| Human Disease |
Granulomatous Disease, Chronic, X-Linked; CGD OMIM ID: 306400 |
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| Synonyms | Cytochrome B-Negative Granulomatous Disease, Chronic, X-Linked | |||||||||||||||||||||
| 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 |
| Cybbtm1Din/Cybbtm1Din |
B6.129S-Cybbtm1Din | J:146231 | View |
| Cybbtm1Din/Y |
involves: 129S/SvEv * C57BL/6 | J:22868 | 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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