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Symbol
Name
ID
Slc12a6
solute carrier family 12, member 6
MGI:2135960
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Flexion contracture
Facial diplegia
Limb muscle weakness
Skeletal muscle atrophy
Generalized hypotonia
Neonatal hypotonia
EMG: chronic denervation signs
Disease(s) Associated with SLC12A6
agenesis of the corpus callosum with peripheral neuropathy

Mouse Phenotypes
muscle hypertonia
Availability Mouse Genotype
Slc12a6tm1Tjj/Slc12a6tm1Tjj

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/05/2019
MGI 6.13
The Jackson Laboratory