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Symbol
Name
ID

Slc12a3
solute carrier family 12, member 3
MGI:108114

Phenotype annotations related to homeostasis/metabolism

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 chloride ion level	increased urine potassium level	decreased urine sodium level	decreased urine calcium level	increased urine magnesium level	abnormal physiological response to xenobiotic	decreased physiological sensitivity to xenobiotic
Availability	Mouse Genotype	decreased circulating magnesium level	hypokalemia	decreased urine chloride ion level	increased urine potassium level	decreased urine sodium level	decreased urine calcium level	increased urine magnesium level	abnormal physiological response to xenobiotic	decreased physiological sensitivity to xenobiotic
	Slc12a3^em3Gpt/Slc12a3^em3Gpt
	Slc12a3^em4Gpt/Slc12a3^em4Gpt
	Slc12a3^tm1Ges/Slc12a3^tm1Ges
	Slc12a3^em3Gpt/Slc12a3^em4Gpt

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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