SLC6A4 c.838-155G>A

Variant ID: 17-28543389-C-T

NM_001045.5(SLC6A4):c.838-155G>A

This variant was identified in 32 publications

View GRCh38 version.




Publications:


Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits.

Psychiatric Genetics
Castellini, Giovanni G; Merola, Giuseppe Pierpaolo GP; Baccaredda, Ottone Boy OB; Pecoraro, Vincenzo V; Bozza, Bernardo B; Cassioli, Emanuele E; Rossi, Eleonora E; Bessi, Valentina V; Sorbi, Sandro S; Nacmias, Benedetta B; Ricca, Valdo V
Publication Date: 2022-12-20

Variant appearance in text: rs140700
PubMed Link: 36729042
Variant Present in the following documents:
  • Main text
  • pg-33-79.pdf
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Interplay between Serotonin, Immune Response, and Intestinal Dysbiosis in Inflammatory Bowel Disease.

International Journal Of Molecular Sciences
González Delgado, Samantha S; Garza-Veloz, Idalia I; Trejo-Vazquez, Fabiola F; Martinez-Fierro, Margarita L ML
Publication Date: 2022-12-09

Variant appearance in text: rs140700
PubMed Link: 36555276
Variant Present in the following documents:
  • Main text
  • ijms-23-15632.pdf
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Major Depressive Disorder: Existing Hypotheses about Pathophysiological Mechanisms and New Genetic Findings.

Genes
Kamran, Muhammad M; Bibi, Farhana F; Ur Rehman, Asim A; Morris, Derek W DW
Publication Date: 2022-04-06

Variant appearance in text: rs140700
PubMed Link: 35456452
Variant Present in the following documents:
  • Main text
  • genes-13-00646.pdf
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Genetic Variation and Hot Flashes: A Systematic Review.

The Journal Of Clinical Endocrinology And Metabolism
Crandall, Carolyn J CJ; Diamant, Allison L AL; Maglione, Margaret M; Thurston, Rebecca C RC; Sinsheimer, Janet J
Publication Date: 2020-12-01

Variant appearance in text: rs140700
PubMed Link: 32797194
Variant Present in the following documents:
  • Main text
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Association Between FoxO1, A2M, and TGF-β1, Environmental Factors, and Major Depressive Disorder.

Frontiers In Psychiatry
Zhao, Mingzhe M; Chen, Lu L; Qiao, Zhengxue Z; Zhou, Jiawei J; Zhang, Tianyu T; Zhang, Wenxin W; Ke, Siyuan S; Zhao, Xiaoyun X; Qiu, Xiaohui X; Song, Xuejia X; Zhao, Erying E; Pan, Hui H; Yang, Yanjie Y; Yang, Xiuxian X
Publication Date: 2020

Variant appearance in text: rs140700
PubMed Link: 32792993
Variant Present in the following documents:
  • Main text
  • fpsyt-11-00675.pdf
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Association between the SLC6A4 gene and schizophrenia: an updated meta-analysis.

Neuropsychiatric Disease And Treatment
Xu, Feng-Ling FL; Wang, Bao-Jie BJ; Yao, Jun J
Publication Date: 2019

Variant appearance in text: rs140700
PubMed Link: 30643413
Variant Present in the following documents:
  • Main text
  • ndt-15-143.pdf
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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs140700
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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Genotype-dependent associations between serotonin transporter gene (SLC6A4) DNA methylation and late-life depression.

Bmc Psychiatry
Lam, Dilys D; Ancelin, Marie-Laure ML; Ritchie, Karen K; Freak-Poli, Rosanne R; Saffery, Richard R; Ryan, Joanne J
Publication Date: 2018-09-04

Variant appearance in text: rs140700
PubMed Link: 30180828
Variant Present in the following documents:
  • Main text
  • 12888_2018_Article_1850.pdf
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Genetic profile and patient-reported outcomes in chronic obstructive pulmonary disease: A systematic review.

Plos One
Melro, Hélder H; Gomes, Jorge J; Moura, Gabriela G; Marques, Alda A
Publication Date: 2018

Variant appearance in text: rs140700
PubMed Link: 29927965
Variant Present in the following documents:
  • Main text
  • pone.0198920.pdf
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Relationship of Genetic Variants With Procedural Pain, Anxiety, and Distress in Children.

Biological Research For Nursing
Ersig, Anne L AL; Schutte, Debra L DL; Standley, Jennifer J; Leslie, Elizabeth E; Zimmerman, Bridget B; Kleiber, Charmaine C; Hanrahan, Kirsten K; Murray, Jeffrey C JC; McCarthy, Ann Marie AM
Publication Date: 2017-05

Variant appearance in text: rs140700
PubMed Link: 28413930
Variant Present in the following documents:
  • Main text
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The rs11191580 variant of the NT5C2 gene is associated with schizophrenia and symptom severity in a South Chinese Han population: evidence from GWAS.

Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)
Li, Zhen Z; Jiang, Juan J; Long, Jianxiong J; Ling, Weijun W; Huang, Guifeng G; Guo, Xiaojing X; Su, Li L
Publication Date: 2017

Variant appearance in text: rs140700
PubMed Link: 27901213
Variant Present in the following documents:
  • Main text
  • bjp-39-02-104.pdf
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Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.

Molecular Psychiatry
Bonvicini, C C; Faraone, S V SV; Scassellati, C C
Publication Date: 2016-07

Variant appearance in text: rs140700
PubMed Link: 27217152
Variant Present in the following documents:
View BVdb publication page



Postpartum depression: A systematic review of the genetics involved.

World Journal Of Psychiatry
Couto, Tiago Castro E TC; Brancaglion, Mayra Yara Martins MY; Alvim-Soares, António A; Moreira, Lafaiete L; Garcia, Frederico Duarte FD; Nicolato, Rodrigo R; Aguiar, Regina Amélia Lopes P RA; Leite, Henrique Vitor HV; Corrêa, Humberto H
Publication Date: 2015-03-22

Variant appearance in text: rs140700
PubMed Link: 25815259
Variant Present in the following documents:
  • Main text
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Assessment of genetic and nongenetic interactions for the prediction of depressive symptomatology: an analysis of the Wisconsin Longitudinal Study using machine learning algorithms.

American Journal Of Public Health
Roetker, Nicholas S NS; Page, C David CD; Yonker, James A JA; Chang, Vicky V; Roan, Carol L CL; Herd, Pamela P; Hauser, Taissa S TS; Hauser, Robert M RM; Atwood, Craig S CS
Publication Date: 2013-10

Variant appearance in text: rs140700
PubMed Link: 23927508
Variant Present in the following documents:
  • Main text
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Serotonin transporter gene (SLC6A4) variations are associated with poor survival in colorectal cancer patients.

Plos One
Savas, Sevtap S; Hyde, Angela A; Stuckless, Susan N SN; Parfrey, Patrick P; Younghusband, H Banfield HB; Green, Roger R
Publication Date: 2012

Variant appearance in text: rs140700
PubMed Link: 22911682
Variant Present in the following documents:
  • Main text
  • pone.0038953.pdf
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AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study.

Plos One
Morley, Andrew P AP; Narayanan, Madan M; Mines, Rebecca R; Molokhia, Ashraf A; Baxter, Sebastian S; Craig, Gavin G; Lewis, Cathryn M CM; Craig, Ian I
Publication Date: 2012

Variant appearance in text: rs140700
PubMed Link: 22384070
Variant Present in the following documents:
  • Main text
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Examining associations between disordered eating and serotonin transporter gene polymorphisms.

The International Journal Of Eating Disorders
Munn-Chernoff, Melissa A MA; McQueen, Matthew B MB; Stetler, Gary L GL; Haberstick, Brett C BC; Rhee, Soo Hyun SH; Sobik, Laura E LE; Corley, Robin P RP; Smolen, Andrew A; Hewitt, John K JK; Stallings, Michael C MC
Publication Date: 2012-05

Variant appearance in text: rs140700
PubMed Link: 22271047
Variant Present in the following documents:
  • Main text
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The genetics of attention deficit/hyperactivity disorder in adults, a review.

Molecular Psychiatry
Franke, B B; Faraone, S V SV; Asherson, P P; Buitelaar, J J; Bau, C H D CH; Ramos-Quiroga, J A JA; Mick, E E; Grevet, E H EH; Johansson, S S; Haavik, J J; Lesch, K-P KP; Cormand, B B; Reif, A A; ,
Publication Date: 2012-10

Variant appearance in text: rs140700
PubMed Link: 22105624
Variant Present in the following documents:
  • Main text
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Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort.

Bmj Open
Nyman, Emma S ES; Sulkava, Sonja S; Soronen, Pia P; Miettunen, Jouko J; Loukola, Anu A; Leppä, Virpi V; Joukamaa, Matti M; Mäki, Pirjo P; Järvelin, Marjo-Riitta MR; Freimer, Nelson N; Peltonen, Leena L; Veijola, Juha J; Paunio, Tiina T
Publication Date: 2011-08-27

Variant appearance in text: rs140700
PubMed Link: 22021758
Variant Present in the following documents:
  • Main text
  • bmjopen-2011-000087.pdf
  • bmjopen-2011-000087.draft_revisions.pdf
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Serotonin transporter gene, depressive symptoms, and interleukin-6.

Circulation. Cardiovascular Genetics
Su, Shaoyong S; Zhao, Jinying J; Bremner, J Douglas JD; Miller, Andrew H AH; Tang, Weining W; Bouzyk, Mark M; Snieder, Harold H; Novik, Olga O; Afzal, Nadeem N; Goldberg, Jack J; Vaccarino, Viola V
Publication Date: 2009-12

Variant appearance in text: rs140700
PubMed Link: 20031642
Variant Present in the following documents:
  • Main text
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Pharmacogenetics studies in STAR*D: strengths, limitations, and results.

Psychiatric Services (Washington, D.C.)
Laje, Gonzalo G; Perlis, Roy H RH; Rush, A John AJ; McMahon, Francis J FJ
Publication Date: 2009-11

Variant appearance in text: rs140700
PubMed Link: 19880459
Variant Present in the following documents:
  • Main text
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Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.

Molecular Psychiatry
Voyiaziakis, E E; Evgrafov, O O; Li, D D; Yoon, H-J HJ; Tabares, P P; Samuels, J J; Wang, Y Y; Riddle, M A MA; Grados, M A MA; Bienvenu, O J OJ; Shugart, Y Y YY; Liang, K-Y KY; Greenberg, B D BD; Rasmussen, S A SA; Murphy, D L DL; Wendland, J R JR; McCracken, J T JT; Piacentini, J J; Rauch, S L SL; Pauls, D L DL; Nestadt, G G; Fyer, A J AJ; Knowles, J A JA
Publication Date: 2011-01

Variant appearance in text: rs140700
PubMed Link: 19806148
Variant Present in the following documents:
  • Main text
  • nihms-139943.pdf
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Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.

Croatian Medical Journal
Pal, Prodipto P; Mihanović, Mate M; Molnar, Sven S; Xi, Huifeng H; Sun, Guangyun G; Guha, Saurav S; Jeran, Nina N; Tomljenović, Andrea A; Malnar, Ana A; Missoni, Sasa S; Deka, Ranjan R; Rudan, Pavao P
Publication Date: 2009-08

Variant appearance in text: rs140700
PubMed Link: 19673036
Variant Present in the following documents:
  • Main text
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Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures.

Biological Psychiatry
Wray, Naomi R NR; James, Michael R MR; Gordon, Scott D SD; Dumenil, Troy T; Ryan, Leanne L; Coventry, William L WL; Statham, Dixie J DJ; Pergadia, Michele L ML; Madden, Pamela A F PA; Heath, Andrew C AC; Montgomery, Grant W GW; Martin, Nicholas G NG
Publication Date: 2009-09-01

Variant appearance in text: rs140700
PubMed Link: 19541292
Variant Present in the following documents:
  • Main text
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Variants of the serotonin transporter gene and NEO-PI-R Neuroticism: No association in the BLSA and SardiNIA samples.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Terracciano, Antonio A; Balaci, Lenuta L; Thayer, Jason J; Scally, Matthew M; Kokinos, Sarah S; Ferrucci, Luigi L; Tanaka, Toshiko T; Zonderman, Alan B AB; Sanna, Serena S; Olla, Nazario N; Zuncheddu, Maria Antonietta MA; Naitza, Silvia S; Busonero, Fabio F; Uda, Manuela M; Schlessinger, David D; Abecasis, Gonçalo R GR; Costa, Paul T PT
Publication Date: 2009-12-05

Variant appearance in text: rs140700
PubMed Link: 19199283
Variant Present in the following documents:
  • Main text
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Examination of association of genes in the serotonin system to autism.

Neurogenetics
Anderson, B M BM; Schnetz-Boutaud, N C NC; Bartlett, J J; Wotawa, A M AM; Wright, H H HH; Abramson, R K RK; Cuccaro, M L ML; Gilbert, J R JR; Pericak-Vance, M A MA; Haines, J L JL
Publication Date: 2009-07

Variant appearance in text: rs140700
PubMed Link: 19184136
Variant Present in the following documents:
  • Main text
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Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Biederman, Joseph J; Kim, Jang Woo JW; Doyle, Alysa E AE; Mick, Eric E; Fagerness, Jesen J; Smoller, Jordan W JW; Faraone, Stephen V SV
Publication Date: 2008-12-05

Variant appearance in text: rs140700
PubMed Link: 18937309
Variant Present in the following documents:
  • Main text
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SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Kollins, S H SH; Anastopoulos, A D AD; Lachiewicz, A M AM; FitzGerald, D D; Morrissey-Kane, E E; Garrett, M E ME; Keatts, S L SL; Ashley-Koch, A E AE
Publication Date: 2008-12-05

Variant appearance in text: rs140700
PubMed Link: 18821566
Variant Present in the following documents:
  • Main text
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Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR).

Molecular Psychiatry
Strug, L J LJ; Suresh, R R; Fyer, A J AJ; Talati, A A; Adams, P B PB; Li, W W; Hodge, S E SE; Gilliam, T C TC; Weissman, M M MM
Publication Date: 2010-02

Variant appearance in text: rs140700
PubMed Link: 18663369
Variant Present in the following documents:
  • Main text
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Physiogenomic analysis of localized FMRI brain activity in schizophrenia.

Annals Of Biomedical Engineering
Windemuth, Andreas A; Calhoun, Vince D VD; Pearlson, Godfrey D GD; Kocherla, Mohan M; Jagannathan, Kanchana K; Ruaño, Gualberto G
Publication Date: 2008-06

Variant appearance in text: rs140700
PubMed Link: 18330705
Variant Present in the following documents:
  • Main text
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Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables.

American Journal Of Human Genetics
Mei, H H; Cuccaro, M L ML; Martin, E R ER
Publication Date: 2007-12

Variant appearance in text: rs140700
PubMed Link: 17999363
Variant Present in the following documents:
  • Main text
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Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

American Journal Of Human Genetics
Sutcliffe, James S JS; Delahanty, Ryan J RJ; Prasad, Harish C HC; McCauley, Jacob L JL; Han, Qiao Q; Jiang, Lan L; Li, Chun C; Folstein, Susan E SE; Blakely, Randy D RD
Publication Date: 2005-08

Variant appearance in text: rs140700
PubMed Link: 15995945
Variant Present in the following documents:
  • Main text
View BVdb publication page