Symbol Name ID |
Slc12a6
solute carrier family 12, member 6 MGI:2135960 |
Darker colors indicate more annotations |
Human Phenotypes | Facial diplegia |
Limb muscle weakness |
Flexion contracture |
Hypotonia |
Neonatal hypotonia |
EMG: chronic denervation signs |
Skeletal muscle atrophy |
Disease(s) Associated with SLC12A6 | |||||||
agenesis of the corpus callosum with peripheral neuropathy |
Mouse Phenotypes | muscle hypertonia |
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Availability | Mouse Genotype | |
Slc12a6tm1Tjj/Slc12a6tm1Tjj |
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 08/02/2024 MGI 6.24 |
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