Symbol Name ID |
Ryr2
ryanodine receptor 2, cardiac MGI:99685 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Seizure |
Disease(s) Associated with RYR2 | |
catecholaminergic polymorphic ventricular tachycardia 1 |
Mouse Phenotypes | nervous system phenotype |
increased susceptibility to pharmacologically induced seizures |
tonic-clonic seizures |
abnormal nervous system electrophysiology |
abnormal action potential |
abnormal afterhyperpolarization |
abnormal brain wave pattern |
abnormal miniature excitatory postsynaptic currents |
decreased paired-pulse ratio |
|
Availability | Mouse Genotype | |||||||||
Ryr2tm1.1Hnis/Ryr2tm1.1Hnis | * | |||||||||
Ryr2tm2Amks/Ryr2tm2Amks | ||||||||||
Ryr2em1Swch/Ryr2+ | ||||||||||
Ryr2tm1Slh/Ryr2+ | ||||||||||
Ryr2tm2Amks/Ryr2+ | * |
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 08/02/2024 MGI 6.24 |
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