| Human Disease |
Neurodegeneration with Brain Iron Accumulation 3; NBIA3 OMIM ID: 606159 |
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| Synonyms | Basal Ganglia Disease, Adult-Onset; Neuroferritinopathy | |||||||||||||||||||||
| 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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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 |
| Tg(Prnp-FTL*)4Ruvi/Tg(Prnp-FTL*)4Ruvi |
B6.C3Fe-Tg(Prnp-FTL*)4Ruvi | J:131053 | 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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