| Human Disease |
Acth-Independent Macronodular Adrenal Hyperplasia; AIMAH OMIM ID: 219080 |
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| Synonyms | Acth-Independent Cushing Syndrome; Acth-Independent Macronodular Adrenocortical Hyperplasia; Adrenocorticotropic Hormone-Independent Macronodular Adrenal Hyperplasia; Corticotropin-Independent Macronodular Adrenal Hyperplasia; Cushing Syndrome, Adrenal, Due to Aimah | ||||||||||||||||||||||||||||
| 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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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 |
| Nr3c1tm2Gsc/Nr3c1tm2Gsc Tg(Nes-cre)1Kln/0 |
involves: 129P2/OlaHsd * C57BL/6J * SJL | J:57315 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Crh)227.1Pbl/0 |
C57BL/6 | J:92996 | 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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