Symbol Name ID |
Nlrp3
NLR family, pyrin domain containing 3 MGI:2653833 |
Darker colors indicate more annotations |
Human Phenotypes | Meningitis |
Cranial nerve paralysis |
EEG abnormality |
Increased intracranial pressure |
Intellectual disability |
Headache |
Migraine |
Global developmental delay |
Seizure |
Disease(s) Associated with NLRP3 | |||||||||
autosomal dominant nonsyndromic deafness 34 | |||||||||
CINCA Syndrome | |||||||||
familial cold autoinflammatory syndrome 1 | |||||||||
Muckle-Wells syndrome |
Mouse Phenotypes | meningitis |
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Availability | Mouse Genotype | |
Nlrp3tm3.1Hhf/Nlrp3+ |
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 08/02/2024 MGI 6.24 |
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