| Human Disease |
Hyperostosis Corticalis Generalisata OMIM ID: 239100 |
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| Synonyms | Endosteal Hyperostosis, Autosomal Recessive; Hyperphosphatasemia Tarda; Van Buchem Disease; VBCH | |||||||||||||||||||||
| 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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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 |
| Sosttm1(KOMP)Vlcg/Sosttm1(KOMP)Vlcg |
involves: C57BL/6NTac | J:188586 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Rr20tm1.1Vlcg/Rr20tm1.1Vlcg |
involves: 129S6/SvEvTac * C57BL/6NTac | J:188586 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(RP11-209M4)#Gglo/Tg(RP11-209M4)#Gglo |
FVB-Tg(RP11-209M4)#Gglo | J:99965 | View |
| Tg(RP11-209M4)#Gglo/0 |
FVB-Tg(RP11-209M4)#Gglo | J:99965 | 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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