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Symbol
Name
ID

Nr3c1
nuclear receptor subfamily 3, group C, member 1
MGI:95824

Phenotype annotations related to skeleton

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Osteoporosis	Gout
Disease(s) Associated with NR3C1	Osteoporosis	Gout
coronary artery disease

Mouse Phenotypes		skeleton phenotype	abnormal osteoblast differentiation	abnormal osteoblast physiology	abnormal bone mineral density	decreased bone mineral density	decreased bone trabecula number	increased bone trabecular spacing	osteoporosis	abnormal bone ossification
Availability	Mouse Genotype	skeleton phenotype	abnormal osteoblast differentiation	abnormal osteoblast physiology	abnormal bone mineral density	decreased bone mineral density	decreased bone trabecula number	increased bone trabecular spacing	osteoporosis	abnormal bone ossification
	Nr3c1^tm2.1Gsc/Nr3c1^tm2.1Gsc	*
	Nr3c1^tm3Gsc/Nr3c1^tm3Gsc	*
	Nr3c1^tm2Gsc/Nr3c1^tm2Gsc Tg(Nes-cre)1Kln/0 (conditional)
	Nr3c1^tm2Gsc/Nr3c1^tm2Gsc Tg(Runx2-icre)1Jtuc/0 (conditional)	*
	Nr3c1^tm2Gsc/Nr3c1^tm2Gsc Lyz2^tm1(cre)Ifo/Lyz2⁺ (conditional)	*

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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