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Allele : Gria2<tm1.1Bviss> glutamate receptor, ionotropic, AMPA2 (alpha 2); targeted mutation 1.1, Bryce Vissel

Primary Identifier  MGI:7643535 Allele Type  Targeted
Gene  Gria2 Transmission  Germline
Strain of Origin  129S/SvEv-Gpi1<c> Is Recombinase  false
Is Wild Type  false
molecularNote  Glutamine codon 607 (CAG) in exon 11 was changed to arginine (CGG) (p.Q607R) and a loxP site flanked neomycin resistance gene cassette was inserted into intron 11. The neo cassette was removed through subsequent Cre-mediated recombination. The mutation mimics the RNA editing at that codon from CAG to CIG, which is translated as a CGG codon, in the brain.
  • mutations:
  • Insertion,
  • Single point mutation
  • synonyms:
  • Gria2<G>,
  • Gria2<tm1BViss>,
  • Gria2<G>,
  • Gria2<tm1BViss>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories

Trail: Allele