irregular vertebral endplates Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An irregular surface of the vertebral end plates, which are normally relatively smooth. (Human Phenotype Ontology, HP_0003301)
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14 genes associated with the irregular vertebral endplates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACP5 acid phosphatase 5, tartrate resistant
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL10A1 collagen, type X, alpha 1
COL2A1 collagen, type II, alpha 1
COMP cartilage oligomeric matrix protein
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
GNPAT glyceronephosphate O-acyltransferase
KIF22 kinesin family member 22
MMP13 matrix metallopeptidase 13
PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2
SLC39A13 solute carrier family 39 (zinc transporter), member 13
TRAPPC2 trafficking protein particle complex 2
ZBTB20 zinc finger and BTB domain containing 20