benign paroxysmal positional nystagmus Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

24 genes co-occuring with the disease benign paroxysmal positional nystagmus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
OTOP1 otopetrin 1 1.94031
HHLA1 HERV-H LTR-associating 1 1.93139
CBLN1 cerebellin 1 precursor 1.51721
SH3RF1 SH3 domain containing ring finger 1 1.43903
FBXO2 F-box protein 2 1.2765
OCM2 oncomodulin 2 1.15453
OCM oncomodulin 1.13416
FBXW2 F-box and WD repeat domain containing 2 1.12151
RGS5 regulator of G-protein signaling 5 1.07614
EN1 engrailed homeobox 1 0.987693
KCNJ13 potassium channel, inwardly rectifying subfamily J, member 13 0.901978
HPN hepsin 0.891308
ARHGEF1 Rho guanine nucleotide exchange factor (GEF) 1 0.788852
PRSS21 protease, serine, 21 (testisin) 0.779841
ASPSCR1 alveolar soft part sarcoma chromosome region, candidate 1 0.705547
NDUFS7 NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase) 0.686291
MPZ myelin protein zero 0.578106
PIDD1 p53-induced death domain protein 1 0.57305
LRP5 low density lipoprotein receptor-related protein 5 0.562169
FLNA filamin A, alpha 0.498085
CETP cholesteryl ester transfer protein, plasma 0.472604
F11R F11 receptor 0.412405
BCR breakpoint cluster region 0.290821
VCAM1 vascular cell adhesion molecule 1 0.190476