Symbol Name ID |
Ryr2
ryanodine receptor 2, cardiac MGI:99685 |
Darker colors indicate more annotations |
Human Phenotypes | Sudden cardiac death |
Disease(s) Associated with RYR2 | |
catecholaminergic polymorphic ventricular tachycardia 1 |
Mouse Phenotypes | increased susceptibility to induced morbidity/mortality |
decreased survivor rate |
premature death |
lethality throughout fetal growth and development, incomplete penetrance |
postnatal lethality, complete penetrance |
embryonic lethality during organogenesis, complete penetrance |
embryonic lethality, complete penetrance |
prenatal lethality, complete penetrance |
preweaning lethality, complete penetrance |
|
Availability | Mouse Genotype | |||||||||
Ryr2em1Swch/Ryr2em1Swch | ||||||||||
Ryr2tm1.1Hta/Ryr2tm1.1Hta | ||||||||||
Ryr2tm1.1Msnr/Ryr2tm1.1Msnr | ||||||||||
Ryr2tm1b(KOMP)Wtsi/Ryr2tm1b(KOMP)Wtsi | ||||||||||
Ryr2tm2.1Swch/Ryr2tm2.1Swch | ||||||||||
Ryr2tm2.1Wex/Ryr2tm2.1Wex | ||||||||||
Ryr2tm2Amks/Ryr2tm2Amks | ||||||||||
Ryr2tm2Hhv/Ryr2tm2Hhv | ||||||||||
Ryr2tm3.1Hhv/Ryr2tm3.1Hhv | ||||||||||
Ryr2tm3.1Swch/Ryr2tm3.1Swch | ||||||||||
Ryr2tm1Slh/Ryr2+ | ||||||||||
Ryr2tm2Amks/Ryr2+ | ||||||||||
Ryr2tm1Krbr/Ryr2tm1Krbr A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ (conditional) |
||||||||||
Ryr2tm1Krbr/Ryr2tm3.1Swch A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 08/02/2024 MGI 6.24 |
![]() |
|