| Human Disease |
Hyperuricemic Nephropathy, Familial Juvenile, 1; HNFJ1 OMIM ID: 162000 |
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| Synonyms | Familial Juvenile Hyperuricemic Nephropathy; FJHN; Gouty Nephropathy, Familial Juvenile; Hyperuricemic Nephropathy, Familial Juvenile; HNFJ; Nephropathy, Familial, with Gout | |||||||||||||||||||||
| 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Umodtm1Kuma/Umodtm1Kuma |
Not Specified | J:96653 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Umod*C147W)958Lura/0 |
involves: FVB | J:161532 | 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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