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 |
|
Availability | Mouse Genotype | |
Slc52a3tm1.1Said/Slc52a3tm1.1Said Tg(Vil1-cre)997Gum/0 (conditional) |
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 05/28/2024 MGI 6.13 |
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