erectile abnormalities Gene Set
Genes
32 genes associated with the erectile abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABCD1
|
ATP-binding cassette, sub-family D (ALD), member 1
|
|
AIP
|
aryl hydrocarbon receptor interacting protein
|
|
ANOS1
|
anosmin 1
|
|
AR
|
androgen receptor
|
|
CHD7
|
chromodomain helicase DNA binding protein 7
|
|
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
|
|
FMR1
|
fragile X mental retardation 1
|
|
GBE1
|
glucan (1,4-alpha-), branching enzyme 1
|
|
GUCY1A3
|
guanylate cyclase 1, soluble, alpha 3
|
|
HBB
|
hemoglobin, beta
|
|
HESX1
|
HESX homeobox 1
|
|
HEXB
|
hexosaminidase B (beta polypeptide)
|
|
HFE
|
hemochromatosis
|
|
HS6ST1
|
heparan sulfate 6-O-sulfotransferase 1
|
|
IL17RD
|
interleukin 17 receptor D
|
|
KISS1R
|
KISS1 receptor
|
|
LMNB1
|
lamin B1
|
|
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
|
|
TTR
|
transthyretin
|
|
WDR11
|
WD repeat domain 11
|
