PLX247357

GSE65772: Transcriptome profiling in knock-in mouse models of Huntington's disease [Liver_mRNA]

• Organsim mouse
• Type RNASEQ
• Target gene
• Project ARCHS4

Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder that is characterized by motor, cognitive, and psychiatric alterations. The mutation responsible for this disease is an abnormally expanded and unstable CAG repeat within the coding region of the gene encoding huntingtin (Htt). Knock-in mouse models of HD with human exon 1 containing expanded CAG repeats inserted in the murine huntingtin gene (Hdh) provide a genetic reconstruction of the human causative mutation within the mouse model. The goal of this study is RNA expression profiling by RNA sequencing (RNA-seq) in 2, 6, and 10 month old knock-in mice with CAG lengths of 20, 80, 92, 111, 140, 175 along with littermate control wild-type animals SOURCE: Jeff Aaronson (jeff.aaronson@chdifoundation.org) - CHDI