| Human Disease |
Ciliary Dyskinesia, Primary, 3; CILD3 OMIM ID: 608644 |
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| Synonyms | Ciliary Dyskinesia, Primary, 3, with or without Situs Inversus | |||||||||||||||||||||
| 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 |
| Dnahc5Tg1Htz/Dnahc5Tg1Htz |
involves: C57BL/6 * CBA/J | J:76189 | View |
| Dnahc5hlb612/Dnahc5hlb612 |
involves: C57BL/6J | J:130755 | 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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