Il1rap exon 3 KO_hAbeta_APOE4_Trem2.R47H

syn22251858

Created By Mette Peters Mette

url: https://www.jax.org/strain/032777
grant: U54AG054345
program: MODEL-AD
summary: This model has a CRISPR/cas9-generated deletion of ex3 of the Il1rap gene. The IL1RAP intronic variant rs12053868 is associated with amyloid accumulation in the ADNI cohort. This was created on a sensitized model expressing: a humanized APOE4 KI; a CRISPR/Cas9-generated App allele with a humanized Abeta1-42 region (G601R, F606Y, R609H in the mouse gene, corresponding to aa positions 676, 681, 684 in the human APP locus) and a CRISPR/cas9-generated R47H point mutation in the mouse Trem2 gene.
toolType: Mouse Model
modelType: Late Onset Alzheimer's disease
strainDetails: [View](https://www.jax.org/strain/032777)
targetedGenes: IL1RAP APOE APP TREM2
backgroundStrain: C57BL/6J

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