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Symbol Name ID |
Slc38a3
solute carrier family 38, member 3 MGI:1923507 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
| Disease(s) Associated with SLC38A3 | |
| developmental and epileptic encephalopathy 102 |
| Mouse Phenotypes | abnormal bone structure |
increased bone mineral content |
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| Availability | Mouse Genotype | ||
| Slc38a3em1(IMPC)Bay/Slc38a3+ | |||
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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