| Human Disease |
Split-Hand/Foot Malformation 3; SHFM3 OMIM ID: 246560 |
| Synonyms | Chromosome 10q24 Duplication Syndrome; Limb Deficiencies, Distal, with Micrognathia; Shsf3 |
| View all models | View ALL (2) mouse models for this human disease. |
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Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Fbxw4Dac-2J/Fbxw4+ mdac/mdac |
CBy.MRL-Fbxw4Dac-2J/J | J:133888 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Fbxw4Dac/Fbxw4+ mdac/mdac |
involves: SM/Ckc | J:29220, J:133888 | 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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