abnormality of the vertebral endplates Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the vertebral end plates, which are the top and bottom portions of the vertebral bodies that interface with the vertebral discs. (Human Phenotype Ontology, HP_0005106)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005106
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Genes

18 genes associated with the abnormality of the 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
CLCN7 chloride channel, voltage-sensitive 7
COL10A1 collagen, type X, alpha 1
COL2A1 collagen, type II, alpha 1
COL9A1 collagen, type IX, 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
SOST sclerostin
TRAPPC2 trafficking protein particle complex 2
WISP3 WNT1 inducible signaling pathway protein 3
ZBTB20 zinc finger and BTB domain containing 20