WNT2 c.*124G>A

Variant ID: 7-116918085-C-T

NM_003391.2(WNT2):c.*124G>A

This variant was identified in 6 publications

View GRCh38 version.




Publications:


JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research
Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K
Publication Date: 2022-11-21

Variant appearance in text: rs2228946
PubMed Link: 36409824
Variant Present in the following documents:
  • can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1
View BVdb publication page



A translational exploration of the effects of WNT2 variants on altered cortical structures in autism spectrum disorder.

Journal Of Psychiatry & Neuroscience : Jpn
Chien, Yi-Ling YL; Chen, Yu-Chieh YC; Chiu, Yen-Nan YN; Tsai, Wen-Che WC; Gau, Susan Shur-Fen SS
Publication Date: 2021

Variant appearance in text: rs2228946
PubMed Link: 34862305
Variant Present in the following documents:
  • Main text
  • 46-6-E647.pdf
View BVdb publication page



Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer
Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC
Publication Date: 2021-05-29

Variant appearance in text: rs2228946
PubMed Link: 34051734
Variant Present in the following documents:
  • 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page



Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.

Investigative Ophthalmology & Visual Science
Shaaban, Sherin S; MacKinnon, Sarah S; Andrews, Caroline C; Staffieri, Sandra E SE; Maconachie, Gail D E GDE; Chan, Wai-Man WM; Whitman, Mary C MC; Morton, Sarah U SU; Yazar, Seyhan S; MacGregor, Stuart S; Elder, James E JE; Traboulsi, Elias I EI; Gottlob, Irene I; Hewitt, Alex W AW; , ; Hunter, David G DG; Mackey, David A DA; Engle, Elizabeth C EC
Publication Date: 2018-08-01

Variant appearance in text: rs2228946
PubMed Link: 30098192
Variant Present in the following documents:
  • i1552-5783-59-10-4054.pdf
View BVdb publication page



Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.

The Pharmacogenomics Journal
Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X
Publication Date: 2014-12

Variant appearance in text: rs2228946
PubMed Link: 24980784
Variant Present in the following documents:
  • Main text
View BVdb publication page



Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes.

Plos One
Yuen, Ryan K C RK; Avila, Luana L; PeƱaherrera, Maria S MS; von Dadelszen, Peter P; Lefebvre, Louis L; Kobor, Michael S MS; Robinson, Wendy P WP
Publication Date: 2009-10-19

Variant appearance in text: rs2228946
PubMed Link: 19838307
Variant Present in the following documents:
  • Main text
  • pone.0007389.pdf
View BVdb publication page