Osteochondritis Dissecans Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An ischemic bone disease that results_in necrosis located_in epiphysis. (Human Disease Ontology, DOID_84)
External Link https://www.disgenet.org/browser/0/1/0/C0029421
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Genes

22 genes associated with the disease Osteochondritis Dissecans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACAN aggrecan
ALCAM activated leukocyte cell adhesion molecule
ARHGEF2 Rho/Rac guanine nucleotide exchange factor (GEF) 2
BDNF brain-derived neurotrophic factor
CD34 CD34 molecule
COL9A2 collagen, type IX, alpha 2
COMT catechol-O-methyltransferase
DLGAP3 discs, large (Drosophila) homolog-associated protein 3
FGFR3 fibroblast growth factor receptor 3
MCAM melanoma cell adhesion molecule
MMP13 matrix metallopeptidase 13
MMP3 matrix metallopeptidase 3
ORC1 origin recognition complex, subunit 1
PIP prolactin-induced protein
PYCARD PYD and CARD domain containing
SGCE sarcoglycan, epsilon
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SMAD3 SMAD family member 3
TNF tumor necrosis factor
TPSG1 tryptase gamma 1
TYMS thymidylate synthetase