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Symbol
Name
ID
Slc12a6
solute carrier family 12, member 6
MGI:2135960
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Psychosis
Disease(s) Associated with SLC12A6
agenesis of the corpus callosum with peripheral neuropathy

Mouse Phenotypes
behavior/neurological phenotype
increased susceptibility to pharmacologically induced seizures
decreased exploration in new environment
increased coping response
abnormal startle reflex
limb grasping
ataxia
impaired coordination
impaired limb coordination
abnormal physical strength
weakness
paraparesis
abnormal limb posture
limp posture
abnormal locomotor behavior
akinesia
hyperactivity
abnormal gait
decreased chemical nociceptive threshold
Availability Mouse Genotype
Slc12a6em1Dlp/Slc12a6em1Dlp
Slc12a6gaxp/Slc12a6gaxp
Slc12a6Gt(OST458419)Lex/Slc12a6Gt(OST458419)Lex
Slc12a6tm1.1Garo/Slc12a6tm1.1Garo
Slc12a6tm1Dlp/Slc12a6tm1Dlp
Slc12a6tm1Tjj/Slc12a6tm1Tjj
Slc12a6tm1Dlp/Slc12a6+
Slc12a6tm1Garo/Slc12a6tm1Garo
Tg(Syn1-cre)671Jxm/0  (conditional)
Scn10atm2(cre)Jnw/Scn10a+
Slc12a6tm2.1Dlp/Slc12a6tm2.1Dlp  (conditional)
*
Slc12a6tm2.1Dlp/Slc12a6tm2.1Dlp
Tg(Dhh-cre)1Mejr/0  (conditional)
*
Slc12a6tm2.1Dlp/Slc12a6tm2.1Dlp
Tg(Eno2-cre)39Jme/0  (conditional)
*
Pvalbtm1(cre)Arbr/Pvalb+
Slc12a6tm2.1Dlp/Slc12a6tm2.1Dlp  (conditional)

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
02/12/2019
MGI 6.13
The Jackson Laboratory