GENE - TERM ANNOTATION REPORT
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction
is comprised of a complex set of reactions and/or regulatory events, possibly involving
additional chemicals and/or gene products.
Object Symbol | Qualifier | Evidence | With | Reference | Source | Notes | Original Reference(s) | Oprm1 | | ISO | OPRM1 (Homo sapiens) | 9068941 | RGD | DNA:missense mutation:exon:p.N40D (118A>G) (rs 1799971) (human) | PMID:28976288 REF_RGD_ID:401831044 | Oprm1 | | ISO | OPRM1 (Homo sapiens) | 9068941 | RGD | DNA:SNP, haplotype: :rs483481 (human) | PMID:32189578 REF_RGD_ID:401827950 | Oprm1 | | ISO | OPRM1 (Homo sapiens) | 9068941 | RGD | mRNA:splice variants:prefrontal cortex | PMID:32506472 REF_RGD_ID:401831047 | Oprm1 | no_association | ISO | OPRM1 (Homo sapiens) | 9068941 | RGD | DNA:missense mutation:exon:p.N40D (118A>G) (rs 1799971) (human) | PMID:11424981 REF_RGD_ID:401827953 | Oprm1 | severity | ISO | OPRM1 (Homo sapiens) | 9068941 | RGD | DNA:SNPs, haplotypes: :rs696522, rs1381376, rs3778151 (human) | PMID:17157823 REF_RGD_ID:401827940 | Oprm1 | susceptibility | ISO | OPRM1 (Homo sapiens) | 9068941 | RGD | DNA:SNPs, haplotypes: :multiple | PMID:28692418 REF_RGD_ID:401831045 | Oprm1 | | ISO | OPRM1 (Homo sapiens) | 9068941 | CTD | CTD Direct Evidence: marker/mechanism | PMID:20201854 | |
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