Retinoic Acid Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0860564
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Genes

28 genes associated with the disease Retinoic Acid Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AHR aryl hydrocarbon receptor
ANPEP alanyl (membrane) aminopeptidase
ATN1 atrophin 1
BCR breakpoint cluster region
CCL5 chemokine (C-C motif) ligand 5
CD34 CD34 molecule
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
CSF3 colony stimulating factor 3 (granulocyte)
CXCL2 chemokine (C-X-C motif) ligand 2
CXCL8 chemokine (C-X-C motif) ligand 8
CXCR4 chemokine (C-X-C motif) receptor 4
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
DDIT3 DNA-damage-inducible transcript 3
HMGB1 high mobility group box 1
ICAM1 intercellular adhesion molecule 1
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
IL1B interleukin 1, beta
IL6 interleukin 6
MAP2K1 mitogen-activated protein kinase kinase 1
MAP2K7 mitogen-activated protein kinase kinase 7
MMP2 matrix metallopeptidase 2
NCF1 neutrophil cytosolic factor 1
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PECAM1 platelet/endothelial cell adhesion molecule 1
TGM2 transglutaminase 2
THBD thrombomodulin
WDR26 WD repeat domain 26