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Symbol
Name
ID

Slc26a4
solute carrier family 26, member 4
MGI:1346029

Phenotype annotations related to renal/urinary system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Nephropathy
Disease(s) Associated with SLC26A4	Nephropathy
Pendred Syndrome

Mouse Phenotypes		renal/urinary system phenotype	increased urine ammonia level	decreased urine pH
Availability	Mouse Genotype	renal/urinary system phenotype	increased urine ammonia level	decreased urine pH
	Slc26a4^tm1.1Dontu/Slc26a4^tm1.1Dontu	*
	Slc26a4^tm1Sole/Slc26a4^tm1Sole
	Slc26a4^tm2.1Dontu/Slc26a4^tm2.1Dontu	*
	Slc26a4^tm1.1Dontu/Slc26a4^tm2.1Dontu	*

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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