Symbol Name ID |
Slc12a3
solute carrier family 12, member 3 MGI:108114 |
Darker colors indicate more annotations |
Human Phenotypes | Hypomagnesemia |
Hypokalemia |
Hypokalemic alkalosis |
Recurrent fever |
Renal magnesium wasting |
Renal potassium wasting |
Hypocalciuria |
Chondrocalcinosis |
Disease(s) Associated with SLC12A3 | ||||||||
Gitelman syndrome |
Mouse Phenotypes | decreased circulating magnesium level |
hypokalemia |
decreased urine calcium level |
decreased urine chloride ion level |
increased urine potassium level |
decreased urine sodium level |
increased urine magnesium level |
abnormal physiological response to xenobiotic |
decreased physiological sensitivity to xenobiotic |
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Availability | Mouse Genotype | |||||||||
Slc12a3em3Gpt/Slc12a3em3Gpt | ||||||||||
Slc12a3em4Gpt/Slc12a3em4Gpt | ||||||||||
Slc12a3tm1Ges/Slc12a3tm1Ges | ||||||||||
Slc12a3em3Gpt/Slc12a3em4Gpt |
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 09/03/2024 MGI 6.24 |
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