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Symbol
Name
ID

Slc7a9
solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
MGI:1353656

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Hyperuricemia	Abnormality of amino acid metabolism	Hematuria	Hyperlysinuria	Argininuria	Cystinuria	Ornithinuria
Disease(s) Associated with SLC7A9
cystinuria

Mouse Phenotypes		argininuria	abnormal circulating amino acid level	hyperglutaminuria	lysinuria	ornithinuria	aminoaciduria	cystinuria	crystalluria
Availability	Mouse Genotype	argininuria	abnormal circulating amino acid level	hyperglutaminuria	lysinuria	ornithinuria	aminoaciduria	cystinuria	crystalluria
	Slc7a9^tm1Nune/Slc7a9^tm1Nune
	Slc7a9^tm1Nune/Slc7a9⁺

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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