Gonadotropin Deficiency Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A reduced ability to secrete gonadotropins, which are protein hormones secreted by gonadotrope cells of the anterior pituitary gland, including the hormones follitropin (FSH) and luteinizing hormone (LH). (Human Phenotype Ontology, HP_0008213)
External Link https://www.disgenet.org/browser/0/1/0/C4552011
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Genes

25 genes associated with the disease Gonadotropin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BRD2 bromodomain containing 2
CHD7 chromodomain helicase DNA binding protein 7
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FSHB follicle stimulating hormone, beta polypeptide
GH1 growth hormone 1
GK glycerol kinase
GLI3 GLI family zinc finger 3
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GNRHR gonadotropin-releasing hormone receptor
KISS1R KISS1 receptor
LHX3 LIM homeobox 3
NR0B1 nuclear receptor subfamily 0, group B, member 1
OTC ornithine carbamoyltransferase
PCSK1 proprotein convertase subtilisin/kexin type 1
POMC proopiomelanocortin
POU1F1 POU class 1 homeobox 1
PRL prolactin
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SLC20A1 solute carrier family 20 (phosphate transporter), member 1
SOX2 SRY (sex determining region Y)-box 2
SRY sex determining region Y
TAC3 tachykinin 3
TACR3 tachykinin receptor 3
TBX3 T-box 3