abnormality of the odontoid process Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of the dens of the axis, which is also known as the odontoid process. (Human Phenotype Ontology, HP_0003310)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003310
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20 genes associated with the abnormality 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
DLL3 delta-like 3 (Drosophila)
DYM dymeclin
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
FGD1 FYVE, RhoGEF and PH domain containing 1
FLNA filamin A, alpha
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
HES7 hes family bHLH transcription factor 7
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