|
Symbol Name ID |
Casr
calcium-sensing receptor MGI:1351351 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypermagnesiuria |
Hyperphosphaturia |
Hypercalciuria |
Hypocalciuria |
Hyperoxaluria |
Nephrocalcinosis |
Nephrolithiasis |
Calcium oxalate nephrolithiasis |
Polycystic kidney dysplasia |
Decreased glomerular filtration rate |
Renal insufficiency |
Acute kidney injury |
Nephroblastoma |
Papillary renal cell carcinoma |
Renal cortical adenoma |
Ureteropelvic junction obstruction |
| Disease(s) Associated with CASR | ||||||||||||||||
| autosomal dominant hypocalcemia | ||||||||||||||||
| autosomal dominant hypocalcemia 1 | ||||||||||||||||
| calcium oxalate nephrolithiasis | ||||||||||||||||
| familial hypocalciuric hypercalcemia 1 | ||||||||||||||||
| hyperparathyroidism |
| Mouse Phenotypes | renal/urinary system phenotype |
decreased urine calcium level |
increased urine calcium level |
decreased urine phosphate level |
nephrocalcinosis |
|
| Availability | Mouse Genotype | |||||
| CasrNuf/CasrNuf | ||||||
| Casrtm1Ces/Casrtm1Ces | ||||||
| Casrtm1Ces/Casr+ | * | |||||
| Casrtm1Wch/Casrtm1Wch Tg(PTH-cre)4167Slib/0 (conditional) |
||||||
| Casrtm1Wch/Casr+ Tg(PTH-cre)4167Slib/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) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools