Disease Info Card

Thalassemia Trait

Information about Thalassemia Trait: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Thalassemia Trait

Most recent studies have shown that Thalassemia Trait shares some biological mechanisms with alpha-thalassemia, alpha-trait-thalassemia, anemia, anemia-hemolytic, anemia-sickle-cell, beta-thalassemia, beta-thalassemia-trait, cooleys-anemia, deficiency-anaemia, glucosephosphate-dehydrogenase-deficiency, hemoglobinopathies, hypochromia, hypochromic-anemia, iron-deficiency, iron-deficiency-anemia, microcytic-anemia, pregnancy-complications-hematologic, sickle-cell-trait, thalassemia, thalassemia-intermedia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Thalassemia Trait, and have been seen in publications frequently: Erythrocyte Aggregation, Immune Response, Intestinal Absorption, Menarche, Oxidative Phosphorylation, Oxygen Transport, Phagocytosis, Platelet Formation, Translation, Transport

Quite a number of genes have been found to play important roles in Thalassemia Trait, such as ACD, ATP6V0A2, G6PD, GPHA2, HBA1, HBB, HBG2, LIPA, PMCH, SCN2A, SGCA, TF, UBL4A. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.