| Human Disease |
Kleefstra Syndrome OMIM ID: 610253 |
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| Synonyms | 9q Subtelomeric Deletion Syndrome; 9q- Syndrome; Chromosome 9q34.3 Deletion Syndrome | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Ehmt1tm1Yshk/Ehmt1+ |
involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj | J:157021, J:192316 | View |
| Ehmt1tm1.1Tara/Ehmt1tm1.1Tara Tg(Camk2a-cre)2Gsc/0 |
involves: 129P2/OlaHsd * C57BL/6 * FVB/N | J:155739 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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