oocyte degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a retrogressive impairment of function or destruction of the female germ cells (Mammalian Phenotype Ontology, MP_0009093)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009093
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Genes

7 gene mutations causing the oocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXC1 forkhead box C1
FOXO3 forkhead box O3
FSHR follicle stimulating hormone receptor
NOBOX NOBOX oogenesis homeobox
SPO11 SPO11 meiotic protein covalently bound to DSB
TBPL2 TATA box binding protein like 2
WNT4 wingless-type MMTV integration site family, member 4