| Human Disease |
Beckwith-Wiedemann Syndrome; BWS OMIM ID: 130650 |
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| Synonyms | EMG Syndrome; Exomphalos-Macroglossia-Gigantism Syndrome | |||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 |
| Cdkn1ctm1Sje/Cdkn1ctm1Sje |
involves: 129S7/SvEvBrd * C57BL/6 | J:40203 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Cdkn1ctm1Bbd/Cdkn1ctm1Bbd |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:40142 | View |
| Cdkn1ctm1Kat/Cdkn1ctm1Kat |
involves: 129P2/OlaHsd * C57BL/6 | J:61190 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Sptbn1tm1Mish/Sptbn1+ |
involves: 129S6/SvEvTac | J:166879 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Kcnq1tm1Apf/Kcnq1tm1Apf |
involves: 129P2/OlaHsd * C57BL/6 | J:66428 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(YACW408A5)1952Ricc/0 |
involves: 129/Sv * SD7 | J:96366 | 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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