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siRNA Id: | aspsirna2195
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siRNA Name: | 8A–14G
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Gene: | Collagen type VI alpha 1 (COL6A1) |
Disease: | Ullrich congenital muscular dystrophy (UCMD),Bethlem myopathy (BM) |
Wild allele/target (5'->3'): | AGAAGCCGGAGAUCCUGGA
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Mutant allele/target (5'->3'): | AGAAGCCAGAGAUGCUGGA
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Target Mutation: | c.850G>A, p.G284R
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Wild siRNA (As strand): | UCUUCGGCCUCUAGGACCU
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ASP-siRNA (As strand): | UCUUCGGUCUCUACGACCU
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Mismatch position in siRNA: | U12C,C6G |
Mutant allele (5'->3'): | AGAAGCCAGAGAUGCUGGA
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ASP-siRNA (As strand): | UCUUCGGUCUCUACGACCU
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ASP-siRNA efficacy for mutant allele: | 5
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Wild allele (5'->3'): | AGAAGCCGGAGAUCCUGGA
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ASP-siRNA (As strand): | UCUUCGGUCUCUACGACCU
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ASP-siRNA efficacy for wild allele: | 10
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Percentage discrimination for ASP-siRNA: | -5
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Wild allele (5'->3'): | AGAAGCCGGAGAUCCUGGA
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Wild siRNA (As strand): | UCUUCGGCCUCUAGGACCU
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Wild sirna efficacy for wild allele: | 80
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Wild allele (5'->3'): | AGAAGCCGGAGAUCCUGGA
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ASP-siRNA (As strand): | UCUUCGGUCUCUACGACCU
|
Wild sirna efficacy for mutant allele: | 40
|
Percentage discrimination for wild siRNA: | 40
|
Concentration: | 80nM |
Orientation: | Sense |
Mismatch in: | siRNA |
UniProt ID: | P12109 |
Target sequence: | AGGGAGAAGCCGGAGAUCCUGGAA |
Genbank Accesion: | NM_001848.2 |
Cell-line: | NIH3T3 |
Experimental technique used: | RT-PCR |
Transfection method: | Lipofectamine 2000 |
siRNA expression method: | Invitrogen |
Post-transfection duration: | 24 hours |
OMID ID: | 254090 |
KEGG disease ID: | H01341 |
Reference: | 24959844 |