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Prnpem1Aag
Endonuclease-mediated Allele Detail
Summary
Symbol: Prnpem1Aag
Name: prion protein; endonuclease-mediated mutation 1, Adriano Aguzzi
MGI ID: MGI:5819099
Synonyms: PrnpZH3
Gene: Prnp  Location: Chr2:131751848-131780349 bp, + strand  Genetic Position: Chr2, 64.07 cM
Alliance: Prnpem1Aag page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsA TALEN pair was used to target a site in close proximity to the start codon. An 8-bp deletion was identified in exon 3. The frame shift introduced a premature stop codon in the sequence coding for the secretory signal peptide. Homozygous mice show no detectable protein expression in central nervous system (CNS) tissues, as assessed by Western blotting. (J:233015)
Expression
In Mice Carrying this Mutation: 2 RNA-Seq or microarray experiment(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Prnp Mutation:  143 strains or lines available
References
Original:  J:233015 Nuvolone M, et al., Strictly co-isogenic C57BL/6J-Prnp-/- mice: A rigorous resource for prion science. J Exp Med. 2016 Mar 7;213(3):313-27
All:  13 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/30/2025
MGI 6.24
The Jackson Laboratory