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Symbol
Name
ID
Kcnq2
potassium voltage-gated channel, subfamily Q, member 2
MGI:1309503
Phenotype annotations related to behavior/neurological
*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
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)

Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory