INSR c.653-15155T>C

Variant ID: 19-7199803-A-G

NM_000208.2(INSR):c.653-15155T>C

This variant was identified in 8 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: rs1035942
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Novel Insights into the Effects of Genetic Variants on Serum Urate Response to an Acute Fructose Challenge: A Pilot Study.

Nutrients
Zhang, Xinruo X; Mass, Baba B BB; Talevi, Valentina V; Hou, Ruixue R; North, Kari E KE; Voruganti, Venkata Saroja VS
Publication Date: 2022-09-28

Variant appearance in text: rs1035942
PubMed Link: 36235682
Variant Present in the following documents:
  • Main text
  • nutrients-14-04030.pdf
View BVdb publication page



Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution.

The Journal Of Clinical Endocrinology And Metabolism
Koprulu, Mine M; Zhao, Yajie Y; Wheeler, Eleanor E; Dong, Liang L; Rocha, Nuno N; Li, Chen C; Griffin, John D JD; Patel, Satish S; Van de Streek, Marcel M; Glastonbury, Craig A CA; Stewart, Isobel D ID; Day, Felix R FR; Luan, Jian'an J; Bowker, Nicholas N; Wittemans, Laura B L LBL; Kerrison, Nicola D ND; Cai, Lina L; Lucarelli, Debora M E DME; Barroso, InĂªs I; McCarthy, Mark I MI; Scott, Robert A RA; Saudek, Vladimir V; Small, Kerrin S KS; Wareham, Nicholas J NJ; Semple, Robert K RK; Perry, John R B JRB; O'Rahilly, Stephen S; Lotta, Luca A LA; Langenberg, Claudia C; Savage, David B DB
Publication Date: 2022-03-24

Variant appearance in text: rs1035942
PubMed Link: 34875679
Variant Present in the following documents:
  • Main text
View BVdb publication page



The genetic susceptibility profile of type 2 diabetes and reflection of its possible role related to reproductive dysfunctions in the southern Indian population of Hyderabad.

Bmc Medical Genomics
Irgam, Kumuda K; Reddy, Battini Sriteja BS; Hari, Sai Gayathri SG; Banapuram, Swathi S; Reddy, Battini Mohan BM
Publication Date: 2021-11-16

Variant appearance in text: rs1035942
PubMed Link: 34784930
Variant Present in the following documents:
  • Main text
  • 12920_2021_Article_1129.pdf
View BVdb publication page



Genetic and Physiological Effects of Insulin on Human Urate Homeostasis.

Frontiers In Physiology
Mandal, Asim K AK; Leask, Megan P MP; Estiverne, Christopher C; Choi, Hyon K HK; Merriman, Tony R TR; Mount, David B DB
Publication Date: 2021

Variant appearance in text: rs1035942
PubMed Link: 34408667
Variant Present in the following documents:
  • Main text
  • fphys-12-713710.pdf
View BVdb publication page



Chronic heavy alcohol consumption influences the association between genetic variants of GCK or INSR and the development of diabetes in men: A 12-year follow-up study.

Scientific Reports
Jang, Han Byul HB; Go, Min Jin MJ; Park, Sang Ick SI; Lee, Hye-Ja HJ; Cho, Seong Beom SB
Publication Date: 2019-12-27

Variant appearance in text: rs1035942
PubMed Link: 31882596
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_56011.pdf
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs1035942
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



The association between polymorphism of INSR and polycystic ovary syndrome: a meta-analysis.

International Journal Of Molecular Sciences
Feng, Chun C; Lv, Ping-Ping PP; Yu, Tian-Tian TT; Jin, Min M; Shen, Jin-Ming JM; Wang, Xue X; Zhou, Feng F; Jiang, Shi-Wen SW
Publication Date: 2015-01-22

Variant appearance in text: rs1035942
PubMed Link: 25622255
Variant Present in the following documents:
  • Main text
  • ijms-16-02403.pdf
View BVdb publication page