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Symbol
Name
ID
Ryr2
ryanodine receptor 2, cardiac
MGI:99685
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Sudden death
Disease(s) Associated with RYR2
arrhythmogenic right ventricular dysplasia 2
catecholaminergic polymorphic ventricular tachycardia 1

Mouse Phenotypes
increased sensitivity 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
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/0  (conditional)
Ryr2tm1Krbr/Ryr2tm3.1Swch
A1cfTg(Myh6-cre/Esr1*)1Jmk/0  (conditional)

Contributing Projects:
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
07/09/2019
MGI 6.14
The Jackson Laboratory