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