| Human Disease |
Canavan Disease OMIM ID: 271900 |
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| Synonyms | ACY2 Deficiency; Aminoacylase 2 Deficiency; ASP Deficiency; ASPA Deficiency; Aspartoacylase Deficiency; Canavan-Van Bogaert-Bertrand Disease; Spongy Degeneration of Central Nervous System | ||||||||||||||||||||||||||||
| 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 |
| Aspanur7/Aspanur7 |
involves: C57BL/6J | J:143201 | View |
| Aspatm1Mata/Aspatm1Mata |
involves: 129S5/SvEvBrd | J:89100, J:89099 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Sod2tm1Cje/Sod2tm1Cje |
involves: C57BL/6J | J:45913 | 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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