Symbol Name ID |
Kcnh3
potassium voltage-gated channel, subfamily H (eag-related), member 3 MGI:1341723 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Mouse Phenotypes | behavior/neurological phenotype |
increased susceptibility to pharmacologically induced seizures |
abnormal long-term object recognition memory |
abnormal spatial reference memory |
abnormal spatial working memory |
hyperactivity |
nonconvulsive seizures |
abnormal spike wave discharge |
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Availability | Mouse Genotype | ||||||||
Kcnh3tm1.1(KOMP)Vlcg/Kcnh3tm1.1(KOMP)Vlcg | |||||||||
Kcnh3tm1.2Tije/Kcnh3tm1.2Tije | * | ||||||||
Kcnh3tm1Akmi/Kcnh3tm1Akmi | |||||||||
Kcnh3tm1.2Tije/Kcnh3+ | |||||||||
Kcnh3tm1Akmi/Kcnh3+ |
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 04/30/2024 MGI 6.23 |
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