creutzfeldt-jakob disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11949)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:11949
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Genes

16 genes associated with the disease creutzfeldt-jakob disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
PRNP prion protein 2.05547
SERPINF2 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 2 1.55738
MTMR7 myotubularin related protein 7 1.39396
RGS7 regulator of G-protein signaling 7 1.25451
PLCXD3 phosphatidylinositol-specific phospholipase C, X domain containing 3 1.23342
PKNOX2 PBX/knotted 1 homeobox 2 1.14463
RPGRIP1L RPGRIP1-like 1.09584
ZNF74 zinc finger protein 74 1.01205
NTRK3 neurotrophic tyrosine kinase, receptor, type 3 0.972876
KIAA0368 KIAA0368 0.831182
PCDHGB4 protocadherin gamma subfamily B, 4 0.813443
ANK2 ankyrin 2, neuronal 0.796329
CATSPERD catsper channel auxiliary subunit delta 0.78695
TCF4 transcription factor 4 0.784733
LAMA3 laminin, alpha 3 0.755798
SYT1 synaptotagmin I 0.755533