| Human Disease |
Asplenia with Cardiovascular Anomalies OMIM ID: 208530 |
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| View all models | View ALL (3) 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 |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Cfc1tm1Cbm/Cfc1tm1Cbm |
Not Specified | J:58530 | View |
| Cfc1tm1Mms/Cfc1tm1Mms |
either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J) | J:58104 | 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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