scoliosis Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) (Experimental Factor Ontology, EFO_0004273)
Similar Terms
Downloads & Tools

Genes

25 genes associated with the disease scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AANAT aralkylamine N-acetyltransferase
CALM1 calmodulin 1 (phosphorylase kinase, delta)
CHD7 chromodomain helicase DNA binding protein 7
DPP9 dipeptidyl-peptidase 9
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
FBN3 fibrillin 3
GH1 growth hormone 1
GHR growth hormone receptor
GPR50 G protein-coupled receptor 50
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
IGF1 insulin-like growth factor 1 (somatomedin C)
MATN1 matrilin 1, cartilage matrix protein
MMP3 matrix metallopeptidase 3
MTNR1A melatonin receptor 1A
MTNR1B melatonin receptor 1B
PAX1 paired box 1
SIM2 single-minded family bHLH transcription factor 2
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SNTG1 syntrophin, gamma 1
TBX6 T-box 6
TIMP2 TIMP metallopeptidase inhibitor 2
TPH1 tryptophan hydroxylase 1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor