| Human Disease |
Hypophosphatasia, Adult OMIM ID: 146300 |
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| View all models | View ALL (8) 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 |
| Alpltm1Sor/Alpltm1Sor |
either: (involves: 129S7/SvEvBrd-Alpltm1Sor) or (involves: 129S7/SvEvBrd * C57BL/6) | J:28394 | View |
| AlplHpp/AlplHpp |
involves: BALB/cAnN * C3H/HeH | J:122319 | View |
| AlplMhdabap020/AlplMhdabap020 |
C3HeB/FeJ-AlplBAP020 | J:183993 | View |
| AlplBAP023/AlplBAP023 |
C3HeB/FeJ-AlplBAP023 | J:183993 | View |
| AlplBAP026/AlplBAP026 |
C3HeB/FeJ-AlplBAP026 | J:183993 | View |
| AlplBAP027/AlplBAP027 |
C3HeB/FeJ-AlplBAP027 | J:183993 | View |
| AlplBAP032/AlplBAP032 |
C3HeB/FeJ-AlplBAP032 | J:183993 | View |
| AlplHpp/Alpl+ |
involves: BALB/cAnN * C3H/HeH | J:122319 | 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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