| Human Disease |
Lubs X-Linked Mental Retardation Syndrome; MRXSL OMIM ID: 300260 |
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| Synonyms | Mecp2 Duplication Syndrome; Mental Retardation, X-Linked, Syndromic, Lubs Type; Mental Retardation, X-Linked, with Recurrent Respiratory Infections | ||||||||||||||||||||||||||||
| 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 |
| Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae |
B6.Cg-Mapttm1(Mecp2)Jae | J:182685 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(MECP2)1Hzo/0 |
either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1 | J:181213 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(MECP2)3Hzo/0 |
either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1 | J:181213 | 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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