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Symbol
Name
ID
Slc12a6
solute carrier family 12, member 6
MGI:2135960
Phenotype annotations related to hearing/vestibular/ear
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

Contributing Projects:
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
10/15/2019
MGI 6.14
The Jackson Laboratory