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MGI:Grin1

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Grin1 ( synonyms: GluRzeta1, M100174, Nmdar, NMDAR1, NR1, Rgsc174 )
Protein Name(s) glutamate receptor, ionotropic, NMDA1 (zeta 1),
External Links
MGI MGI:95819

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0001661

conditioned taste aversion

MGI:MGI:3589959
PMID:16101757[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:3038374

P

From MGI

GO:0001964

startle response

MGI:MGI:1858680
PMID:10818139[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928283
MGI:MGI:1928284

P

From MGI

GO:0001967

suckling behavior

MGI:MGI:2137201
PMID:10777815[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0001967

suckling behavior

MGI:MGI:65431
PMID:8313466[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0001967

suckling behavior

MGI:MGI:85962
PMID:8713451[5]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:3629445
PMID:16638606[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928280

P

From MGI

GO:0001975

response to amphetamine

MGI:MGI:3784348
PMID:15467708[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928280

P

From MGI

GO:0004872

receptor activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0675

F

From MGI

GO:0004872

receptor activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001508

F

From MGI

GO:0004970

ionotropic glutamate receptor activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:1888650
PMID:10963597[8]

IMP: Inferred from Mutant Phenotype

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:1928326
PMID:8060614[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928327

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:2182479
PMID:12040087[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2387441

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:2667460
PMID:12832526[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:3579211
PMID:15745956[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:3703316
PMID:17313573[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3611337
MGI:MGI:2448952

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:49860
PMID:1377365[14]

IDA: Inferred from Direct Assay

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:49860
PMID:1377365[14]

IGI: Inferred from Genetic Interaction

MGI:MGI:95820

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:49860
PMID:1377365[14]

IGI: Inferred from Genetic Interaction

MGI:MGI:95821

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:49860
PMID:1377365[14]

IGI: Inferred from Genetic Interaction

MGI:MGI:95822

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:50809
PMID:1532151[15]

IDA: Inferred from Direct Assay

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:51718
PMID:1385220[16]

IDA: Inferred from Direct Assay

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:65431
PMID:8313466[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:65947
PMID:1374164[17]

IDA: Inferred from Direct Assay

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:65947
PMID:1374164[17]

IGI: Inferred from Genetic Interaction

MGI:MGI:95820

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:68623
PMID:7929101[18]

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0004972

N-methyl-D-aspartate selective glutamate receptor activity

MGI:MGI:69304
PMID:7531804[19]

IGI: Inferred from Genetic Interaction

MGI:MGI:95821

F

From MGI

GO:0005102

receptor binding

MGI:MGI:2155580
PMID:11754835[20]

IPI: Inferred from Physical Interaction

UniProtKB:P54763

F

From MGI

GO:0005215

transporter activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001638

F

From MGI

GO:0005216

ion channel activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0407

F

From MGI

GO:0005216

ion channel activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001508

F

From MGI

GO:0005234

extracellular-glutamate-gated ion channel activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR019594
InterPro:IPR001320
InterPro:IPR001508

F

From MGI

GO:0005261

cation channel activity

MGI:MGI:69304
PMID:7531804[19]

IGI: Inferred from Genetic Interaction

MGI:MGI:95821

F

From MGI

GO:0005262

calcium channel activity

MGI:MGI:50809
PMID:1532151[15]

IDA: Inferred from Direct Assay

F

From MGI

GO:0005262

calcium channel activity

MGI:MGI:65947
PMID:1374164[17]

IDA: Inferred from Direct Assay

F

From MGI

GO:0005262

calcium channel activity

MGI:MGI:65947
PMID:1374164[17]

IGI: Inferred from Genetic Interaction

MGI:MGI:95820

F

From MGI

GO:0005509

calcium ion binding

MGI:MGI:3526504
PMID:15663482[21]

IDA: Inferred from Direct Assay

F

From MGI

GO:0005515

protein binding

MGI:MGI:1195436
PMID:9458051[22]

IPI: Inferred from Physical Interaction

UniProtKB:Q01098
UniProtKB:Q62108

F

From MGI

GO:0005515

protein binding

MGI:MGI:1860431
PMID:10862698[23]

IPI: Inferred from Physical Interaction

UniProtKB:Q62108

F

From MGI

GO:0005515

protein binding

MGI:MGI:2155580
PMID:11754835[20]

IPI: Inferred from Physical Interaction

UniProtKB:P54763

F

From MGI

GO:0005515

protein binding

MGI:MGI:2682163
PMID:14645471[24]

IPI: Inferred from Physical Interaction

UniProtKB:P35436

F

From MGI

GO:0005515

protein binding

MGI:MGI:3526504
PMID:15663482[21]

IPI: Inferred from Physical Interaction

UniProtKB:Q9QVP4

F

From MGI

GO:0005515

protein binding

MGI:MGI:3619820
PMID:16554481[25]

IPI: Inferred from Physical Interaction

UniProtKB:P35436
UniProtKB:Q01097

F

From MGI

GO:0005515

protein binding

MGI:MGI:3692803
PMID:17018287[26]

IPI: Inferred from Physical Interaction

MGI:MGI:104684

F

From MGI

GO:0005515

protein binding

MGI:MGI:3694290
PMID:16332682[27]

IPI: Inferred from Physical Interaction

UniProtKB:Q924X6

F

From MGI

GO:0005515

protein binding

MGI:MGI:3835254
PMID:18945678[28]

IPI: Inferred from Physical Interaction

UniProtKB:Q6ZWQ9

F

From MGI

GO:0005515

protein binding

MGI:MGI:4359331
PMID:19455133[29]

IPI: Inferred from Physical Interaction

UniProtKB:Q62108

F

From MGI

GO:0005515

protein binding

MGI:MGI:5315347
PMID:16635246[30]

IPI: Inferred from Physical Interaction

UniProtKB:Q62108

F

From MGI

GO:0005515

protein binding

MGI:MGI:80545
PMID:8595214[31]

IPI: Inferred from Physical Interaction

UniProtKB:Q01097
UniProtKB:Q01098

F

From MGI

GO:0005515

protein binding

MGI:MGI:85255
PMID:9003035[32]

IPI: Inferred from Physical Interaction

UniProtKB:P35436
UniProtKB:Q01097

F

From MGI

GO:0005516

calmodulin binding

MGI:MGI:3526504
PMID:15663482[21]

IDA: Inferred from Direct Assay

F

From MGI

GO:0005624

membrane fraction

MGI:MGI:1859430
PMID:10846156[33]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:3690398
PMID:17093100[34]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:81821
PMID:8840015[35]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005624

membrane fraction

MGI:MGI:85255
PMID:9003035[32]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:2445233
PMID:12414093[36]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005886

plasma membrane

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-1003

C

From MGI

GO:0005887

integral to plasma membrane

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

C

From MGI

GO:0006810

transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0813

P

From MGI

GO:0006810

transport

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001638

P

From MGI

GO:0006811

ion transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0406

P

From MGI

GO:0006811

ion transport

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001508

P

From MGI

GO:0006812

cation transport

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

P

From MGI

GO:0006812

cation transport

MGI:MGI:69304
PMID:7531804[19]

IGI: Inferred from Genetic Interaction

MGI:MGI:95821

P

From MGI

GO:0006816

calcium ion transport

MGI:MGI:3622400
PMID:15576450[37]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2178083
MGI:MGI:2181422

P

From MGI

GO:0006816

calcium ion transport

MGI:MGI:50809
PMID:1532151[15]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006874

cellular calcium ion homeostasis

MGI:MGI:1928326
PMID:8060614[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928327

P

From MGI

GO:0007268

synaptic transmission

MGI:MGI:1859430
PMID:10846156[33]

TAS: Traceable Author Statement

P

From MGI

GO:0007585

respiratory gaseous exchange

MGI:MGI:65431
PMID:8313466[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0007585

respiratory gaseous exchange

MGI:MGI:85962
PMID:8713451[5]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0007611

learning or memory

MGI:MGI:3664028
PMID:17004940[38]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2387441

P

From MGI

GO:0007612

learning

MGI:MGI:3691363
PMID:17015831[39]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3692441

P

From MGI

GO:0007613

memory

MGI:MGI:1353841
PMID:10700255[40]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2177650

P

From MGI

GO:0007613

memory

MGI:MGI:1353881
PMID:10719900[41]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0007613

memory

MGI:MGI:3715411
PMID:17556551[42]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0007616

long-term memory

MGI:MGI:3036924
PMID:15003177[43]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2177650

P

From MGI

GO:0008021

synaptic vesicle

MGI:MGI:1859430
PMID:10846156[33]

IDA: Inferred from Direct Assay

C

From MGI

GO:0008306

associative learning

MGI:MGI:2182479
PMID:12040087[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2387441

P

From MGI

GO:0008306

associative learning

MGI:MGI:3621679
PMID:12718863[44]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2387441

P

From MGI

GO:0008344

adult locomotory behavior

MGI:MGI:1343743
PMID:10481908[45]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928280

P

From MGI

GO:0008344

adult locomotory behavior

MGI:MGI:1858680
PMID:10818139[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928283
MGI:MGI:1928284

P

From MGI

GO:0008355

olfactory learning

MGI:MGI:1353841
PMID:10700255[40]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2177650

P

From MGI

GO:0008355

olfactory learning

MGI:MGI:1931991
PMID:11248114[46]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2177650

P

From MGI

GO:0008542

visual learning

MGI:MGI:1858680
PMID:10818139[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928283
MGI:MGI:1928284

P

From MGI

GO:0008542

visual learning

MGI:MGI:3623866
PMID:16611824[47]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0008542

visual learning

MGI:MGI:3703316
PMID:17313573[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3611337
MGI:MGI:2448952

P

From MGI

GO:0008542

visual learning

MGI:MGI:84850
PMID:8980238[48]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2177650

P

From MGI

GO:0008542

visual learning

MGI:MGI:86085
PMID:9054942[49]

IGI: Inferred from Genetic Interaction

MGI:MGI:97306

P

From MGI

GO:0008542

visual learning

MGI:MGI:893741
PMID:9246451[50]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0009986

cell surface

MGI:MGI:3765383
PMID:17229826[51]

IDA: Inferred from Direct Assay

C

From MGI

GO:0010646

regulation of cell communication

MGI:MGI:3610881
PMID:16299502[52]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0010942

positive regulation of cell death

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

P

From MGI

GO:0014069

postsynaptic density

MGI:MGI:3054180
PMID:15317856[53]

IDA: Inferred from Direct Assay

C

From MGI

GO:0014069

postsynaptic density

MGI:MGI:3531593
PMID:15748150[54]

IDA: Inferred from Direct Assay

C

From MGI

GO:0014069

postsynaptic density

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0016020

membrane

MGI:MGI:50809
PMID:1532151[15]

IC: Inferred by Curator

GO:0004972

C

From MGI

GO:0016021

integral to membrane

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0812

C

From MGI

GO:0016594

glycine binding

MGI:MGI:3687923
PMID:12586454[55]

IMP: Inferred from Mutant Phenotype

F

From MGI

GO:0016594

glycine binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0016594

glycine binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

F

From MGI

GO:0016595

glutamate binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0016595

glutamate binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

F

From MGI

GO:0017146

N-methyl-D-aspartate selective glutamate receptor complex

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0017146

N-methyl-D-aspartate selective glutamate receptor complex

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

C

From MGI

GO:0017146

N-methyl-D-aspartate selective glutamate receptor complex

MGI:MGI:85255
PMID:9003035[32]

IPI: Inferred from Physical Interaction

UniProtKB:P35436
UniProtKB:Q01097

C

From MGI

GO:0019233

sensory perception of pain

MGI:MGI:2667460
PMID:12832526[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0019717

synaptosome

MGI:MGI:2682163
PMID:14645471[24]

IDA: Inferred from Direct Assay

C

From MGI

GO:0019899

enzyme binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0021586

pons maturation

MGI:MGI:65431
PMID:8313466[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0021987

cerebral cortex development

MGI:MGI:1888650
PMID:10963597[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:1928281

P

From MGI

GO:0021987

cerebral cortex development

MGI:MGI:2654367
PMID:12657691[56]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2655237
MGI:MGI:2655232

P

From MGI

GO:0022843

voltage-gated cation channel activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0030054

cell junction

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0965

C

From MGI

GO:0030288

outer membrane-bounded periplasmic space

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001638

C

From MGI

GO:0030425

dendrite

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

C

From MGI

GO:0030426

growth cone

MGI:MGI:1344968
PMID:10480904[57]

NAS: Non-traceable Author Statement

C

From MGI

GO:0032590

dendrite membrane

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0407

P

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:1888650
PMID:10963597[8]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:1928326
PMID:8060614[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928327

P

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001508

P

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:2182479
PMID:12040087[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2387441

P

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:2667460
PMID:12832526[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:3579211
PMID:15745956[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:3703316
PMID:17313573[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3611337
MGI:MGI:2448952

P

From MGI

GO:0034220

ion transmembrane transport

MGI:MGI:65431
PMID:8313466[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0034765

regulation of ion transmembrane transport

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:Q62683

P

From MGI

GO:0035176

social behavior

MGI:MGI:1343743
PMID:10481908[45]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928280

P

From MGI

GO:0035235

ionotropic glutamate receptor signaling pathway

MGI:MGI:3604036
PMID:16025111[58]

IDA: Inferred from Direct Assay

P

From MGI

GO:0035235

ionotropic glutamate receptor signaling pathway

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

P

From MGI

GO:0035249

synaptic transmission, glutamatergic

MGI:MGI:1888650
PMID:10963597[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:1928281

P

From MGI

GO:0035249

synaptic transmission, glutamatergic

MGI:MGI:65431
PMID:8313466[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0035254

glutamate receptor binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0042165

neurotransmitter binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

F

From MGI

GO:0042391

regulation of membrane potential

MGI:MGI:1928326
PMID:8060614[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928327

P

From MGI

GO:0042391

regulation of membrane potential

MGI:MGI:2182479
PMID:12040087[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2387441

P

From MGI

GO:0042391

regulation of membrane potential

MGI:MGI:2654367
PMID:12657691[56]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2655237
MGI:MGI:2655232

P

From MGI

GO:0042391

regulation of membrane potential

MGI:MGI:2667460
PMID:12832526[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0042391

regulation of membrane potential

MGI:MGI:3622400
PMID:15576450[37]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2178083
MGI:MGI:2181422

P

From MGI

GO:0042391

regulation of membrane potential

MGI:MGI:3703316
PMID:17313573[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3611337
MGI:MGI:2448952

P

From MGI

GO:0042391

regulation of membrane potential

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

P

From MGI

GO:0042391

regulation of membrane potential

MGI:MGI:50809
PMID:1532151[15]

IDA: Inferred from Direct Assay

P

From MGI

GO:0043065

positive regulation of apoptotic process

MGI:MGI:3757796
PMID:17803966[59]

IGI: Inferred from Genetic Interaction

MGI:MGI:95820
MGI:MGI:1096575

P

From MGI

GO:0043083

synaptic cleft

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0043195

terminal button

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0043197

dendritic spine

MGI:MGI:3526504
PMID:15663482[21]

IDA: Inferred from Direct Assay

C

From MGI

GO:0043197

dendritic spine

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0043278

response to morphine

MGI:MGI:3797147
PMID:18423864[60]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0043523

regulation of neuron apoptotic process

MGI:MGI:1344923
PMID:10479699[61]

IGI: Inferred from Genetic Interaction

MGI:MGI:95815

P

From MGI

GO:0043523

regulation of neuron apoptotic process

MGI:MGI:3655891
PMID:16906136[62]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:3695621
PMID:17077143[63]

IGI: Inferred from Genetic Interaction

MGI:MGI:99702

P

From MGI

GO:0043524

negative regulation of neuron apoptotic process

MGI:MGI:3695621
PMID:17077143[63]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0043576

regulation of respiratory gaseous exchange

MGI:MGI:2137201
PMID:10777815[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0045202

synapse

MGI:MGI:2154458

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0045202

synapse

MGI:MGI:3530687
PMID:15681343[64]

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0045202

synapse

MGI:MGI:3604036
PMID:16025111[58]

IDA: Inferred from Direct Assay

C

From MGI

GO:0045202

synapse

MGI:MGI:3701026
PMID:16710293[65]

IDA: Inferred from Direct Assay

C

From MGI

GO:0045211

postsynaptic membrane

MGI:MGI:2155573
PMID:11754836[66]

IDA: Inferred from Direct Assay

C

From MGI

GO:0045211

postsynaptic membrane

MGI:MGI:2669049
PMID:12890763[67]

IDA: Inferred from Direct Assay

C

From MGI

GO:0045211

postsynaptic membrane

MGI:MGI:3054180
PMID:15317856[53]

IDA: Inferred from Direct Assay

C

From MGI

GO:0045471

response to ethanol

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

P

From MGI

GO:0045944

positive regulation of transcription from RNA polymerase II promoter

MGI:MGI:65181
PMID:7907365[68]

IDA: Inferred from Direct Assay

P

From MGI

GO:0048167

regulation of synaptic plasticity

MGI:MGI:3036924
PMID:15003177[43]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2177650

P

From MGI

GO:0048167

regulation of synaptic plasticity

MGI:MGI:84849
PMID:8980239[69]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0048167

regulation of synaptic plasticity

MGI:MGI:84850
PMID:8980238[48]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2177650

P

From MGI

GO:0048167

regulation of synaptic plasticity

MGI:MGI:893741
PMID:9246451[50]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279

P

From MGI

GO:0048168

regulation of neuronal synaptic plasticity

MGI:MGI:3622400
PMID:15576450[37]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2178083
MGI:MGI:2181422

P

From MGI

GO:0048169

regulation of long-term neuronal synaptic plasticity

MGI:MGI:1858680
PMID:10818139[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928283
MGI:MGI:1928284

P

From MGI

GO:0048169

regulation of long-term neuronal synaptic plasticity

MGI:MGI:3691363
PMID:17015831[39]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3692441

P

From MGI

GO:0048169

regulation of long-term neuronal synaptic plasticity

MGI:MGI:3703316
PMID:17313573[13]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3611337
MGI:MGI:2448952

P

From MGI

GO:0048511

rhythmic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

P

From MGI

GO:0048814

regulation of dendrite morphogenesis

MGI:MGI:3579211
PMID:15745956[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0050770

regulation of axonogenesis

MGI:MGI:3579211
PMID:15745956[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0050905

neuromuscular process

MGI:MGI:65431
PMID:8313466[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928270

P

From MGI

GO:0051963

regulation of synapse assembly

MGI:MGI:2654367
PMID:12657691[56]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2655237
MGI:MGI:2655232

P

From MGI

GO:0055074

calcium ion homeostasis

MGI:MGI:65181
PMID:7907365[68]

IDA: Inferred from Direct Assay

P

From MGI

GO:0060076

excitatory synapse

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

C

From MGI

GO:0060079

regulation of excitatory postsynaptic membrane potential

MGI:MGI:2682163
PMID:14645471[24]

IGI: Inferred from Genetic Interaction

MGI:MGI:95821

P

From MGI

GO:0060079

regulation of excitatory postsynaptic membrane potential

MGI:MGI:3036924
PMID:15003177[43]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928279
MGI:MGI:2177650

P

From MGI

GO:0060134

prepulse inhibition

MGI:MGI:3051067
PMID:15265649[70]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928280

P

From MGI

GO:0060179

male mating behavior

MGI:MGI:1343743
PMID:10481908[45]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1928280

P

From MGI

GO:0070588

calcium ion transmembrane transport

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q05586

P

From MGI

GO:2000463

positive regulation of excitatory postsynaptic membrane potential

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

UniProtKB:P35439

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. ↑ Cui Z et al. (2005) Requirement of NMDA receptor reactivation for consolidation and storage of nondeclarative taste memory revealed by inducible NR1 knockout. Eur J Neurosci 22: 755-63 PubMed GONUTS page
  2. ↑ 2.0 2.1 2.2 2.3 Kew JN et al. (2000) Functional consequences of reduction in NMDA receptor glycine affinity in mice carrying targeted point mutations in the glycine binding site. J Neurosci 20: 4037-49 PubMed GONUTS page
  3. ↑ 3.0 3.1 Poon CS et al. (2000) NMDA receptor activity in utero averts respiratory depression and anomalous long-term depression in newborn mice. J Neurosci 20: RC73 PubMed GONUTS page
  4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 Li Y et al. (1994) Whisker-related neuronal patterns fail to develop in the trigeminal brainstem nuclei of NMDAR1 knockout mice. Cell 76: 427-37 PubMed GONUTS page
  5. ↑ 5.0 5.1 Tokita Y et al. (1996) Characterization of excitatory amino acid neurotoxicity in N-methyl-D-aspartate receptor-deficient mouse cortical neuronal cells. Eur J Neurosci 8: 69-78 PubMed GONUTS page
  6. ↑ Moy SS et al. (2006) Amphetamine-induced disruption of prepulse inhibition in mice with reduced NMDA receptor function. Brain Res 1089: 186-94 PubMed GONUTS page
  7. ↑ Miyamoto S et al. (2004) Amphetamine-induced Fos is reduced in limbic cortical regions but not in the caudate or accumbens in a genetic model of NMDA receptor hypofunction. Neuropsychopharmacology 29: 2180-8 PubMed GONUTS page
  8. ↑ 8.0 8.1 8.2 8.3 Iwasato T et al. (2000) Cortex-restricted disruption of NMDAR1 impairs neuronal patterns in the barrel cortex. Nature 406: 726-31 PubMed GONUTS page
  9. ↑ 9.0 9.1 9.2 9.3 Forrest D et al. (1994) Targeted disruption of NMDA receptor 1 gene abolishes NMDA response and results in neonatal death. Neuron 13: 325-38 PubMed GONUTS page
  10. ↑ 10.0 10.1 10.2 10.3 Nakazawa K et al. (2002) Requirement for hippocampal CA3 NMDA receptors in associative memory recall. Science 297: 211-8 PubMed GONUTS page
  11. ↑ 11.0 11.1 11.2 11.3 South SM et al. (2003) A conditional deletion of the NR1 subunit of the NMDA receptor in adult spinal cord dorsal horn reduces NMDA currents and injury-induced pain. J Neurosci 23: 5031-40 PubMed GONUTS page
  12. ↑ 12.0 12.1 12.2 12.3 Lee LJ et al. (2005) NMDA receptor-dependent regulation of axonal and dendritic branching. J Neurosci 25: 2304-11 PubMed GONUTS page
  13. ↑ 13.0 13.1 13.2 13.3 13.4 Niewoehner B et al. (2007) Impaired spatial working memory but spared spatial reference memory following functional loss of NMDA receptors in the dentate gyrus. Eur J Neurosci 25: 837-46 PubMed GONUTS page
  14. ↑ 14.0 14.1 14.2 14.3 Kutsuwada T et al. (1992) Molecular diversity of the NMDA receptor channel. Nature 358: 36-41 PubMed GONUTS page
  15. ↑ 15.0 15.1 15.2 15.3 15.4 Yamazaki M et al. (1992) Cloning, expression and modulation of a mouse NMDA receptor subunit. FEBS Lett 300: 39-45 PubMed GONUTS page
  16. ↑ Ikeda K et al. (1992) Cloning and expression of the epsilon 4 subunit of the NMDA receptor channel. FEBS Lett 313: 34-8 PubMed GONUTS page
  17. ↑ 17.0 17.1 17.2 17.3 Meguro H et al. (1992) Functional characterization of a heteromeric NMDA receptor channel expressed from cloned cDNAs. Nature 357: 70-4 PubMed GONUTS page
  18. ↑ Chazot PL et al. (1994) Molecular characterization of N-methyl-D-aspartate receptors expressed in mammalian cells yields evidence for the coexistence of three subunit types within a discrete receptor molecule. J Biol Chem 269: 24403-9 PubMed GONUTS page
  19. ↑ 19.0 19.1 19.2 Tsuzuki K et al. (1994) Ion permeation properties of the cloned mouse epsilon 2/zeta 1 NMDA receptor channel. Brain Res Mol Brain Res 26: 37-46 PubMed GONUTS page
  20. ↑ 20.0 20.1 Grunwald IC et al. (2001) Kinase-independent requirement of EphB2 receptors in hippocampal synaptic plasticity. Neuron 32: 1027-40 PubMed GONUTS page
  21. ↑ 21.0 21.1 21.2 21.3 Amparan D et al. (2005) Direct interaction of myosin regulatory light chain with the NMDA receptor. J Neurochem 92: 349-61 PubMed GONUTS page
  22. ↑ Sprengel R et al. (1998) Importance of the intracellular domain of NR2 subunits for NMDA receptor function in vivo. Cell 92: 279-89 PubMed GONUTS page
  23. ↑ Husi H et al. (2000) Proteomic analysis of NMDA receptor-adhesion protein signaling complexes. Nat Neurosci 3: 661-9 PubMed GONUTS page
  24. ↑ 24.0 24.1 24.2 Köhr G et al. (2003) Intracellular domains of NMDA receptor subtypes are determinants for long-term potentiation induction. J Neurosci 23: 10791-9 PubMed GONUTS page
  25. ↑ Son GH et al. (2006) Maternal stress produces learning deficits associated with impairment of NMDA receptor-mediated synaptic plasticity. J Neurosci 26: 3309-18 PubMed GONUTS page
  26. ↑ Offenhäuser N et al. (2006) Increased ethanol resistance and consumption in Eps8 knockout mice correlates with altered actin dynamics. Cell 127: 213-26 PubMed GONUTS page
  27. ↑ Hoe HS et al. (2006) Apolipoprotein E receptor 2 interactions with the N-methyl-D-aspartate receptor. J Biol Chem 281: 3425-31 PubMed GONUTS page
  28. ↑ Bajaj G et al. (2009) N-methyl-D-aspartate receptor subunits are non-myosin targets of myosin regulatory light chain. J Biol Chem 284: 1252-66 PubMed GONUTS page
  29. ↑ Fernández E et al. (2009) Targeted tandem affinity purification of PSD-95 recovers core postsynaptic complexes and schizophrenia susceptibility proteins. Mol Syst Biol 5: 269 PubMed GONUTS page
  30. ↑ Collins MO et al. (2006) Molecular characterization and comparison of the components and multiprotein complexes in the postsynaptic proteome. J Neurochem 97 Suppl 1: 16-23 PubMed GONUTS page
  31. ↑ Didier M et al. (1995) Differential expression and co-assembly of NMDA zeta 1 and epsilon subunits in the mouse cerebellum during postnatal development. Neuroreport 6: 2255-9 PubMed GONUTS page
  32. ↑ 32.0 32.1 32.2 Chazot PL & Stephenson FA (1997) Biochemical evidence for the existence of a pool of unassembled C2 exon-containing NR1 subunits of the mammalian forebrain NMDA receptor. J Neurochem 68: 507-16 PubMed GONUTS page
  33. ↑ 33.0 33.1 33.2 Setou M et al. (2000) Kinesin superfamily motor protein KIF17 and mLin-10 in NMDA receptor-containing vesicle transport. Science 288: 1796-802 PubMed GONUTS page
  34. ↑ Lai C et al. (2006) Amyotrophic lateral sclerosis 2-deficiency leads to neuronal degeneration in amyotrophic lateral sclerosis through altered AMPA receptor trafficking. J Neurosci 26: 11798-806 PubMed GONUTS page
  35. ↑ Snell LD et al. (1996) Regional and subunit specific changes in NMDA receptor mRNA and immunoreactivity in mouse brain following chronic ethanol ingestion. Brain Res Mol Brain Res 40: 71-8 PubMed GONUTS page
  36. ↑ Puyal J et al. (2002) Distribution of alpha-amino-3-hydroxy-5-methyl-4 isoazolepropionic acid and N-methyl-D-aspartate receptor subunits in the vestibular and spiral ganglia of the mouse during early development. Brain Res Dev Brain Res 139: 51-7 PubMed GONUTS page
  37. ↑ 37.0 37.1 37.2 Pawlak V et al. (2005) Impaired synaptic scaling in mouse hippocampal neurones expressing NMDA receptors with reduced calcium permeability. J Physiol 562: 771-83 PubMed GONUTS page
  38. ↑ Cravens CJ et al. (2006) CA3 NMDA receptors are crucial for rapid and automatic representation of context memory. Eur J Neurosci 24: 1771-80 PubMed GONUTS page
  39. ↑ 39.0 39.1 Dang MT et al. (2006) Disrupted motor learning and long-term synaptic plasticity in mice lacking NMDAR1 in the striatum. Proc Natl Acad Sci U S A 103: 15254-9 PubMed GONUTS page
  40. ↑ 40.0 40.1 Rampon C et al. (2000) Enrichment induces structural changes and recovery from nonspatial memory deficits in CA1 NMDAR1-knockout mice. Nat Neurosci 3: 238-44 PubMed GONUTS page
  41. ↑ Huerta PT et al. (2000) Formation of temporal memory requires NMDA receptors within CA1 pyramidal neurons. Neuron 25: 473-80 PubMed GONUTS page
  42. ↑ McHugh TJ et al. (2007) Dentate gyrus NMDA receptors mediate rapid pattern separation in the hippocampal network. Science 317: 94-9 PubMed GONUTS page
  43. ↑ 43.0 43.1 43.2 Cui Z et al. (2004) Inducible and reversible NR1 knockout reveals crucial role of the NMDA receptor in preserving remote memories in the brain. Neuron 41: 781-93 PubMed GONUTS page
  44. ↑ Nakazawa K et al. (2003) Hippocampal CA3 NMDA receptors are crucial for memory acquisition of one-time experience. Neuron 38: 305-15 PubMed GONUTS page
  45. ↑ 45.0 45.1 45.2 Mohn AR et al. (1999) Mice with reduced NMDA receptor expression display behaviors related to schizophrenia. Cell 98: 427-36 PubMed GONUTS page
  46. ↑ Rondi-Reig L et al. (2001) CA1-specific N-methyl-D-aspartate receptor knockout mice are deficient in solving a nonspatial transverse patterning task. Proc Natl Acad Sci U S A 98: 3543-8 PubMed GONUTS page
  47. ↑ Rondi-Reig L et al. (2006) Impaired sequential egocentric and allocentric memories in forebrain-specific-NMDA receptor knock-out mice during a new task dissociating strategies of navigation. J Neurosci 26: 4071-81 PubMed GONUTS page
  48. ↑ 48.0 48.1 Tsien JZ et al. (1996) The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory. Cell 87: 1327-38 PubMed GONUTS page
  49. ↑ Silva AJ et al. (1997) A mouse model for the learning and memory deficits associated with neurofibromatosis type I. Nat Genet 15: 281-4 PubMed GONUTS page
  50. ↑ 50.0 50.1 Tonegawa S et al. (1996) Hippocampal CA1-region-restricted knockout of NMDAR1 gene disrupts synaptic plasticity, place fields, and spatial learning. Cold Spring Harb Symp Quant Biol 61: 225-38 PubMed GONUTS page
  51. ↑ Qiu S & Weeber EJ (2007) Reelin signaling facilitates maturation of CA1 glutamatergic synapses. J Neurophysiol 97: 2312-21 PubMed GONUTS page
  52. ↑ Arumugam H et al. (2005) NMDA receptors regulate developmental gap junction uncoupling via CREB signaling. Nat Neurosci 8: 1720-6 PubMed GONUTS page
  53. ↑ 53.0 53.1 Abe M et al. (2004) NMDA receptor GluRepsilon/NR2 subunits are essential for postsynaptic localization and protein stability of GluRzeta1/NR1 subunit. J Neurosci 24: 7292-304 PubMed GONUTS page
  54. ↑ Trinidad JC et al. (2005) Phosphorylation state of postsynaptic density proteins. J Neurochem 92: 1306-16 PubMed GONUTS page
  55. ↑ Kiefer F et al. (2003) Involvement of NMDA receptors in alcohol-mediated behavior: mice with reduced affinity of the NMDA R1 glycine binding site display an attenuated sensitivity to ethanol. Biol Psychiatry 53: 345-51 PubMed GONUTS page
  56. ↑ 56.0 56.1 56.2 Rudhard Y et al. (2003) Absence of Whisker-related pattern formation in mice with NMDA receptors lacking coincidence detection properties and calcium signaling. J Neurosci 23: 2323-32 PubMed GONUTS page
  57. ↑ Chen LT et al. (1999) A candidate target for G protein action in brain. J Biol Chem 274: 26931-8 PubMed GONUTS page
  58. ↑ 58.0 58.1 Snyder EM et al. (2005) Regulation of NMDA receptor trafficking by amyloid-beta. Nat Neurosci 8: 1051-8 PubMed GONUTS page
  59. ↑ Taniura H et al. (2007) Tex261 modulates the excitotoxic cell death induced by N-methyl-D-aspartate (NMDA) receptor activation. Biochem Biophys Res Commun 362: 1096-100 PubMed GONUTS page
  60. ↑ Quintero GC et al. (2008) Evaluation of morphine analgesia and motor coordination in mice following cortex-specific knockout of the N-methyl-D-aspartate NR1-subunit. Neurosci Lett 437: 55-8 PubMed GONUTS page
  61. ↑ Jensen P et al. (1999) Rescue of cerebellar granule cells from death in weaver NR1 double mutants. J Neurosci 19: 7991-8 PubMed GONUTS page
  62. ↑ Tashiro A et al. (2006) NMDA-receptor-mediated, cell-specific integration of new neurons in adult dentate gyrus. Nature 442: 929-33 PubMed GONUTS page
  63. ↑ 63.0 63.1 de Rivero Vaccari JC et al. (2006) NMDA receptors promote survival in somatosensory relay nuclei by inhibiting Bax-dependent developmental cell death. Proc Natl Acad Sci U S A 103: 16971-6 PubMed GONUTS page
  64. ↑ Chih B et al. (2005) Control of excitatory and inhibitory synapse formation by neuroligins. Science 307: 1324-8 PubMed GONUTS page
  65. ↑ Nakazawa T et al. (2006) NR2B tyrosine phosphorylation modulates fear learning as well as amygdaloid synaptic plasticity. EMBO J 25: 2867-77 PubMed GONUTS page
  66. ↑ Henderson JT et al. (2001) The receptor tyrosine kinase EphB2 regulates NMDA-dependent synaptic function. Neuron 32: 1041-56 PubMed GONUTS page
  67. ↑ Tao YX et al. (2003) Impaired NMDA receptor-mediated postsynaptic function and blunted NMDA receptor-dependent persistent pain in mice lacking postsynaptic density-93 protein. J Neurosci 23: 6703-12 PubMed GONUTS page
  68. ↑ 68.0 68.1 Bulleit RF et al. (1994) NMDA receptor activation in differentiating cerebellar cell cultures regulates the expression of a new POU gene, Cns-1. J Neurosci 14: 1584-95 PubMed GONUTS page
  69. ↑ McHugh TJ et al. (1996) Impaired hippocampal representation of space in CA1-specific NMDAR1 knockout mice. Cell 87: 1339-49 PubMed GONUTS page
  70. ↑ Duncan GE et al. (2004) Deficits in sensorimotor gating and tests of social behavior in a genetic model of reduced NMDA receptor function. Behav Brain Res 153: 507-19 PubMed GONUTS page
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