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MGI:Drd1a

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Drd1a ( synonyms: D1 receptor, Drd-1, Drd1, Gpcr15 )
Protein Name(s) dopamine receptor D1A,
External Links
MGI MGI:99578

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:1098091
PMID:9387887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:1927281
PMID:11069937[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:2679747
PMID:12930822[3]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:3586401
PMID:13679419[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:3626135
PMID:12097513[5]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:3689286
PMID:16962565[6]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:64569
PMID:8294904[7]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:69539
PMID:7954836[8]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:69969
PMID:7809078[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:76570
PMID:7566118[10]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001588

dopamine receptor activity, coupled via Gs

MGI:MGI:80600
PMID:8738226[11]

IDA: Inferred from Direct Assay

F

From MGI

GO:0001659

temperature homeostasis

MGI:MGI:3797707
PMID:18486343[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0001661

conditioned taste aversion

MGI:MGI:3590453
PMID:15932618[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0001662

behavioral fear response

MGI:MGI:1930467
PMID:11172752[14]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0001662

behavioral fear response

MGI:MGI:2136089
PMID:11409899[15]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0001963

synaptic transmission, dopaminergic

MGI:MGI:3663985
PMID:16908842[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0001963

synaptic transmission, dopaminergic

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:1195902
PMID:9261820[17]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:1351083
PMID:10661513[18]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:2137377
PMID:10222120[19]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:3610905
PMID:11823893[20]

IGI: Inferred from Genetic Interaction

MGI:MGI:94927

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:3626135
PMID:12097513[5]

IGI: Inferred from Genetic Interaction

MGI:MGI:94924
MGI:MGI:94925

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:3711455
PMID:16014726[21]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3527157

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:3797707
PMID:18486343[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0004871

signal transducer activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0807

F

From MGI

GO:0004872

receptor activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0675

F

From MGI

GO:0004930

G-protein coupled receptor activity

MGI:MGI:3032880
PMID:14712229[22]

IDA: Inferred from Direct Assay

F

From MGI

GO:0004930

G-protein coupled receptor activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

F

From MGI

GO:0004952

dopamine receptor activity

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

F

From MGI

GO:0004952

dopamine receptor activity

MGI:MGI:3811680
PMID:18671743[23]

IDA: Inferred from Direct Assay

F

From MGI

GO:0005515

protein binding

MGI:MGI:85829
PMID:9016340[24]

IPI: Inferred from Physical Interaction

UniProtKB:Q6R0H7
UniProtKB:P21279

F

From MGI

GO:0005622

intracellular

MGI:MGI:2387279
PMID:12223546[25]

IGI: Inferred from Genetic Interaction

MGI:MGI:99673

C

From MGI

GO:0005622

intracellular

MGI:MGI:3701153
PMID:17194762[26]

IGI: Inferred from Genetic Interaction

MGI:MGI:94924
MGI:MGI:95776
MGI:MGI:95766

C

From MGI

GO:0005622

intracellular

MGI:MGI:3797712
PMID:18496528[27]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

C

From MGI

GO:0005622

intracellular

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0005622

intracellular

MGI:MGI:85829
PMID:9016340[24]

IMP: Inferred from Mutant Phenotype

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:69969
PMID:7809078[9]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:80600
PMID:8738226[11]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:85829
PMID:9016340[24]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:1098091
PMID:9387887[1]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005783

endoplasmic reticulum

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0005886

plasma membrane

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0005886

plasma membrane

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

C

From MGI

GO:0005901

caveola

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0006469

negative regulation of protein kinase activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0006606

protein import into nucleus

MGI:MGI:3797712
PMID:18496528[27]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0006886

intracellular protein transport

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0006936

muscle contraction

MGI:MGI:3703826
PMID:17360497[28]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3707260
MGI:MGI:2181426

P

From MGI

GO:0007165

signal transduction

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0807

P

From MGI

GO:0007186

G-protein coupled receptor signaling pathway

MGI:MGI:3032880
PMID:14712229[22]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007186

G-protein coupled receptor signaling pathway

MGI:MGI:3719553
PMID:11404425[29]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007187

G-protein signaling, coupled to cyclic nucleotide second messenger

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

GO:0007189

activation of adenylate cyclase activity by G-protein signaling pathway

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

GO:0007190

activation of adenylate cyclase activity

MGI:MGI:2450485
PMID:12488442[30]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007190

activation of adenylate cyclase activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0007190

activation of adenylate cyclase activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

GO:0007191

activation of adenylate cyclase activity by dopamine receptor signaling pathway

MGI:MGI:2178201
PMID:11923452[31]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007191

activation of adenylate cyclase activity by dopamine receptor signaling pathway

MGI:MGI:2387279
PMID:12223546[25]

IGI: Inferred from Genetic Interaction

MGI:MGI:99673

P

From MGI

GO:0007191

activation of adenylate cyclase activity by dopamine receptor signaling pathway

MGI:MGI:2660986
PMID:12665504[32]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007191

activation of adenylate cyclase activity by dopamine receptor signaling pathway

MGI:MGI:3701153
PMID:17194762[26]

IGI: Inferred from Genetic Interaction

MGI:MGI:95774
MGI:MGI:95777

P

From MGI

GO:0007191

activation of adenylate cyclase activity by dopamine receptor signaling pathway

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0007191

activation of adenylate cyclase activity by dopamine receptor signaling pathway

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

GO:0007191

activation of adenylate cyclase activity by dopamine receptor signaling pathway

MGI:MGI:80600
PMID:8738226[11]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007191

activation of adenylate cyclase activity by dopamine receptor signaling pathway

MGI:MGI:85829
PMID:9016340[24]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0007212

dopamine receptor signaling pathway

MGI:MGI:2181304
PMID:11089973[33]

IGI: Inferred from Genetic Interaction

MGI:MGI:94924

P

From MGI

GO:0007212

dopamine receptor signaling pathway

MGI:MGI:3626135
PMID:12097513[5]

IGI: Inferred from Genetic Interaction

MGI:MGI:94924
MGI:MGI:94925

P

From MGI

GO:0007212

dopamine receptor signaling pathway

MGI:MGI:3663985
PMID:16908842[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0007212

dopamine receptor signaling pathway

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:1927281
PMID:11069937[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:2679747
PMID:12930822[3]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:3626135
PMID:12097513[5]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:3689286
PMID:16962565[6]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:3811680
PMID:18671743[23]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:64569
PMID:8294904[7]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:69539
PMID:7954836[8]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:76570
PMID:7566118[10]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:80600
PMID:8738226[11]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007610

behavior

MGI:MGI:1932164
PMID:11251190[34]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007610

behavior

MGI:MGI:3575240
PMID:11985822[35]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007610

behavior

MGI:MGI:3703826
PMID:17360497[28]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3707260
MGI:MGI:2181426

P

From MGI

GO:0007610

behavior

MGI:MGI:69969
PMID:7809078[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007612

learning

MGI:MGI:3530728
PMID:15684065[36]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0007613

memory

MGI:MGI:3607825
PMID:10585522[37]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007617

mating behavior

MGI:MGI:1314754
PMID:9829800[38]

IDA: Inferred from Direct Assay

P

From MGI

GO:0007625

grooming behavior

MGI:MGI:1313196
PMID:9749770[39]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007625

grooming behavior

MGI:MGI:1339880
PMID:9988094[40]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:1195902
PMID:9261820[17]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:1274984
PMID:9692749[41]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:1351083
PMID:10661513[18]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:1929539
PMID:11150348[42]

IGI: Inferred from Genetic Interaction

MGI:MGI:94862

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:2137377
PMID:10222120[19]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3050733
PMID:15272078[43]

IGI: Inferred from Genetic Interaction

MGI:MGI:94924

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3530728
PMID:15684065[36]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3586401
PMID:13679419[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3607822
PMID:10884517[44]

IGI: Inferred from Genetic Interaction

MGI:MGI:1857159

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3664164
PMID:8001143[45]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:3703826
PMID:17360497[28]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3707260
MGI:MGI:2181426

P

From MGI

GO:0007626

locomotory behavior

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0007628

adult walking behavior

MGI:MGI:1098940
PMID:9354330[46]

IGI: Inferred from Genetic Interaction

MGI:MGI:94925
MGI:MGI:94924

P

From MGI

GO:0007628

adult walking behavior

MGI:MGI:3610833
PMID:12652349[47]

IGI: Inferred from Genetic Interaction

MGI:MGI:94925

P

From MGI

GO:0007628

adult walking behavior

MGI:MGI:69539
PMID:7954836[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0007631

feeding behavior

MGI:MGI:3050733
PMID:15272078[43]

IGI: Inferred from Genetic Interaction

MGI:MGI:94924

P

From MGI

GO:0008144

drug binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

F

From MGI

GO:0008306

associative learning

MGI:MGI:1274984
PMID:9692749[41]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0008306

associative learning

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0008542

visual learning

MGI:MGI:1274984
PMID:9692749[41]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0008542

visual learning

MGI:MGI:3530728
PMID:15684065[36]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0008542

visual learning

MGI:MGI:3607822
PMID:10884517[44]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857159

P

From MGI

GO:0008542

visual learning

MGI:MGI:3607825
PMID:10585522[37]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0008542

visual learning

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0014002

astrocyte development

MGI:MGI:3703826
PMID:17360497[28]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3707260
MGI:MGI:2181426

P

From MGI

GO:0015872

dopamine transport

MGI:MGI:3719553
PMID:11404425[29]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0016020

membrane

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0472

C

From MGI

GO:0016021

integral to membrane

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0019226

transmission of nerve impulse

MGI:MGI:2667765
PMID:12867509[48]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0019228

regulation of action potential in neuron

MGI:MGI:3663985
PMID:16908842[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0019722

calcium-mediated signaling

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0021542

dentate gyrus development

MGI:MGI:3703826
PMID:17360497[28]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3707260
MGI:MGI:2181426

P

From MGI

GO:0021756

striatum development

MGI:MGI:3703826
PMID:17360497[28]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3707260
MGI:MGI:2181426

P

From MGI

GO:0021766

hippocampus development

MGI:MGI:3703826
PMID:17360497[28]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3707260
MGI:MGI:2181426

P

From MGI

GO:0021853

cerebral cortex GABAergic interneuron migration

MGI:MGI:3709536
PMID:17409246[49]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857875

P

From MGI

GO:0030335

positive regulation of cell migration

MGI:MGI:3709536
PMID:17409246[49]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857875

P

From MGI

GO:0030336

negative regulation of cell migration

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0030424

axon

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0030425

dendrite

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0030432

peristalsis

MGI:MGI:3050733
PMID:15272078[43]

IGI: Inferred from Genetic Interaction

MGI:MGI:94924

P

From MGI

GO:0030819

positive regulation of cAMP biosynthetic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0030819

positive regulation of cAMP biosynthetic process

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

GO:0031161

phosphatidylinositol catabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0035106

operant conditioning

MGI:MGI:3622838
PMID:12603275[50]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0035106

operant conditioning

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0035240

dopamine binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

F

From MGI

GO:0042053

regulation of dopamine metabolic process

MGI:MGI:2136539
PMID:11438590[51]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0042220

response to cocaine

MGI:MGI:1098091
PMID:9387887[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0042220

response to cocaine

MGI:MGI:1351083
PMID:10661513[18]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0042220

response to cocaine

MGI:MGI:2137377
PMID:10222120[19]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0042220

response to cocaine

MGI:MGI:3663985
PMID:16908842[16]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0042220

response to cocaine

MGI:MGI:3761901
PMID:12354293[52]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0042220

response to cocaine

MGI:MGI:3765089
PMID:18045908[53]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0042321

negative regulation of circadian sleep/wake cycle, sleep

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0042493

response to drug

MGI:MGI:1932164
PMID:11251190[34]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0042493

response to drug

MGI:MGI:77732
PMID:7549459[54]

IDA: Inferred from Direct Assay

P

From MGI

GO:0042755

eating behavior

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0043025

neuronal cell body

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0043197

dendritic spine

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

C

From MGI

GO:0043269

regulation of ion transport

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0045762

positive regulation of adenylate cyclase activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0046323

glucose import

MGI:MGI:1932164
PMID:11251190[34]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0046488

phosphatidylinositol metabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0046960

sensitization

MGI:MGI:3610905
PMID:11823893[20]

IGI: Inferred from Genetic Interaction

MGI:MGI:94927

P

From MGI

GO:0048148

behavioral response to cocaine

MGI:MGI:3711455
PMID:16014726[21]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3527157

P

From MGI

GO:0048148

behavioral response to cocaine

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0048169

regulation of long-term neuronal synaptic plasticity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P18901

P

From MGI

GO:0051281

positive regulation of release of sequestered calcium ion into cytosol

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

GO:0051482

elevation of cytosolic calcium ion concentration involved in G-protein signaling coupled to IP3 second messenger

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

GO:0051968

positive regulation of synaptic transmission, glutamatergic

MGI:MGI:82736
PMID:8795639[55]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0060158

activation of phospholipase C activity by dopamine receptor signaling pathway

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

GO:0060158

activation of phospholipase C activity by dopamine receptor signaling pathway

MGI:MGI:3621386
PMID:15016423[56]

IDA: Inferred from Direct Assay

P

From MGI

GO:0060158

activation of phospholipase C activity by dopamine receptor signaling pathway

MGI:MGI:3701153
PMID:17194762[26]

IGI: Inferred from Genetic Interaction

MGI:MGI:94924
MGI:MGI:95776
MGI:MGI:95766

P

From MGI

GO:0060291

long-term synaptic potentiation

MGI:MGI:3036431
PMID:14981263[57]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0060291

long-term synaptic potentiation

MGI:MGI:3586401
PMID:13679419[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2159306

P

From MGI

GO:0060291

long-term synaptic potentiation

MGI:MGI:3610662
PMID:9427321[58]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0060292

long term synaptic depression

MGI:MGI:3036431
PMID:14981263[57]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

GO:0071870

cellular response to catecholamine stimulus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P21728

P

From MGI

NOT

GO:0001964

startle response

MGI:MGI:3721754
PMID:17324452[59]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

NOT

GO:0001964

startle response

MGI:MGI:3757792
PMID:17712281[60]

IMP: Inferred from Mutant Phenotype

P

From MGI

NOT

GO:0060134

prepulse inhibition

MGI:MGI:3654415
PMID:12417685[61]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

NOT

GO:0060134

prepulse inhibition

MGI:MGI:3721754
PMID:17324452[59]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1857158

P

From MGI

NOT

GO:0060134

prepulse inhibition

MGI:MGI:3757792
PMID:17712281[60]

IMP: Inferred from Mutant Phenotype

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. ↑ 1.0 1.1 1.2 Bender M et al. (1997) D1 receptors mediate dopamine action in the fetal suprachiasmatic nuclei: studies of mice with targeted deletion of the D1 dopamine receptor gene. Brain Res Mol Brain Res 49: 271-7 PubMed GONUTS page
  2. ↑ 2.0 2.1 Wang Y et al. (2000) Dopamine D2 long receptor-deficient mice display alterations in striatum-dependent functions. J Neurosci 20: 8305-14 PubMed GONUTS page
  3. ↑ 3.0 3.1 Goldberg MS et al. (2003) Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons. J Biol Chem 278: 43628-35 PubMed GONUTS page
  4. ↑ 4.0 4.1 4.2 Centonze D et al. (2003) Distinct roles of D1 and D5 dopamine receptors in motor activity and striatal synaptic plasticity. J Neurosci 23: 8506-12 PubMed GONUTS page
  5. ↑ 5.0 5.1 5.2 5.3 Glickstein SB et al. (2002) Mice lacking dopamine D2 and D3 receptors have spatial working memory deficits. J Neurosci 22: 5619-29 PubMed GONUTS page
  6. ↑ 6.0 6.1 Leonard SK et al. (2006) Low affinity binding of the classical D1 antagonist SCH23390 in rodent brain: potential interaction with A2A and D2-like receptors. Brain Res 1117: 25-37 PubMed GONUTS page
  7. ↑ 7.0 7.1 Qin ZH et al. (1994) Lesions of mouse striatum induced by 6-hydroxydopamine differentially alter the density, rate of synthesis, and level of gene expression of D1 and D2 dopamine receptors. J Neurochem 62: 411-20 PubMed GONUTS page
  8. ↑ 8.0 8.1 8.2 Xu M et al. (1994) Dopamine D1 receptor mutant mice are deficient in striatal expression of dynorphin and in dopamine-mediated behavioral responses. Cell 79: 729-42 PubMed GONUTS page
  9. ↑ 9.0 9.1 9.2 Drago J et al. (1994) Altered striatal function in a mutant mouse lacking D1A dopamine receptors. Proc Natl Acad Sci U S A 91: 12564-8 PubMed GONUTS page
  10. ↑ 10.0 10.1 Baik JH et al. (1995) Parkinsonian-like locomotor impairment in mice lacking dopamine D2 receptors. Nature 377: 424-8 PubMed GONUTS page
  11. ↑ 11.0 11.1 11.2 11.3 Noble F & Cox BM (1996) Differences among mouse strains in the regulation by mu, delta 1 and delta 2 opioid receptors of striatal adenylyl cyclases activated by dopamine D1 or adenosine A2a receptors. Brain Res 716: 107-17 PubMed GONUTS page
  12. ↑ 12.0 12.1 Ito M et al. (2008) Hyperthermic and lethal effects of methamphetamine: roles of dopamine D1 and D2 receptors. Neurosci Lett 438: 327-9 PubMed GONUTS page
  13. ↑ Cannon CM et al. (2005) Mice lacking dopamine D1 receptors express normal lithium chloride-induced conditioned taste aversion for salt but not sucrose. Eur J Neurosci 21: 2600-4 PubMed GONUTS page
  14. ↑ El-Ghundi M et al. (2001) Prolonged fear responses in mice lacking dopamine D1 receptor. Brain Res 892: 86-93 PubMed GONUTS page
  15. ↑ Kojima T et al. (2001) Genomic organization of the Shc-related phosphotyrosine adapters and characterization of the full-length Sck/ShcB: specific association of p68-Sck/ShcB with pp135. Biochem Biophys Res Commun 284: 1039-47 PubMed GONUTS page
  16. ↑ 16.0 16.1 16.2 16.3 Naccache SN et al. (2006) Binding of internalized receptors to the PDZ domain of GIPC/synectin recruits myosin VI to endocytic vesicles. Proc Natl Acad Sci U S A 103: 12735-40 PubMed GONUTS page
  17. ↑ 17.0 17.1 Crawford CA et al. (1997) Effects of repeated amphetamine treatment on the locomotor activity of the dopamine D1A-deficient mouse. Neuroreport 8: 2523-7 PubMed GONUTS page
  18. ↑ 18.0 18.1 18.2 Xu M et al. (2000) Behavioral responses to cocaine and amphetamine administration in mice lacking the dopamine D1 receptor. Brain Res 852: 198-207 PubMed GONUTS page
  19. ↑ 19.0 19.1 19.2 Dracheva S et al. (1999) Paradoxical locomotor behavior of dopamine D1 receptor transgenic mice. Exp Neurol 157: 169-79 PubMed GONUTS page
  20. ↑ 20.0 20.1 Karper PE et al. (2002) Role of D1-like receptors in amphetamine-induced behavioral sensitization: a study using D1A receptor knockout mice. Psychopharmacology (Berl) 159: 407-14 PubMed GONUTS page
  21. ↑ 21.0 21.1 Heusner CL & Palmiter RD (2005) Expression of mutant NMDA receptors in dopamine D1 receptor-containing cells prevents cocaine sensitization and decreases cocaine preference. J Neurosci 25: 6651-7 PubMed GONUTS page
  22. ↑ 22.0 22.1 Weissman JT et al. (2004) G-protein-coupled receptor-mediated activation of rap GTPases: characterization of a novel Galphai regulated pathway. Oncogene 23: 241-9 PubMed GONUTS page
  23. ↑ 23.0 23.1 Bailey A et al. (2008) Decrease of D2 receptor binding but increase in D2-stimulated G-protein activation, dopamine transporter binding and behavioural sensitization in brains of mice treated with a chronic escalating dose 'binge' cocaine administration paradigm. Eur J Neurosci 28: 759-70 PubMed GONUTS page
  24. ↑ 24.0 24.1 24.2 24.3 Friedman E et al. (1997) D1-like dopaminergic activation of phosphoinositide hydrolysis is independent of D1A dopamine receptors: evidence from D1A knockout mice. Mol Pharmacol 51: 6-11 PubMed GONUTS page
  25. ↑ 25.0 25.1 Lee KW et al. (2002) Impaired D2 dopamine receptor function in mice lacking type 5 adenylyl cyclase. J Neurosci 22: 7931-40 PubMed GONUTS page
  26. ↑ 26.0 26.1 26.2 Rashid AJ et al. (2007) D1-D2 dopamine receptor heterooligomers with unique pharmacology are coupled to rapid activation of Gq/11 in the striatum. Proc Natl Acad Sci U S A 104: 654-9 PubMed GONUTS page
  27. ↑ 27.0 27.1 Stipanovich A et al. (2008) A phosphatase cascade by which rewarding stimuli control nucleosomal response. Nature 453: 879-84 PubMed GONUTS page
  28. ↑ 28.0 28.1 28.2 28.3 28.4 28.5 28.6 Gantois I et al. (2007) Ablation of D1 dopamine receptor-expressing cells generates mice with seizures, dystonia, hyperactivity, and impaired oral behavior. Proc Natl Acad Sci U S A 104: 4182-7 PubMed GONUTS page
  29. ↑ 29.0 29.1 Hervé D et al. (2001) Galpha(olf) levels are regulated by receptor usage and control dopamine and adenosine action in the striatum. J Neurosci 21: 4390-9 PubMed GONUTS page
  30. ↑ Schwindinger WF et al. (2003) Loss of G protein gamma 7 alters behavior and reduces striatal alpha(olf) level and cAMP production. J Biol Chem 278: 6575-9 PubMed GONUTS page
  31. ↑ Drouin C et al. (2002) Alpha1b-adrenergic receptors control locomotor and rewarding effects of psychostimulants and opiates. J Neurosci 22: 2873-84 PubMed GONUTS page
  32. ↑ Iwamoto T et al. (2003) Motor dysfunction in type 5 adenylyl cyclase-null mice. J Biol Chem 278: 16936-40 PubMed GONUTS page
  33. ↑ Usiello A et al. (2000) Distinct functions of the two isoforms of dopamine D2 receptors. Nature 408: 199-203 PubMed GONUTS page
  34. ↑ 34.0 34.1 34.2 Miyamoto S et al. (2001) Blunted brain metabolic response to ketamine in mice lacking D(1A) dopamine receptors. Brain Res 894: 167-80 PubMed GONUTS page
  35. ↑ Tomiyama K et al. (2002) Phenotypic resolution of spontaneous and D1-like agonist-induced orofacial movement topographies in congenic dopamine D1A receptor 'knockout' mice. Neuropharmacology 42: 644-52 PubMed GONUTS page
  36. ↑ 36.0 36.1 36.2 Tran AH et al. (2005) Dopamine D1 receptors involved in locomotor activity and accumbens neural responses to prediction of reward associated with place. Proc Natl Acad Sci U S A 102: 2117-22 PubMed GONUTS page
  37. ↑ 37.0 37.1 El-Ghundi M et al. (1999) Spatial learning deficit in dopamine D(1) receptor knockout mice. Eur J Pharmacol 383: 95-106 PubMed GONUTS page
  38. ↑ Szczypka MS et al. (1998) Dopamine-stimulated sexual behavior is testosterone dependent in mice. Behav Neurosci 112: 1229-35 PubMed GONUTS page
  39. ↑ Cromwell HC et al. (1998) Action sequencing is impaired in D1A-deficient mutant mice. Eur J Neurosci 10: 2426-32 PubMed GONUTS page
  40. ↑ Drago F et al. (1999) The expression of neuropeptide-induced excessive grooming behavior in dopamine D1 and D2 receptor-deficient mice. Eur J Pharmacol 365: 125-31 PubMed GONUTS page
  41. ↑ 41.0 41.1 41.2 Smith DR et al. (1998) Behavioural assessment of mice lacking D1A dopamine receptors. Neuroscience 86: 135-46 PubMed GONUTS page
  42. ↑ Ralph RJ et al. (2001) Prepulse inhibition deficits and perseverative motor patterns in dopamine transporter knock-out mice: differential effects of D1 and D2 receptor antagonists. J Neurosci 21: 305-13 PubMed GONUTS page
  43. ↑ 43.0 43.1 43.2 Kobayashi M et al. (2004) Simultaneous absence of dopamine D1 and D2 receptor-mediated signaling is lethal in mice. Proc Natl Acad Sci U S A 101: 11465-70 PubMed GONUTS page
  44. ↑ 44.0 44.1 Karasinska JM et al. (2000) Modification of dopamine D(1) receptor knockout phenotype in mice lacking both dopamine D(1) and D(3) receptors. Eur J Pharmacol 399: 171-81 PubMed GONUTS page
  45. ↑ Xu M et al. (1994) Elimination of cocaine-induced hyperactivity and dopamine-mediated neurophysiological effects in dopamine D1 receptor mutant mice. Cell 79: 945-55 PubMed GONUTS page
  46. ↑ Xu M et al. (1997) Dopamine D3 receptor mutant mice exhibit increased behavioral sensitivity to concurrent stimulation of D1 and D2 receptors. Neuron 19: 837-48 PubMed GONUTS page
  47. ↑ Wong JY et al. (2003) Essential conservation of D1 mutant phenotype at the level of individual topographies of behaviour in mice lacking both D1 and D3 dopamine receptors. Psychopharmacology (Berl) 167: 167-73 PubMed GONUTS page
  48. ↑ Centonze D et al. (2003) Receptor subtypes involved in the presynaptic and postsynaptic actions of dopamine on striatal interneurons. J Neurosci 23: 6245-54 PubMed GONUTS page
  49. ↑ 49.0 49.1 Crandall JE et al. (2007) Dopamine receptor activation modulates GABA neuron migration from the basal forebrain to the cerebral cortex. J Neurosci 27: 3813-22 PubMed GONUTS page
  50. ↑ El-Ghundi M et al. (2003) Attenuation of sucrose reinforcement in dopamine D1 receptor deficient mice. Eur J Neurosci 17: 851-62 PubMed GONUTS page
  51. ↑ Parish CL et al. (2001) The role of dopamine receptors in regulating the size of axonal arbors. J Neurosci 21: 5147-57 PubMed GONUTS page
  52. ↑ Zhang D et al. (2002) The dopamine D1 receptor is a critical mediator for cocaine-induced gene expression. J Neurochem 82: 1453-64 PubMed GONUTS page
  53. ↑ Caine SB et al. (2007) Lack of self-administration of cocaine in dopamine D1 receptor knock-out mice. J Neurosci 27: 13140-50 PubMed GONUTS page
  54. ↑ Verma A & Kulkarni SK (1995) Role of D1/D2 dopamine and N-methyl-D-aspartate (NMDA) receptors in morphine tolerance and dependence in mice. Eur Neuropsychopharmacol 5: 81-7 PubMed GONUTS page
  55. ↑ Levine MS et al. (1996) Modulatory actions of dopamine on NMDA receptor-mediated responses are reduced in D1A-deficient mutant mice. J Neurosci 16: 5870-82 PubMed GONUTS page
  56. ↑ Mizuo K et al. (2004) Enhancement of dopamine-induced signaling responses in the forebrain of mice lacking dopamine D3 receptor. Neurosci Lett 358: 13-6 PubMed GONUTS page
  57. ↑ 57.0 57.1 Huang YY et al. (2004) Genetic evidence for the bidirectional modulation of synaptic plasticity in the prefrontal cortex by D1 receptors. Proc Natl Acad Sci U S A 101: 3236-41 PubMed GONUTS page
  58. ↑ Matthies H et al. (1997) Dopamine D1-deficient mutant mice do not express the late phase of hippocampal long-term potentiation. Neuroreport 8: 3533-5 PubMed GONUTS page
  59. ↑ 59.0 59.1 Vinkers CH et al. (2007) Role of dopamine D1 and D2 receptors in CRF-induced disruption of sensorimotor gating. Pharmacol Biochem Behav 86: 550-8 PubMed GONUTS page
  60. ↑ 60.0 60.1 Mohr D et al. (2007) Accumbal dopamine D2 receptors are important for sensorimotor gating in C3H mice. Neuroreport 18: 1493-7 PubMed GONUTS page
  61. ↑ Ralph-Williams RJ et al. (2002) Differential effects of direct and indirect dopamine agonists on prepulse inhibition: a study in D1 and D2 receptor knock-out mice. J Neurosci 22: 9604-11 PubMed GONUTS page
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