| Human Disease |
Hermansky-Pudlak Syndrome 2; HPS2 OMIM ID: 608233 |
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| View all models | View ALL (4) 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 |
| Ap3b1pe-rim2/Ap3b1pe-rim2 |
involves: B10.A(R201) * C57BL/10Slc | J:42685 | View |
| Ap3b1pe/Ap3b1pe |
involves: C3H/He | J:52879, J:80751 | View |
| Ap3b1pe/Ap3b1pe Hps1ep/Hps1ep |
involves: C3H/He * C3HeB/FeJ * C57BL/6J | J:85431 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ap3d1mh/Ap3d1mh |
B6.C3-Grxcr1pi | J:29151 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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