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Prnpb
Spontaneous Allele Detail
Summary
Symbol: Prnpb
Name: prion protein; b
MGI ID: MGI:3045031
Gene: Prnp  Location: Chr2:131751848-131780349 bp, + strand  Genetic Position: Chr2, 64.07 cM
Alliance: Prnpb page
Mutation
origin
Strain of Origin:  I/LnJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Nucleotide substitutions
 
Mutation detailsIn this allele, amino acid residue 108 is Phenylalanine (F) and amino acid residue 189 is Valine (V). This allele was initially sequenced using DNA from the I/LnJ strain. The same allele has been identified in P/J, IM, and BDP/J. (J:8918)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Prnp Mutation:  150 strains or lines available
References
Original:  J:8918 Westaway D, et al., Distinct prion proteins in short and long scrapie incubation period mice. Cell. 1987 Nov 20;51(4):651-62
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
04/30/2024
MGI 6.23
The Jackson Laboratory