| Human Disease |
Vitamin E, Familial Isolated Deficiency Of; VED OMIM ID: 277460 |
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| Synonyms | Ataxia, Friedreich-Like, with Selective Vitamin E Deficiency; AVED; Friedreich-Like Ataxia | |||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ttpatm1Far/Ttpatm1Far |
involves: 129S4/SvJae * C57BL/6 | J:66419 | View |
| Ttpatm1Hsz/Ttpatm1Hsz |
involves: 129S7/SvEvBrd * C57BL/6J | J:67046 | View |
| Ttpatm1Far/Ttpa+ |
involves: 129S4/SvJae * C57BL/6 | J:66419 | 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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