ovoid vertebral bodies Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description When viewed in lateral radiographs, vertebral bodies have a roughly rectangular configuration. This term applies if the vertebral body appears rounded or oval. (Human Phenotype Ontology, HP_0003300)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003300
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Genes

21 genes associated with the ovoid vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
ARSB arylsulfatase B
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
COL2A1 collagen, type II, alpha 1
COMP cartilage oligomeric matrix protein
FBN1 fibrillin 1
GALNS galactosamine (N-acetyl)-6-sulfatase
GLB1 galactosidase, beta 1
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GNS glucosamine (N-acetyl)-6-sulfatase
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
IHH indian hedgehog
MATN3 matrilin 3
NAGLU N-acetylglucosaminidase, alpha
NPR2 natriuretic peptide receptor 2
PCYT1A phosphate cytidylyltransferase 1, choline, alpha
SBDS Shwachman-Bodian-Diamond syndrome
SGSH N-sulfoglucosamine sulfohydrolase
SLC35D1 solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
TBX15 T-box 15