abnormal primary polar body morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the small cell formed by the first meiotic division of oocytes (Mammalian Phenotype Ontology, MP_0012737)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012737
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4 gene mutations causing the abnormal primary polar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FMN2 formin 2
MOS v-mos Moloney murine sarcoma viral oncogene homolog
NOS3 nitric oxide synthase 3 (endothelial cell)
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)