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Disease Info Card
Dextrocardia
Information about Dextrocardia: 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 Dextrocardia
Most recent studies have shown that Dextrocardia shares some biological mechanisms with atresia, congenital-abnormality, congenital-heart-defects, congenital-heart-disease, heart-diseases, heart-failure, heart-septal-defects, hypoplasia, kartagener-syndrome, levocardia, myocardial-infarction, pulmonary-stenosis, pulmonary-valve-stenosis, scimitar-syndrome, situs-inversus, stenosis, tetralogy-of-fallot, transposition-of-great-vessels, ventricular-septal-defects.
Among the many pathways, these few ones have gauged particular interests from scientists studying Dextrocardia, and have been seen in publications frequently: Cardiac Conduction, Cell Migration, Chemotaxis, Coagulation, Developmental Process, Embryo Development, Fibrinolysis, Gastrulation, Heart Formation, Localization, Lung Development, Ossification, Pathogenesis, Segmentation, Spermatogenesis, Swimming, Transport, Transposition, Tube Fusion, Vasoconstriction
Quite a number of genes have been found to play important roles in Dextrocardia, such as AMY2A, BLOC1S6, CFC1, CS, DNAH5, DNAI1, EPB42, GDF1, IGKV1-5, INVS, PAH, PCBD1, PRH1, TBX1, UVRAG, ZIC3. 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.