Abnormality Of The Cranial Nerves Gene Set
Genes
17 genes associated with the disease Abnormality Of The Cranial Nerves in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
COX8A
|
cytochrome c oxidase subunit VIIIA (ubiquitous)
|
|
EGR2
|
early growth response 2
|
|
FGD4
|
FYVE, RhoGEF and PH domain containing 4
|
|
FGF3
|
fibroblast growth factor 3
|
|
GDF3
|
growth differentiation factor 3
|
|
GDF6
|
growth differentiation factor 6
|
|
GNAQ
|
guanine nucleotide binding protein (G protein), q polypeptide
|
|
HTR2A
|
5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
|
|
HTR6
|
5-hydroxytryptamine (serotonin) receptor 6, G protein-coupled
|
|
MEOX1
|
mesenchyme homeobox 1
|
|
NOD2
|
nucleotide-binding oligomerization domain containing 2
|
|
OSMR
|
oncostatin M receptor
|
|
OTX2
|
orthodenticle homeobox 2
|
|
PRRX1
|
paired related homeobox 1
|
|
SBF1
|
SET binding factor 1
|
|
SH3TC2
|
SH3 domain and tetratricopeptide repeats 2
|
|
SLC29A3
|
solute carrier family 29 (equilibrative nucleoside transporter), member 3
|
