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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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