Symbol Name ID |
Nr3c1
nuclear receptor subfamily 3, group C, member 1 MGI:95824 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Sudden cardiac death |
Disease(s) Associated with NR3C1 | |
coronary artery disease |
Mouse Phenotypes | increased susceptibility to induced morbidity/mortality |
lethality, complete penetrance |
decreased survivor rate |
premature death |
neonatal lethality, complete penetrance |
neonatal lethality, incomplete penetrance |
perinatal lethality, complete penetrance |
perinatal lethality, incomplete penetrance |
postnatal lethality, complete penetrance |
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Availability | Mouse Genotype | |||||||||
Nr3c1Gt(ESKN92)Hgs/Nr3c1Gt(ESKN92)Hgs | ||||||||||
Nr3c1tm1Gsc/Nr3c1tm1Gsc | ! | |||||||||
Nr3c1tm1Ljm/Nr3c1tm1Ljm | ||||||||||
Nr3c1tm2.1Gsc/Nr3c1tm2.1Gsc | ||||||||||
Nr3c1tm1.1Jaci/Nr3c1tm1.1Jaci Tg(Myh6-cre)2182Mds/0 (conditional) |
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Nr3c1tm1.1Mvc/Nr3c1tm1.1Mvc Tg(Sim1-cre)1Lowl/0 (conditional) |
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Nr3c1tm2Ljm/Nr3c1tm2Ljm Tg(Lck-cre)548Jxm/? (conditional) |
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 06/12/2024 MGI 6.13 |
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