| Human Disease |
Pyloric Stenosis, Infantile Hypertrophic, 1; IHPS1 OMIM ID: 179010 |
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| Synonyms | Pyloric Stenosis, Infantile; Pyloric Stenosis, Infantile Hypertrophic; IHPS | |||||||||||||||||||||||||
| 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 * C57BL/6 | J:16390 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Nos1tm1Plh/Nos1tm1Plh |
involves: 129S4/SvJae * C57BL/6J | J:64225 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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