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Ryr2tm1.1Msnr
Targeted Allele Detail
Summary
Symbol: Ryr2tm1.1Msnr
Name: ryanodine receptor 2, cardiac; targeted mutation 1.1, Gerhard Meissner
MGI ID: MGI:3713774
Synonyms: Ryr2ADA, Ryr2tm1Msnr
Gene: Ryr2  Location: Chr13:11567988-12121831 bp, - strand  Genetic Position: Chr13, 4.38 cM, cytoband A1-A2
Alliance: Ryr2tm1.1Msnr page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:122033
Parent Cell Line:  TC1/TC-1 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Not Specified)
Mutation:    Nucleotide substitutions
 
Mutation detailsA targeting vector was designed to insert the W3587A/L3591AD/F3603A mutations into exon 75. A floxed neo was subsequently removed via cre mediated recombination. (J:122033)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Ryr2 Mutation:  325 strains or lines available
References
Original:  J:122033 Yamaguchi N, et al., Early cardiac hypertrophy in mice with impaired calmodulin regulation of cardiac muscle Ca release channel. J Clin Invest. 2007 May;117(5):1344-53
All:  5 reference(s)

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
04/09/2024
MGI 6.23
The Jackson Laboratory