hypoplasia of the odontoid process Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Developmental hypoplasia of the dens of the axis. (Human Phenotype Ontology, HP_0003311)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0003311
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Genes

17 genes associated with the hypoplasia of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ARSB	arylsulfatase B
COL2A1	collagen, type II, alpha 1
COMP	cartilage oligomeric matrix protein
DDR2	discoidin domain receptor tyrosine kinase 2
DYM	dymeclin
EIF2AK3	eukaryotic translation initiation factor 2-alpha kinase 3
FGD1	FYVE, RhoGEF and PH domain containing 1
FLNB	filamin B, beta
GALNS	galactosamine (N-acetyl)-6-sulfatase
GLB1	galactosidase, beta 1
GNPTAB	N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GUSB	glucuronidase, beta
IDUA	iduronidase, alpha-L-
NFIX	nuclear factor I/X (CCAAT-binding transcription factor)
RAB33B	RAB33B, member RAS oncogene family
TRAPPC2	trafficking protein particle complex 2
TRPV4	transient receptor potential cation channel, subfamily V, member 4