Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Nlrp3tm1Hhf
Name:	NLR family, pyrin domain containing 3; targeted mutation 1, Hal M Hoffman
MGI ID:	MGI:3850011
Synonyms:	Nlrp3A350VneoR
Gene:	Nlrp3  Location: Chr11:59432395-59457781 bp, + strand  Genetic Position: Chr11, 37.73 cM, cytoband B1.3
Alliance:	Nlrp3tm1Hhf page

Germline Transmission:	Earliest citation of germline transmission: J:150054
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	129/Sv

Allele Type:    Targeted (Conditional ready, Humanized sequence, No functional change) Mutations:    Insertion, Nucleotide substitutions   Mutation details: The alanine 352 to valine human mutation associated with Muckle-Wells syndrome was produced in mice by changing the equivalent alanine at position 350 to a valine (A350V). A floxed neomycin cassette was inserted in the reverse orientation into intron 2, which is upstream of the point mutation in exon 3. Sequence analysis of transcripts isolated from heterozygote mice demonstrate the mutant allele is not expressed due to the presence of the neomycin cassette. In the presence of cre recombinase, the neomycin cassette is removed and the mutant allele is expressed. (J:150054)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

3 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Nlrp3 Mutation:	61 strains or lines available

Original:	J:150054 Brydges SD, et al., Inflammasome-mediated disease animal models reveal roles for innate but not adaptive immunity. Immunity. 2009 Jun 19;30(6):875-87
All:	34 reference(s)