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Prndtm1Sbp
Targeted Allele Detail
Summary
Symbol: Prndtm1Sbp
Name: prion like protein doppel; targeted mutation 1, Stanley B Prusiner
MGI ID: MGI:6508088
Gene: Prnd  Location: Chr2:131792781-131798050 bp, + strand  Genetic Position: Chr2, 64.07 cM
Alliance: Prndtm1Sbp page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:300211
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    A loxP-flanked PGK/neomycin cassette replaced the entireopen reading frame (ORF) within exon 2. (J:300211)
Expression
In Mice Carrying this Mutation: 30 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Prnd Mutation:  6 strains or lines available
References
Original:  J:300211 Tamguney G, et al., Genes contributing to prion pathogenesis. J Gen Virol. 2008 Jul;89(Pt 7):1777-1788
All:  1 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
05/07/2024
MGI 6.23
The Jackson Laboratory