About   Help   FAQ
Nr3c2tm2.1Gsc
Targeted Allele Detail
Summary
Symbol: Nr3c2tm2.1Gsc
Name: nuclear receptor subfamily 3, group C, member 2; targeted mutation 2.1, Gunther Schutz
MGI ID: MGI:3613035
Synonyms: MRnull
Gene: Nr3c2  Location: Chr8:77626070-77971641 bp, + strand  Genetic Position: Chr8, 36.34 cM
Alliance: Nr3c2tm2.1Gsc page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:104549
Parent Cell Line:  E14.1 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCre mediated excision was used to remove exon 3, which which encode the first zinc finger of the mineralocorticoid receptor DNA binding domain. (J:104549)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
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 Nr3c2 Mutation:  51 strains or lines available
References
Original:  J:104549 Berger S, et al., Loss of the limbic mineralocorticoid receptor impairs behavioral plasticity. Proc Natl Acad Sci U S A. 2006 Jan 3;103(1):195-200
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/09/2024
MGI 6.23
The Jackson Laboratory