OPRM1, opioid receptor mu 1, 4988

N. diseases: 370; N. variants: 42
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1323040
rs1323040
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE The rs1799971 and rs1323040 polymorphisms of the <i>OPRM1</i> gene and rs2032582 and rs1128503 polymorphisms of the <i>ABCB1</i> gene are related to the analgesic effect and consumed dose of sufentanil in Chinese Han patients undergoing radical operation of lung cancer. 30455395 2019
dbSNP: rs1323040
rs1323040
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE The rs1799971 and rs1323040 polymorphisms of the <i>OPRM1</i> gene and rs2032582 and rs1128503 polymorphisms of the <i>ABCB1</i> gene are related to the analgesic effect and consumed dose of sufentanil in Chinese Han patients undergoing radical operation of lung cancer. 30455395 2019
dbSNP: rs1323040
rs1323040
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE The rs1799971 and rs1323040 polymorphisms of the <i>OPRM1</i> gene and rs2032582 and rs1128503 polymorphisms of the <i>ABCB1</i> gene are related to the analgesic effect and consumed dose of sufentanil in Chinese Han patients undergoing radical operation of lung cancer. 30455395 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0033860
Disease:
Psoriasis
0.010 GeneticVariation BEFREE While effect allele 'G' of rs1799971 (OPRM1) also associated with increased risk of early onset and familial aggregation of psoriasis in the additive and dominant models (OR<sub>additive</sub> = 1.75, 95% CI 1.27-2.43, p = 0.001, OR<sub>dominant</sub> = 1.82, 95% CI 1.26-2.63, p = 0.001). 31011876 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0030662
Disease:
Gambling, Pathological
0.010 GeneticVariation BEFREE This study aimed to investigate the associations among the A118G polymorphism in the <i>OPRM1</i> gene, psychiatric symptoms, and quantitative electroencephalography (qEEG) findings in patients with gambling disorder. 31553235 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1611743
Disease:
Familial (FPAH)
0.010 GeneticVariation BEFREE The OPRM1 (rs1799971) polymorphism was investigated in an association study of a group of ADS patients (n = 177) and in subgroups (delirium tremens and/or seizures, age at onset <26 years, dissocial alcoholics, positive familial history of alcoholism, delirium tremens, and seizures). 30085428 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE The rs1799971 and rs1323040 polymorphisms of the <i>OPRM1</i> gene and rs2032582 and rs1128503 polymorphisms of the <i>ABCB1</i> gene are related to the analgesic effect and consumed dose of sufentanil in Chinese Han patients undergoing radical operation of lung cancer. 30455395 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0005586
Disease:
Bipolar Disorder
0.010 GeneticVariation BEFREE No genetic association between A118G polymorphism of μ-opioid receptor gene and schizophrenia and bipolar disorders. 29497192 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0085625
Disease:
Hypoalgesia
0.010 GeneticVariation BEFREE In this study, we expanded on previous findings related to the 3 SNPs in the opioid receptor mu subunit (OPRM1 rs1799971), catechol-O-methyltransferase (COMT rs4680), and fatty acid amide hydrolase (FAAH rs324420) genes associated with placebo hypoalgesia and tested the effect of a 3-way interaction on placebo hypoalgesia. 31335650 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0687132
Disease:
heavy drinking
0.010 GeneticVariation BEFREE The study's primary objective was to examine the association of the Asn40Asp OPRM1 single nucleotide polymorphism (SNP) with naltrexone's effects on smoking quit rate, weight gain, and heavy drinking behavior during a double-blind, randomized clinical trial in 280 adult DSM-IV nicotine-dependent participants. 31206155 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0001957
Disease:
Alcohol Withdrawal Delirium
0.010 GeneticVariation BEFREE The OPRM1 (rs1799971) polymorphism was investigated in an association study of a group of ADS patients (n = 177) and in subgroups (delirium tremens and/or seizures, age at onset <26 years, dissocial alcoholics, positive familial history of alcoholism, delirium tremens, and seizures). 30085428 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0520679
Disease:
Sleep Apnea, Obstructive
0.010 GeneticVariation BEFREE Patients with OSA and the A118G OPRM1 polymorphism of A/A and A/G had a significantly different morphine effect on awake ventilatory chemosensitivity and T90 during sleep. 30166422 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0278139
Disease:
Moderate pain
0.010 GeneticVariation BEFREE The frequency of the wild-type allele of SNP rs1799971 was higher in patients with mild to moderate pain (p:0.04). 30973927 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0036572
Disease:
Seizures
0.010 GeneticVariation BEFREE The OPRM1 (rs1799971) polymorphism was investigated in an association study of a group of ADS patients (n = 177) and in subgroups (delirium tremens and/or seizures, age at onset <26 years, dissocial alcoholics, positive familial history of alcoholism, delirium tremens, and seizures). 30085428 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0438696
Disease:
Suicidal
0.010 GeneticVariation BEFREE Polymorphism A118G of opioid receptor mu 1 (OPRM1) is associated with emergence of suicidal ideation at antidepressant onset in a large naturalistic cohort of depressed outpatients. 30796320 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE The rs1799971 and rs1323040 polymorphisms of the <i>OPRM1</i> gene and rs2032582 and rs1128503 polymorphisms of the <i>ABCB1</i> gene are related to the analgesic effect and consumed dose of sufentanil in Chinese Han patients undergoing radical operation of lung cancer. 30455395 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE The rs1799971 and rs1323040 polymorphisms of the <i>OPRM1</i> gene and rs2032582 and rs1128503 polymorphisms of the <i>ABCB1</i> gene are related to the analgesic effect and consumed dose of sufentanil in Chinese Han patients undergoing radical operation of lung cancer. 30455395 2019
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0338908
Disease:
Mixed anxiety and depressive disorder
0.010 GeneticVariation BEFREE From the neuroendocrine system, OPRM1 rs1799971 correlated increasing levels of female's Anxiety, depression and Social Dysfunction scores. 30656852 2019
dbSNP: rs111339162
rs111339162
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1842981
Disease:
NEUROTICISM
0.010 GeneticVariation BEFREE The personality domains and hair cortisol levels were heritable and associated with genotypes: the short form of AVPR1a was associated with lower Neuroticism and the AA genotype of the A111T SNP of OPRM1 was related to lower Dominance, lower Neuroticism, and higher hair cortisol level. 29980755 2018
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0085159
Disease:
Seasonal Affective Disorder
0.010 GeneticVariation BEFREE In the current study (N = 44), we expand upon what is known about children's genetic and environmental risk for anxiety by examining the unique and interactive effects of mother-child LSM and the OPRM1 polymorphism A118G on school-aged children's separation anxiety disorder (SAD) symptoms. 29576267 2018
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0233702
Disease:
Algophobia
0.010 GeneticVariation BEFREE In addition, the interaction between OPRM1 (rs1799971) and fear of pain as well as COMT (rs4818) and pain catastrophizing provided strong statistical evidence for predicting strength loss. 30425562 2018
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0520905
Disease:
Vomiting, Postoperative
0.010 GeneticVariation BEFREE OPRM1-A118G polymorphism (A > G) is associated with a reduced risk of postoperative vomiting, but not nausea, pruritus and dizziness. 30323865 2018
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0027796
Disease:
Neuralgia
0.010 GeneticVariation 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
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0003477
Disease:
Separation Anxiety Disorder
0.010 GeneticVariation BEFREE In the current study (N = 44), we expand upon what is known about children's genetic and environmental risk for anxiety by examining the unique and interactive effects of mother-child LSM and the OPRM1 polymorphism A118G on school-aged children's separation anxiety disorder (SAD) symptoms. 29576267 2018
dbSNP: rs6902403
rs6902403
Entrez Id: 4988;26034
Gene Symbol: OPRM1;IPCEF1
OPRM1;IPCEF1
CUI: C0242510
Disease:
Drug usage
0.010 GeneticVariation BEFREE <b>Conclusion:</b> Dosage of methadone, plasma methadone concentration, several SNPs (rs3192723, rs6912029, rs6902403) of the <i>OPRM1</i> gene, and age of first drug use were associated with better MMT outcomes. 30420869 2018