c1-c2 subluxation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A partial dislocation of the atlantoaxial joints. (Human Phenotype Ontology, HP_0003320)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003320
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Genes

4 genes associated with the c1-c2 subluxation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
DDR2 discoidin domain receptor tyrosine kinase 2
IDUA iduronidase, alpha-L-
MMP2 matrix metallopeptidase 2