About   Help   FAQ
Symbol
Name
ID
Slc12a6
solute carrier family 12, member 6
MGI:2135960
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Abnormality of retinal pigmentation
Hypertelorism
Strabismus
Nystagmus
Myopia
Ptosis
Disease(s) Associated with SLC12A6
agenesis of the corpus callosum with peripheral neuropathy

Mouse Phenotypes
abnormal optic stalk morphology
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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/08/2019
MGI 6.14
The Jackson Laboratory