c1-c2 vertebral abnormality Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the atlas and the axis. (Human Phenotype Ontology, HP_0008440)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008440
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5 genes associated with the c1-c2 vertebral abnormality 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
SKI SKI proto-oncogene