Aortic Rupture Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0003496
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Genes

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

Symbol Name
ADAMTS3 ADAM metallopeptidase with thrombospondin type 1 motif, 3
ADAMTS4 ADAM metallopeptidase with thrombospondin type 1 motif, 4
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ANGPT2 angiopoietin 2
APOE apolipoprotein E
ATP7A ATPase, Cu++ transporting, alpha polypeptide
CCN2 cellular communication network factor 2
CSF3 colony stimulating factor 3 (granulocyte)
CXCL1 chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha)
CXCR2 chemokine (C-X-C motif) receptor 2
FBN1 fibrillin 1
KLF15 Kruppel-like factor 15
MAPK3 mitogen-activated protein kinase 3
MMP2 matrix metallopeptidase 2
MMP9 matrix metallopeptidase 9
PLK1 polo-like kinase 1
PRKCB protein kinase C, beta
RCAN1 regulator of calcineurin 1
SMAD3 SMAD family member 3
STAT1 signal transducer and activator of transcription 1, 91kDa
VKORC1 vitamin K epoxide reductase complex, subunit 1
VPS51 vacuolar protein sorting 51 homolog (S. cerevisiae)