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: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0003467
Disease:
Anxiety
0.030 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875 2004
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0003469
Disease:
Anxiety Disorders
0.030 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875 2004
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0233477
Disease:
Dysphoric mood
0.010 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875 2004
dbSNP: rs769540300
rs769540300
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0003469
Disease:
Anxiety Disorders
0.010 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875 2004
dbSNP: rs769540300
rs769540300
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0085281
Disease:
Addictive Behavior
0.010 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875 2004
dbSNP: rs769540300
rs769540300
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0003467
Disease:
Anxiety
0.010 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875 2004
dbSNP: rs769540300
rs769540300
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0233477
Disease:
Dysphoric mood
0.010 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875 2004
dbSNP: rs769540300
rs769540300
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.010 GeneticVariation BEFREE Functional alleles that alter alcoholism-related intermediate phenotypes include common alcohol dehydrogenase 1B and aldehyde dehydrogenase 2 variants that cause the aversive flushing reaction; catechol-O-methyltransferase (COMT) Val158Met leading to differences in three aspects of neurobiology: executive cognitive function, stress/anxiety response, and opioid function; opioid receptor micro1 (OPRM1) Asn40Asp, which may serve as a gatekeeper molecule in the action of naltrexone, a drug used in alcoholism treatment; and HTTLPR, which alters serotonin transporter function and appears to affect stress response and anxiety/dysphoria, which are factors relevant to initial vulnerability, the process of addiction, and relapse. 15584875 2004
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0030193
Disease:
Pain
0.100 GeneticVariation BEFREE This study examines the association of the A118G SNP of OPRM1 to experimental pain sensitivity. 15772909 2005
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C1510472
Disease:
Drug Dependence
0.060 GeneticVariation BEFREE Genetic variants of OPRM1 have been implicated in predisposition to drug addiction, in particular the single nucleotide polymorphism A118G, leading to an N40D substitution, with an allele frequency of 10-32%, and uncertain functions. 16046395 2005
dbSNP: rs648007
rs648007
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE In single SNP association analyses, rs648007 demonstrated significant evidence of association with T2DM (P=0.013). 16140553 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0038580
Disease:
Substance Dependence
0.060 GeneticVariation BEFREE The Asn40Asp SNP in OPRM1 does not appear to affect risk for SD. 16387451 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0030201
Disease:
Pain, Postoperative
0.070 GeneticVariation BEFREE These results suggest that the A118G SNP may moderate but not mediate the effects of anger-out on postoperative pain responses. 16400534 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0013384
Disease:
Dyskinetic syndrome
0.010 GeneticVariation BEFREE Carrying the G-allele of the A118G single nucleotide coding region polymorphism of the mu opioid receptor, as well as a history of never smoking, were independently associated with increased risk of earlier onset of dyskinesia (P=0.05 and 0.02, respectively). 16435402 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.100 GeneticVariation BEFREE In the present study, we compared the frequencies of the polymorphism OPRM1 A118G between patients with alcohol dependence and healthy control subjects living in a Japanese provincial prefecture. 16679777 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0600241
Disease:
heroin abuse
0.010 GeneticVariation BEFREE Mu opioid receptors are critical for heroin dependence, and A118G SNP of the mu opioid receptor gene (OPRM1) has been linked with heroin abuse. 16682632 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0563625
Disease:
Agnosia for Pain
0.100 GeneticVariation BEFREE Human opioid receptor A118G polymorphism affects intravenous patient-controlled analgesia morphine consumption after total abdominal hysterectomy. 16871067 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0563625
Disease:
Agnosia for Pain
0.100 GeneticVariation BEFREE Association of mu-opioid receptor gene polymorphism (A118G) with variations in morphine consumption for analgesia after total knee arthroplasty. 16879459 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0563625
Disease:
Agnosia for Pain
0.100 GeneticVariation BEFREE The mu-opioid receptor gene polymorphism 118A>G depletes alfentanil-induced analgesia and protects against respiratory depression in homozygous carriers. 16906017 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0270850
Disease:
Idiopathic generalized epilepsy
0.010 GeneticVariation BEFREE Our results provide no support for association of A118G with either IAE or IGE and also exclude association in our sample of a small-to-moderate gene effect with IGE from a large part of OPRM1. 17054695 2006
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.100 GeneticVariation BEFREE These results do not support association of the OPRM1 Asn40Asp polymorphism with NTX treatment response for AD. 17374034 2007
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0524662
Disease:
Opiate Addiction
0.100 GeneticVariation BEFREE Although a role of OPRM1 polymorphisms in determining risk for opioid dependence cannot be entirely discounted, a major contribution of the Asn40Asp polymorphism seems unlikely. 17416470 2007
dbSNP: rs1799971
rs1799971
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0740858
Disease:
Substance abuse problem
0.010 GeneticVariation BEFREE Two of these, C17T and A118G, have been reported to be associated with substance abuse. 18181266 2007
dbSNP: rs1799972
rs1799972
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0740858
Disease:
Substance abuse problem
0.010 GeneticVariation BEFREE Two of these, C17T and A118G, have been reported to be associated with substance abuse. 18181266 2007
dbSNP: rs1799972
rs1799972
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1
CUI: C0524662
Disease:
Opiate Addiction
0.010 GeneticVariation BEFREE A significant association was observed between the 118G allele and no association was seen with C17T polymorphism and opioid dependence. 18181266 2007