| Human Disease |
Periodic Fever, Familial, Autosomal Dominant OMIM ID: 142680 |
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| Synonyms | Familial Hibernian Fever; FPF; Hibernian Fever, Familial; FHF; TNF Receptor-Associated Periodic Syndrome; Tumor Necrosis Factor Receptor-Associated Periodic Syndrome; TRAPS | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Tnfrsf1atm2.1Rsie/Tnfrsf1a+ |
B6.Cg-Tnfrsf1atm2.1Rsie | J:160543 | View |
| Tnfrsf1atm1Rsie/Tnfrsf1a+ |
B6.Cg-Tnfrsf1atm1Rsie | J:160543 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tnfrsf1atm1Imx/Tnfrsf1atm1Imx |
involves: 129S7/SvEvBrd * C57BL/6 | J:45147 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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