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Symbol Name ID |
Slc7a7
solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 MGI:1337120 |
| Darker colors indicate more annotations |
| Human Phenotypes | Oroticaciduria |
Proteinuria |
Aminoaciduria |
Hyperlysinuria |
Argininuria |
Ornithinuria |
Renal amyloidosis |
Glomerulonephritis |
Membranous nephropathy |
Abnormal renal tubule morphology |
Tubulointerstitial nephritis |
Renal fibrosis |
Decreased glomerular filtration rate |
Stage 5 chronic kidney disease |
| Disease(s) Associated with SLC7A7 | ||||||||||||||
| lysinuric protein intolerance |
| Mouse Phenotypes | argininuria |
lysinuria |
aminoaciduria |
kidney cortex atrophy |
delayed kidney development |
abnormal proximal convoluted tubule morphology |
dilated renal tubule |
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| Availability | Mouse Genotype | |||||||
| Slc7a7em1Lbu/Slc7a7em1Lbu | ||||||||
| Slc7a7Gt(OST41878)Lex/Slc7a7Gt(OST41878)Lex | ||||||||
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 05/21/2024 MGI 6.23 |
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