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Prnptm2Cwe
Targeted Allele Detail
Summary
Symbol: Prnptm2Cwe
Name: prion protein; targeted mutation 2, Charles Weissmann
MGI ID: MGI:2682347
Synonyms: Prnp lox2
Gene: Prnp  Location: Chr2:131751848-131780349 bp, + strand  Genetic Position: Chr2, 64.07 cM
Alliance: Prnptm2Cwe page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:67593
Parent Cell Line:  E14.1 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
    Exon 3 was flanked by single loxP sites in intron 2 and following exon 3. (J:67593)
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:67593 Rossi D, et al., Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain. EMBO J. 2001 Feb 15;20(4):694-702
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
04/23/2024
MGI 6.23
The Jackson Laboratory