abnormal rib ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly if the process of rib bone formation. (Human Phenotype Ontology, HP_0012306)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012306
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6 genes associated with the abnormal rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMPER BMP binding endothelial regulator
COL10A1 collagen, type X, alpha 1
LBR lamin B receptor
MGP matrix Gla protein
SBDS Shwachman-Bodian-Diamond syndrome
SLC26A2 solute carrier family 26 (anion exchanger), member 2