decreased ovulation rate Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the frequency in which an ovum (or ova) is/are released from a rupturing ovarian follicle(s) (Mammalian Phenotype Ontology, MP_0003355)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003355
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Genes

23 gene mutations causing the decreased ovulation rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
BMP15 bone morphogenetic protein 15
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CSF1 colony stimulating factor 1 (macrophage)
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
GHR growth hormone receptor
GJA1 gap junction protein, alpha 1, 43kDa
HR hair growth associated
LIPC lipase, hepatic
NCOA3 nuclear receptor coactivator 3
NHLH2 nescient helix loop helix 2
NOS3 nitric oxide synthase 3 (endothelial cell)
PABPC1L poly(A) binding protein, cytoplasmic 1-like
PTGER2 prostaglandin E receptor 2 (subtype EP2), 53kDa
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
PTX3 pentraxin 3, long
TNFAIP6 tumor necrosis factor, alpha-induced protein 6
TSHR thyroid stimulating hormone receptor
ZP3 zona pellucida glycoprotein 3 (sperm receptor)