abnormal tarsal 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 of the tarsal bones, seven bones of the foot comprising the calcaneus, talus, cuboid, navicular, and the cuneiform bones. (Human Phenotype Ontology, HP_0008369)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0008369
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Genes

8 genes associated with the abnormal tarsal 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
HOXA13	homeobox A13
MATN3	matrilin 3
PTH1R	parathyroid hormone 1 receptor
SLC35D1	solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1