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Allele : Ryr2<tm2.1Wex> ryanodine receptor 2, cardiac; targeted mutation 2.1, Xander Wehrens

Primary Identifier  MGI:5571850 Allele Type  Targeted
Attribute String  Constitutively active Gene  Ryr2
Transmission  Germline Strain of Origin  129S7/SvEvBrd-Hprt1<b-m2>
Is Recombinase  false Is Wild Type  false
molecularNote  Exon 56 was replaced with one containing nucleotide substitutions that result in the amino acid substitution of aspartic acid for serine at position 2814 (S2814D). This mutation produces a constitutively active protein. The modified exon was followed by a floxed neo cassette that was removed by subsequent cre-mediated recombination.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • RyR2-S2814D,
  • RyR2-S2814D
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

11 Publication categories