vestibulocochlear nerve disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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23 genes co-occuring with the disease vestibulocochlear nerve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
BET1 Bet1 golgi vesicular membrane trafficking protein 1.32629
MCAT malonyl CoA:ACP acyltransferase (mitochondrial) 1.22865
FBXW2 F-box and WD repeat domain containing 2 1.14263
FEV FEV (ETS oncogene family) 1.10426
KCNJ13 potassium channel, inwardly rectifying subfamily J, member 13 0.922561
HPN hepsin 0.911433
IFT122 intraflagellar transport 122 0.900335
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like 0.834378
NTRK1 neurotrophic tyrosine kinase, receptor, type 1 0.826589
NDUFS7 NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase) 0.706351
HRH1 histamine receptor H1 0.697109
TES testin LIM domain protein 0.684692
KMT2A lysine (K)-specific methyltransferase 2A 0.581606
CYGB cytoglobin 0.572273
DLL1 delta-like 1 (Drosophila) 0.53928
HTR3A 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic 0.535796
PER1 period circadian clock 1 0.481325
LCK LCK proto-oncogene, Src family tyrosine kinase 0.418019
GDNF glial cell derived neurotrophic factor 0.409414
CD38 CD38 molecule 0.296571
CD40 CD40 molecule, TNF receptor superfamily member 5 0.247852
CD19 CD19 molecule 0.185612
CD68 CD68 molecule 0.178682