Nlrp3tm2.1(NLRP3)Bhk
Targeted Allele Detail
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Symbol: |
Nlrp3tm2.1(NLRP3)Bhk |
Name: |
NLR family, pyrin domain containing 3; targeted mutation 2.1, Beverly H Koller |
MGI ID: |
MGI:5910169 |
Synonyms: |
NLRP3 |
Gene: |
Nlrp3 Location: Chr11:59432395-59457781 bp, + strand Genetic Position: Chr11, 37.73 cM, cytoband B1.3
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Alliance: |
Nlrp3tm2.1(NLRP3)Bhk page
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Germline Transmission: |
Earliest citation of germline transmission:
J:241705
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
129S6/SvEvTac
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Allele Type: |
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Targeted (Humanized sequence, Inserted expressed sequence, No functional change, Null/knockout) |
Mutations: |
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Insertion, Intragenic deletion
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Nlrp3tm2.1(NLRP3)Bhk expresses
1 gene
Knock-in expresses:
Organism |
Expressed Gene |
Homolog in Mouse |
Note |
human |
NLRP3 (114548) |
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Mutation details: A Replacer vector containing a mutated loxP site and the human ortholog of the mouse gene was injected into Nlrp3tm1Bhk ES cells. In these ES cells the endogenous locus was replaced with an FRT site flanked neomycin resistance gene cassette which was then removed through flp-mediated recombination. The cells also contain the same mutated loxP site as the Replacer vector. The injected ES cells were subjected to cre-mediated recombination to integrate the vector into the genome. The resulting allele corrects the null allele of the ES cells by inserting the human ortholog into the location of the endogenous gene. The inserted gene is flanked by an upstream mutated loxP site and a downstream FRT site. Expression of the inserted sequence was confirmed by qPCR.
(J:241705)
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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 Nlrp3 Mutation: |
66 strains or lines available
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Original: |
J:241705 Snouwaert JN, et al., An NLRP3 Mutation Causes Arthropathy and Osteoporosis in Humanized Mice. Cell Rep. 2016 Dec 13;17(11):3077-3088 |
All: |
1 reference(s) |
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