abnormal vertebral ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the formation and mineralization of one or more vertebrae. (Human Phenotype Ontology, HP_0100569)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100569
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Genes

17 genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
BMPER BMP binding endothelial regulator
COL2A1 collagen, type II, alpha 1
FLNB filamin B, beta
HSPG2 heparan sulfate proteoglycan 2
INPPL1 inositol polyphosphate phosphatase-like 1
LBR lamin B receptor
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
NKX3-2 NK3 homeobox 2
RMRP RNA component of mitochondrial RNA processing endoribonuclease
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SOX9 SRY (sex determining region Y)-box 9
TRIP11 thyroid hormone receptor interactor 11
TRPV4 transient receptor potential cation channel, subfamily V, member 4
WNT3 wingless-type MMTV integration site family, member 3