| Human Disease |
Encephalopathy, Familial, with Neuroserpin Inclusion Bodies; FENIB OMIM ID: 604218 |
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| Synonyms | Encephalopathy, Familial, with Collins Bodies | |||||||||||||||||||||
| View all models | View ALL (3) 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 |
| Serpini1tm1Dpw/Serpini1tm1Dpw |
involves: 129/Sv * C57BL/6JBom | J:84427 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Thy1-SERPINI1*G392E)333Icka/Tg(Thy1-SERPINI1*G392E)333Icka |
involves: C57BL * CD-1 * DBA | J:144649 | View |
| Tg(Thy1-SERPINI1*G392E)333Icka/0 |
involves: C57BL * CD-1 * DBA | J:144649 | 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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