| Human Disease |
Muckle-Wells Syndrome; MWS OMIM ID: 191900 |
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| Synonyms | Cryopyrin-Associated Periodic Syndrome 2; CAPS2; UDA Syndrome; Urticaria-Deafness-Amyloidosis Syndrome | |||||||||||||||||||||
| View all models | View ALL (5) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Nlrp3tm1Wstr/Nlrp3+ |
involves: C57BL/6 | J:150053 | View |
| Nlrp3tm1Hhf/Nlrp3+ Lyz2tm1(cre)Ifo/Lyz2+ |
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 | J:150054 | View |
| Nlrp3tm1Flv/Nlrp3tm1Hhf Lyz2tm1(cre)Ifo/Lyz2+ |
involves: 129 * C57BL/6 | J:150054 | View |
| Nlrp3tm1Hhf/Nlrp3+ Tg(CAG-cre/Esr1*)5Amc/? |
involves: 129/Sv * C57BL/6 * CBA | J:150054 | View |
| Nlrp3tm1Hhf/Nlrp3+ Tg(Zp3-cre)3Mrt/? |
involves: 129/Sv * FVB/N | J:150054 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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