dentin sensitivity Gene Set

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

14 genes co-occuring with the disease dentin sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TRPM3 transient receptor potential cation channel, subfamily M, member 3 1.73869
NT5M 5',3'-nucleotidase, mitochondrial 1.66285
KCNK4 potassium channel, two pore domain subfamily K, member 4 1.58314
KCNK10 potassium channel, two pore domain subfamily K, member 10 1.57824
TRPA1 transient receptor potential cation channel, subfamily A, member 1 1.52732
CSN3 casein kappa 1.42235
TRPV4 transient receptor potential cation channel, subfamily V, member 4 1.33283
ENTPD2 ectonucleoside triphosphate diphosphohydrolase 2 1.30008
TRPV3 transient receptor potential cation channel, subfamily V, member 3 1.29746
TRPV2 transient receptor potential cation channel, subfamily V, member 2 1.21089
TRPV1 transient receptor potential cation channel, subfamily V, member 1 1.08957
INA internexin neuronal intermediate filament protein, alpha 0.874919
GJA1 gap junction protein, alpha 1, 43kDa 0.503824
TRPM8 transient receptor potential cation channel, subfamily M, member 8 0.398216