Nfkbiatm1.1Pjc
Targeted Allele Detail
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Symbol: |
Nfkbiatm1.1Pjc |
Name: |
nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha; targeted mutation 1.1, Paul J Chiao |
MGI ID: |
MGI:4829878 |
Synonyms: |
IkappaBalphaM, IkBaM |
Gene: |
Nfkbia Location: Chr12:55536195-55539432 bp, - strand Genetic Position: Chr12, 24.0 cM, cytoband C1-C3
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Alliance: |
Nfkbiatm1.1Pjc page
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Germline Transmission: |
Earliest citation of germline transmission:
J:163686
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
Not Specified
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Allele Type: |
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Targeted (Modified regulatory region) |
Mutations: |
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Insertion, Nucleotide substitutions
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Mutation details: Two well defined NFKB binding sites (M1 and M2) and 4 NFKB like binding sites (M3 - M6) in the promoter region were mutated, a FLAG tag was attached to exon 1, and a floxed neo cassette was inserted in intron 1 via homologous recombination. Cre mediated recombination removed the neo cassette. The locations of and mutations in the 6 binding sites are as follows: -115 - -93, a TCC motif changed to a CCG (M1); -143 - -122, a CCC motif changed to an AGT (M2); -227 - -205, a TCT motif changed to a CAC (M3); -292 - -271, a CC motif changed to a AA (M4); -319 - -297, a GGG motif changed to a TTT (M5); -387 - -365, a CCC motif changed to a GGG (M6). Chromatin immunoprecipitation analysis confirmed the loss of kappa B enhancer function in MEFs from homozygous mice.
(J:163686)
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View phenotypes and curated references for all genotypes (concatenated display).
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Original: |
J:163686 Peng B, et al., Defective feedback regulation of NF-kappaB underlies Sjogren's syndrome in mice with mutated kappaB enhancers of the IkappaBalpha promoter. Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15193-8 |
All: |
3 reference(s) |
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