| Human Disease |
Achalasia, Familial Esophageal OMIM ID: 200400 |
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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 |
| Nos1tm1Plh/Nos1tm1Plh |
involves: 129S4/SvJae | J:70182 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Spry2tm1Ayos/Spry2tm1Ayos |
B6.Cg-Spry2tm1Ayos | J:99827 | 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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