About   Help   FAQ
Prnpc
Spontaneous Allele Detail
Summary
Symbol: Prnpc
Name: prion protein; c
MGI ID: MGI:3045033
Gene: Prnp  Location: Chr2:131751848-131780349 bp, + strand  Genetic Position: Chr2, 64.07 cM
Alliance: Prnpc page
Mutation
origin
Strain of Origin:  MAI/Pas
Mutation
description
Allele Type:    Spontaneous
Mutation:    Nucleotide substitutions
 
Mutation detailsAmino acid residue 108 is Phenylalanine and amino acid residue 189 is Threonine. This allele was identified by sequencing DNA from the MAI/Pas strain of mice. (J:90099)
Phenotypes
Loading...
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:  142 strains or lines available
References
Original:  J:90099 Lloyd SE, et al., Identification and characterization of a novel mouse prion gene allele. Mamm Genome. 2004 May;15(5):383-9
All:  2 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory