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Symbol
Name
ID
Slc12a6
solute carrier family 12, member 6
MGI:2135960
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Flexion contracture
Hypoplasia of the maxilla
Microcephaly
Brachycephaly
Craniosynostosis
Turricephaly
Long fingers
Tapered finger
2-3 toe syndactyly
Scoliosis
Disease(s) Associated with SLC12A6
agenesis of the corpus callosum with peripheral neuropathy

Mouse Phenotypes
type I spiral ligament fibrocyte degeneration
type III spiral ligament fibrocyte degeneration
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
10/08/2019
MGI 6.14
The Jackson Laboratory