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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) |
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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 04/16/2024 MGI 6.23 |
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