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 |
|
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) |
||
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 02/23/2021 MGI 6.16 |
![]() |
|