About Help FAQ

Symbol
Name
ID

Ryr1
ryanodine receptor 1, skeletal muscle
MGI:99659

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Hepatomegaly	Short stature	Failure to thrive
Disease(s) Associated with RYR1	Hepatomegaly	Short stature	Failure to thrive
congenital myopathy 1B
primary pulmonary hypertension

Mouse Phenotypes		cleft secondary palate	decreased birth weight	decreased birth body size	decreased body weight	increased body weight	omphalocele	pectus excavatum	decreased body length	fetal growth retardation	increased spleen weight
Availability	Mouse Genotype	cleft secondary palate	decreased birth weight	decreased birth body size	decreased body weight	increased body weight	omphalocele	pectus excavatum	decreased body length	fetal growth retardation	increased spleen weight
	Ryr1^m1Bei/Ryr1^m1Bei
	Ryr1^tm1.1Dhm/Ryr1^tm1.1Dhm
	Ryr1^tm1Slh/Ryr1^tm1Slh
	Ryr1^tm1.1Dhm/Ryr1⁺
	Ryr1^{tm1b(EUCOMM)Hmgu}/Ryr1⁺

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, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/09/2024 MGI 6.23