biconcave vertebral bodies Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Exaggerated concavity of the anterior or posterior surface of the vertebral body, i.e., the upper and lower vertebral endplates are hollowed inward. (Human Phenotype Ontology, HP_0004586)
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12 genes associated with the biconcave vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
CBS cystathionine-beta-synthase
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
FKBP10 FK506 binding protein 10, 65 kDa
GORAB golgin, RAB6-interacting
IDUA iduronidase, alpha-L-
IFITM5 interferon induced transmembrane protein 5
KIF22 kinesin family member 22
NOTCH2 notch 2
SERPINF1 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1
ZBTB20 zinc finger and BTB domain containing 20