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