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Trp53tm3.1Glo
Targeted Allele Detail
Summary
Symbol: Trp53tm3.1Glo
Name: transformation related protein 53; targeted mutation 3.1, Guillermina Lozano
MGI ID: MGI:3528279
Synonyms: p53515A, p53H, p53R172H
Gene: Trp53  Location: Chr11:69471185-69482699 bp, + strand  Genetic Position: Chr11, 42.83 cM, cytoband B2-C
Alliance: Trp53tm3.1Glo page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:95318
Parent Cell Line:  AB1 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1+
Mutation
description
Allele Type:    Targeted (Dominant negative, Humanized sequence)
Mutations:    Insertion, Single point mutation
 
Mutation detailsArginine codon 172 (CGC) was changed to histidine (CAC) (c.515G>A, p.R172H, equivalent to p.R175H in humans) and a loxP site flanked neomycin resistance gene cassette was inserted into intron 4. The neo cassette was excised via Cre-mediated recombination. Western blot analysis of homozygous MEFs detected mutant protein. (J:95318)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 3 anatomical structure(s)
Tumor Data
List all tumor models in MMHCdb carrying Trp53tm3.1Glo
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 Trp53 Mutation:  232 strains or lines available
References
Original:  J:95318 Lang GA, et al., Gain of function of a p53 hot spot mutation in a mouse model of Li-Fraumeni syndrome. Cell. 2004 Dec 17;119(6):861-72
All:  35 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
04/16/2024
MGI 6.23
The Jackson Laboratory