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Symbol Name ID |
Nr3c2
nuclear receptor subfamily 3, group C, member 2 MGI:99459 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties |
| Disease(s) Associated with NR3C2 | |
| autosomal dominant pseudohypoaldosteronism type 1 |
| Mouse Phenotypes | behavior/neurological phenotype |
abnormal spatial learning |
abnormal spatial working memory |
abnormal response to novel object |
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| Availability | Mouse Genotype | ||||
| Nr3c2tm2Gsc/Nr3c2tm2Gsc Tg(Camk2a-cre)2Gsc/0 (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 04/16/2024 MGI 6.23 |
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