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Symbol Name ID |
Slc12a6
solute carrier family 12, member 6 MGI:2135960 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of retinal pigmentation |
Hypertelorism |
Strabismus |
Esotropia |
Nystagmus |
Myopia |
Ptosis |
| Disease(s) Associated with SLC12A6 | |||||||
| agenesis of the corpus callosum with peripheral neuropathy |
| Mouse Phenotypes | abnormal optic stalk morphology |
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| Availability | Mouse Genotype | |
| Slc12a6tm1Tjj/Slc12a6tm1Tjj | ||
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 04/23/2024 MGI 6.23 |
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