abnormal polar body morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of one of the small cells that are produced during the development of an oocyte and ultimately degenerate; a polar body contains one of the nuclei derived from the first or second meiotic division but little or no cytoplasm (Mammalian Phenotype Ontology, MP_0012736)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012736
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5 gene mutations causing the abnormal polar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CTTN cortactin
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)