| Human Disease |
Hermansky-Pudlak Syndrome 1; HPS1 OMIM ID: 203300 |
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| Synonyms | Albinism with Hemorrhagic Diathesis and Pigmented Reticuloendothelial Cells; Delta Storage Pool Disease | |||||||||||||||||||||
| 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 |
| Hps1ep/Hps1ep |
B6.C3Fe-Hps1ep/J | J:80751 | View |
| Hps1ep/Hps1ep |
involves: C3HeB/FeJ * C57BL/6J | J:7416 | View |
| Ap3b1pe/Ap3b1pe Hps1ep/Hps1ep |
involves: C3H/He * C3HeB/FeJ * C57BL/6J | J:85431 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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