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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	Fetal akinesia sequence	Feeding difficulties	Feeding difficulties in infancy	Fatigue	Chest pain	Exercise-induced myalgia
Disease(s) Associated with RYR1	Decreased fetal movement	Fetal akinesia sequence	Feeding difficulties	Feeding difficulties in infancy	Fatigue	Chest pain	Exercise-induced myalgia
congenital myopathy 1A
congenital myopathy 1B
primary pulmonary hypertension

Mouse Phenotypes		enhanced behavioral response to xenobiotic	unresponsive to tactile stimuli	decreased grip strength	abnormal posture	abnormal locomotor behavior	paralysis	hindlimb paralysis	no spontaneous movement
Availability	Mouse Genotype	enhanced behavioral response to xenobiotic	unresponsive to tactile stimuli	decreased grip strength	abnormal posture	abnormal locomotor behavior	paralysis	hindlimb paralysis	no spontaneous movement
	Ryr1^tm1.1Dhm/Ryr1^tm1.1Dhm
	Ryr1^tm1Tno/Ryr1^tm1Tno
	Ryr1^m1Nisw/Ryr1⁺
	Ryr1^tm1.1Dhm/Ryr1⁺
	Ryr1^tm1Slh/Ryr1⁺
	Ryr1^tm2.1Itl/?

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)
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