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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 | Hypotonia |
Infantile muscular hypotonia |
Muscle weakness |
Skeletal muscle atrophy |
| Disease(s) Associated with SLC7A7 | ||||
| lysinuric protein intolerance |
| Mouse Phenotypes | hypotonia |
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| Availability | Mouse Genotype | |
| 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 04/16/2024 MGI 6.23 |
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