This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Holt-oram Syndrome
Information about Holt-oram Syndrome: 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 Holt-oram Syndrome
Most recent studies have shown that Holt-oram Syndrome shares some biological mechanisms with anemia, aplasia-nos, atrial-septal-defects, cardiac-arrhythmia, congenital-abnormality, congenital-hand-deformities, congenital-heart-defects, congenital-heart-disease, cytogenetic-abnormality, hand-deformities-acquired, haploinsufficiency, heart-block, heart-diseases, heart-septal-defects, hypoplasia, limb-defect, limb-deformities-congenital, patent-ductus-arteriosus, ventricular-septal-defects.
Among the many pathways, these few ones have gauged particular interests from scientists studying Holt-oram Syndrome, and have been seen in publications frequently: Cardiac Conduction, Cell Growth, Cell Migration, Cell Proliferation, Chondrocyte Differentiation, Fertilization, Fin Development, Heart Development, Heart Formation, Heart Morphogenesis, Induction Of Apoptosis, Limb Development, Limb Morphogenesis, Localization, Mesoderm Formation, Ossification, Paraxial Mesoderm Formation, Pathogenesis, Pectoral Fin Development, Transposition
Quite a number of genes have been found to play important roles in Holt-oram Syndrome, such as BMP4, FBXW11, GATA4, GJA5, HESX1, MYH6, NKX2-5, NPPA, PCNA, PGD, PGR, PSMD9, SALL4, SRSF2, TBX1, TBX3, TBX5. 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.