irregular epiphyses Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An alteration of the normally smooth contour of the epiphysis leading to an irregular appearance. (Human Phenotype Ontology, HP_0010582)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010582
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Genes

12 genes associated with the irregular epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTSL2 ADAMTS-like 2
CDC6 cell division cycle 6
COL11A1 collagen, type XI, alpha 1
COL2A1 collagen, type II, alpha 1
COL9A2 collagen, type IX, alpha 2
COL9A3 collagen, type IX, alpha 3
COMP cartilage oligomeric matrix protein
DYM dymeclin
KIF22 kinesin family member 22
MATN3 matrilin 3
SLC26A2 solute carrier family 26 (anion exchanger), member 2
TRAPPC2 trafficking protein particle complex 2