| Human Disease |
Heterotaxy, Visceral, 4, Autosomal; HTX4 OMIM ID: 613751 |
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| View all models | View ALL (1) 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 |
| Acvr2btm1Enl/Acvr2btm1Enl |
either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J) | J:42018 | 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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