NUCKS1 c.*2056A>G

Variant ID: 1-205685352-T-C

NM_022731.4(NUCKS1):c.*2056A>G

This variant was identified in 12 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: rs951366
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Tissue-specific multi-omics analysis of atrial fibrillation.

Nature Communications
Assum, Ines I; Krause, Julia J; Scheinhardt, Markus O MO; Müller, Christian C; Hammer, Elke E; Börschel, Christin S CS; Völker, Uwe U; Conradi, Lenard L; Geelhoed, Bastiaan B; Zeller, Tanja T; Schnabel, Renate B RB; Heinig, Matthias M
Publication Date: 2022-01-21

Variant appearance in text: rs951366
PubMed Link: 35064145
Variant Present in the following documents:
  • 41467_2022_27953_MOESM1_ESM.pdf
View BVdb publication page



Tissue-specific multi-omics analysis of atrial fibrillation.

Nature Communications
Assum, Ines I; Krause, Julia J; Scheinhardt, Markus O MO; Müller, Christian C; Hammer, Elke E; Börschel, Christin S CS; Völker, Uwe U; Conradi, Lenard L; Geelhoed, Bastiaan B; Zeller, Tanja T; Schnabel, Renate B RB; Heinig, Matthias M
Publication Date: 2022-01-21

Variant appearance in text: rs951366
PubMed Link: 35064145
Variant Present in the following documents:
  • 41467_2022_27953_MOESM1_ESM.pdf
View BVdb publication page



Nucks1 gene polymorphism rs823114 is associated with the positive symptoms and neurocognitive function of patients with schizophrenia in parts of southern China.

Psychiatric Genetics
Wen, Xia X; Xu, Xusan X; Luo, Xudong X; Yin, Jinwen J; Liang, Chunmei C; Zhu, Jinyuan J; Nong, Xueyan X; Zhu, Xiudeng X; Ning, Fan F; Gu, Shanshan S; Xiong, Susu S; Fu, Jiawu J; Zhu, Dongjian D; Dai, Zhun Z; Lv, Dong D; Lin, Zhixiong Z; Lin, Juda J; Li, You Y; Ma, Guoda G; Wang, Yajun Y
Publication Date: 2021-08-01

Variant appearance in text: rs951366
PubMed Link: 34030174
Variant Present in the following documents:
  • Main text
View BVdb publication page



The genetic architecture of the human thalamus and its overlap with ten common brain disorders.

Nature Communications
Elvsåshagen, Torbjørn T; Shadrin, Alexey A; Frei, Oleksandr O; van der Meer, Dennis D; Bahrami, Shahram S; Kumar, Vinod Jangir VJ; Smeland, Olav O; Westlye, Lars T LT; Andreassen, Ole A OA; Kaufmann, Tobias T
Publication Date: 2021-05-18

Variant appearance in text: rs951366
PubMed Link: 34006833
Variant Present in the following documents:
  • Main text
  • 41467_2021_Article_23175.pdf
View BVdb publication page



Allele-specific expression of Parkinson's disease susceptibility genes in human brain.

Scientific Reports
Langmyhr, Margrete M; Henriksen, Sandra Pilar SP; Cappelletti, Chiara C; van de Berg, Wilma D J WDJ; Pihlstrøm, Lasse L; Toft, Mathias M
Publication Date: 2021-01-12

Variant appearance in text: rs951366
PubMed Link: 33436766
Variant Present in the following documents:
  • Main text
  • 41598_2020_79990_MOESM1_ESM.pdf
  • 41598_2020_Article_79990.pdf
View BVdb publication page



Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.

Nature Communications
Teumer, Alexander A; Chaker, Layal L; Groeneweg, Stefan S; Li, Yong Y; Di Munno, Celia C; Barbieri, Caterina C; Schultheiss, Ulla T UT; Traglia, Michela M; Ahluwalia, Tarunveer S TS; Akiyama, Masato M; Appel, Emil Vincent R EVR; Arking, Dan E DE; Arnold, Alice A; Astrup, Arne A; Beekman, Marian M; Beilby, John P JP; Bekaert, Sofie S; Boerwinkle, Eric E; Brown, Suzanne J SJ; De Buyzere, Marc M; Campbell, Purdey J PJ; Ceresini, Graziano G; Cerqueira, Charlotte C; Cucca, Francesco F; Deary, Ian J IJ; Deelen, Joris J; Eckardt, Kai-Uwe KU; Ekici, Arif B AB; Eriksson, Johan G JG; Ferrrucci, Luigi L; Fiers, Tom T; Fiorillo, Edoardo E; Ford, Ian I; Fox, Caroline S CS; Fuchsberger, Christian C; Galesloot, Tessel E TE; Gieger, Christian C; Gögele, Martin M; De Grandi, Alessandro A; Grarup, Niels N; Greiser, Karin Halina KH; Haljas, Kadri K; Hansen, Torben T; Harris, Sarah E SE; van Heemst, Diana D; den Heijer, Martin M; Hicks, Andrew A AA; den Hollander, Wouter W; Homuth, Georg G; Hui, Jennie J; Ikram, M Arfan MA; Ittermann, Till T; Jensen, Richard A RA; Jing, Jiaojiao J; Jukema, J Wouter JW; Kajantie, Eero E; Kamatani, Yoichiro Y; Kasbohm, Elisa E; Kaufman, Jean-Marc JM; Kiemeney, Lambertus A LA; Kloppenburg, Margreet M; Kronenberg, Florian F; Kubo, Michiaki M; Lahti, Jari J; Lapauw, Bruno B; Li, Shuo S; Liewald, David C M DCM; , ; Lim, Ee Mun EM; Linneberg, Allan A; Marina, Michela M; Mascalzoni, Deborah D; Matsuda, Koichi K; Medenwald, Daniel D; Meisinger, Christa C; Meulenbelt, Ingrid I; De Meyer, Tim T; Meyer Zu Schwabedissen, Henriette E HE; Mikolajczyk, Rafael R; Moed, Matthijs M; Netea-Maier, Romana T RT; Nolte, Ilja M IM; Okada, Yukinori Y; Pala, Mauro M; Pattaro, Cristian C; Pedersen, Oluf O; Petersmann, Astrid A; Porcu, Eleonora E; Postmus, Iris I; Pramstaller, Peter P PP; Psaty, Bruce M BM; Ramos, Yolande F M YFM; Rawal, Rajesh R; Redmond, Paul P; Richards, J Brent JB; Rietzschel, Ernst R ER; Rivadeneira, Fernando F; Roef, Greet G; Rotter, Jerome I JI; Sala, Cinzia F CF; Schlessinger, David D; Selvin, Elizabeth E; Slagboom, P Eline PE; Soranzo, Nicole N; Sørensen, Thorkild I A TIA; Spector, Timothy D TD; Starr, John M JM; Stott, David J DJ; Taes, Youri Y; Taliun, Daniel D; Tanaka, Toshiko T; Thuesen, Betina B; Tiller, Daniel D; Toniolo, Daniela D; Uitterlinden, Andre G AG; Visser, W Edward WE; Walsh, John P JP; Wilson, Scott G SG; Wolffenbuttel, Bruce H R BHR; Yang, Qiong Q; Zheng, Hou-Feng HF; Cappola, Anne A; Peeters, Robin P RP; Naitza, Silvia S; Völzke, Henry H; Sanna, Serena S; Köttgen, Anna A; Visser, Theo J TJ; Medici, Marco M
Publication Date: 2018-10-26

Variant appearance in text: rs951366
PubMed Link: 30367059
Variant Present in the following documents:
  • 41467_2018_6356_MOESM1_ESM.pdf
View BVdb publication page



Roles of NUCKS1 in Diseases: Susceptibility, Potential Biomarker, and Regulatory Mechanisms.

Biomed Research International
Huang, Pengru P; Cai, Yujie Y; Zhao, Bin B; Cui, Lili L
Publication Date: 2018

Variant appearance in text: rs951366
PubMed Link: 29619377
Variant Present in the following documents:
  • Main text
  • BMRI2018-7969068.pdf
View BVdb publication page



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: rs951366
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page



Age at menarche and lung function: a Mendelian randomization study.

European Journal Of Epidemiology
Gill, Dipender D; Sheehan, Nuala A NA; Wielscher, Matthias M; Shrine, Nick N; Amaral, Andre F S AFS; Thompson, John R JR; Granell, Raquel R; Leynaert, Bénédicte B; Real, Francisco Gómez FG; Hall, Ian P IP; Tobin, Martin D MD; Auvinen, Juha J; Ring, Susan M SM; Jarvelin, Marjo-Riitta MR; Wain, Louise V LV; Henderson, John J; Jarvis, Deborah D; Minelli, Cosetta C
Publication Date: 2017-08

Variant appearance in text: rs951366
PubMed Link: 28624884
Variant Present in the following documents:
  • 10654_2017_272_MOESM2_ESM.pdf
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs951366
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Publication Date: 2014

Variant appearance in text: rs951366
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Evolutionary signatures of common human cis-regulatory haplotypes.

Plos One
Ouyang, Ching C; Smith, David D DD; Krontiris, Theodore G TG
Publication Date: 2008

Variant appearance in text: rs951366
PubMed Link: 18846218
Variant Present in the following documents:
  • Main text
  • pone.0003362.pdf
View BVdb publication page