Infarction, Lacunar Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0333559
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Genes

35 genes associated with the disease Infarction, Lacunar in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial)
ANGPT2 angiopoietin 2
APOC3 apolipoprotein C-III
APOE apolipoprotein E
APOH apolipoprotein H (beta-2-glycoprotein I)
ATP6AP2 ATPase, H+ transporting, lysosomal accessory protein 2
BAD BCL2-associated agonist of cell death
COL3A1 collagen, type III, alpha 1
CRP C-reactive protein, pentraxin-related
EDN1 endothelin 1
FBN2 fibrillin 2
FOXC1 forkhead box C1
GPI glucose-6-phosphate isomerase
HP haptoglobin
IL6 interleukin 6
MMP9 matrix metallopeptidase 9
NOS3 nitric oxide synthase 3 (endothelial cell)
NOTCH3 notch 3
PLAT plasminogen activator, tissue
PLIN1 perilipin 1
PON1 paraoxonase 1
PRKCH protein kinase C, eta
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
PTX3 pentraxin 3, long
REN renin
RPSA ribosomal protein SA
SERPINA3 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3
SHC2 SHC (Src homology 2 domain containing) transforming protein 2
SORBS1 sorbin and SH3 domain containing 1
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B