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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 | Hepatic amyloidosis |
Hepatosplenomegaly |
Hepatomegaly |
Cirrhosis |
| Disease(s) Associated with SLC7A7 | ||||
| lysinuric protein intolerance |
| Mouse Phenotypes | delayed hepatic development |
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| Availability | Mouse Genotype | |
| Slc7a7em1Lbu/Slc7a7em1Lbu | ||
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 04/23/2024 MGI 6.23 |
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