| Human Disease |
Aicardi-Goutieres Syndrome 1; AGS1 OMIM ID: 225750 |
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| Synonyms | Ags; Blcpmg; Cree Encephalitis; Encephalopathy, Familial Infantile, with Intracranial Calcification and Chronic Cerebrospinal Fluid Lymphocytosis; Pseudo-TORCH Syndrome | |||||||||||||||||||||
| View all models | View ALL (1) 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 |
| Trex1tm1Tld/Trex1tm1Tld |
involves: 129P2/OlaHsd | J:145466 | 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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