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Symbol Name ID |
Slc25a15
solute carrier family 25 (mitochondrial carrier ornithine transporter), member 15 MGI:1342274 |
| Darker colors indicate more annotations |
| Human Phenotypes | Chorioretinal atrophy |
Hypopigmentation of the fundus |
| Disease(s) Associated with SLC25A15 | ||
| ornithine translocase deficiency |
| Mouse Phenotypes | abnormal lens morphology |
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| Availability | Mouse Genotype | |
| Slc25a15tm1b(EUCOMM)Hmgu/Slc25a15+ | ||
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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