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) |
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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) |
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last database update 07/05/2024 MGI 6.24 |
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