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Disease Info Card
Situs Inversus
Information about Situs Inversus: 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 Situs Inversus
Most recent studies have shown that Situs Inversus shares some biological mechanisms with accessory-spleen, atresia, bronchiectasis, ciliary-motility-disorders, congenital-abnormality, congenital-heart-defects, congenital-heart-disease, dextrocardia, dyskinetic-syndrome, heart-diseases, heart-septal-defects, kartagener-syndrome, levocardia, pulmonary-stenosis, pulmonary-valve-stenosis, sinusitis, situs-ambiguus, stenosis, transposition-of-great-vessels, ventricular-septal-defects.
Among the many pathways, these few ones have gauged particular interests from scientists studying Situs Inversus, and have been seen in publications frequently: Cell Division, Cell Proliferation, Chemotaxis, Dehiscence, Developmental Process, Gastrulation, Heart Development, Heart Looping, Intraflagellar Transport, Localization, Mating, Neural Tube Closure, Ossification, Pathogenesis, Secretion, Segmentation, Sperm Motility, Transport, Transposition, Tube Closure
Quite a number of genes have been found to play important roles in Situs Inversus, such as BLOC1S6, COL18A1, DNAH5, DNAI1, GDF1, INVS, LMLN, NODAL, OXSM, PCBD1, PITX2, PKD2, PMEL, SHH, SI, SS18L1, 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.