| Human Disease |
Hypocalciuric Hypercalcemia, Familial, Type I; HHC1 OMIM ID: 145980 |
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| Synonyms | Familial Benign Hypercalcemia 1; FBH1; FHH1 | |||||||||||||||||||||
| View all models | View ALL (7) 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 |
| CasrBCH004/CasrBCH004 |
C3HeB/FeJ-CasrBCH004 | J:183993 | View |
| CasrBCH007/CasrBCH007 |
C3HeB/FeJ-CasrBCH007 | J:183993 | View |
| CasrBCH011/CasrBCH011 |
C3HeB/FeJ-CasrBCH011 | J:183993 | View |
| CasrBCH013/CasrBCH013 |
C3HeB/FeJ-CasrBCH013 | J:183993 | View |
| CasrBCH002/CasrBCH002 |
C3HeB/FeJ-CasrBCH002 | J:183993 | View |
| CasrBCH003/CasrBCH003 |
C3HeB/FeJ-CasrBCH003 | J:183993 | View |
| Casrtm1Ces/Casr+ |
involves: 129X1/SvJ * Black Swiss | J:29900 | 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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