| Human Disease |
Factor X Deficiency OMIM ID: 227600 |
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| Synonyms | F10 Deficiency; Stuart-Prower Factor Deficiency | |||||||||||||||||||||
| 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 |
| F10tm1Edr/F10tm1Edr |
involves: 129S1/Sv * 129X1/SvJ * Swiss | J:61230 | View |
| F10tm1Ccmt/F10tm1Ccmt |
involves: 129P2/OlaHsd * C57BL/6 | J:145092 | View |
| F10tm2Ccmt/F10tm2Ccmt |
involves: 129P2/OlaHsd * C57BL/6 | J:145092 | 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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