Symbol Name ID |
Nlrp3
NLR family, pyrin domain containing 3 MGI:2653833 |
Darker colors indicate more annotations |
Human Phenotypes | Purpura |
Urticaria |
Skin rash |
Maculopapular exanthema |
Papule |
Ichthyosis |
Disease(s) Associated with NLRP3 | ||||||
autosomal dominant nonsyndromic deafness 34 | ||||||
CINCA Syndrome | ||||||
familial cold autoinflammatory syndrome 1 | ||||||
Muckle-Wells syndrome |
Mouse Phenotypes | dermatitis |
hairless |
reddish skin |
scaly skin |
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Availability | Mouse Genotype | ||||
Nlrp3tm1Wstr/Nlrp3+ | |||||
Nlrp3tm1Hhf/Nlrp3+ Lyz2tm1(cre)Ifo/Lyz2+ (conditional) |
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Nlrp3tm1Hhf/Nlrp3+ Tg(Zp3-cre)3Mrt/? (conditional) |
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 05/14/2024 MGI 6.23 |
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