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Rxrgem1Nses
Endonuclease-mediated Allele Detail
Summary
Symbol: Rxrgem1Nses
Name: retinoid X receptor gamma; endonuclease-mediated mutation 1, Nenad Sestan
MGI ID: MGI:7425386
Gene: Rxrg  Location: Chr1:167425953-167467192 bp, + strand  Genetic Position: Chr1, 74.99 cM
Alliance: Rxrgem1Nses page
Mutation
origin
Strain of Origin:  (C57BL/6J x SJL/J)F1/J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
    CRISPR-cas9 mediated recombination using guide RNAs created a deletion spanning exons 3 and 4. (J:325971)
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
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 Rxrg Mutation:  28 strains or lines available
References
Original:  J:325971 Shibata M, et al., Regulation of prefrontal patterning and connectivity by retinoic acid. Nature. 2021 Oct;598(7881):483-488
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
12/30/2025
MGI 6.24
The Jackson Laboratory