Symbol Name ID |
Cntn2
contactin 2 MGI:104518 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hippocampal sclerosis |
Myoclonus |
Tremor |
Interictal epileptiform activity |
Bilateral tonic-clonic seizure |
Focal impaired awareness seizure |
Focal sensory seizure with visual features |
Disease(s) Associated with CNTN2 | |||||||
familial adult myoclonic epilepsy 5 |
Mouse Phenotypes | nervous system phenotype |
increased susceptibility to pharmacologically induced seizures |
sporadic seizures |
abnormal sensory neuron innervation pattern |
abnormal spinal cord dorsal horn morphology |
abnormal somatic nervous system physiology |
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Availability | Mouse Genotype | ||||||
Cntn2tm1Fuka/Cntn2tm1Fuka | * | ||||||
Cntn2tm1Furl/Cntn2tm1Furl | |||||||
Cntn2tm2Furl/Cntn2tm2Furl |
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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