aspsirna0011 details

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ASPsiRNA information siRNA Id:aspsirna0011
siRNA Name: YS-Ds
Mismatch information Wild siRNA (As strand 3'->5'):AACACUUGGACGAGAUACU
ASP-siRNA (As strand 3'->5'):AACACUUGGACGAGUCGCU
Mismatch position in siRNA: C4U,G3A,U5A
Gene Information Gene Name Type 1 ryanodine receptor (RyR1)
Target Sequence (5'->3'):TTGTGAACCTGCTCAGCGA
Wild allele (5'->3'):UUGUGAACCUGCUCUAUGA
Mutant allele (5'->3'):UUGUGAACCUGCUCAGCGA
Position of siRNA on target gene: NA
Respective Gene/Protein Resources GenBank Accession:NM_000540.2
Cytogenic location:19q13.2
Chromosomal coordinates:19:38,924,339-39,078,203
UniProt ID:P21817
HUGO ID:10483
Reference SNp(RefSNP): rs11819216
Disease/Mutation information Target Mutation: c.1565A>C,p.Tyr522Ser
Matation type/variant: Single nucleotide variant/Missense variant
Mutation at gene level: NG_008866.1:g.26660A>C
Pathogenic status of mutation: Disease causing
Disease:Central core disease (CCD)
Clinical Resources ClinVar ID:12993
KEGG disease ID:H00699
OMIM ID: 117000
COSMIC: RyR1
DECIPHER: RyR1
GeneTests: RyR1
ASP siRNA details Mutant allele (5'->3'): UUGUGAACCUGCUCAGCGA
ASP-siRNA (As strand 3'->5'):AACACUUGGACGAGUCGCU
Percentage efficacy of ASP-siRNA for mutant allele:67
Wild allele (5'->3'): UUGUGAACCUGCUCUAUGA
ASP-siRNA (As strand 3'->5'):AACACUUGGACGAGUCGCU
Percentage efficacy of ASP-siRNA for wild allele:38
Relative difference:29
Wild siRNA details Wild allele (5'->3'): UUGUGAACCUGCUCUAUGA
Wild siRNA (As strand 3'->5'):AACACUUGGACGAGAUACU
Percentage efficacy of wild siRNA for wild allele:40
Wild allele (5'->3'): UUGUGAACCUGCUCUAUGA
ASP-siRNA (As strand 3'->5'):AACACUUGGACGAGUCGCU
Percentage efficacy of Wild sirna for mutant allele:19
Relative difference :21
General information Mismatch incorporated in siRNA/Target:siRNA
Cell-line used: HEK293
Experimental technique used: RT-PCR
Transfection method: Lipofectamine 2000
siRNA expression method: Dharmacon
Post-transfection duration: 48 hours
Concentration used:200pmol
Reference:23152933
Delivery method:Electroporation
Article title:Allele-specific gene silencing in two mouse models of autosomal dominant skeletal myopathy.
Authors:Loy RE1, Lueck JD, Mostajo-Radji MA, Carrell EM, Dirksen RT.
Journal Reference:PLoS One. 2012;7(11):e49757. doi: 10.1371/journal.pone.0049757. Epub 2012 Nov 12.