Bone Necrosis Gene Set

Dataset DisGeNET Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link https://www.disgenet.org/browser/0/1/0/C0029445
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Genes

23 genes associated with the phenotype Bone Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ANXA2 annexin A2
BACH1 BTB and CNC homology 1, basic leucine zipper transcription factor 1
BMP6 bone morphogenetic protein 6
CREBBP CREB binding protein
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CYP2C8 cytochrome P450, family 2, subfamily C, polypeptide 8
F5 coagulation factor V (proaccelerin, labile factor)
GRIK1 glutamate receptor, ionotropic, kainate 1
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
IL17A interleukin 17A
IL23R interleukin 23 receptor
KL klotho
MMP2 matrix metallopeptidase 2
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS3 nitric oxide synthase 3 (endothelial cell)
PON1 paraoxonase 1
PPARG peroxisome proliferator-activated receptor gamma
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SREBF1 sterol regulatory element binding transcription factor 1
TFPI tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)
TP53 tumor protein p53
ZFHX3 zinc finger homeobox 3