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Usp7tm1Wgu
Targeted Allele Detail
Summary
Symbol: Usp7tm1Wgu
Name: ubiquitin specific peptidase 7; targeted mutation 1, Wei Gu
MGI ID: MGI:4941831
Synonyms: hausp-, hauspdeltaEx14
Gene: Usp7  Location: Chr16:8506586-8574931 bp, - strand  Genetic Position: Chr16, 4.28 cM
Alliance: Usp7tm1Wgu page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:168184
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsAn IRES LacZ-neo cassette is inserted into exon 14 of the gene and 29 nucleotides are deleted within exon 14 by targeted homologous recombination. The resulting mutation causes C-terminal truncation and partial deletion of DUB active site domain due to a reading frame shift in protein translation. Western blot confirmed absence of protein product in E8.5 embryo. This is a null allele. (J:168184)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 8 assay results
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 Usp7 Mutation:  63 strains or lines available
References
Original:  J:168184 Kon N, et al., Inactivation of HAUSP in vivo modulates p53 function. Oncogene. 2010 Mar 4;29(9):1270-9
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)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory