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Prkntm1Ykt
Targeted Allele Detail
Summary
Symbol: Prkntm1Ykt
Name: parkin RBR E3 ubiquitin protein ligase; targeted mutation 1, Yasuko Kitao
MGI ID: MGI:3698054
Gene: Prkn  Location: Chr17:11059271-12282248 bp, + strand  Genetic Position: Chr17, 7.8 cM, cytoband A3.2-A3.3
Alliance: Prkntm1Ykt page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:117737
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 3 was replaced with a floxed pgk-neomycin cassette. Absence of protein was confirmed by Western blot analysis. (J:117737)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 2 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 Prkn Mutation:  54 strains or lines available
References
Original:  J:117737 Kitao Y, et al., Pael receptor induces death of dopaminergic neurons in the substantia nigra via endoplasmic reticulum stress and dopamine toxicity, which is enhanced under condition of parkin inactivation. Hum Mol Genet. 2007 Jan 1;16(1):50-60
All:  5 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
11/12/2024
MGI 6.24
The Jackson Laboratory