| Human Disease |
Aspartylglucosaminuria; AGU OMIM ID: 208400 |
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| Synonyms | AGA Deficiency; Aspartylglucosaminidase Deficiency; Aspartylglycosaminuria; Glycoasparaginase; Glycosylasparaginase Deficiency | |||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Agatm1Pltn/Agatm1Pltn |
involves: 129S4/SvJae * C57BL/6 | J:45587 | View |
| Agatm1Vk/Agatm1Vk |
involves: 129S1/Sv * 129X1/SvJ * Black Swiss | J:37022 | 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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