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Symbol Name ID |
Slc12a6
solute carrier family 12, member 6 MGI:2135960 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties |
| 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 |
abnormal limb posture |
limp posture |
abnormal locomotor behavior |
akinesia |
abnormal gait |
increased locomotor activity |
paraparesis |
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) |
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| Scn10atm2(cre)Jwo/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) |
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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 05/07/2024 MGI 6.23 |
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