impaired luteinization Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description atypical transformation of the mature ovarian follicle and its theca interna into a corpus luteum after ovulation (Mammalian Phenotype Ontology, MP_0003356)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003356
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Genes

11 gene mutations causing the impaired luteinization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDK4 cyclin-dependent kinase 4
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
FADS2 fatty acid desaturase 2
FZD4 frizzled class receptor 4
GHR growth hormone receptor
GJA1 gap junction protein, alpha 1, 43kDa
PGR progesterone receptor
TSHR thyroid stimulating hormone receptor
UBE3A ubiquitin protein ligase E3A