About   Help   FAQ
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
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/05/2019
MGI 6.13
The Jackson Laboratory