دورية أكاديمية
Investigation of missense mutation-related type 1 diabetes mellitus through integrating genomic databases and bioinformatic approach.
| العنوان: | Investigation of missense mutation-related type 1 diabetes mellitus through integrating genomic databases and bioinformatic approach. |
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| المؤلفون: | Pakha DN; Department of Pharmacology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, 57126, Indonesia., Yudhani RD; Department of Pharmacology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, 57126, Indonesia. ratihyudhani@staff.uns.ac.id., Irham LM; Faculty of Pharmacy, Universitas Ahmad Dahlan, Yogyakarta, 55166, Indonesia. |
| المصدر: | Genomics & informatics [Genomics Inform] 2024 Jun 26; Vol. 22 (1), pp. 8. Date of Electronic Publication: 2024 Jun 26. |
| نوع المنشور: | Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Korea Genome Organization Country of Publication: Korea (South) NLM ID: 101223836 Publication Model: Electronic Cited Medium: Print ISSN: 1598-866X (Print) Linking ISSN: 1598866X NLM ISO Abbreviation: Genomics Inform Subsets: PubMed not MEDLINE |
| أسماء مطبوعة: | Original Publication: Seoul : Korea Genome Organization |
| مستخلص: | Though genes are already known to be responsible for type 1 diabetes mellitus (T1DM), the knowledge of missense mutation of that disease gene has still to be under covered. A genomic database and a bioinformatics-based approach are integrated in the present study in order to address this issue. Initially, nine variants associated with T1DM were retrieved from the GWAS catalogue. Different genomic algorithms such as PolyPhen2.0, SNPs and GTEx analyser programs were used to study the structural and functional effects of these mutations. Subsequently, SNPnexus was also employed to understand the effect of these mutations on the function of the expressed protein. Nine missense variants of T1DM were identified using the GWAS catalogue database. Among these nine SNPs, three were predicted to be related to the progression of T1DM disease by affecting the protein level. TYK2 gene variants with SNP rs34536443 were thought to have a probably damaging effect. Meanwhile, both COL4A3 and IFIH1 genes with SNPs rs55703767 and rs35667974, respectively, might alter protein function through a possibly damaging prediction. Among the variants of the three genes, the TYK2 gene with SNP rs34536443 had the strongest contribution in affecting the development of T1DM, with a score of 0.999. We sincerely hope that the results could be of immense importance in understanding the genetic basis of T1DM. (© 2024. The Author(s).) |
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| فهرسة مساهمة: | Keywords: Bioinformatics; Genomic database; Genomic variant; T1DM |
| تواريخ الأحداث: | Date Created: 20240626 Latest Revision: 20240705 |
| رمز التحديث: | 20240705 |
| مُعرف محوري في PubMed: | PMC11201337 |
| DOI: | 10.1186/s44342-024-00005-4 |
| PMID: | 38926794 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder | تدمد: | 1598-866X |
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| DOI: | 10.1186/s44342-024-00005-4 |