abnormal foot bone ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the formation and mineralization of any bone of the skeleton of foot. (Human Phenotype Ontology, HP_0010675)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010675
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11 genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CANT1 calcium activated nucleotidase 1
COL2A1 collagen, type II, alpha 1
EBP emopamil binding protein (sterol isomerase)
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
FLNA filamin A, alpha
HOXA13 homeobox A13
LBR lamin B receptor
MATN3 matrilin 3
PTH1R parathyroid hormone 1 receptor
SLC35D1 solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1
TRIP11 thyroid hormone receptor interactor 11