vertebral compression fractures Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002953
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Genes

12 genes associated with the vertebral compression fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
CRTAP cartilage associated protein
FKBP10 FK506 binding protein 10, 65 kDa
GBA glucosidase, beta, acid
GORAB golgin, RAB6-interacting
MMP2 matrix metallopeptidase 2
NOTCH2 notch 2
P3H1 prolyl 3-hydroxylase 1
SERPINF1 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1
SQSTM1 sequestosome 1
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator
UROS uroporphyrinogen III synthase