Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
0.400 GeneticVariation phenotype BEFREE Effect of naltrexone on neuropathic pain in mice locally transfected with the mutant μ-opioid receptor gene in spinal cord. 24866991 2015
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
0.400 GeneticVariation phenotype BEFREE In the meta-analysis, polymorphisms in HLA-DRB1*13 (odds ratio [OR], 2.96; confidence interval [CI], 1.93-4.56), HLA-DRB1*04 (OR, 1.40; CI, 1.02-1.93), HLA-DQB1*03 (OR, 2.86; CI, 1.57-5.21), HLA-A*33 (OR, 2.32; CI, 1.42-3.80), and HLA-B*44 (OR, 3.17; CI, 2.22-4.55) were associated with significantly increased risk of developing NP, whereas HLA-A*02 (OR, 0.64; CI, 0.47-0.87) conferred reduced risk and neither rs1799971 in OPRM1 (OR, 0.55; CI, 0.27-1.11) nor rs4680 in COMT (OR, 0.95; CI, 0.81-1.13) were significantly associated with NP. 29351172 2018
Entrez Id: 6335
Gene Symbol: SCN9A
SCN9A
0.350 GeneticVariation phenotype BEFREE To investigate mutations in the SCN9A gene in patients with chronic non-paroxysmal neuropathic pain. 21094958 2011
Entrez Id: 6335
Gene Symbol: SCN9A
SCN9A
0.350 GeneticVariation phenotype BEFREE The exonic regions of SCN9A were sequenced in a subset of 244 patients with neuropathic pain, and the variants discovered were compared with POPRES control (stage 1). 25585270 2015
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
0.320 GeneticVariation phenotype BEFREE We report here a patient with painful diabetic peripheral neuropathy and negative genetic screening for mutations in SCN9A, SCN10A, and SCN11A-genes encoding sodium channel α-subunit that have been previously linked to the development of neuropathic pain. 31041876 2020
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.220 GeneticVariation phenotype BEFREE Genetic regulation of DRD2 function by 957C>T polymorphism thus seems to influence thermal and pain sensitivity, its modulation by rTMS, and susceptibility to neuropathic pain. 25180011 2014
Entrez Id: 7442
Gene Symbol: TRPV1
TRPV1
0.100 GeneticVariation phenotype BEFREE It was suggested that the TRPV1-variant rs8065080 (1911A>G) plays a pivotal role in patients with neuropathic pain syndromes. 28817717 2017
Entrez Id: 4803
Gene Symbol: NGF
NGF
0.100 GeneticVariation phenotype BEFREE Inhibition of the NGF/TrkA interaction presents an interesting alternative to the use of non-steroidal anti-inflammatories and/or opioids for the control of inflammatory, chronic and neuropathic pain. 30700786 2019
Entrez Id: 3700
Gene Symbol: ITIH4
ITIH4
0.100 GeneticVariation phenotype BEFREE Moreover, 2-261 reversed thermal hyperalgesia and partially reversed tactile allodynia in the gp120 model of HIV-related neuropathic pain. 30204648 2019
Entrez Id: 10280
Gene Symbol: SIGMAR1
SIGMAR1
0.100 GeneticVariation phenotype BEFREE This study indicates lack of association of SIGMAR1 -297G>T and 5A>C genetic variants to susceptibility to develop chronic pain, but significant modulation of somatosensory function in neuropathic pain patients. 30266269 2019
Entrez Id: 5027
Gene Symbol: P2RX7
P2RX7
0.100 GeneticVariation phenotype BEFREE Disruption of the P2X7 purinoceptor gene abolishes chronic inflammatory and neuropathic pain. 15777864 2005
Entrez Id: 2166
Gene Symbol: FAAH
FAAH
0.100 GeneticVariation phenotype BEFREE Here, we designed dual inhibitors targeting the enzymes FAAH and soluble epoxide hydrolase (sEH), which are targets previously shown to synergize at reducing inflammatory and neuropathic pain. 30411058 2018
Entrez Id: 5027
Gene Symbol: P2RX7
P2RX7
0.100 GeneticVariation phenotype BEFREE Our present results confirm the physiological relevance of some of the SNPs in the P2RX7 gene and show that the presence of these genetic variants correlates with pain sensitivity also in a diabetic neuropathic pain patient population. 24934217 2014
Entrez Id: 627
Gene Symbol: BDNF
BDNF
0.100 GeneticVariation phenotype BEFREE It has been suggested that the disruption of complex behaviors and mood seen in some neuropathic pain patients is mediated in part by alterations of BDNF in this cortical region. 28609560 2017
Entrez Id: 1808
Gene Symbol: DPYSL2
DPYSL2
0.090 GeneticVariation phenotype BEFREE Spinal administration of a SUMOylation incompetent CRMP2 (CRMP2 K374A) significantly attenuated pain behavior in the spared nerve injury (SNI) model of neuropathic pain, underscoring the importance of SUMOylation of CRMP2 as a pathologic event in chronic pain. 30081699 2018
Entrez Id: 1808
Gene Symbol: DPYSL2
DPYSL2
0.090 GeneticVariation phenotype BEFREE ST2-104, a nona-arginine (R9)-conjugated CBD3 peptide derived from CRMP2, exerts a beneficial effect on neuropathic pain; however, the effect of ST2-104 on AD and its mechanism of action have not been studied. 30871964 2019
Entrez Id: 79054
Gene Symbol: TRPM8
TRPM8
0.060 GeneticVariation phenotype BEFREE We have previously demonstrated the contribution of enhanced activity of transient receptor potential melastatin 8 (TRPM8) to cold hyperalgesia in neuropathic pain using a rat model of chronic constriction injury (CCI) to the sciatic nerve. 28867384 2017
Entrez Id: 1312
Gene Symbol: COMT
COMT
0.050 GeneticVariation phenotype BEFREE Our study concludes that functional Val158Met polymorphism of COMT gene is not associated to increased susceptibility to neuropathic pain. 15862471 2005
Entrez Id: 1312
Gene Symbol: COMT
COMT
0.050 GeneticVariation phenotype BEFREE Catechol-O-methyltransferase polymorphism Val158Met is associated with distal neuropathic pain in HIV-associated sensory neuropathy. 31021849 2019
Entrez Id: 6624
Gene Symbol: FSCN1
FSCN1
0.050 GeneticVariation phenotype BEFREE The representative compound 17h showed comparable in vivo efficacy to gabapentin in the SNL model, which indicates T-type calcium channel inhibitors can be developed as effective therapeutics for neuropathic pain. 30928197 2019
Entrez Id: 1312
Gene Symbol: COMT
COMT
0.050 GeneticVariation phenotype BEFREE In the meta-analysis, polymorphisms in HLA-DRB1*13 (odds ratio [OR], 2.96; confidence interval [CI], 1.93-4.56), HLA-DRB1*04 (OR, 1.40; CI, 1.02-1.93), HLA-DQB1*03 (OR, 2.86; CI, 1.57-5.21), HLA-A*33 (OR, 2.32; CI, 1.42-3.80), and HLA-B*44 (OR, 3.17; CI, 2.22-4.55) were associated with significantly increased risk of developing NP, whereas HLA-A*02 (OR, 0.64; CI, 0.47-0.87) conferred reduced risk and neither rs1799971 in OPRM1 (OR, 0.55; CI, 0.27-1.11) nor rs4680 in COMT (OR, 0.95; CI, 0.81-1.13) were significantly associated with NP. 29351172 2018
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.040 GeneticVariation phenotype BEFREE AM1710 (3-(1,1-dimethyl-heptyl)-1-hydroxy-9-methoxy-benzo(c) chromen-6-one), a cannabilactone cannabinoid receptor 2 (CB2) agonist, suppresses chemotherapy-induced neuropathic pain in rodents without producing tolerance or unwanted side effects associated with CB1 receptors; however, the signaling profile of AM1710 remains incompletely characterized. 30504240 2019
Entrez Id: 2643
Gene Symbol: GCH1
GCH1
0.040 GeneticVariation phenotype BEFREE GTP cyclohydrolase 1 (GCH1) gene, which encodes the rate-limiting enzyme in tetrahydrobiopterin synthesis, has been strongly implicated to be associated with neuropathic pain in previous animal and human studies. 31486149 2019
Entrez Id: 1993
Gene Symbol: ELAVL2
ELAVL2
0.040 GeneticVariation phenotype BEFREE Noteworthy, 13 hub genes associated with neuropathic pain and nerve regeneration, including Ccl12, Ppp1r15a, Cdkn1a, Atf3, Nts, Dusp1, Ccl7, Csf, Gadd45a, Serpine1, Timp1 were rarely reported in PubMed database, these genes may provide us the new orientation in experimental research and clinical study. 29672183 2020
Entrez Id: 7454
Gene Symbol: WAS
WAS
0.040 GeneticVariation phenotype BEFREE These studies involved patients with diverse etiologies of neuropathic pain and included medical cannabis with different THC concentrations and routes of administration. 29388063 2018