abnormal hand 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 hand. (Human Phenotype Ontology, HP_0010660)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010660
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Genes

20 genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
CANT1 calcium activated nucleotidase 1
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
DDR2 discoidin domain receptor tyrosine kinase 2
EBP emopamil binding protein (sterol isomerase)
FLNB filamin B, beta
GPC3 glypican 3
HOXA13 homeobox A13
IHH indian hedgehog
MATN3 matrilin 3
PIGV phosphatidylinositol glycan anchor biosynthesis, class V
PTCH1 patched 1
PTCH2 patched 2
PTH1R parathyroid hormone 1 receptor
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SLC35D1 solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1
SUFU suppressor of fused homolog (Drosophila)
TRIP11 thyroid hormone receptor interactor 11
TRPV4 transient receptor potential cation channel, subfamily V, member 4
XYLT1 xylosyltransferase I