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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
Argininuria
Cystinuria
Hyperlysinuria
Ornithinuria
Disease(s) Associated with SLC7A9
cystinuria

Mouse Phenotypes
argininuria
abnormal circulating amino acid level
hyperglutaminuria
lysinuria
ornithinuria
aminoaciduria
cystinuria
crystalluria
Availability Mouse Genotype
Slc7a9tm1Nune/Slc7a9tm1Nune
Slc7a9tm1Nune/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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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory