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Nr3c2tm1Krst
Targeted Allele Detail
Summary
Symbol: Nr3c2tm1Krst
Name: nuclear receptor subfamily 3, group C, member 2; targeted mutation 1, Henk Karst
MGI ID: MGI:3613053
Synonyms: MRloxP
Gene: Nr3c2  Location: Chr8:77626070-77971641 bp, + strand  Genetic Position: Chr8, 36.34 cM
Alliance: Nr3c2tm1Krst page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:104691
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsLoxP sites flanked exon 3, which encodes the first zinc finger of the mineralocorticoid receptor DNA binding domain. (J:104691)
Phenotypes
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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: 0 strains available      Cell Lines: 0 lines available
Carrying any Nr3c2 Mutation:  51 strains or lines available
References
Original:  J:104691 Karst H, et al., Mineralocorticoid receptors are indispensable for nongenomic modulation of hippocampal glutamate transmission by corticosterone. Proc Natl Acad Sci U S A. 2005 Dec 27;102(52):19204-7
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
04/16/2024
MGI 6.23
The Jackson Laboratory