| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | abnormal numbers of the ovarian follicle prior to the appearance of an antrum, normally marked by developmental changes in the primary oocyte and follicular cells so that the latter form one or more layers of cuboidal or columnar cells; the follicle becomes surrounded by a sheath of stroma, the theca (Mammalian Phenotype Ontology, MP_0011123) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011123 |
| Similar Terms | |
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4 gene mutations causing the abnormal primary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| CCDC169-SOHLH2 | CCDC169-SOHLH2 readthrough |
| FSHR | follicle stimulating hormone receptor |
| PRLR | prolactin receptor |
| RANBP9 | RAN binding protein 9 |
