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Symbol
Name
ID
Slc12a6
solute carrier family 12, member 6
MGI:2135960
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Low anterior hairline
Disease(s) Associated with SLC12A6
agenesis of the corpus callosum with peripheral neuropathy


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
05/07/2024
MGI 6.23
The Jackson Laboratory