| Human Disease |
Intestinal Atresia, Multiple; MINAT OMIM ID: 243150 |
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| Synonyms | Familial Intestinal Polyatresia Syndrome; FIPA | |||||||||||||||||||||||||
| 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 |
| Fgf10tm1Ska/Fgf10tm1Ska |
involves: C57BL/6 * CBA | J:92361 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn |
involves: 129P2/OlaHsd * C57BL/6 | J:92361 | 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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