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Symbol Name ID |
Kcnb1
potassium voltage gated channel, Shab-related subfamily, member 1 MGI:96666 |
| Darker colors indicate more annotations |
| Human Phenotypes | Stereotypical hand wringing |
| Disease(s) Associated with KCNB1 | |
| developmental and epileptic encephalopathy 26 |
| Mouse Phenotypes | increased exploration in new environment |
abnormal locomotor behavior |
abnormal gait |
hyperactivity |
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| Availability | Mouse Genotype | ||||
| Kcnb1tm1b(EUCOMM)Hmgu/Kcnb1tm1b(EUCOMM)Hmgu | |||||
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 |
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