IGF2 c.*29C>G

Variant ID: 11-2154188-G-C

NM_000612.4(IGF2):c.*29C>G

This variant was identified in 10 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: rs2230949
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Large parental differences in chromatin organization in pancreatic beta cell line explaining diabetes susceptibility effects.

Nature Communications
Jian, Xing X; Felsenfeld, Gary G
Publication Date: 2021-07-15

Variant appearance in text: rs2230949
PubMed Link: 34267199
Variant Present in the following documents:
  • Main text
  • 41467_2021_24635_MOESM1_ESM.pdf
  • 41467_2021_Article_24635.pdf
View BVdb publication page



Genotyping data of routinely processed matched primary/metastatic tumor samples.

Data In Brief
Kotoula, Vassiliki V; Chatzopoulos, Kyriakos K; Papadopoulou, Kyriaki K; Giannoulatou, Eleni E; Koliou, Georgia-Angeliki GA; Karavasilis, Vasilios V; Pazarli, Elissavet E; Pervana, Stavroula S; Kafiri, Georgia G; Tsoulfas, Georgios G; Chrisafi, Sofia S; Sgouramali, Helen H; Papakostas, Pavlos P; Pectasides, Dimitrios D; Hytiroglou, Prodromos P; Pentheroudakis, George G; Fountzilas, George G
Publication Date: 2021-02

Variant appearance in text: rs2230949
PubMed Link: 33365374
Variant Present in the following documents:
  • mmc1.xlsx, sheet 3
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: rs2230949
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
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: rs2230949
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs2230949
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 2
View BVdb publication page



Gefitinib in Combination with Weekly Docetaxel in Patients with Metastatic Breast Cancer Caused Unexpected Toxicity: Results from a Randomized Phase II Clinical Trial.

Isrn Oncology
Engebraaten, Olav O; Edvardsen, Hege H; Løkkevik, Erik E; Naume, Bjørn B; Kristensen, Vessela V; Ottestad, Lars L; Natarajan, Vasanti V
Publication Date: 2012

Variant appearance in text: rs2230949
PubMed Link: 22666610
Variant Present in the following documents:
  • Main text
  • ISRN.ONCOLOGY2012-176789.pdf
View BVdb publication page



Loss of imprinting and marked gene elevation are 2 forms of aberrant IGF2 expression in colorectal cancer.

International Journal Of Cancer
Cheng, Yu-Wei YW; Idrees, Kamran K; Shattock, Richard R; Khan, Sajid A SA; Zeng, Zhaoshi Z; Brennan, Cameron W CW; Paty, Philip P; Barany, Francis F
Publication Date: 2010-08-01

Variant appearance in text: rs2230949
PubMed Link: 19957330
Variant Present in the following documents:
  • Main text
View BVdb publication page



Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1.

Plos One
Cironi, Luisa L; Provero, Paolo P; Riggi, Nicola N; Janiszewska, Michalina M; Suva, Domizio D; Suva, Mario-Luca ML; Kindler, Vincent V; Stamenkovic, Ivan I
Publication Date: 2009-11-19

Variant appearance in text: rs2230949
PubMed Link: 19936258
Variant Present in the following documents:
  • Main text
  • pone.0007904.pdf
View BVdb publication page



Genetic variation in insulin-like growth factors and brain tumor risk.

Neuro-Oncology
Lönn, Stefan S; Rothman, Nathaniel N; Shapiro, William R WR; Fine, Howard A HA; Selker, Robert G RG; Black, Peter M PM; Loeffler, Jay S JS; Hutchinson, Amy A AA; Inskip, Peter D PD
Publication Date: 2008-08

Variant appearance in text: rs2230949
PubMed Link: 18562769
Variant Present in the following documents:
  • Main text
View BVdb publication page