| Human Disease |
Fatal Familial Insomnia; FFI OMIM ID: 600072 |
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| Synonyms | Insomnia, Fatal Familial | |||||||||||||||||||||
| View all models | View ALL (1) 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 |
| Prnptm2Lnq/Prnptm2Lnq |
involves: 129P2/OlaHsd * C57BL/6 | J:154937 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Prnptm1Edin/Prnptm1Edin |
129P2/OlaHsd-Prnptm1Edin | J:58820 | View |
| Prnptm1Rcm/Prnptm1Rcm |
129P2/OlaHsd-Prnptm1Rcm | J:45908 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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