GRIN2B c.*409T>C

Variant ID: 12-13715308-A-G

NM_000834.3(GRIN2B):c.*409T>C

This variant was identified in 31 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs890
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
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Effects of psychosis-associated genetic markers on brain volumetry: a systematic review of replicated findings and an independent validation.

Psychological Medicine
Vouga Ribeiro, Nuno N; Tavares, Vânia V; Bramon, Elvira E; Toulopoulou, Timothea T; Valli, Isabel I; Shergill, Sukhi S; Murray, Robin R; Prata, Diana D
Publication Date: 2022-09-28

Variant appearance in text: rs890
PubMed Link: 36168994
Variant Present in the following documents:
View BVdb publication page



Genetic variables of the glutamatergic system associated with treatment-resistant depression: A review of the literature.

World Journal Of Psychiatry
Saez, Estela E; Erkoreka, Leire L; Moreno-Calle, Teresa T; Berjano, Belen B; Gonzalez-Pinto, Ana A; Basterreche, Nieves N; Arrue, Aurora A
Publication Date: 2022-07-19

Variant appearance in text: rs890
PubMed Link: 36051601
Variant Present in the following documents:
  • WJP-12-884.pdf
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Genes of the Glutamatergic System and Tardive Dyskinesia in Patients with Schizophrenia.

Diagnostics (Basel, Switzerland)
Fedorenko, Olga Yu OY; Paderina, Diana Z DZ; Kornetova, Elena G EG; Poltavskaya, Evgeniya G EG; Pozhidaev, Ivan V IV; Goncharova, Anastasiia A AA; Freidin, Maxim B MB; Bocharova, Anna V AV; Bokhan, Nikolay A NA; Loonen, Anton J M AJM; Ivanova, Svetlana A SA
Publication Date: 2022-06-22

Variant appearance in text: rs890
PubMed Link: 35885427
Variant Present in the following documents:
  • Main text
  • diagnostics-12-01521.pdf
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Evidence for the Association between the Intronic Haplotypes of Ionotropic Glutamate Receptors and First-Episode Schizophrenia.

Journal Of Personalized Medicine
Hirschfeldova, Katerina K; Cerny, Jiri J; Bozikova, Paulina P; Kuchtiak, Viktor V; Rausch, Tobias T; Benes, Vladimir V; Spaniel, Filip F; Gregus, David D; Horacek, Jiri J; Vyklicky, Ladislav L; Balik, Ales A
Publication Date: 2021-11-25

Variant appearance in text: rs890
PubMed Link: 34945722
Variant Present in the following documents:
  • Main text
  • jpm-11-01250.pdf
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Evidence for the Association between the Intronic Haplotypes of Ionotropic Glutamate Receptors and First-Episode Schizophrenia.

Journal Of Personalized Medicine
Hirschfeldova, Katerina K; Cerny, Jiri J; Bozikova, Paulina P; Kuchtiak, Viktor V; Rausch, Tobias T; Benes, Vladimir V; Spaniel, Filip F; Gregus, David D; Horacek, Jiri J; Vyklicky, Ladislav L; Balik, Ales A
Publication Date: 2021-11-25

Variant appearance in text: rs890
PubMed Link: 34945722
Variant Present in the following documents:
  • Main text
  • jpm-11-01250.pdf
View BVdb publication page



Genetic variation of rs12918566 affects GRIN2A expression and is associated with spontaneous movement response during sevoflurane anesthesia induction.

Brain And Behavior
Chen, Ming-Hua MH; Fang, Chao C; Wu, Na-Yiyuan NY; Xia, Yu-Hao YH; Zeng, You-Jie YJ; Ouyang, Wen W
Publication Date: 2021-08

Variant appearance in text: rs890
PubMed Link: 34291608
Variant Present in the following documents:
  • Main text
  • BRB3-11-e02165.pdf
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Pharmacogenetics of Antipsychotic Drug Treatment: Update and Clinical Implications.

Molecular Neuropsychiatry
Yoshida, Kazunari K; Müller, Daniel J DJ
Publication Date: 2020-04

Variant appearance in text: rs890
PubMed Link: 32399466
Variant Present in the following documents:
  • Main text
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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs890
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Biological Predictors of Clozapine Response: A Systematic Review.

Frontiers In Psychiatry
Samanaite, Ruta R; Gillespie, Amy A; Sendt, Kyra-Verena KV; McQueen, Grant G; MacCabe, James H JH; Egerton, Alice A
Publication Date: 2018

Variant appearance in text: rs890
PubMed Link: 30093869
Variant Present in the following documents:
  • fpsyt-09-00327.pdf
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Dysregulation of miRNA and its potential therapeutic application in schizophrenia.

Cns Neuroscience & Therapeutics
Cao, Ting T; Zhen, Xue-Chu XC
Publication Date: 2018-07

Variant appearance in text: rs890
PubMed Link: 29529357
Variant Present in the following documents:
  • Main text
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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs890
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
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Genetic Studies on the Tripartite Glutamate Synapse in the Pathophysiology and Therapeutics of Mood Disorders.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology
de Sousa, Rafael T RT; Loch, Alexandre A AA; Carvalho, André F AF; Brunoni, André R AR; Haddad, Marie Reine MR; Henter, Ioline D ID; Zarate, Carlos A CA; Machado-Vieira, Rodrigo R
Publication Date: 2017-03

Variant appearance in text: rs890
PubMed Link: 27510426
Variant Present in the following documents:
  • Main text
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Genetic variation within GRIN2B in adolescents with alcohol use disorder may be associated with larger left posterior cingulate cortex volume.

Acta Neuropsychiatrica
Dalvie, Shareefa S; Brooks, Samantha J SJ; Cardenas, Valerie V; Fein, George G; Ramesar, Raj R; Stein, Dan J DJ
Publication Date: 2017-08

Variant appearance in text: rs890
PubMed Link: 27498914
Variant Present in the following documents:
  • Main text
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Targets of polyamine dysregulation in major depression and suicide: Activity-dependent feedback, excitability, and neurotransmission.

Neuroscience And Biobehavioral Reviews
Limon, Agenor A; Mamdani, Firoza F; Hjelm, Brooke E BE; Vawter, Marquis P MP; Sequeira, Adolfo A
Publication Date: 2016-07

Variant appearance in text: rs890
PubMed Link: 27108532
Variant Present in the following documents:
  • Main text
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Genetic Effects on Longitudinal Changes from Healthy to Adverse Weight and Metabolic Status – The HUNT Study.

Plos One
Kvaløy, Kirsti K; Holmen, Jostein J; Hveem, Kristian K; Holmen, Turid Lingaas TL
Publication Date: 2015

Variant appearance in text: rs890
PubMed Link: 26445370
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease.

Journal Of Huntington'S Disease
Correia, Kevin K; Harold, Denise D; Kim, Kyung-Hee KH; Holmans, Peter P; Jones, Lesley L; Orth, Michael M; Myers, Richard H RH; Kwak, Seung S; Wheeler, Vanessa C VC; MacDonald, Marcy E ME; Gusella, James F JF; Lee, Jong-Min JM
Publication Date: 2015

Variant appearance in text: rs890
PubMed Link: 26444025
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms in MicroRNA Genes And Genes Involving in NMDAR Signaling and Schizophrenia: A Case-Control Study in Chinese Han Population.

Scientific Reports
Zhang, Yanxia Y; Fan, Mei M; Wang, Qingzhong Q; He, Guang G; Fu, Yingmei Y; Li, Huafang H; Yu, Shunying S
Publication Date: 2015-08-10

Variant appearance in text: rs890
PubMed Link: 26257337
Variant Present in the following documents:
  • Main text
View BVdb publication page



Exploring Genetic Factors Involved in Huntington Disease Age of Onset: E2F2 as a New Potential Modifier Gene.

Plos One
Valcárcel-Ocete, Leire L; Alkorta-Aranburu, Gorka G; Iriondo, Mikel M; Fullaondo, Asier A; García-Barcina, María M; Fernández-García, José Manuel JM; Lezcano-García, Elena E; Losada-Domingo, José María JM; Ruiz-Ojeda, Javier J; Álvarez de Arcaya, Amaia A; Pérez-Ramos, José María JM; Roos, Raymund A C RA; Nielsen, Jørgen E JE; Saft, Carsten C; , ; Zubiaga, Ana M AM; Aguirre, Ana A
Publication Date: 2015

Variant appearance in text: rs890
PubMed Link: 26148071
Variant Present in the following documents:
  • Main text
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Association Study of N-Methyl-D-Aspartate Receptor Subunit 2B (GRIN2B) Polymorphisms and Schizophrenia Symptoms in the Han Chinese Population.

Plos One
Yang, Yongfeng Y; Li, Wenqiang W; Zhang, Hongxing H; Yang, Ge G; Wang, Xiujuan X; Ding, Minli M; Jiang, Tianzi T; Lv, Luxian L
Publication Date: 2015

Variant appearance in text: rs890
PubMed Link: 26020650
Variant Present in the following documents:
  • Main text
  • pone.0125925.pdf
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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs890
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Modulation at age of onset in tunisian huntington disease patients: implication of new modifier genes.

Genetics Research International
Hmida-Ben Brahim, Dorra D; Chourabi, Marwa M; Ben Amor, Sana S; Harrabi, Imed I; Trabelsi, Saoussen S; Haddaji-Mastouri, Marwa M; Gribaa, Moez M; Sassi, Sihem S; Gahbiche, Fatma Ezzahra FE; Lamouchi, Turkia T; Mougou-Zereli, Soumaya S; Ben Ammou, Sofiane S; Saad, Ali A
Publication Date: 2014

Variant appearance in text: rs890
PubMed Link: 25254119
Variant Present in the following documents:
  • Main text
  • GRI2014-210418.pdf
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Molecular actions and clinical pharmacogenetics of lithium therapy.

Pharmacology, Biochemistry, And Behavior
Can, Adem A; Schulze, Thomas G TG; Gould, Todd D TD
Publication Date: 2014-08

Variant appearance in text: rs890
PubMed Link: 24534415
Variant Present in the following documents:
  • Main text
View BVdb publication page



GRIN2B gene and associated brain cortical white matter changes in bipolar disorder: a preliminary combined platform investigation.

Biomed Research International
Kuswanto, Carissa Nadia CN; Sum, Min Yi MY; Thng, Christopher Ren Zhi CR; Zhang, Yi Bin YB; Yang, Guo Liang GL; Nowinski, Wieslaw Lucjan WL; Sitoh, Yih Yian YY; Low, Chian Ming CM; Sim, Kang K
Publication Date: 2013

Variant appearance in text: rs890
PubMed Link: 24490167
Variant Present in the following documents:
  • Main text
  • BMRI2013-635131.pdf
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An integrated genetic linkage map for white clover (Trifolium repens L.) with alignment to Medicago.

Bmc Genomics
Griffiths, Andrew G AG; Barrett, Brent A BA; Simon, Deborah D; Khan, Anar K AK; Bickerstaff, Paul P; Anderson, Craig B CB; Franzmayr, Benjamin K BK; Hancock, Kerry R KR; Jones, Chris S CS
Publication Date: 2013-06-10

Variant appearance in text: rs890
PubMed Link: 23758831
Variant Present in the following documents:
  • 1471-2164-14-388.pdf
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Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.

Neurogenetics
Ramos, Eliana Marisa EM; Latourelle, Jeanne C JC; Gillis, Tammy T; Mysore, Jayalakshmi S JS; Squitieri, Ferdinando F; Di Pardo, Alba A; Di Donato, Stefano S; Gellera, Cinzia C; Hayden, Michael R MR; Morrison, Patrick J PJ; Nance, Martha M; Ross, Christopher A CA; Margolis, Russell L RL; Gomez-Tortosa, Estrella E; Ayuso, Carmen C; Suchowersky, Oksana O; Trent, Ronald J RJ; McCusker, Elizabeth E; Novelletto, Andrea A; Frontali, Marina M; Jones, Randi R; Ashizawa, Tetsuo T; Frank, Samuel S; Saint-Hilaire, Marie-Helene MH; Hersch, Steven M SM; Rosas, Herminia D HD; Lucente, Diane D; Harrison, Madaline B MB; Zanko, Andrea A; Abramson, Ruth K RK; Marder, Karen K; Gusella, James F JF; Lee, Jong-Min JM; Alonso, Isabel I; Sequeiros, Jorge J; Myers, Richard H RH; Macdonald, Marcy E ME
Publication Date: 2013-11

Variant appearance in text: rs890
PubMed Link: 23644918
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of 94 candidate genes and 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia.

The American Journal Of Psychiatry
Greenwood, Tiffany A TA; Lazzeroni, Laura C LC; Murray, Sarah S SS; Cadenhead, Kristin S KS; Calkins, Monica E ME; Dobie, Dorcas J DJ; Green, Michael F MF; Gur, Raquel E RE; Gur, Ruben C RC; Hardiman, Gary G; Kelsoe, John R JR; Leonard, Sherry S; Light, Gregory A GA; Nuechterlein, Keith H KH; Olincy, Ann A; Radant, Allen D AD; Schork, Nicholas J NJ; Seidman, Larry J LJ; Siever, Larry J LJ; Silverman, Jeremy M JM; Stone, William S WS; Swerdlow, Neal R NR; Tsuang, Debby W DW; Tsuang, Ming T MT; Turetsky, Bruce I BI; Freedman, Robert R; Braff, David L DL
Publication Date: 2011-09

Variant appearance in text: rs890
PubMed Link: 21498463
Variant Present in the following documents:
  • Main text
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Glutamate system genes associated with ventral prefrontal and thalamic volume in pediatric obsessive-compulsive disorder.

Brain Imaging And Behavior
Arnold, Paul Daniel PD; Macmaster, Frank P FP; Hanna, Gregory L GL; Richter, Margaret A MA; Sicard, Tricia T; Burroughs, Eliza E; Mirza, Yousha Y; Easter, Phillip C PC; Rose, Michelle M; Kennedy, James L JL; Rosenberg, David R DR
Publication Date: 2009-03-01

Variant appearance in text: rs890
PubMed Link: 21031159
Variant Present in the following documents:
  • Main text
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Incorporating age at onset of smoking into genetic models for nicotine dependence: evidence for interaction with multiple genes.

Addiction Biology
Grucza, Richard A RA; Johnson, Eric O EO; Krueger, Robert F RF; Breslau, Naomi N; Saccone, Nancy L NL; Chen, Li-Shiun LS; Derringer, Jaime J; Agrawal, Arpana A; Lynskey, Michael M; Bierut, Laura J LJ
Publication Date: 2010-07

Variant appearance in text: rs890
PubMed Link: 20624154
Variant Present in the following documents:
  • Main text
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Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.

Neuroimage
Stein, Jason L JL; Hua, Xue X; Morra, Jonathan H JH; Lee, Suh S; Hibar, Derrek P DP; Ho, April J AJ; Leow, Alex D AD; Toga, Arthur W AW; Sul, Jae Hoon JH; Kang, Hyun Min HM; Eskin, Eleazar E; Saykin, Andrew J AJ; Shen, Li L; Foroud, Tatiana T; Pankratz, Nathan N; Huentelman, Matthew J MJ; Craig, David W DW; Gerber, Jill D JD; Allen, April N AN; Corneveaux, Jason J JJ; Stephan, Dietrich A DA; Webster, Jennifer J; DeChairo, Bryan M BM; Potkin, Steven G SG; Jack, Clifford R CR; Weiner, Michael W MW; Thompson, Paul M PM; ,
Publication Date: 2010-06

Variant appearance in text: rs890
PubMed Link: 20197096
Variant Present in the following documents:
  • Main text
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Glutamate receptor gene (GRIN2B) associated with reduced anterior cingulate glutamatergic concentration in pediatric obsessive-compulsive disorder.

Psychiatry Research
Arnold, Paul Daniel PD; Macmaster, Frank P FP; Richter, Margaret A MA; Hanna, Gregory L GL; Sicard, Tricia T; Burroughs, Eliza E; Mirza, Yousha Y; Easter, Phillip C PC; Rose, Michelle M; Kennedy, James L JL; Rosenberg, David R DR
Publication Date: 2009-05-15

Variant appearance in text: rs890
PubMed Link: 19324536
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder.

Genes, Brain, And Behavior
Dorval, K M KM; Wigg, K G KG; Crosbie, J J; Tannock, R R; Kennedy, J L JL; Ickowicz, A A; Pathare, T T; Malone, M M; Schachar, R R; Barr, C L CL
Publication Date: 2007-07

Variant appearance in text: rs890
PubMed Link: 17010153
Variant Present in the following documents:
  • Main text
View BVdb publication page