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Prnp/Prndtm1Dwm
Targeted Allele Detail
Summary
Symbol: Prnp/Prndtm1Dwm
Name: prion like protein doppel; targeted mutation 1, David W Milton
MGI ID: MGI:3047064
Synonyms: Prnp-/Prnd-
Gene: Prnd  Location: Chr2:131792781-131798050 bp, + strand  Genetic Position: Chr2, 64.07 cM
Alliance: Prnp/Prndtm1Dwm page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:91094
Parent Cell Line:  HM-1 (ES Cell)
Strain of Origin:  129P2/OlaHsd-Hprt1b-m3
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intergenic deletion
 
Mutation detailsBoth coding regions were ablated by replacement with an Hprt minigene. Western blot of mutant testes lysates show absence of both proteins. (J:91094)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Prnd Mutation:  6 strains or lines available
References
Original:  J:91094 Paisley D, et al., Male infertility and DNA damage in Doppel knockout and prion protein/Doppel double-knockout mice. Am J Pathol. 2004 Jun;164(6):2279-88
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
04/09/2024
MGI 6.23
The Jackson Laboratory