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Symbol Name ID |
Kcnq3
potassium voltage-gated channel, subfamily Q, member 3 MGI:1336181 |
| Darker colors indicate more annotations |
| Human Phenotypes | Lack of spontaneous play |
Reduced ability to form peer relationships |
Autism |
Motor stereotypy |
Inflexible adherence to routines |
Restrictive behavior |
| Disease(s) Associated with KCNQ3 | ||||||
| autistic disorder |
| Mouse Phenotypes | increased exploration in new environment |
hyperactivity |
seizures |
abnormal seizure response to electrical stimulation |
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| Availability | Mouse Genotype | ||||
| Kcnq3em1(IMPC)H/Kcnq3em1(IMPC)H | |||||
| Kcnq3tm1.1Naas/Kcnq3tm1.1Naas | |||||
| Kcnq3tm1.1Naas/Kcnq3+ | |||||
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 05/26/2026 MGI 6.24 |
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