Cadasil 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/C0751587
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Genes

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

Symbol Name
ACTB actin, beta
ACTG2 actin, gamma 2, smooth muscle, enteric
APCS amyloid P component, serum
APOE apolipoprotein E
APP amyloid beta (A4) precursor protein
BGN biglycan
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CLU clusterin
COL18A1 collagen, type XVIII, alpha 1
COL4A1 collagen, type IV, alpha 1
CSF1R colony stimulating factor 1 receptor
CSF3 colony stimulating factor 3 (granulocyte)
CTSA cathepsin A
DCN decorin
DVL1 dishevelled segment polarity protein 1
EGF epidermal growth factor
ELN elastin
FBN1 fibrillin 1
FN1 fibronectin 1
GFAP glial fibrillary acidic protein
HTRA1 HtrA serine peptidase 1
JAG1 jagged 1
KDR kinase insert domain receptor
LPA lipoprotein, Lp(a)
MRS2 MRS2 magnesium transporter
NEFL neurofilament, light polypeptide
NOTCH1 notch 1
NOTCH2 notch 2
NOTCH3 notch 3
NOX5 NADPH oxidase, EF-hand calcium binding domain 5
PLXNA2 plexin A2
PROC protein C (inactivator of coagulation factors Va and VIIIa)
RBPJ recombination signal binding protein for immunoglobulin kappa J region
RNF213 ring finger protein 213
SOD1 superoxide dismutase 1, soluble
TGFB1 transforming growth factor, beta 1
THBD thrombomodulin
TREX1 three prime repair exonuclease 1