| Human Disease |
Hirschsprung Disease, Susceptibility to, 1; HSCR1 OMIM ID: 142623 |
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| Synonyms | Aganglionic Megacolon; Hirschsprung Disease; HSCR; Megacolon, Aganglionic; MGC | |||||||||||||||||||||
| View all models | View ALL (4) 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 |
| Rettm2.1Heno/Rettm2.1Heno |
involves: 129S/Sv * C57BL/6 * FVB/N | J:135153 | View |
| Rettm1Cos/Rettm1Cos |
involves: 129S/Sv * C57BL/6 | J:135153 | View |
| Rettm1Cos/Rettm1Cos |
involves: 129S/SvEv * MF1 | J:23852, J:30389 | View |
| Rettm1Cos/Rettm2(RET)Jmi |
involves: 129S/Sv * C57BL/6 | J:135153 | 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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