Symbol Name ID |
Kcnq2
potassium voltage-gated channel, subfamily Q, member 2 MGI:1309503 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Disease(s) Associated with KCNQ2 | |
developmental and epileptic encephalopathy 7 |
Mouse Phenotypes | behavior/neurological phenotype |
increased susceptibility to pharmacologically induced seizures |
decreased exploration in new environment |
impaired spatial learning |
seizures |
abnormal seizure response to electrical stimulation |
clonic seizures |
tonic-clonic seizures |
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Availability | Mouse Genotype | ||||||||
Kcnq2Nmf134/Kcnq2Nmf134 | |||||||||
Kcnq2tm1.1Naas/Kcnq2tm1.1Naas | |||||||||
Kcnq2tm2.1Snhr/Kcnq2tm2.1Snhr | * | ||||||||
Kcnq2Nmf134/Kcnq2+ | |||||||||
Kcnq2tm1.1Lvi/Kcnq2+ | * | ||||||||
Kcnq2tm1.1Naas/Kcnq2+ | |||||||||
Kcnq2tm1Dgen/Kcnq2+ | |||||||||
Kcnq2tm1Hsa/Kcnq2+ | * | ||||||||
Kcnq2tm2.1Snhr/Kcnq2+ | |||||||||
Kcnq2tm3.1Snhr/Kcnq2+ | |||||||||
Emx1tm1(cre)Krj/? Kcnq2tm1.1Avtz/Kcnq2tm1.1Avtz (conditional) |
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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