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Symbol Name ID |
Slc39a8
solute carrier family 39 (metal ion transporter), member 8 MGI:1914797 |
| Darker colors indicate more annotations |
| Human Phenotypes | Astigmatism |
Strabismus |
Nystagmus |
Visual fixation instability |
Hypermetropia |
| Disease(s) Associated with SLC39A8 | |||||
| congenital disorder of glycosylation type IIn |
| Mouse Phenotypes | abnormal retina morphology |
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| Availability | Mouse Genotype | |
| Slc39a8tm1b(EUCOMM)Wtsi/Slc39a8+ | ||
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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