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Prnptm1Rcm
Targeted Allele Detail
Summary
Symbol: Prnptm1Rcm
Name: prion protein; targeted mutation 1, Richard C Moore
MGI ID: MGI:1934273
Synonyms: Prnpa[108F189V], PrP gtB
Gene: Prnp  Location: Chr2:131751848-131780349 bp, + strand  Genetic Position: Chr2, 64.07 cM
Alliance: Prnptm1Rcm page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:45908
Parent Cell Line:  HM-1 (ES Cell)
Strain of Origin:  129P2/OlaHsd-Hprt1b-m3
Mutation
description
Allele Type:    Targeted
Mutation:    Nucleotide substitutions
 
Mutation detailsThe 129P2/OlaHsd strain normally carries the PrP A allotype, with leucine and threonine at residues 108 and 189. In this allele, the sequences encoding these amino acids were altered to instead encode phenylalanine and valine. These changes alter the allotype to one identical to PrP B. (J:29021)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Prnp Mutation:  142 strains or lines available
References
Original:  J:45908 Moore RC, et al., Mice with gene targetted prion protein alterations show that Prnp, Sinc and Prni are congruent [see comments]. Nat Genet. 1998 Feb;18(2):118-25
All:  4 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
11/12/2024
MGI 6.24
The Jackson Laboratory