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| Nomenclature |
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Symbol:
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Rxratm2Ipc
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Name:
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retinoid X receptor alpha;
targeted mutation 2, Pierre Chambon
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MGI ID: |
MGI:2136274 |
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Synonyms: |
RXR-alpha- |
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Gene:
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Rxra
Location:
Chr2:27676440-27762957 bp, + strand
Genetic Position: Chr2,
19.38 cM
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:20550
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129/Sv
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Mutation description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: Replacement of exon 4 with a PGK-Neo cassette. Western analysis using a polyclonal antibody directed against the N-terminus failed to detect the protein in homozygous mutant animals. (J:20550)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Rxra Mutation:
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6 strains or lines available |
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Notes |
Two ES cell lines were used: D3 and H1
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| References |
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Original: |
J:20550
Kastner P et al.,
"Genetic analysis of RXR alpha developmental function: convergence of RXR and RAR signaling pathways in heart and eye morphogenesis."
Cell 1994 Sep 23;78(6):987-1003
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All: |
16 reference(s)
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