| Human Disease |
Hirschsprung Disease, Susceptibility to, 3; HSCR3 OMIM ID: 613711 |
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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 |
| Gdnftm1Lmgd/Gdnftm1Lmgd |
either: (involves: 129S4/SvJae) or (involves: 129S1/Sv * 129X1/SvJ) | J:33810 | View |
| Gdnftm1Lmgd/Gdnf+ |
either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * CD-1) | J:73922 | View |
| Gdnftm1Rosl/Gdnf+ |
involves: 129S2/SvPas * C57BL/6 | J:82456 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/12/2013 MGI 5.14 |
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