RGD DISEASE ONTOLOGY - ANNOTATIONS
RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term: opiate dependence
Accession: DOID:2559
browse the term
Definition: A drug dependence that involves the continued use of opiate drugs despite despite problems related to use of the substance. (DO)
Synonyms: exact_synonym: Disorder, Opioid-Related; Narcotic Abuse; Narcotic Abuses; Narcotic Addiction; Narcotic Dependence; ODS1; Opiate Addiction; Opioid-Related Disorders; opioid addiction; opioid dependence; opioid type dependence
related_synonym: OPIOID DEPENDENCE, SUSCEPTIBILITY TO, 1
primary_id: MESH:D009293
alt_id: OMIM:610064
xref: EFO:0005611 ; ICD10CM:F11.2 ; ICD9CM:304.00
For additional species annotation, visit the
Alliance of Genome Resources .
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Abcb1a
ATP binding cassette subfamily B member 1A
severity susceptibility treatment
ISO
DNA:SNP: :3435C>T (rs1045642) (human) DNA:SNP:: (rs9282564) DNA:SNPs::rs1045642, rs2032582(human) DNA:haplotype::
RGD
PMID:27061230 PMID:24950410 PMID:24086514 PMID:17178268
RGD:401959589 , RGD:401827941 , RGD:401901242 , RGD:401901190
NCBI chr 4:25,357,467...25,529,941
Ensembl chr 4:25,158,362...25,442,709
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Ankk1
ankyrin repeat and kinase domain containing 1
susceptibility
ISO
DNA:SNP,haplotype:exon:rs1800497(human)
RGD
PMID:19373123
RGD:401959309
NCBI chr 8:49,779,862...49,788,024
Ensembl chr 8:49,779,862...49,788,024
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Arrb2
arrestin, beta 2
treatment
ISO
DNA:SNPs: :rs3786047, rs1045280, rs2036657(human) protein:decreased expression:pre-frontal cortex
RGD
PMID:20514076 PMID:14969742
RGD:401901595 , RGD:401901596
NCBI chr10:55,146,887...55,154,854
Ensembl chr10:55,146,818...55,154,850
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Bdnf
brain-derived neurotrophic factor
ISO
protein:increased expression:serum
RGD
PMID:21890593
RGD:405850248
NCBI chr 3:96,165,042...96,215,621
Ensembl chr 3:96,165,042...96,215,615
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Bmper
BMP-binding endothelial regulator
susceptibility
ISO
CTD Direct Evidence: marker/mechanism DNA:SNP:: (rs731844) (human)
CTD RGD
PMID:18438686 PMID:18438686
RGD:401851917
NCBI chr 8:21,732,225...21,977,261
Ensembl chr 8:21,732,225...21,977,256
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C9
complement C9
susceptibility
ISO
CTD Direct Evidence: marker/mechanism DNA:SNP:: (rs476569) (human)
CTD RGD
PMID:18438686 PMID:18438686
RGD:401851917
NCBI chr 2:55,573,094...55,621,345
Ensembl chr 2:55,572,992...55,621,338
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Ces1d
carboxylesterase 1D
ISO
CTD Direct Evidence: therapeutic
CTD
PMID:12679808
NCBI chr19:13,873,490...13,912,035
Ensembl chr19:13,796,623...13,912,035
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Comt
catechol-O-methyltransferase
severity treatment
ISO
DNA:SNP:cd: p.V158M (rs4680) (human)
RGD
PMID:27061230 PMID:32407152
RGD:401959589 , RGD:401959744
NCBI chr11:82,568,052...82,587,642
Ensembl chr11:82,568,025...82,587,642
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Cyp2d4
cytochrome P450, family 2, subfamily d, polypeptide 4
treatment
ISO
RGD
PMID:10653207
RGD:401901270
NCBI chr 7:113,882,584...113,891,754
Ensembl chr 7:113,881,618...113,891,759
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Drd2
dopamine receptor D2
treatment susceptibility
ISO
DNA:SNP: :rs6275(human) DNA:SNP,haplotype: :rs1076560,rs6275(human)
RGD
PMID:19373123 PMID:19373123
RGD:401959309 , RGD:401959309
NCBI chr 8:49,708,927...49,772,876
Ensembl chr 8:49,708,927...49,772,875
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Gal
galanin and GMAP prepropeptide
susceptibility
ISO
DNA:SNP: :rs948854(human)
RGD
PMID:24086514
RGD:401901242
NCBI chr 1:200,650,439...200,655,302
Ensembl chr 1:200,650,439...200,654,959
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Grk2
G protein-coupled receptor kinase 2
ISO
protein:decreased expression:pre-frontal cortex
RGD
PMID:14969742
RGD:401901596
NCBI chr 1:201,580,823...201,601,580
Ensembl chr 1:201,581,480...201,601,582
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Grk6
G protein-coupled receptor kinase 6
ISO
protein:decreased expression:pre-frontal cortex
RGD
PMID:14969742
RGD:401901596
NCBI chr17:9,177,018...9,192,813
Ensembl chr17:9,177,019...9,192,644
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Nav3
neuron navigator 3
susceptibility
ISO
CTD Direct Evidence: marker/mechanism DNA:SNP:: (rs770124) (human)
CTD RGD
PMID:18438686 PMID:18438686
RGD:401851917
NCBI chr 7:45,052,206...45,840,471
Ensembl chr 7:45,054,296...45,840,698
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Ngf
nerve growth factor
ISO
DNA:hypermethylation:promoter,exon:blood protein:decreased expression:brain
RGD
PMID:29224006 PMID:26440527
RGD:401976280 , RGD:401976545
NCBI chr 2:189,901,058...189,954,452
Ensembl chr 2:189,901,058...189,954,452
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Npy1r
neuropeptide Y receptor Y1
susceptibility
ISO
DNA:SNP, haplotype:enhancer: (rs4128839) (human) DNA:SNP, haplotype:intron: (rs4691910) (human)
RGD
PMID:31689297 PMID:32757697
RGD:402463939 , RGD:402463942
NCBI chr16:23,037,788...23,047,330
Ensembl chr16:23,037,789...23,046,759
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Oprd1
opioid receptor, delta 1
susceptibility treatment
ISO
DNA:SNP: :rs1042114 (human) DNA:SNPs, haplotype:intron 1:multiple (human) associated with neonatal abstinence syndrome in offspring;DNA:SNP:intron (rs204076) (human) associated with African American;DNA:SNP:intron (rs678849) (human) associated with methadone treatment;DNA:SNP:intron (rs204076) (human) DNA:SNP:intron (rs10753331, rs581111) (human) DNA:SNP,haplotype:multiple (multiple)(human) DNA:SNP, haplotype: (rs678849|rs2236857|rs2236855|rs760589) (human) DNA:SNP: :rs2236861(human)
RGD
PMID:28656735 PMID:24533225 PMID:26233486 PMID:23612435 PMID:37531661 PMID:22795689 PMID:17622222 PMID:28632076 PMID:24086514 More...
RGD:401850580 , RGD:402525443 , RGD:11079504 , RGD:402463973 , RGD:401977581 , RGD:401976559 , RGD:401976552 , RGD:401976541 , RGD:401901242
NCBI chr 5:144,306,188...144,340,960
Ensembl chr 5:144,306,188...144,340,960
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Oprk1
opioid receptor, kappa 1
no_association
ISO
DNA:SNP: :rs702764 (human) DNA:SNP,haplotype:multiple (multiple GGCTTCT) (human)
RGD
PMID:28656735 PMID:17622222
RGD:401850580 , RGD:401976552
NCBI chr 5:13,860,016...13,877,823
Ensembl chr 5:13,860,021...13,877,823
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Oprm1
opioid receptor, mu 1
susceptibility treatment no_association
ISO
ClinVar Annotator: match by term: Opioid dependence, susceptibility to, 1 protein:decreased expression:pre-frontal cortex DNA:SNP: :rs9479757(human) DNA:SNP, haplotype:3' utr:rs10485058 (human) associated with Chronic Pain;DNA:missense mutation:exon:p.N40D (118A>G) (rs 1799971) (human) DNA:altered methylation:promoter DNA:SNPs: :multiple associated with alcohol dependence:DNA:SNP, haplotypes: :-2044C>A (human) DNA:SNPs: :172G>T (rs6912029), 1510G>A (rs12205732) (human) DNA:hypermethylation:promoter DNA:SNP:exon:17C>T (rs 1799972) (human) DNA:SNP:exon:118A>G (rs 1799971) (human)
ClinVar RGD
PMID:9193881 PMID:9689128 PMID:11134674 PMID:11773858 PMID:11773859 PMID:15037869 PMID:15086512 PMID:16046395 PMID:16387451 PMID:16682632 PMID:16906017 PMID:19528658 PMID:14969742 PMID:24086514 PMID:27958381 PMID:29781244 PMID:29564682 PMID:31853823 PMID:32492095 PMID:19429175 PMID:12815747 PMID:23226066 PMID:28121474 PMID:12960749 PMID:18181266 PMID:18181266 More...
RGD:401901596 , RGD:401901242 , RGD:401831043 , RGD:401831042 , RGD:401831040 , RGD:401827954 , RGD:401827948 , RGD:401827945 , RGD:401827942 , RGD:401827937 , RGD:401827935 , RGD:401827933 , RGD:401827929 , RGD:401827929
NCBI chr 1:43,160,057...43,413,409
Ensembl chr 1:43,160,057...43,413,409
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Pdyn
prodynorphin
sexual_dimorphism no_association susceptibility
ISO
DNA:SNP: :rs1022563 (human) DNA:SNPs:promoter, 3' utr:rs1997794, rs102256 DNA:SNP: :rs199774, rs1022563 (human) DNA:SNP: :rs910080 (human) DNA:SNP: :rs910080, rs199774 (human)
RGD
PMID:22443215 PMID:19298317 PMID:28656735 PMID:28656735 PMID:22443215
RGD:401850569 , RGD:401850586 , RGD:401850580 , RGD:401850580 , RGD:401850569
NCBI chr 3:116,900,990...116,913,334
Ensembl chr 3:116,900,992...116,913,334
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Penk
proenkephalin
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:10321497
NCBI chr 5:17,183,799...17,189,160
Ensembl chr 5:17,183,806...17,189,129
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Ttc9
tetratricopeptide repeat domain 9
susceptibility
ISO
CTD Direct Evidence: marker/mechanism DNA:SNP:: (rs8688) (human)
CTD RGD
PMID:18438686 PMID:18438686
RGD:401851917
NCBI chr 6:101,333,274...101,368,110
Ensembl chr 6:101,333,141...101,368,110
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Vegfa
vascular endothelial growth factor A
ISO
DNA:hypermethylation:exon:blood
RGD
PMID:29224006
RGD:401976280
NCBI chr 9:14,955,300...14,970,641
Ensembl chr 9:14,955,300...14,970,641
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Abat
4-aminobutyrate aminotransferase
IMP
RGD
PMID:10900239
RGD:10046064
NCBI chr10:6,996,688...7,092,835
Ensembl chr10:6,999,819...7,092,835
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Abcb1a
ATP binding cassette subfamily B member 1A
treatment
ISO
associated with methadone treatment;DNA:SNP:intron (rs1128503) (human)
RGD
PMID:29173032
RGD:401976557
NCBI chr 4:25,357,467...25,529,941
Ensembl chr 4:25,158,362...25,442,709
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Adipoq
adiponectin, C1Q and collagen domain containing
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:15717844
NCBI chr11:77,721,912...77,735,644
Ensembl chr11:77,721,912...77,735,564
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Adra1a
adrenoceptor alpha 1A
susceptibility
ISO
DNA:SNP:exon 4: p.R347C (rs1048101) (human)
RGD
PMID:33577997
RGD:401940110
NCBI chr15:40,830,125...40,935,902
Ensembl chr15:40,832,534...40,927,500
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Aldh2
aldehyde dehydrogenase 2 family member
susceptibility
ISO
DNA:polymorphism: :
RGD
PMID:21723677
RGD:401959204
NCBI chr12:34,949,549...34,982,527
Ensembl chr12:34,901,219...34,982,521
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Ankk1
ankyrin repeat and kinase domain containing 1
onset susceptibility
ISO
DNA:SNPS:exon:rs17115439, rs7118900, rs1800497 (human) DNA:SNPs:5'UTR,exon:rs877138, rs4938013(human) DNA:SNP:exon:rs1800497(human) DNA:SNPs, haplotypes:intron, 3'flanking:rs11214598, rs2859545(human)
RGD
PMID:28854834 PMID:23303482 PMID:23840506 PMID:29550268
RGD:401959202 , RGD:401959304 , RGD:401959223 , RGD:401959205
NCBI chr 8:49,779,862...49,788,024
Ensembl chr 8:49,779,862...49,788,024
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Arrb2
arrestin, beta 2
treatment
ISO
DNA:polymorphism: :rs1045280(human) associated with methadone treatment;DNA:SNP:intron (rs1045280) (human)
RGD
PMID:33783060 PMID:29173032
RGD:401901593 , RGD:401976557
NCBI chr10:55,146,887...55,154,854
Ensembl chr10:55,146,818...55,154,850
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Bche
butyrylcholinesterase
ISO
protein:increased activity:blood plasma (human)
RGD
PMID:30707402
RGD:401960085
NCBI chr 2:158,308,674...158,401,148
Ensembl chr 2:158,307,584...158,401,148
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Bdnf
brain-derived neurotrophic factor
ISO
CTD Direct Evidence: marker/mechanism protein:decreased expression:serum
CTD RGD
PMID:17715210 PMID:17715210
RGD:401976440
NCBI chr 3:96,165,042...96,215,621
Ensembl chr 3:96,165,042...96,215,615
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Chrm2
cholinergic receptor, muscarinic 2
ISO
DNA:SNP:intron:rs2350780 (human)
RGD
PMID:19500151
RGD:5509583
NCBI chr 4:65,015,408...65,149,104
Ensembl chr 4:65,014,144...65,149,103
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Comt
catechol-O-methyltransferase
severity onset susceptibility
ISO
DNA:SNP:exon 5: (rs769224) (human) DNA:SNP:cd: p.V158M (human) DNA:SNP:: (rs737866) (Human) DNA:SNP:-287A>G (human) DNA:SNP:exon 1: (rs737866) (Human) DNA:SNP:exon 4: (rs4680) p.V158M (human)
RGD
PMID:33577997 PMID:33544778 PMID:23155402 PMID:12476424 PMID:21857968 PMID:20728009 More...
RGD:401940110 , RGD:401959602 , RGD:401959234 , RGD:401940154 , RGD:401940140 , RGD:401940113
NCBI chr11:82,568,052...82,587,642
Ensembl chr11:82,568,025...82,587,642
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Creb1
cAMP responsive element binding protein 1
treatment
IDA ISO
DNA:SNP:exon:rs35349697
RGD
PMID:21362452 PMID:24704376 PMID:23062870
RGD:401901181 , RGD:401938627 , RGD:401901182
NCBI chr 9:65,903,511...65,972,562
Ensembl chr 9:65,903,547...65,970,816
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Cyp2b3
cytochrome P450, family 2, subfamily b, polypeptide 3
treatment
ISO
DNA:polymorphisms: :785A>G (rs2279343), 516G>T (rs3745274)(human)
RGD
PMID:21790905
RGD:11097675
NCBI chr 1:81,652,762...81,732,153
Ensembl chr 1:81,652,787...81,732,143
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Cyp2c6
cytochrome P450, family 2, subfamily C, polypeptide 6
treatment
ISO
DNA:SNP:exon:CYP2C19*2 (681G>A,rs4244285)(human) DNA:SNPs::CYP2C19*2, CYP2C19*3(human)
RGD
PMID:24016178 PMID:24956251
RGD:401960868 , RGD:401960881
NCBI chr 1:237,938,521...237,976,238
Ensembl chr 1:237,693,094...238,057,596
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Drd1
dopamine receptor D1
IEP
RGD
PMID:28598964
RGD:13506959
NCBI chr17:10,540,440...10,544,971
Ensembl chr17:10,540,558...10,545,002
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Drd2
dopamine receptor D2
susceptibility onset
ISO IEP
CTD Direct Evidence: marker/mechanism DNA:SNP:intron:rs1079597(human) DNA:SNPS:exon, intron:multiples(human)
CTD RGD
PMID:11751029 PMID:23840506 PMID:28854834 PMID:28598964
RGD:401959223 , RGD:401959202 , RGD:13506959
NCBI chr 8:49,708,927...49,772,876
Ensembl chr 8:49,708,927...49,772,875
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Drd3
dopamine receptor D3
IEP
RGD
PMID:28598964
RGD:13506959
NCBI chr11:56,879,689...56,931,901
Ensembl chr11:56,879,689...56,940,596
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Drd4
dopamine receptor D4
susceptibility onset
ISO
DNA:SNPs:5promoter:rs1800955,rs936462(human) DNA:SNP,methylation::rs3758653(human) DNA:polymorphism:promoter:-521G>A(human)
RGD
PMID:23840506 PMID:34864042 PMID:18991844
RGD:401959223 , RGD:401959595 , RGD:401959594
NCBI chr 1:196,396,366...196,400,824
Ensembl chr 1:196,396,366...196,399,553
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Fas
Fas cell surface death receptor
IEP
protein:increased expression:cerebral cortex (rat)
RGD
PMID:14530904
RGD:8686423
NCBI chr 1:231,798,963...231,832,591
Ensembl chr 1:231,798,960...231,832,591
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Fkbp5
FKBP prolyl isomerase 5
susceptibility
ISO
DNA:SNPs:intron,3'utr: (rs1360780,rs3800373) (human)
RGD
PMID:24845178
RGD:401976498
NCBI chr20:6,457,207...6,575,404
Ensembl chr20:6,457,216...6,541,674
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Fosb
FosB proto-oncogene, AP-1 transcription factor subunit
ameliorates
IDA
RGD
PMID:21362452 PMID:23062870
RGD:401901181 , RGD:401901182
NCBI chr 1:78,954,312...78,961,492
Ensembl chr 1:78,954,115...78,961,465
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Gabbr1
gamma-aminobutyric acid type B receptor subunit 1
susceptibility
ISO
DNA:SNP:intron: C>G (rs29220) (human)
RGD
PMID:26727527
RGD:11552767
NCBI chr20:1,464,534...1,494,114
Ensembl chr20:1,464,534...1,493,994
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Gabra2
gamma-aminobutyric acid type A receptor subunit alpha 2
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:19833324
NCBI chr14:37,097,251...37,230,030
Ensembl chr14:37,097,279...37,228,944
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Gabrg2
gamma-aminobutyric acid type A receptor subunit gamma 2
ISO
DNA:SNP:intron: (rs211014) (human)
RGD
PMID:17440936
RGD:402525444
NCBI chr10:26,374,693...26,463,937
Ensembl chr10:26,374,694...26,464,346
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Gad1
glutamate decarboxylase 1
treatment susceptibility
ISO
DNA:SNPs, haplotype:multiple: DNA:SNP,haplotype: :rs2058725(human) DNA:SNPs,haplotypes:promoter,exon:rs1978340, rs3791878, rs11542313 (human)
RGD
PMID:31866536 PMID:19500151 PMID:22564729
RGD:401900128 , RGD:5509583 , RGD:401900156
NCBI chr 3:55,369,704...55,410,335
Ensembl chr 3:55,369,704...55,410,333
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Gad2
glutamate decarboxylase 2
susceptibility
ISO
DNA:SNP: ::rs8190646(human)
RGD
PMID:19500151
RGD:5509583
NCBI chr17:84,763,630...84,826,155
Ensembl chr17:84,763,628...84,826,155
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Gdnf
glial cell derived neurotrophic factor
ISO
DNA:SNP: :rs2910709
RGD
PMID:24022000
RGD:405849398
NCBI chr 2:56,894,022...56,919,935
Ensembl chr 2:56,895,010...56,917,209
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Gria1
glutamate ionotropic receptor AMPA type subunit 1
treatment
ISO IEP
mRNA:increased expression:ventral striatum (human)
RGD
PMID:27863698 PMID:19940171
RGD:405096665 , RGD:4107717
NCBI chr10:41,210,713...41,527,283
Ensembl chr10:41,210,713...41,527,283
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Grin2a
glutamate ionotropic receptor NMDA type subunit 2A
susceptibility
ISO
DNA:repeats,SNPs,haplotype:introns:(GT)26, rs3219790,rs1102972,rs1650420,rs3104703 (human) DNA:repeats: :(GT)26 (human)
RGD
PMID:23940648 PMID:25366762
RGD:401938628 , RGD:401938629
NCBI chr10:5,629,683...6,053,262
Ensembl chr10:5,631,369...6,044,637
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Grm2
glutamate metabotropic receptor 2
IMP
RGD
PMID:30283001
RGD:38501063
NCBI chr 8:107,280,099...107,293,159
Ensembl chr 8:107,280,099...107,293,146
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Grm2em1
glutamate metabotropic receptor 2; endonuclease induced mutant 1
IMP
KO compared to wild-type rats
RGD
PMID:30283001
RGD:38501063
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Hcrt
hypocretin neuropeptide precursor
treatment
ISO
RGD
PMID:35984180
RGD:401960075
NCBI chr10:85,689,979...85,691,214
Ensembl chr10:85,689,465...85,691,210
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Htr3a
5-hydroxytryptamine receptor 3A
ISO
DSNA:SNPs:promoter, intron, CDS:g.113974819C>T, g.113985089A>G, g.113989703A>G (rs1150226, rs897687, rs1176713) (human) DNA:SNPs, haplotype:multiple (human)
RGD
PMID:26227246 PMID:19500151
RGD:405096480 , RGD:5509583
NCBI chr 8:49,242,018...49,254,475
Ensembl chr 8:49,242,020...49,254,389
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Kcnj6
potassium inwardly-rectifying channel, subfamily J, member 6
ISO
DNA:SNP: :rs2070995 (human)
RGD
PMID:20220551
RGD:6483055
NCBI chr11:34,061,702...34,308,758
Ensembl chr11:34,061,708...34,308,758
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Lep
leptin
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:15717844
NCBI chr 4:57,661,127...57,675,262
Ensembl chr 4:57,661,131...57,675,262
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Ngf
nerve growth factor
treatment
ISO
CTD Direct Evidence: marker/mechanism protein:decreased expression:serum DNA:SNP:intron:rs2239622
CTD RGD
PMID:17715210 PMID:17715210 PMID:21358750
RGD:401976440 , RGD:401965390
NCBI chr 2:189,901,058...189,954,452
Ensembl chr 2:189,901,058...189,954,452
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Npy1r
neuropeptide Y receptor Y1
susceptibility
ISO
DNA:SNP, haplotype:intron: (rs4234955) (human) DNA:SNP:intron: (rs4518200) (human)
RGD
PMID:29465008 PMID:24845178
RGD:402463944 , RGD:401976498
NCBI chr16:23,037,788...23,047,330
Ensembl chr16:23,037,789...23,046,759
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Oprd1
opioid receptor, delta 1
onset treatment
ISO
DNA:SNP: :rs508448 (human) associated with stress-related disorder;DNA:SNP:coding synonymous,intron (rs2234918, rs2236857) (human) associated with methadone treatment;DNA:SNP:intron (rs529520) (human) DNA:SNP, haplotype:intron 1 (multiple) (human) DNA:SNP, haplotype:multiple (multiple) (human) DNA:SNP:CDS:intron 1 (rs204047|rs797397) (human)
RGD
PMID:28692418 PMID:30171993 PMID:29173032 PMID:22500942 PMID:34031368 PMID:31907389 More...
RGD:401831045 , RGD:401977579 , RGD:401976557 , RGD:401976535 , RGD:401976533 , RGD:401976443
NCBI chr 5:144,306,188...144,340,960
Ensembl chr 5:144,306,188...144,340,960
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Oprk1
opioid receptor, kappa 1
treatment
IMP ISO
DNA:SNP: :rs3802279, rs3802281, and rs963549 (human)
RGD
PMID:24725195 PMID:24305833 PMID:31940240
RGD:9831447 , RGD:401850592 , RGD:401827951
NCBI chr 5:13,860,016...13,877,823
Ensembl chr 5:13,860,021...13,877,823
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Oprm1
opioid receptor, mu 1
susceptibility no_association severity
ISO
CTD Direct Evidence: marker/mechanism mRNA:splice variants:prefrontal cortex DNA:SNPs, haplotypes: :multiple DNA:missense mutation:exon:p.N40D (118A>G) (rs 1799971) (human) DNA:SNP, haplotype: :rs483481 (human) DNA:SNPs, haplotypes: :rs696522, rs1381376, rs3778151 (human)
CTD RGD
PMID:20201854 PMID:32506472 PMID:28692418 PMID:28976288 PMID:11424981 PMID:32189578 PMID:17157823 More...
RGD:401831047 , RGD:401831045 , RGD:401831044 , RGD:401827953 , RGD:401827950 , RGD:401827940
NCBI chr 1:43,160,057...43,413,409
Ensembl chr 1:43,160,057...43,413,409
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Pdyn
prodynorphin
onset susceptibility no_association
ISO
DNA:repeat:promoter:rs35286251 (human) DNA:VNTR, SNPs:rs1022563, rs2235749, rs910080 (human) DNA:VNTR:promoter DNA:SNPs, repeat:promoter:rs2281285, rs2235749, rs35286251 (human) DNA:SNP: :rs910080 (human) mRNA:decreased expression:periamygdaloid cortex
RGD
PMID:30936032 PMID:21382455 PMID:30138645 PMID:29911117 PMID:29911117 PMID:35271823 PMID:24231353 More...
RGD:401850549 , RGD:401850577 , RGD:401850562 , RGD:401850561 , RGD:401850561 , RGD:401850556 , RGD:401850554
NCBI chr 3:116,900,990...116,913,334
Ensembl chr 3:116,900,992...116,913,334
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Penk
proenkephalin
IMP
RGD
PMID:22683090
RGD:10003025
NCBI chr 5:17,183,799...17,189,160
Ensembl chr 5:17,183,806...17,189,129
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Pomc
proopiomelanocortin
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:18201294
NCBI chr 6:26,939,844...26,945,666
Ensembl chr 6:26,939,837...26,945,664
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Retn
resistin
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:15717844
NCBI chr12:1,710,881...1,712,621
Ensembl chr12:1,710,881...1,712,620
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Slc6a3
solute carrier family 6 member 3
IEP
RGD
PMID:28598964
RGD:13506959
NCBI chr 1:29,709,443...29,750,413
Ensembl chr 1:29,709,443...29,750,413
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Ttc12
tetratricopeptide repeat domain 12
susceptibility
ISO
DNA:SNP:5'UTR,intron:rs7130431(human)
RGD
PMID:23303482
RGD:401959304
NCBI chr 8:49,799,916...49,847,940
Ensembl chr 8:49,799,920...49,847,087
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Adra2a
adrenoceptor alpha 2A
IEP
mRNA:increases expression:cerebral cortex (rat)
RGD
PMID:9105684
RGD:401976538
NCBI chr 1:253,061,480...253,064,280
Ensembl chr 1:253,060,218...253,064,365
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Ago2
argonaute RISC catalytic component 2
IEP
RGD
PMID:23927484
RGD:401900655
NCBI chr 7:105,018,202...105,105,118
Ensembl chr 7:105,029,120...105,104,974
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Arc
activity-regulated cytoskeleton-associated protein
ameliorates
IMP
RGD
PMID:21549764 PMID:25746394
RGD:401851922 , RGD:11087075
NCBI chr 7:106,555,968...106,559,697
Ensembl chr 7:106,555,785...106,559,378
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Bax
BCL2 associated X, apoptosis regulator
treatment
IDA
RGD
PMID:24906198
RGD:10054248
NCBI chr 1:95,940,001...95,945,407
Ensembl chr 1:95,938,808...95,945,368
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Bcl2
BCL2, apoptosis regulator
treatment
IEP
RGD
PMID:24906198
RGD:10054248
NCBI chr13:22,689,783...22,853,920
Ensembl chr13:22,684,989...22,853,743 Ensembl chr13:22,684,989...22,853,743
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Bdnf
brain-derived neurotrophic factor
treatment
ISO IEP
protein:decreased expression:nucleus accumbens
RGD
PMID:27461790 PMID:32428531
RGD:401940145 , RGD:401959372
NCBI chr 3:96,165,042...96,215,621
Ensembl chr 3:96,165,042...96,215,615
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Cnr1
cannabinoid receptor 1
treatment
ISO
RGD
PMID:27461790
RGD:401940145
NCBI chr 5:48,408,543...48,436,099
Ensembl chr 5:48,408,574...48,435,099
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Comt
catechol-O-methyltransferase
susceptibility
ISO
DNA:SNP:cd: (rs4680) p.V158M (human)
RGD
PMID:30211780
RGD:401940137
NCBI chr11:82,568,052...82,587,642
Ensembl chr11:82,568,025...82,587,642
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Creb1
cAMP responsive element binding protein 1
treatment
ISO IDA IEP
CTD Direct Evidence: marker/mechanism protein:increased expression:neuron, brain protein:increased phosphorylation:central amygdaloid nucleus protein:increased phosphorylation:hypothalamus, ventral tegmental area mRNA, protein:increased expression:hippocampus, prefrontal cortex
CTD RGD
PMID:11717377 PMID:27053349 PMID:29024786 PMID:19108758 PMID:19052216 PMID:18772347 PMID:26313266 PMID:32113678 PMID:27461790 PMID:24073333 PMID:33609567 PMID:19341783 More...
RGD:401959748 , RGD:401959607 , RGD:401959375 , RGD:401959374 , RGD:401950487 , RGD:401940184 , RGD:401940182 , RGD:401940145 , RGD:401940122 , RGD:401940121 , RGD:401940119
NCBI chr 9:65,903,511...65,972,562
Ensembl chr 9:65,903,547...65,970,816
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Drd2
dopamine receptor D2
IEP
protein:decreased expression:hippocampus (rat)
RGD
PMID:18276072
RGD:2311587
NCBI chr 8:49,708,927...49,772,876
Ensembl chr 8:49,708,927...49,772,875
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Fadd
Fas associated via death domain
severity
IDA
RGD
PMID:21088039
RGD:11341805
NCBI chr 1:199,743,200...199,745,746
Ensembl chr 1:199,739,994...199,745,653
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Fos
Fos proto-oncogene, AP-1 transcription factor subunit
treatment
IDA IEP IMP
RGD
PMID:27053349 PMID:12225868 PMID:10998122
RGD:401959748 , RGD:405255651 , RGD:405100721
NCBI chr 6:105,121,170...105,124,036
Ensembl chr 6:105,121,170...105,124,036
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Fosb
FosB proto-oncogene, AP-1 transcription factor subunit
ameliorates
IEP
protein:increased expression:brain (rat) associated with pregnancy complications; protein:increased expression:brain (rat)
RGD
PMID:23185589 PMID:33592274
RGD:401851068 , RGD:401901281
NCBI chr 1:78,954,312...78,961,492
Ensembl chr 1:78,954,115...78,961,465
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Gad1
glutamate decarboxylase 1
IEP
mRNA:increased expression:dentate gyrus granule cell layer
RGD
PMID:15673448
RGD:401900167
NCBI chr 3:55,369,704...55,410,335
Ensembl chr 3:55,369,704...55,410,333
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Gria1
glutamate ionotropic receptor AMPA type subunit 1
treatment exacerbates
ISO IEP IMP
CTD Direct Evidence: marker/mechanism protein:increased expression:shell of nucleus accumbens, cell surface (rat) protein:decreased phosphorylation:caudate-putamen, nucleus accumbens (rat) protein:altered expression:prefrontal cortex, membrane (rat) rat gene in a mouse model protein:increased phosphorylation:nucleus accumbens (rat)
CTD RGD
PMID:11404432 PMID:25746394 PMID:34390773 PMID:15287884 PMID:31209728 PMID:16775132 PMID:22072679 PMID:32717192 PMID:31863796 PMID:24201449 PMID:25716866 More...
RGD:11087075 , RGD:405818276 , RGD:405650198 , RGD:405649863 , RGD:405649739 , RGD:405101690 , RGD:405100728 , RGD:405100238 , RGD:405096668 , RGD:401976466
NCBI chr10:41,210,713...41,527,283
Ensembl chr10:41,210,713...41,527,283
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Grin2a
glutamate ionotropic receptor NMDA type subunit 2A
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:12878694
NCBI chr10:5,629,683...6,053,262
Ensembl chr10:5,631,369...6,044,637
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Htr1b
5-hydroxytryptamine receptor 1B
treatment
ISO
RGD
PMID:35447543
RGD:405650692
NCBI chr 8:82,513,572...82,534,670
Ensembl chr 8:82,517,360...82,534,549
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Htr2a
5-hydroxytryptamine receptor 2A
ISO
protein:increased expression:prefrontal cortex
RGD
PMID:28082900
RGD:401900741
NCBI chr15:49,950,035...50,022,188
Ensembl chr15:49,950,804...50,020,928
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Mapk1
mitogen activated protein kinase 1
treatment
ISO IDA
protein:increased phosphorylation:central amygdaloid nucleus
RGD
PMID:33609567 PMID:29024786 PMID:19052216 PMID:18772347 PMID:27461790
RGD:401940121 , RGD:401959607 , RGD:401959374 , RGD:401950487 , RGD:401940145
NCBI chr11:83,957,813...84,023,629
Ensembl chr11:83,957,813...84,023,616
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Mapk3
mitogen activated protein kinase 3
treatment
ISO IDA
protein:increased phosphorylation:central amygdaloid nucleus
RGD
PMID:33609567 PMID:29024786 PMID:19052216 PMID:18772347 PMID:27461790
RGD:401940121 , RGD:401959607 , RGD:401959374 , RGD:401950487 , RGD:401940145
NCBI chr 1:181,366,646...181,372,863
Ensembl chr 1:181,366,637...181,372,863
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Mmp9
matrix metallopeptidase 9
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:20519536
NCBI chr 3:153,684,158...153,692,118
Ensembl chr 3:153,683,858...153,692,120
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Ncam1
neural cell adhesion molecule 1
IEP
protein:decreased expression, altered form:hippocampus (rat)
RGD
PMID:15673448
RGD:401900167
NCBI chr 8:49,865,629...50,165,687
Ensembl chr 8:49,865,633...50,166,014
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Ngf
nerve growth factor
IEP
mRNA,protein:increased expression:central amygdaloid nucleus
RGD
PMID:22871918
RGD:401965392
NCBI chr 2:189,901,058...189,954,452
Ensembl chr 2:189,901,058...189,954,452
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Nos1
nitric oxide synthase 1
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:17989510
NCBI chr12:38,615,111...38,795,492
Ensembl chr12:38,626,714...38,710,945
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Nps
neuropeptide S
IDA
RGD
PMID:23684726
RGD:9831198
NCBI chr 1:190,077,040...190,080,821
Ensembl chr 1:190,077,040...190,080,821
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Npsr1
neuropeptide S receptor 1
IEP
RGD
PMID:23684726
RGD:9831198
NCBI chr 8:22,606,946...22,831,558
Ensembl chr 8:22,606,946...22,831,558
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Nr3c2
nuclear receptor subfamily 3, group C, member 2
treatment
IMP
RGD
PMID:22304485
RGD:401965468
NCBI chr19:30,715,634...31,059,885
Ensembl chr19:30,715,648...31,059,885
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Oprl1
opioid related nociceptin receptor 1
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:11027224
NCBI chr 3:168,831,934...168,839,920
Ensembl chr 3:168,834,003...168,839,920
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Oprm1
opioid receptor, mu 1
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:3720824
NCBI chr 1:43,160,057...43,413,409
Ensembl chr 1:43,160,057...43,413,409
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Pdyn
prodynorphin
treatment
IEP
RGD
PMID:15976090
RGD:401850590
NCBI chr 3:116,900,990...116,913,334
Ensembl chr 3:116,900,992...116,913,334
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Rack1
receptor for activated C kinase 1
ISO
mRNA, protein:increased expression:hippocampus, prefrontal cortex
RGD
PMID:19341783
RGD:401940119
NCBI chr10:33,169,415...33,174,896
Ensembl chr10:33,169,169...33,174,975
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