About   Help   FAQ
Ryr2tm5.1Amks
Targeted Allele Detail
Summary
Symbol: Ryr2tm5.1Amks
Name: ryanodine receptor 2, cardiac; targeted mutation 5.1, Andrew R Marks
MGI ID: MGI:5796177
Synonyms: RyR2-S2808D
Gene: Ryr2  Location: Chr13:11567988-12121831 bp, - strand  Genetic Position: Chr13, 4.38 cM, cytoband A1-A2
Alliance: Ryr2tm5.1Amks page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:171862
Parent Cell Line:  MM13 (ES Cell)
Strain of Origin:  129S/SvEv
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsExon 55 was replaced wiht one in which nucleotide substitution(s) result(s) in the amino acid substitution of aspartic acid for serine at position 2808 (S2808D). A self-excising neomycin resistance cassette is removed from the final allele. (J:171862)
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:  330 strains or lines available
References
Original:  J:171862 Shan J, et al., Role of chronic ryanodine receptor phosphorylation in heart failure and beta-adrenergic receptor blockade in mice. J Clin Invest. 2010 Dec 1;120(12):4375-87
All:  3 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/30/2025
MGI 6.24
The Jackson Laboratory