CLEC16A c.2116+4006G>A

Variant ID: 16-11158885-G-A

NM_015226.2(CLEC16A):c.2116+4006G>A

This variant was identified in 12 publications

View GRCh38 version.




Publications:


CLEC16A-An Emerging Master Regulator of Autoimmunity and Neurodegeneration.

International Journal Of Molecular Sciences
Pandey, Rahul R; Bakay, Marina M; Hakonarson, Hakon H
Publication Date: 2023-05-04

Variant appearance in text: rs887864
PubMed Link: 37175930
Variant Present in the following documents:
  • ijms-24-08224.pdf
View BVdb publication page



CLEC16A variants conferred a decreased risk to allergic rhinitis in the Chinese population.

Frontiers In Genetics
Niu, Yongliang Y; Wang, Haiying H; Li, Zhengqing Z; Shamsi, Bilal Haider BH; Liu, Mingxia M; Liu, Juan J; Wang, Qiang Q; Liu, Yonglin Y
Publication Date: 2022

Variant appearance in text: rs887864
PubMed Link: 36588789
Variant Present in the following documents:
  • Main text
  • fgene-13-1053761.pdf
View BVdb publication page



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: rs887864
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs887864
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Detection and interpretation of shared genetic influences on 42 human traits.

Nature Genetics
Pickrell, Joseph K JK; Berisa, Tomaz T; Liu, Jimmy Z JZ; Ségurel, Laure L; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2016-07

Variant appearance in text: rs887864
PubMed Link: 27182965
Variant Present in the following documents:
  • NIHMS780506-supplement-5.pdf
View BVdb publication page



Genetic Loci Associated with Allergic Sensitization in Lithuanians.

Plos One
Šaulienė, Ingrida I; Greičiuvienė, Jūratė J; Šukienė, Laura L; Juškevičiūtė, Neringa N; Benner, Christian C; Zinkevičienė, Auksė A; Ripatti, Samuli S; Donner, Kati K; Kainov, Denis D
Publication Date: 2015

Variant appearance in text: rs887864
PubMed Link: 26214689
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells.

Nature Communications
Li, Jin J; Jørgensen, Silje F SF; Maggadottir, S Melkorka SM; Bakay, Marina M; Warnatz, Klaus K; Glessner, Joseph J; Pandey, Rahul R; Salzer, Ulrich U; Schmidt, Reinhold E RE; Perez, Elena E; Resnick, Elena E; Goldacker, Sigune S; Buchta, Mary M; Witte, Torsten T; Padyukov, Leonid L; Videm, Vibeke V; Folseraas, Trine T; Atschekzei, Faranaz F; Elder, James T JT; Nair, Rajan P RP; Winkelmann, Juliane J; Gieger, Christian C; Nöthen, Markus M MM; Büning, Carsten C; Brand, Stephan S; Sullivan, Kathleen E KE; Orange, Jordan S JS; Fevang, Børre B; Schreiber, Stefan S; Lieb, Wolfgang W; Aukrust, Pål P; Chapel, Helen H; Cunningham-Rundles, Charlotte C; Franke, Andre A; Karlsen, Tom H TH; Grimbacher, Bodo B; Hakonarson, Hakon H; Hammarström, Lennart L; Ellinghaus, Eva E
Publication Date: 2015-04-20

Variant appearance in text: rs887864
PubMed Link: 25891430
Variant Present in the following documents:
  • NIHMS669415-supplement-1.pdf
View BVdb publication page



Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype.

The Journal Of Allergy And Clinical Immunology
Ferreira, Manuel A R MA; Matheson, Melanie C MC; Tang, Clara S CS; Granell, Raquel R; Ang, Wei W; Hui, Jennie J; Kiefer, Amy K AK; Duffy, David L DL; Baltic, Svetlana S; Danoy, Patrick P; Bui, Minh M; Price, Loren L; Sly, Peter D PD; Eriksson, Nicholas N; Madden, Pamela A PA; Abramson, Michael J MJ; Holt, Patrick G PG; Heath, Andrew C AC; Hunter, Michael M; Musk, Bill B; Robertson, Colin F CF; Le Souëf, Peter P; Montgomery, Grant W GW; Henderson, A John AJ; Tung, Joyce Y JY; Dharmage, Shyamali C SC; Brown, Matthew A MA; James, Alan A; Thompson, Philip J PJ; Pennell, Craig C; Martin, Nicholas G NG; Evans, David M DM; Hinds, David A DA; Hopper, John L JL; ,
Publication Date: 2014-06

Variant appearance in text: rs887864
PubMed Link: 24388013
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.

Nature Genetics
Hinds, David A DA; McMahon, George G; Kiefer, Amy K AK; Do, Chuong B CB; Eriksson, Nicholas N; Evans, David M DM; St Pourcain, Beate B; Ring, Susan M SM; Mountain, Joanna L JL; Francke, Uta U; Davey-Smith, George G; Timpson, Nicholas J NJ; Tung, Joyce Y JY
Publication Date: 2013-08

Variant appearance in text: rs887864
PubMed Link: 23817569
Variant Present in the following documents:
  • NIHMS489582-supplement-1.pdf
View BVdb publication page



Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.

Plos One
Li, Yi-Ju YJ; Minear, Mollie A MA; Rimmler, Jacqueline J; Zhao, Bei B; Balajonda, Elmer E; Hauser, Michael A MA; Allingham, R Rand RR; Eghrari, Allen O AO; Riazuddin, S Amer SA; Katsanis, Nicholas N; Gottsch, John D JD; Gregory, Simon G SG; Klintworth, Gordon K GK; Afshari, Natalie A NA
Publication Date: 2011-04-20

Variant appearance in text: rs887864
PubMed Link: 21533127
Variant Present in the following documents:
  • Main text
  • pone.0018044.pdf
View BVdb publication page



A generalized family-based association test for dichotomous traits.

American Journal Of Human Genetics
Chen, Wei-Min WM; Manichaikul, Ani A; Rich, Stephen S SS
Publication Date: 2009-09

Variant appearance in text: rs887864
PubMed Link: 19732865
Variant Present in the following documents:
  • Main text
View BVdb publication page



A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3.

Diabetes
Concannon, Patrick P; Onengut-Gumuscu, Suna S; Todd, John A JA; Smyth, Deborah J DJ; Pociot, Flemming F; Bergholdt, Regine R; Akolkar, Beena B; Erlich, Henry A HA; Hilner, Joan E JE; Julier, Cécile C; Morahan, Grant G; Nerup, Jørn J; Nierras, Concepcion R CR; Chen, Wei-Min WM; Rich, Stephen S SS; ,
Publication Date: 2008-10

Variant appearance in text: rs887864
PubMed Link: 18647951
Variant Present in the following documents:
  • Main text
  • 2858.pdf
View BVdb publication page