| Human Disease |
Fragile X Tremor/Ataxia Syndrome; FXTAS OMIM ID: 300623 |
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| 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 |
| Fmr1tm2Cgr/Y |
involves: 129P2/OlaHsd * C57BL/6J * FVB | J:104445 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Pcp2-FMR1*)1Dln/0 |
C57BL/6-Tg(Pcp2-Fmr1*)1Dln | J:149320 | 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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