# Polymorphic variants in DOCK7, ABCG8, UBE2E2, and SYN2 genes associated with type 2 diabetes in the Uzbek population

**Authors:** Darya Zakirova, Alisher Abdullaev, Dilbar Dalimova, Elina Aguryanova, Fazliddin Khonboev, Nilyufar Khushvakova, Nodira Alikhanova, Feruza Takhirova

PMC · DOI: 10.3389/fcdhc.2025.1494128 · Frontiers in Clinical Diabetes and Healthcare · 2025-02-28

## TL;DR

This study identifies genetic variants linked to type 2 diabetes in the Uzbek population, highlighting the role of specific genes in disease risk.

## Contribution

The study reports novel associations between polymorphisms in DOCK7, ABCG8, UBE2E2, and SYN2 genes and type 2 diabetes in the Uzbek population.

## Key findings

- Polymorphisms in DOCK7, ABCG8, UBE2E2, and SYN2 genes were significantly associated with type 2 diabetes.
- Genotype frequencies were consistent with Hardy–Weinberg equilibrium.
- The study emphasizes the importance of ethnic diversity in genetic research on diabetes.

## Abstract

Diabetes is a leading cause of death, affecting nearly half a billion adults worldwide. With projections indicating a significant increase in prevalence, understanding the genetic factors that contribute to diabetes, particularly type 2, is crucial.

This study investigated the association of specific polymorphisms with type 2 diabetes (T2D) in the Uzbek population. A total of 165 individuals, including 125 patients with T2D and 40 controls, were genotyped for variants located in the DOCK7, ABCG8, UBE2E2, SYN2, HNF1A, and IGF2BP2 genes using real-time polymerase chain reaction.

The analysis revealed significant associations between these polymorphisms and T2D under various genetic models. The distribution of the genotype frequencies was consistent with the Hardy–Weinberg equilibrium.

The findings of this study underscore the importance of ethnic and geographical diversity in genetic studies and contribute to the understanding of T2D in the Uzbek population. Further research is needed to explore the clinical implications of these genetic associations.

## Linked entities

- **Genes:** DOCK7 (dedicator of cytokinesis 7) [NCBI Gene 85440], ABCG8 (ATP binding cassette subfamily G member 8) [NCBI Gene 64241], UBE2E2 (ubiquitin conjugating enzyme E2 E2) [NCBI Gene 7325], SYN2 (synapsin II) [NCBI Gene 6854], HNF1A (HNF1 homeobox A) [NCBI Gene 6927], IGF2BP2 (insulin like growth factor 2 mRNA binding protein 2) [NCBI Gene 10644]
- **Diseases:** type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** ABCG8 (ATP binding cassette subfamily G member 8) [NCBI Gene 64241] {aka GBD4, STSL, STSL1}, UBE2E2 (ubiquitin conjugating enzyme E2 E2) [NCBI Gene 7325] {aka UBCH8}, DOCK7 (dedicator of cytokinesis 7) [NCBI Gene 85440] {aka DEE23, EIEE23, ZIR2}, HNF1A (HNF1 homeobox A) [NCBI Gene 6927] {aka HNF-1-alpha, HNF-1A, HNF1, HNF1alpha, IDDM20, LFB1}, SYN2 (synapsin II) [NCBI Gene 6854] {aka SYNII}, IGF2BP2 (insulin like growth factor 2 mRNA binding protein 2) [NCBI Gene 10644] {aka IMP-2, IMP2, VICKZ2}
- **Diseases:** Diabetes (MESH:D003920), T2D (MESH:D003924), death (MESH:D003643)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11906705/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC11906705/full.md

---
Source: https://tomesphere.com/paper/PMC11906705