Erectile Abnormalities Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4022003
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Genes

24 genes associated with the disease Erectile Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ANOS1 anosmin 1
AR androgen receptor
CCDC141 coiled-coil domain containing 141
CHD7 chromodomain helicase DNA binding protein 7
DCC DCC netrin 1 receptor
DUSP6 dual specificity phosphatase 6
FEZF1 FEZ family zinc finger 1
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
HESX1 HESX homeobox 1
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
IL17RD interleukin 17 receptor D
KISS1R KISS1 receptor
NDP Norrie disease (pseudoglioma)
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)
TACR3 tachykinin receptor 3
WDR11 WD repeat domain 11