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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 | Hypsarrhythmia |
Absent speech |
Stereotypical hand wringing |
Epileptic encephalopathy |
Global developmental delay |
Bilateral tonic-clonic seizure |
Bilateral tonic-clonic seizure with focal onset |
Focal impaired awareness seizure |
Atypical absence seizure |
Atonic seizure |
Infantile spasms |
| Disease(s) Associated with KCNB1 | |||||||||||
| developmental and epileptic encephalopathy 26 |
| Mouse Phenotypes | short photoreceptor inner segment |
short photoreceptor outer segment |
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| Availability | Mouse Genotype | ||
| Kcnb1tm1Dgen/Kcnb1tm1Dgen | |||
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 05/14/2024 MGI 6.23 |
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