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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 renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Hematuria
Argininuria
Cystinuria
Hyperlysinuria
Ornithinuria
Nephrolithiasis
Renal insufficiency
Recurrent urinary tract infections
Disease(s) Associated with SLC7A9
cystinuria

Mouse Phenotypes
renal tubular necrosis
argininuria
hyperglutaminuria
lysinuria
ornithinuria
aminoaciduria
cystinuria
crystalluria
tubulointerstitial nephritis
hydronephrosis
abnormal renal tubule morphology
dilated renal tubules
renal cast
increased urinary bladder weight
urolithiasis
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