aspsirna3335 details

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ASPsiRNA information siRNA Id:aspsirna3335
siRNA Name: miSNP50C-18-13mm
Mismatch information Wild siRNA (As strand 3'->5'):UAGAUGACACACGUGAAGUAG
ASP-siRNA (As strand 3'->5'):UAGGUGACCCACGUGAAGUAG
Mismatch position in siRNA: G4A,C9A
Gene Information Gene Name Hungtintin (HTT)
Target Sequence (5'->3'):TTGTGACCCACGCCTGCTCCCTCATCTACTGTGTGCACTTCAT
Wild allele (5'->3'):AUCUACUGUGUGCACUUCAUC
Mutant allele (5'->3'):AUCCACUGGGUGCACUUCAUC
Position of siRNA on target gene: 7244-7264
Respective Gene/Protein Resources GenBank Accession:NM_002111.7
Cytogenic location:4p16.3
Chromosomal coordinates:4:3,076,407-3,245,686
UniProt ID:Q96CV9
HUGO ID:4851
Reference SNp(RefSNP): rs362331
Disease/Mutation information Target Mutation: NM_002111.7:c.6931T>C
Matation type/variant: Single nucleotide variant/Missense variant
Mutation at gene level: NG_009378.1:g.144434T>C
Pathogenic status of mutation: Pathogenic
Disease:Huntington disease (HD)
Clinical Resources ClinVar ID:NA
KEGG disease ID:H00059
OMIM ID: 143100
COSMIC: HTT
DECIPHER: HTT
GeneTests: HTT
ASP siRNA details Mutant allele (5'->3'): AUCCACUGGGUGCACUUCAUC
ASP-siRNA (As strand 3'->5'):UAGGUGACCCACGUGAAGUAG
Percentage efficacy of ASP-siRNA for mutant allele:75
Wild allele (5'->3'): AUCUACUGUGUGCACUUCAUC
ASP-siRNA (As strand 3'->5'):UAGGUGACCCACGUGAAGUAG
Percentage efficacy of ASP-siRNA for wild allele:60
Relative difference:15
Wild siRNA details Wild allele (5'->3'): AUCUACUGUGUGCACUUCAUC
Wild siRNA (As strand 3'->5'):UAGAUGACACACGUGAAGUAG
Percentage efficacy of wild siRNA for wild allele:82
Wild allele (5'->3'): AUCUACUGUGUGCACUUCAUC
ASP-siRNA (As strand 3'->5'):UAGGUGACCCACGUGAAGUAG
Percentage efficacy of Wild sirna for mutant allele:80
Relative difference :2
General information Mismatch incorporated in siRNA/Target:siRNA
Cell-line used: HEK293T
Experimental technique used: Dual luciferase reporter assay
Transfection method: Lipofectamine 2000
siRNA expression method: Chemically synthesized
Post-transfection duration: 48 hours
Concentration used:50 ng
Reference:27003755
Delivery method:Transfection
Article title:Design, Characterization, and Lead Selection of Therapeutic miRNAs Targeting Huntingtin for Development of Gene Therapy for Huntington's Disease
Authors:Miniarikova J,, Zanella I, Huseinovic A, van der Zon T, Hanemaaijer E, Martier R,, Koornneef A, Southwell AL, Hayden MR, van Deventer SJ, Petry H, Konstantinova P.
Journal Reference:Mol Ther Nucleic Acids. 2016 Mar 22;5:e297. doi: 10.1038/mtna.2016.7.