| Human Disease |
Pigmented Nodular Adrenocortical Disease, Primary, 1; PPNAD1 OMIM ID: 610489 |
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| Synonyms | Adrenocortical Nodular Dysplasia, Primary; Cushing Syndrome, Adrenal, Due to Ppnad1; Pigmented Micronodular Adrenocortical Disease, Primary, 1 | |||||||||||||||||||||
| 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 |
| Prkar1atm1Lsk/Prkar1atm1Lsk Tg(Akr1b7-cre)1Anm/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 | J:161521 | 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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