926995
aspsirna3483 GGAAGUCUGCGCCCUUGUG
CCUUCAGACGCGGGAACAC
85 55 30 HTT Huntington disease (HD) NM_002111.6:c.9810C>T rs362307
24926995
aspsirna3488 GGGACAGUACUUCAACGCUU
CCCUGUCAUGAAGUUGCGAA
97 67 30 HTT Huntington disease (HD) NM_002111.7:c.5165C>A rs363125
24926995
aspsirna3493 GGAAGUCUGCGCCCUUGUG
CCUUCAGACGCGGGAACAC
85 55 30 HTT Huntington disease (HD) NM_002111.6:c.9810C>T rs362307
24926995
aspsirna0696 CAGUGGCUCCCCUGAUUAC
GUCACCGAGGGGACUAAUG
76 20 56 HTT Huntington disease (HD) c.52CAG(36_39) rs19392295
22397573
aspsirna0456 AAGUUUGCCCCCUUCAUCG
UUCAAACGGGGGAAGUAGC
30 0 30 KRT5 Epidermolysis bullosa simplex (EBS) c.541T>C ,p.Ser181Pro rs60715293
21716320
aspsirna0494 AAGUUUGCCCCCUUCAUCG
UUCAAACGGGGGAAGUAGC
30 0 30 KRT5 Epidermolysis bullosa simplex (EBS) c.541T>C ,p.Ser181Pro rs60715293
21716320
aspsirna0837 UGGGGACAGUACUUCAACGCU
ACCCCUGUCAUGAAGUUGCGA
NA NA NA HTT Huntington disease (HD) c.52CAG(36_39) rs363125
19361997
aspsirna0839 CAGUACUUCAACGCUAGAAGA
GUCAUGAAGUUGCGAUCUUCU
NA NA NA HTT Huntington disease (HD) c.52CAG(36_39) rs363125
19361997
aspsirna3692 GGUUGGAGGAGAGAUGAUA
CCAACCUCCGCUCUACUAU
90 40 50 PPIB/Cyclophilin B PPIB-Related Osteogenesis Imperfecta (Type IX) NA NA
16489337
Showing 1 to 25 of 25 entries