Sporadic Cjd Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4310512
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Genes

30 genes associated with the disease Sporadic Cjd in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)
AHSP alpha hemoglobin stabilizing protein
APOE apolipoprotein E
BACE1 beta-site APP-cleaving enzyme 1
C4BPA complement component 4 binding protein, alpha
CARD14 caspase recruitment domain family, member 14
CHN2 chimerin 2
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
CTSD cathepsin D
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
EIF2AK2 eukaryotic translation initiation factor 2-alpha kinase 2
ENO2 enolase 2 (gamma, neuronal)
GH1 growth hormone 1
HECTD2 HECT domain containing E3 ubiquitin protein ligase 2
IL6 interleukin 6
LAMC2 laminin, gamma 2
MAPT microtubule-associated protein tau
PLCXD3 phosphatidylinositol-specific phospholipase C, X domain containing 3
PPP1R14B protein phosphatase 1, regulatory (inhibitor) subunit 14B
PRDX2 peroxiredoxin 2
PRNP prion protein
PVALB parvalbumin
RARB retinoic acid receptor, beta
RASA2 RAS p21 protein activator 2
RPSA ribosomal protein SA
S100A1 S100 calcium binding protein A1
S100B S100 calcium binding protein B
STMN2 stathmin 2
YWHAQ tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta
ZBTB38 zinc finger and BTB domain containing 38