Related Experiment Video
Updated: Jul 29, 2025

Generation of High Quality Chromatin Immunoprecipitation DNA Template for High-throughput Sequencing ChIP-seq
Published on: April 19, 2013
The KL genetic polymorphisms Associated with type 2 diabetes Mellitus
Hyun-Seok Jin1, Dongju Jung1,2
1Department of Biomedical Laboratory Science, College of Life and Health Sciences, Hoseo University, 31499 Asan, Chungnam Republic of Korea.
The anti-aging gene Klotho (KL) is linked to Type 2 Diabetes Mellitus (T2DM). Specific KL gene variations (SNPs) were found to increase the risk of developing T2DM in an Asian population.
Area of Science:
- Genetics
- Endocrinology
- Metabolic Diseases
Background:
- The Klotho (KL) gene, known for its anti-aging properties, has been increasingly associated with Type 2 Diabetes Mellitus (T2DM).
- Understanding the genetic basis of this association is crucial for identifying T2DM risk factors.
Purpose of the Study:
- To genetically analyze the association between Klotho (KL) gene single nucleotide polymorphisms (SNPs) and Type 2 Diabetes Mellitus (T2DM) in an Asian cohort.
- To identify specific KL SNPs that may serve as risk markers for T2DM.
Main Methods:
- Utilized data from the Korean Association Resource (KARE) database, examining 20 KL SNPs.
- Performed statistical analyses using additive, dominant, and recessive genetic models.
- Employed imputed KL SNPs from HapMap reference data for further analysis.
Main Results:
- Twelve out of 20 KL SNPs showed a significant association with T2DM under additive and dominant models.
- Odds ratios indicated that these KL SNPs increase susceptibility to T2DM.
- Significant KL SNPs, including imputed ones, were distributed across the KL gene region.
Conclusions:
- Klotho plays a significant role in the development of Type 2 Diabetes Mellitus.
- Identified KL SNPs represent potential risk markers for T2DM in the Asian cohort studied.
More Related Videos
Related Concept Videos
Diabetes Mellitus: Type 2 and Gestational
Genome-wide Association Studies-GWAS
GWAS does not require the identification of the target gene involved in...
Single Nucleotide Polymorphisms-SNPs
Pathophysiology of Diabetes
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
Diabetes Mellitus: Overview and Type I Subtype
Type 1 diabetes is an autoimmune disease in which the immune system mistakenly attacks and destroys the insulin-producing beta cells in the pancreas. As a result, the body is unable to produce sufficient insulin, and individuals with...
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

