| Human Disease |
Neurodegeneration with Brain Iron Accumulation 1; NBIA1 OMIM ID: 234200 |
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| Synonyms | Hallervorden-Spatz Disease; Pantothenate Kinase-Associated Neurodegeneration; PKAN; Pkan Neuroaxonal Dystrophy, Juvenile-Onset | |||||||||||||||||||||
| View all models | View ALL (1) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI. | |||||||||||||||||||||
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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 |
| Pank2tm1Jgt/Pank2tm1Jgt |
involves: 129X1/SvJ * C57BL/6J | J:94753 | 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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