flattened epiphysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal flatness (decreased height) of epiphyses. (Human Phenotype Ontology, HP_0003071)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003071
Similar Terms
Downloads & Tools

Genes

15 genes associated with the flattened epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACAN aggrecan
CANT1 calcium activated nucleotidase 1
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL2A1 collagen, type II, alpha 1
COL9A2 collagen, type IX, alpha 2
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit
IFT122 intraflagellar transport 122
KIF22 kinesin family member 22
MMP13 matrix metallopeptidase 13
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC39A13 solute carrier family 39 (zinc transporter), member 13
TBX4 T-box 4
TRPS1 trichorhinophalangeal syndrome I
WISP3 WNT1 inducible signaling pathway protein 3