| Human Disease |
Oculodentodigital Dysplasia; ODDD OMIM ID: 164200 |
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| Synonyms | Oculodentoosseous Dysplasia; ODOD; ODD Syndrome | |||||||||||||||||||||
| View all models | View ALL (5) 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 |
| Gja1m1Jrt/Gja1+ |
involves: C3H/HeJ * C57BL/6J | J:101733 | View |
| Gja1tm3Gfi/Gja1+ |
involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:130575 | View |
| Gja1m1Jrt/Gja1+ |
involves: C3H/HeJ * C57BL/6J * FVB | J:101733 | View |
| Gja1tm1Dlg/Gja1tm1Dlg Tg(GFAP-cre)1Kdmc/0 |
involves: 129S7/SvEvBrd * C3H * C57BL/6 * C57BL/6J | J:156098 | View |
| Gja1tm8Kwi/Gja1+ Tg(Pgk1-cre)1Lni/0 |
involves: 129S2/SvPas * BALB/c * C57BL/6 | J:132032 | 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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