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Symbol
Name
ID
Ryr1
ryanodine receptor 1, skeletal muscle
MGI:99659
Phenotype annotations related to digestive/alimentary system
Darker colors indicate more annotations
Human Phenotypes
Dysphagia
Disease(s) Associated with RYR1
congenital fiber-type disproportion

Mouse Phenotypes
cleft secondary palate
Availability Mouse Genotype
Ryr1tm1.1Dhm/Ryr1tm1.1Dhm

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
11/12/2019
MGI 6.14
The Jackson Laboratory