Empty Follicle Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1328577
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Genes

13 genes associated with the disease Empty Follicle Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AGRP agouti related neuropeptide
ARTN artemin
CGA glycoprotein hormones, alpha polypeptide
CGB chorionic gonadotropin, beta polypeptide
CGB5 chorionic gonadotropin, beta polypeptide 5
CGB8 chorionic gonadotropin, beta polypeptide 8
LHCGR luteinizing hormone/choriogonadotropin receptor
MAPK3 mitogen-activated protein kinase 3
PLA2G1B phospholipase A2, group IB (pancreas)
PLB1 phospholipase B1
YWHAZ tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta
ZP1 zona pellucida glycoprotein 1 (sperm receptor)
ZP3 zona pellucida glycoprotein 3 (sperm receptor)