Symbol Name ID |
Nlrp12
NLR family, pyrin domain containing 12 MGI:2676630 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Leukocytosis |
Recurrent aphthous stomatitis |
Lymphadenopathy |
Splenomegaly |
Erythema nodosum |
Skin rash |
Disease(s) Associated with NLRP12 | ||||||
familial cold autoinflammatory syndrome 2 |
Mouse Phenotypes | immune system phenotype |
impaired neutrophil chemotaxis |
abnormal leukocyte migration |
increased susceptibility to induced colitis |
enlarged spleen |
decreased neutrophil cell number |
abnormal cytokine level |
abnormal chemokine level |
decreased susceptibility to type IV hypersensitivity reaction |
increased inflammatory response |
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Availability | Mouse Genotype | ||||||||||
Nlrp12tm1Jpyt/Nlrp12tm1Jpyt | * | ||||||||||
Nlrp12tm1Tdk/Nlrp12tm1Tdk |
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 09/03/2024 MGI 6.24 |
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