Congenital 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/C0559260
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Genes

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

Symbol Name
AR androgen receptor
BTK Bruton agammaglobulinemia tyrosine kinase
CD38 CD38 molecule
DLL3 delta-like 3 (Drosophila)
EGFR epidermal growth factor receptor
EGR3 early growth response 3
FBN1 fibrillin 1
FOXO4 forkhead box O4
GDF3 growth differentiation factor 3
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
LMX1A LIM homeobox transcription factor 1, alpha
NOTCH1 notch 1
OLFML1 olfactomedin-like 1
PAX1 paired box 1
SHOX short stature homeobox
SMS spermine synthase
SOX9 SRY (sex determining region Y)-box 9
TBX6 T-box 6
TP63 tumor protein p63