abnormal ovary development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal morphogenesis of the ovarian follicle for the production of female germ cells or the endocrine cells for the production of estrogen and progesterone (Mammalian Phenotype Ontology, MP_0003582)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003582
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6 gene mutations causing the abnormal ovary development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CPEB1 cytoplasmic polyadenylation element binding protein 1
MKS1 Meckel syndrome, type 1
PSMC3IP PSMC3 interacting protein
RSPO1 R-spondin 1
TMPRSS6 transmembrane protease, serine 6
WNT4 wingless-type MMTV integration site family, member 4