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Tg(Prnp*D177N*M128V)G1Rchi
Transgene Detail
Summary
Symbol: Tg(Prnp*D177N*M128V)G1Rchi
Name: transgene insertion G1, Roberto Chiesa
MGI ID: MGI:5614760
Synonyms: Tg(CJD)
Transgene: Tg(Prnp*D177N*M128V)G1Rchi  Location: unknown  
Alliance: Tg(Prnp*D177N*M128V)G1Rchi page
Transgene
origin
Strain of Origin:  (C57BL/6J x CBA/J)F2
Transgene
description
Transgene Type:    Transgenic (Inserted expressed sequence)
Mutation:    Nucleotide substitutions
 
Tg(Prnp*D177N*M128V)G1Rchi expresses 1 gene
 
Mutation detailsThe transgene construct contained a a 12 kb genomic DNA fragment of the mouse Prnp gene, including the promoter and first intron, joined to a cDNA encoding the a variant of mouse prion protein in which aspartic acid is replaced by asparagine at anino acid position 177 (D177N) and methionine by valine at position 128 (M128V), equivalent to the hereditary Creutzfeldt-Jakob disease- (CJD-) associated human D178N/V129 prion protein mutation. Hemizygous mice of transgenic line G1 carry 6 copies of the transgene; western blot analysis detects the mutant prion protein in brains of these mice at 0.15 times the endogenous PRNP level in wild-type brains. The gross pattern of mutant PRNP expression in brains of transgenic mice is similar to that of endogenous PRNP in non-transgenic mice. (J:142098)
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
References
Original:  J:142098 Dossena S, et al., Mutant prion protein expression causes motor and memory deficits and abnormal sleep patterns in a transgenic mouse model. Neuron. 2008 Nov 26;60(4):598-609
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
06/12/2024
MGI 6.13
The Jackson Laboratory