In silico prediction of HBD gene variants in the Iranian population

Egyptian Journal of Medical Human Genetics

Keivan Moradi¹  Mohsen Kazeminia²  Aboozar Mohammadi³ 

[1] Department of Biochemistry, School of Medicine, Kermanshah University of Medical Sciences;Department of Nursing, School of Nursing and Midwifery, Kermanshah University of Medical Sciences;Student Research Committee, Kermanshah University of Medical Sciences;

关键词: Hemoglobin A2;    δ-globin gene;    Variant;    Thalassemia;    Iran;   

DOI  :  10.1186/s43042-021-00137-0

来源: DOAJ

【 摘 要 】

Abstract Background The quantification of hemoglobin A2 (Hb A2; α2δ2) is used as a valuable test to differentiate α- and ß-thal carriers in clinical laboratories. Therefore, the HBD (δ-globin) gene variants could result in reduced levels of Hb A2 and have implications for thalassemia screening programs. The aim of the present study was to predict the consequences of HBD gene variants identified in the Iranome project. Results The highest number of variants was in the Persian Gulf Islanders. The variants of p.Gln132Glu (HBD: c.394C>G), p.Gly17Arg (HBD: c.49G>C), p.Thr5Ile (HBD: c.14C>T), and p.Ala28Ser (HBD: c.82G>T) presented damage results in three or more prediction tools. In addition, it seems that the p.Gly30= (HBD: c.90C>T) decreases the use of authentic splice and, instead, creates a new donor splice site (DSS) or leads to the use of a cryptic DSS. Conclusions Most of these variants have been associated with a decrease in Hb A2 levels. Due to the high mutational diversity in the HBB gene in the Iranian population and the use of Hb A2 quantification to differentiate α- and ß-thal carriers among Iranian clinical laboratories, some attention should be taken to a possible co-inheritance of HBD gene variants to avoid the misdiagnosis of ß-thal carriers.

【 授权许可】

Unknown