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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ryr3tm1Vso
targeted mutation 1, Vincenzo Sorrentino
MGI:2181794
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ryr3tm1Vso/Ryr3tm1Vso involves: 129P2/OlaHsd MGI:3623004
hm2
Ryr3tm1Vso/Ryr3tm1Vso involves: 129P2/OlaHsd * C57BL/6 MGI:3623003


Genotype
MGI:3623004
hm1
Allelic
Composition
Ryr3tm1Vso/Ryr3tm1Vso
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ryr3tm1Vso mutation (1 available); any Ryr3 mutation (261 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• spontaneous discrete events of calcium release in mutant myotubes are of longer duration than those in wild-type




Genotype
MGI:3623003
hm2
Allelic
Composition
Ryr3tm1Vso/Ryr3tm1Vso
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ryr3tm1Vso mutation (1 available); any Ryr3 mutation (261 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• time to peak tension becomes shorter in adult mutant muscle preparations compared to neonatal preparations
• in neonatal (15 day old) mutant mice, the tension developed in a twitch at low frequency or that develop in an unfused tetani is lower than that in wild-type preparations; the force-frequency curve is shifted down and rightward in nulls
• contracture of diaphragm muscle induced by caffeine is strongly reduced in mutant muscle compared to wild-type neonatal muscle; response to caffeine is almost abolished in mutant neonatal diaphragm muscle and significantly reduced in the extensor digitorum longus and soleus muscles





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last database update
08/21/2024
MGI 6.24
The Jackson Laboratory