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Symbol Name ID |
Slc19a3
solute carrier family 19, member 3 MGI:1931307 |
| Darker colors indicate more annotations |
| Human Phenotypes | Vomiting |
Dysphagia |
| Disease(s) Associated with SLC19A3 | ||
| biotin-responsive basal ganglia disease |
| Mouse Phenotypes | abnormal vitamin absorption |
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| Availability | Mouse Genotype | |
| Slc19a3tm1Said/Slc19a3tm1Said | ||
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 04/30/2024 MGI 6.23 |
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