Rxratm1Ipc
Targeted Allele Detail
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Symbol: |
Rxratm1Ipc |
Name: |
retinoid X receptor alpha; targeted mutation 1, Pierre Chambon |
MGI ID: |
MGI:1857511 |
Synonyms: |
Rxr alpha AF2I, Rxralphaaf2(l), Rxr alpha AF2O |
Gene: |
Rxra Location: Chr2:27566452-27652969 bp, + strand Genetic Position: Chr2, 19.38 cM
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Alliance: |
Rxratm1Ipc page
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Rxratm1Ipc/Rxratm4Ipc Rxrbtm1Mma/Rxrbtm1Pcn Tg(KRT14-cre/ERT2)1Ipc/0 mice develop alopecia but no skin inflammation while Rxratm4Ipc/Rxratm4Ipc Rxrbtm1Pcn/Rxrbtm1Pcn Tg(KRT14-cre/ERT2)1Ipc/0 mice show both hair loss and skin inflammation
Show the 1 phenotype image(s) involving this allele.
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Germline Transmission: |
Earliest citation of germline transmission:
J:50515
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Parent Cell Line: |
H1 (ES Cell)
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Strain of Origin: |
129S2/SvPas
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Allele Type: |
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Targeted (Null/knockout) |
Mutations: |
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Insertion, Nucleotide substitutions
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Mutation details: This allele encodes a protein that lacks the final 18 amino acids (position 450 to 467) due to a nonsense mutation introduced into exon 10. The deletion corresponds to the last alpha helical structure (helix 12) of the ligand binding domain. A floxed neo cassette was inserted into intron 9 for selection.
(J:50515)
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View phenotypes and curated references for all genotypes (concatenated display).
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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 Rxra Mutation: |
30 strains or lines available
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Original: |
J:50515 Mascrez B, et al., The RXRalpha ligand-dependent activation function 2 (AF-2) is important for mouse development. Development. 1998 Dec;125(23):4691-707 |
All: |
14 reference(s) |
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