| Human Disease |
Bleeding Disorder, Platelet-Type, 16; BDPLT16 OMIM ID: 187800 |
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| Synonyms | Glanzmann Thrombasthenia, Autosomal Dominant; Thrombasthenia of Glanzmann and Naegeli, Autosomal Dominant | |||||||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Itga2btm1Tlr/Itga2btm1Tlr |
either: (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:63961 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Itgb3tm1Hyn/Itgb3tm1Hyn |
involves: 129S2/SvPas * C57BL/6 | J:52262 | 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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