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Symbol Name ID |
Slc19a2
solute carrier family 19 (thiamine transporter), member 2 MGI:1928761 |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties |
Hoarse voice |
| Disease(s) Associated with SLC19A2 | ||
| megaloblastic anemia | ||
| thiamine-responsive megaloblastic anemia syndrome |
| Mouse Phenotypes | ataxia |
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| Availability | Mouse Genotype | |
| Slc19a2tm1Gelb/Slc19a2tm1Gelb | ||
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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