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Symbol
Name
ID

Slc12a3
solute carrier family 12, member 3
MGI:108114

Phenotype annotations related to renal/urinary system

Darker colors indicate more annotations

Human Phenotypes	Renal magnesium wasting	Renal potassium wasting	Hypocalciuria	Enuresis	Nocturia	Polyuria
Disease(s) Associated with SLC12A3
Gitelman syndrome

Mouse Phenotypes		decreased urine chloride ion level	increased urine potassium level	decreased urine sodium level	decreased urine calcium level	increased urine magnesium level	abnormal distal convoluted tubule morphology	abnormal renal sodium ion transport	polyuria
Availability	Mouse Genotype	decreased urine chloride ion level	increased urine potassium level	decreased urine sodium level	decreased urine calcium level	increased urine magnesium level	abnormal distal convoluted tubule morphology	abnormal renal sodium ion transport	polyuria
	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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