Disease Info Card

Hemoglobinopathies

Information about Hemoglobinopathies: 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 Hemoglobinopathies

Most recent studies have shown that Hemoglobinopathies shares some biological mechanisms with alpha-thalassemia, anemia, anemia-hemolytic, anemia-sickle-cell, beta-thalassemia, cooleys-anemia, diabetes-mellitus, glucosephosphate-dehydrogenase-deficiency, hematological-disease, hemoglobin-c-disease, hemoglobin-f-disease, hemoglobin-sc-disease, hemolysis-(disorder), hereditary-diseases, iron-deficiency, malaria, other-hemoglobinopathies, pregnancy-complications-hematologic, sickle-cell-trait, thalassemia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Hemoglobinopathies, and have been seen in publications frequently: Cell Cycle, Cell Proliferation, Coagulation, Dna Methylation, Excretion, Glomerular Filtration, Hemopoiesis, Hemostasis, Immune Response, Localization, Methylation, Oxygen Transport, Pathogenesis, Phagocytosis, Platelet Aggregation, Proteolysis, Regeneration, Sensitization, Translation, Transport

Quite a number of genes have been found to play important roles in Hemoglobinopathies, such as ASAH1, ATP6V0A2, EPO, ERMAP, G6PD, GPHA2, HBA1, HBB, HBG1, HBG2, PMCH, SCD, 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.

Hemoglobinopathies Related Genes

click to see detail information for each gene

ASAH1 ATP6V0A2 EPO
ERMAP G6PD GPHA2
HBA1 HBB HBG1
HBG2 PMCH SCD
SGCA TF UBL4A