| Human Disease |
Hypophosphatemic Rickets, Autosomal Dominant; ADHR OMIM ID: 193100 |
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| Synonyms | Hypophosphatemia, Autosomal Dominant; Vitamin D-Resistant Rickets, Autosomal Dominant | |||||||||||||||||||||
| 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Fgf23tm1.1Kew/Fgf23tm1.1Kew |
B6.129-Fgf23tm1.1Kew | J:180061 | View |
| Fgf23tm1Blan/Fgf23tm1Blan PhexHyp/Y |
Not Specified | J:94041 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(APOE-FGF23*R176Q)#Ack/0 |
involves: C57BL/6J * CBA | J:93981 | 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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