| Human Disease |
Central Hypoventilation Syndrome, Congenital; CCHS OMIM ID: 209880 |
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| 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 |
| Phox2btm2Jbr/Phox2b+ |
involves: 129S2/SvPas * C57BL/6 | J:131365 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tlx3tm1Sjk/Tlx3tm1Sjk |
involves: 129X1/SvJ | J:60751 | 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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