Idiopathic Scoliosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0595995
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Genes

38 genes associated with the disease Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ACHE acetylcholinesterase (Yt blood group)
ACTB actin, beta
ACTN3 actinin, alpha 3 (gene/pseudogene)
ADGRG6 adhesion G protein-coupled receptor G6
AQP6 aquaporin 6, kidney specific
BCL2 B-cell CLL/lymphoma 2
CELSR2 cadherin, EGF LAG seven-pass G-type receptor 2
CHD7 chromodomain helicase DNA binding protein 7
CHL1 cell adhesion molecule L1-like
COL1A2 collagen, type I, alpha 2
COL2A1 collagen, type II, alpha 1
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
FGF22 fibroblast growth factor 22
GADD45B growth arrest and DNA-damage-inducible, beta
GAPDH glyceraldehyde-3-phosphate dehydrogenase
GHR growth hormone receptor
GJB2 gap junction protein, beta 2, 26kDa
IL1B interleukin 1, beta
IL6 interleukin 6
KIF22 kinesin family member 22
KIF6 kinesin family member 6
LBX1 ladybird homeobox 1
MAPK7 mitogen-activated protein kinase 7
MED13 mediator complex subunit 13
MMP3 matrix metallopeptidase 3
NLRP3 NLR family, pyrin domain containing 3
PAX1 paired box 1
POC5 POC5 centriolar protein
RUNX2 runt-related transcription factor 2
SH3GL1 SH3-domain GRB2-like 1
SLC39A8 solute carrier family 39 (zinc transporter), member 8
SMS spermine synthase
SNTG1 syntrophin, gamma 1
TGFB1 transforming growth factor, beta 1
TIMP2 TIMP metallopeptidase inhibitor 2
TOB2 transducer of ERBB2, 2