| Human Disease |
Holoprosencephaly 2; HPE2 OMIM ID: 157170 |
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| 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 |
| Six3tm1Gco/Six3tm1Gco |
involves: 129S1/Sv | J:81797 | View |
| Six3tm3.1Gco/Six3+ Shhtm1Chg/Shh+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:140315 | View |
| Six3tm3Gco/Six3tm3Gco Foxg1tm1(cre)Skm/Foxg1+ |
involves: 129S1/Sv * C57BL/6 | J:140315 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Six3tm4(cre/ERT2)Gco/Six3+ |
involves: 129S1/Sv * C57BL/6 | J:140315 | 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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