Gria2tm1.1Bviss
Targeted Allele Detail
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| Symbol: |
Gria2tm1.1Bviss |
| Name: |
glutamate receptor, ionotropic, AMPA2 (alpha 2); targeted mutation 1.1, Bryce Vissel |
| MGI ID: |
MGI:7643535 |
| Synonyms: |
Gria2G, Gria2tm1BViss |
| Gene: |
Gria2 Location: Chr3:80588757-80710142 bp, - strand Genetic Position: Chr3, 35.5 cM
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| Alliance: |
Gria2tm1.1Bviss page
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| Germline Transmission: |
Earliest citation of germline transmission:
J:348213
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| Parent Cell Line: |
CCE/EK.CCE (ES Cell)
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| Strain of Origin: |
129S/SvEv-Gpi1c
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| Allele Type: |
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Targeted (Not Applicable) |
| Mutations: |
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Insertion, Single point mutation
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Mutation details: 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.
(J:348213)
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| Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
| Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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| Carrying any Gria2 Mutation: |
78 strains or lines available
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| Original: |
J:348213 Wright AL, et al., The Q/R editing site of AMPA receptor GluA2 subunit acts as an epigenetic switch regulating dendritic spines, neurodegeneration and cognitive deficits in Alzheimer's disease. Mol Neurodegener. 2023 Sep 28;18(1):65 |
| All: |
1 reference(s) |
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