Hepatic Veno-Occlusive Disease Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0019156
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Genes

37 genes associated with the disease Hepatic Veno-Occlusive Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALB albumin
ASPG asparaginase
CABIN1 calcineurin binding protein 1
CD22 CD22 molecule
CSF3 colony stimulating factor 3 (granulocyte)
DPYD dihydropyrimidine dehydrogenase
ERCC1 excision repair cross-complementation group 1
ERCC2 excision repair cross-complementation group 2
F5 coagulation factor V (proaccelerin, labile factor)
FBL fibrillarin
FCN2 ficolin (collagen/fibrinogen domain containing lectin) 2
FOXP3 forkhead box P3
GABPA GA binding protein transcription factor, alpha subunit 60kDa
GSTA1 glutathione S-transferase alpha 1
GSTT1 glutathione S-transferase theta 1
HFE hemochromatosis
HMOX1 heme oxygenase 1
HPSE heparanase
HSPA14 heat shock 70kDa protein 14
HSPD1 heat shock 60kDa protein 1 (chaperonin)
IGF1 insulin-like growth factor 1 (somatomedin C)
IL1B interleukin 1, beta
IL6 interleukin 6
MMP9 matrix metallopeptidase 9
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NFE2L2 nuclear factor, erythroid 2-like 2
OCLN occludin
PML promyelocytic leukemia
SCO2 SCO2 cytochrome c oxidase assembly protein
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1
SP110 SP110 nuclear body protein
THBD thrombomodulin
TNF tumor necrosis factor
TPMT thiopurine S-methyltransferase
TYMP thymidine phosphorylase
TYMS thymidylate synthetase
XYLT2 xylosyltransferase II