About   Help   FAQ
Symbol
Name
ID
Ryr1
ryanodine receptor 1, skeletal muscle
MGI:99659
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Feeding difficulties
Weak cry
Disease(s) Associated with RYR1
congenital fiber-type disproportion

Mouse Phenotypes
enhanced behavioral response to xenobiotic
unresponsive to tactile stimuli
decreased grip strength
abnormal posture
abnormal locomotor behavior
no spontaneous movement
paralysis
hindlimb paralysis
Availability Mouse Genotype
Ryr1tm1.1Dhm/Ryr1tm1.1Dhm
Ryr1tm1Tno/Ryr1tm1Tno
Ryr1m1Nisw/Ryr1+
Ryr1tm1.1Dhm/Ryr1+
Ryr1tm1Slh/Ryr1+
Ryr1tm2.1Itl/?

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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
11/05/2019
MGI 6.14
The Jackson Laboratory