abnormality of carpal bone ossification Gene Set
Genes
16 genes associated with the abnormality of carpal 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
|
|
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
|
|
TRPV4
|
transient receptor potential cation channel, subfamily V, member 4
|
|
XYLT1
|
xylosyltransferase I
|
