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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Genes

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