Varaico: Literature-Extracted Genetic Variants

Gene:OR13G1
Variant:p.I132V
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OR13G1

NM_001005487.2:p.I132V

Associated Papers

High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune profile, clinical outcome and sensitivity to targeted therapies.

Toulmonde M et al.

Ebiomedicine, 2020

33254023 (PubMed )
Supplement: mmc5.xlsx › UPS_somatic_mutations_filtered

Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.

Maguire SL et al.

The Journal of Pathology, 2016

27512948 (PubMed )
Supplement: PATH-240-315-s015.xlsx › Table_S2

Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients.

Reyes-Gibby CC et al.

Scientific Reports, 2016

Genetic score based on high-risk genetic polymorphisms and early onset of ischemic heart disease in an Italian cohort of ischemic patients.

Vecoli C et al.

Thrombosis Research, 2014

Association of a matrix metallopeptidase 1 gene polymorphism with long-term outcome of thoracic aortic aneurysm.

Kato K et al.

International Journal of Molecular Medicine, 2012

Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.

Yoshida T et al.

Genomics, 2009

Usefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemia.

van der Net JB et al.

The American Journal of Cardiology, 2009

Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population.

Yamada Y et al.

Journal of Medical Genetics, 2008

Pharmacogenomics in acute coronary syndrome.

Remmler C et al.

Expert Opinion on Pharmacotherapy, 2008

Identification of four gene variants associated with myocardial infarction.

Shiffman D et al.

American Journal of Human Genetics, 2005

Association of polymorphisms of THBS2 and HSPA8 with hypertension in Japanese individuals with chronic kidney disease.

Oguri M et al.

Molecular Medicine Reports, 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."