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Symbol Name ID |
Slc17a5
solute carrier family 17 (anion/sugar transporter), member 5 MGI:1924105 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypertelorism |
Exotropia |
Nystagmus |
| Disease(s) Associated with SLC17A5 | |||
| sialuria |
| Mouse Phenotypes | abnormal optic nerve morphology |
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| Availability | Mouse Genotype | |
| Slc17a5tm1Lex/Slc17a5tm1Lex | ||
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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