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Symbol
Name
ID
Ryr1
ryanodine receptor 1, skeletal muscle
MGI:99659
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Myopathic facies
Abnormality of masseter muscle
Weakness of facial musculature
Facial palsy
High palate
Disease(s) Associated with RYR1
congenital myopathy 1A
congenital myopathy 1B
malignant hyperthermia

Mouse Phenotypes
domed cranium
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
04/23/2024
MGI 6.23
The Jackson Laboratory