cerebral palsy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A brain disease that is caused by damage to the motor control centers of the developing brain during pregnancy, during childbirth or after birth, which affects muscle movement and balance. (Human Disease Ontology, DOID_1969)
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Genes

34 genes associated with the disease cerebral palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADD1 adducin 1 (alpha)
ADRB2 adrenoceptor beta 2, surface
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
ANXA5 annexin A5
APOE apolipoprotein E
CBS cystathionine-beta-synthase
CXCL8 chemokine (C-X-C motif) ligand 8
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
F7 coagulation factor VII (serum prothrombin conversion accelerator)
FGB fibrinogen beta chain
GNB3 guanine nucleotide binding protein (G protein), beta polypeptide 3
IL10 interleukin 10
IL1B interleukin 1, beta
IL6 interleukin 6
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LTA lymphotoxin alpha
MBL2 mannose-binding lectin (protein C) 2, soluble
MMP3 matrix metallopeptidase 3
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS3 nitric oxide synthase 3 (endothelial cell)
NPPA natriuretic peptide A
PLAT plasminogen activator, tissue
PROCR protein C receptor, endothelial
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
SCNN1A sodium channel, non voltage gated 1 alpha subunit
SELE selectin E
SERPINB2 serpin peptidase inhibitor, clade B (ovalbumin), member 2
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
TFPI tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)
THBD thrombomodulin
TLR4 toll-like receptor 4
TNF tumor necrosis factor