| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | acquired diminution of the size of the uterus associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal changes (Mammalian Phenotype Ontology, MP_0004894) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004894 |
| Similar Terms | |
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9 gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| APC | adenomatous polyposis coli |
| CDK2 | cyclin-dependent kinase 2 |
| CDKN1C | cyclin-dependent kinase inhibitor 1C (p57, Kip2) |
| CYP7B1 | cytochrome P450, family 7, subfamily B, polypeptide 1 |
| FSHR | follicle stimulating hormone receptor |
| KL | klotho |
| LHX9 | LIM homeobox 9 |
| NPC1 | Niemann-Pick disease, type C1 |
| PROKR2 | prokineticin receptor 2 |
