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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 | Splenomegaly |
Hepatosplenomegaly |
Hepatomegaly |
Short stature |
Failure to thrive |
Truncal obesity |
| Disease(s) Associated with SLC7A7 | ||||||
| lysinuric protein intolerance |
| Mouse Phenotypes | cardiac hypertrophy |
cleft palate |
short snout |
embryonic growth retardation |
abnormal embryo size |
decreased embryo size |
decreased birth body size |
increased lean body mass |
slow postnatal weight gain |
weight loss |
postnatal growth retardation |
decreased fetal size |
increased spleen weight |
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| Availability | Mouse Genotype | |||||||||||||
| Slc7a7em1(IMPC)Bay/Slc7a7em1(IMPC)Bay | ||||||||||||||
| Slc7a7em1Lbu/Slc7a7em1Lbu | ||||||||||||||
| Slc7a7Gt(OST41878)Lex/Slc7a7Gt(OST41878)Lex | ||||||||||||||
| Slc7a7em1(IMPC)Bay/Slc7a7+ | ||||||||||||||
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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