| Human Disease |
Polycystic Ovary Syndrome 1; PCOS1 OMIM ID: 184700 |
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| Synonyms | Hyperandrogenemia; PCO1; PCO; PCOS; Stein-Leventhal Syndrome | |||||||||||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Akt2tm1Hem/Akt2tm1Hem |
involves: 129P2/OlaHsd | J:185012 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Insrtm1Khn/Insrtm1Khn Leprtm1.1Chua/Leprtm1.1Chua Tg(Pomc1-cre)16Lowl/0 |
involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N | J:192274 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Insrtm1Khn/Insrtm1Khn Leprtm1.1Chua/Leprtm1.1Chua Tg(Pomc1-cre)16Lowl/0 |
involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N | J:192274 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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