| Human Disease |
Rubinstein-Taybi Syndrome 1; RSTS1 OMIM ID: 180849 |
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| Synonyms | Broad Thumb-Hallux Syndrome; Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation; Rubinstein Syndrome | ||||||||||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| CrebbpGt(U-San)112Imeg/Crebbp+ |
involves: C57BL/6 * CBA | J:53370 | View |
| Crebbptm1Dli/Crebbp+ |
involves: 129S6/SvEvTac * C57BL/6 | J:60630 | View |
| Crebbptm1Sis/Crebbp+ |
either: (involves: BALB/c * C57BL/6 * CBA) or (involves: C57BL/6 * CBA) | J:42932 | View |
| Crebbptm1.2Ltz/Crebbptm1.2Ltz Tg(Camk2a-cre)T29-1Stl/0 |
involves: 129P2/OlaHsd * BALB/c * C57BL * C57BL/6J | J:168984 | 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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