Spondylolisthesis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A bone structure disease that has_material_basis_in displacement located_in set of vertebrae. (Human Disease Ontology, DOID_6682)
External Link https://www.disgenet.org/browser/0/1/0/C0038016
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Genes

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

Symbol Name
ACCS 1-aminocyclopropane-1-carboxylate synthase homolog (Arabidopsis)(non-functional)
ACSS2 acyl-CoA synthetase short-chain family member 2
AGA aspartylglucosaminidase
AMH anti-Mullerian hormone
BMP2 bone morphogenetic protein 2
CTSK cathepsin K
DCT dopachrome tautomerase
FBN1 fibrillin 1
FTH1 ferritin, heavy polypeptide 1
GDF5 growth differentiation factor 5
IDUA iduronidase, alpha-L-
LIF leukemia inhibitory factor
MAN2B1 mannosidase, alpha, class 2B, member 1
MMP3 matrix metallopeptidase 3
PABPN1 poly(A) binding protein, nuclear 1
PLA2G15 phospholipase A2, group XV
RANBP2 RAN binding protein 2
ROM1 retinal outer segment membrane protein 1
RUNX2 runt-related transcription factor 2
SMAD3 SMAD family member 3
SMS spermine synthase
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)
TRPC3 transient receptor potential cation channel, subfamily C, member 3
ZNF469 zinc finger protein 469