| Human Disease |
Alpha-Thalassemia/Mental Retardation Syndrome, X-Linked; ATRX OMIM ID: 301040 |
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| Synonyms | Alpha-Thalassemia/Mental Retardation Syndrome, Nondeletion Type; ATR, Nondeletion Type; ATR-X 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Atrxtm1Pick/Y Tg(Nes-cre)2472Pick/0 |
involves: C57BL/6 * FVB/N | J:95953 | View |
| Atrxtm1Pick/Y Tg(Pax6-cre,GFP)2Pgr/0 |
involves: C57BL/6 * FVB/N | J:145002 | View |
| Atrxtm1Pick/Y Foxg1tm1(cre)Skm/Foxg1+ |
involves: C57BL/6 * FVB/N | J:95953 | 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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