| Human Disease |
Synpolydactyly 1; SPD1 OMIM ID: 186000 |
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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 |
| Hoxd13spdh/Hoxd13spdh |
B6C3Fe a/a-Hoxd13spdh/J | J:47974 | View |
| Hoxd13tm1Ddu/Hoxd13tm1Ddu |
either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * C57BL/6) | J:15507 | View |
| Hoxd13tm1Mrc/Hoxd13tm1Mrc |
involves: 129S7/SvEvBrd | J:32603 | 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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