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All mouse models of adrenal cortex disease with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | X-linked adrenal hypoplasia congenita | Nr0b1tm1.1Lja/Y | involves: 129S1/Sv * 129X1/SvJ | J:51292, J:71710 | View | |||
| | primary pigmented nodular adrenocortical disease |
Prkar1atm1Lsk/Prkar1atm1Lsk Tg(Akr1b7-cre)1Anm/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 | J:161521 | View | |||
| Transgenes and Other Mutations | primary pigmented nodular adrenocortical disease |
Tg(CMV-tTA)3Bjd/0 Tg(tetO-Prkar1a*x2as)1Stra/0 |
involves: C57BL/6 * NMRI * SJL | J:95465 | View | |||