gonadal disease Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An endocrine system disease that is located_in the gonads. (Human Disease Ontology, DOID_2277)
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Genes

25 genes involed in the disease gonadal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
AMH anti-Mullerian hormone
AMHR2 anti-Mullerian hormone receptor, type II
ANOS1 anosmin 1
AR androgen receptor
CHD7 chromodomain helicase DNA binding protein 7
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DUSP6 dual specificity phosphatase 6
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FLRT3 fibronectin leucine rich transmembrane protein 3
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
HSD17B3 hydroxysteroid (17-beta) dehydrogenase 3
IL17RD interleukin 17 receptor D
LHB luteinizing hormone beta polypeptide
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SOX10 SRY (sex determining region Y)-box 10
SPRY4 sprouty homolog 4 (Drosophila)
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
WDR11 WD repeat domain 11