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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nlrp3tm3.1Hhf
targeted mutation 3.1, Hal M Hoffman
MGI:5517707
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Nlrp3tm3.1Hhf/Nlrp3+ involves: 129 MGI:5517789


Genotype
MGI:5517789
ht1
Allelic
Composition
Nlrp3tm3.1Hhf/Nlrp3+
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nlrp3tm3.1Hhf mutation (0 available); any Nlrp3 mutation (64 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Nlrp3tm3.1Hhf/Nlrp3+ mice display joint inflammation

mortality/aging
• mice usually die by 2 to 3 weeks of age

skeleton
• resulting in increased bone resorption
• decreased femur size
• increased relative to small bone size
• whole body as well as cortical and trabecular compartments of the axial and appendicular skeleton
• increased trabecular in the region continguous to the spike but not the region that contains this structure
• in the region continguous to the spike but not the region that contains this structure
• in the region continguous to the spike but not the region that contains this structure
• in the region continuous to the spike area
• in the central zone of the epiphysis, as determined by collagen staining
• stunted skeletal growth
• small skeleton at P13
• higher osteoclast formation potential in the bone marrow
• especially in the mid region
• with tissue spikes that extend into the primary spongiosa of the distal femur
• acellular central structure in the epiphysis of the distal femur and proximal tibia
• due to inflammation
• increased apoptosis particularly in the area surrounding the spike

immune system
N
• mice exhibit normal serum levels of IL1a, IL2, IL10 and IL17
• higher osteoclast formation potential in the bone marrow
• in various tissues, including joints and meninges
• circulating and in the bone marrow
• neutrophilic in the periphery
• inflammatory monocytes in the bone marrow
• increased serum chemokine (eotaxin, KC, MCP-1, MIP-1a, MIP-1b and RANTES) levels
• 3-fold in the bone marrow
• systemic inflammation
• resulting in increased bone resorption

growth/size/body

cellular
• higher osteoclast formation potential in the bone marrow
• of bone marrow cells

nervous system

homeostasis/metabolism
• increased serum chemokine (eotaxin, KC, MCP-1, MIP-1a, MIP-1b and RANTES) levels

hematopoietic system
• higher osteoclast formation potential in the bone marrow
• in various tissues, including joints and meninges
• circulating and in the bone marrow
• neutrophilic in the periphery
• inflammatory monocytes in the bone marrow
• decreased proliferation and survival

limbs/digits/tail
• decreased femur size

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
CINCA Syndrome DOID:0090029 OMIM:607115
J:202147





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory