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Symbol Name ID |
Slc12a6
solute carrier family 12, member 6 MGI:2135960 |
| Darker colors indicate more annotations |
| Human Phenotypes | Macrotia |
| Disease(s) Associated with SLC12A6 | |
| agenesis of the corpus callosum with peripheral neuropathy |
| Mouse Phenotypes | cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
cochlear hair cell degeneration |
organ of Corti degeneration |
type I spiral ligament fibrocyte degeneration |
type III spiral ligament fibrocyte degeneration |
decreased endocochlear potential |
deafness |
sensorineural hearing loss |
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| Availability | Mouse Genotype | |||||||||
| Slc12a6tm1Tjj/Slc12a6tm1Tjj | ||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 03/19/2019 MGI 6.13 |
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