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Symbol Name ID |
Slc52a3
solute carrier protein family 52, member 3 MGI:1916948 |
| Darker colors indicate more annotations |
| Human Phenotypes | External ophthalmoplegia |
Ptosis |
| Disease(s) Associated with SLC52A3 | ||
| Brown-Vialetto-Van Laere syndrome 1 | ||
| Fazio-Londe disease |
| Mouse Phenotypes | abnormal ocular surface morphology |
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| Availability | Mouse Genotype | |
| Slc52a3tm1.1Said/Slc52a3tm1.1Said Tg(Vil1-cre)997Gum/0 (conditional) |
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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 04/09/2024 MGI 6.23 |
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