Septo-Optic Dysplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Underdevelopment of the optic nerve and absence of the septum pellucidum. (Human Phenotype Ontology, HP_0100842)
External Link https://www.disgenet.org/browser/0/1/0/C0338503
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Genes

34 genes associated with the disease Septo-Optic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ANOS1 anosmin 1
ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
CDON cell adhesion associated, oncogene regulated
CHD7 chromodomain helicase DNA binding protein 7
CRX cone-rod homeobox
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FLNA filamin A, alpha
GDF6 growth differentiation factor 6
GH1 growth hormone 1
GLI2 GLI family zinc finger 2
GPR161 G protein-coupled receptor 161
HESX1 HESX homeobox 1
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
MT-CYB cytochrome b
OTX2 orthodenticle homeobox 2
PAX3 paired box 3
POMC proopiomelanocortin
POU1F1 POU class 1 homeobox 1
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
PROP1 PROP paired-like homeobox 1
RALGAPB Ral GTPase activating protein, beta subunit (non-catalytic)
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
RSPO2 R-spondin 2
SLC20A1 solute carrier family 20 (phosphate transporter), member 1
SOX2 SRY (sex determining region Y)-box 2
SOX3 SRY (sex determining region Y)-box 3
TAX1BP3 Tax1 (human T-cell leukemia virus type I) binding protein 3
TUBA1A tubulin, alpha 1a
VAX1 ventral anterior homeobox 1
WDR11 WD repeat domain 11
WNT3 wingless-type MMTV integration site family, member 3