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Prdx6tm3.1Abf
Targeted Allele Detail
Summary
Symbol: Prdx6tm3.1Abf
Name: peroxiredoxin 6; targeted mutation 3.1, Aron B Fisher
MGI ID: MGI:5825152
Synonyms: C47S
Gene: Prdx6  Location: Chr1:161067682-161078780 bp, - strand  Genetic Position: Chr1, 69.75 cM
Alliance: Prdx6tm3.1Abf page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:239138
Parent Cell Line:  EAP6 (ES Cell)
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutation:    Single point mutation
 
Mutation detailsThe targeting vector is designed to insert, by site-directed mutagenesis, a TGC to TCC point mutation followed by a FRT-flanked neomycin cassette in exon 2. The mutation results in an alteration of the corresponding amino acid from cysteine to serine (C47S) at codon 47. Flp-mediated recombination removed the FRT-flanked neo cassette. The mutation does not affect phospholipase A2 activity, but does eliminate peroxidase activity. (J:239138)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Prdx6 Mutation:  52 strains or lines available
References
Original:  J:239138 Li H, et al., Critical role of peroxiredoxin 6 in the repair of peroxidized cell membranes following oxidative stress. Free Radic Biol Med. 2015 Oct;87:356-65
All:  3 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