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Symbol Name ID |
Slc7a9
solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 MGI:1353656 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hematuria |
Hyperlysinuria |
Argininuria |
Cystinuria |
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 tubule |
renal cast |
increased urinary bladder weight |
urolithiasis |
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| Availability | Mouse Genotype | |||||||||||||||
| Slc7a9tm1Nune/Slc7a9tm1Nune | ||||||||||||||||
| Slc7a9tm1Nune/Slc7a9+ | ||||||||||||||||
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 05/14/2024 MGI 6.23 |
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