sensory peripheral neuropathy Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A peripheral neuropathy that involves damage to nerves of the peripheral nervous system. (Human Disease Ontology, DOID_2491)
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17 genes associated with the disease sensory peripheral neuropathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
EPHA5 EPH receptor A5 1.49784
XKR4 XK, Kell blood group complex subunit-related family, member 4 1.37143
PITPNA phosphatidylinositol transfer protein, alpha 1.14671
FGD4 FYVE, RhoGEF and PH domain containing 4 1.11582
LIMK2 LIM domain kinase 2 1.10764
TRIO trio Rho guanine nucleotide exchange factor 1.07599
CACNB2 calcium channel, voltage-dependent, beta 2 subunit 0.980012
GLIS3 GLIS family zinc finger 3 0.933664
PALLD palladin, cytoskeletal associated protein 0.912987
PTPRT protein tyrosine phosphatase, receptor type, T 0.884
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) 0.882764
SPIDR scaffolding protein involved in DNA repair 0.870688
ERBB4 erb-b2 receptor tyrosine kinase 4 0.849872
SLCO1B1 solute carrier organic anion transporter family, member 1B1 0.838141
MISP mitotic spindle positioning 0.832379
PARK2 parkin RBR E3 ubiquitin protein ligase 0.814557
EPHA6 EPH receptor A6 0.813813