| Human Disease |
Peters Anomaly OMIM ID: 604229 |
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| View all models | View ALL (9) 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 |
| Pax6tm1.2Xzh/Pax6tm1.2Xzh |
B6.129S6-Pax6tm1.2Xzh | J:182769 | View |
| Pax6tm2Pgr/Pax6+ Tg(Pax6-cre,GFP)1Pgr/0 |
involves: 129S1/Sv * 129X1/SvJ * FVB | J:163191 | View |
| Pax6Sey-Neu/Pax6+ |
involves: 102 * C3H | J:12101 | View |
| Pax61Jrt/Pax6+ |
C3.B6-Pax61Jrt | J:86523 | View |
| Pax6Sey/Pax6+ |
Not Specified | J:22316 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Pax6Sey-Dey/Pax6+ |
C3H/HeJ-Pax6Sey-Dey | J:10820 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ext1tm1Yama/Ext1tm1Yama Tg(Wnt1-cre)11Rth/0 |
B6.Cg-Ext1tm1Yama Tg(Wnt1-cre)11Rth | J:152572 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Foxe3dyl/Foxe3dyl |
BALB/cLiA-Foxe3dyl | J:6131, J:59880, J:76605 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Msx2tm1Rilm/Msx2tm1Rilm |
involves: 129S4/SvJae | J:184697 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tgfb2tm1Doe/Tgfb2tm1Doe |
involves: 129P2/OlaHsd * Black Swiss | J:73681 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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