Neonatal Encephalopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0235820
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Genes

26 genes associated with the disease Neonatal Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APC adenomatous polyposis coli
ATF2 activating transcription factor 2
CDKL5 cyclin-dependent kinase-like 5
CLPB ClpB homolog, mitochondrial AAA ATPase chaperonin
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
CUL4B cullin 4B
EPO erythropoietin
F5 coagulation factor V (proaccelerin, labile factor)
GFAP glial fibrillary acidic protein
GLS glutaminase
GLUL glutamate-ammonia ligase
GNAO1 guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
IL1RN interleukin 1 receptor antagonist
ITGAM integrin, alpha M (complement component 3 receptor 3 subunit)
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
LAMC2 laminin, gamma 2
LIAS lipoic acid synthetase
LIPT2 lipoyl(octanoyl) transferase 2 (putative)
MECP2 methyl CpG binding protein 2
NOS1 nitric oxide synthase 1 (neuronal)
PROC protein C (inactivator of coagulation factors Va and VIIIa)
S100B S100 calcium binding protein B
SCN2A sodium channel, voltage gated, type II alpha subunit
TLR4 toll-like receptor 4
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
VEGFA vascular endothelial growth factor A