Disease Info Card

Kartagener Syndrome

Information about Kartagener 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 Kartagener Syndrome

Most recent studies have shown that Kartagener Syndrome shares some biological mechanisms with bronchiectasis, bronchitis, chronic-sinusitis, ciliary-motility-disorders, coughing, cystic-fibrosis, dextrocardia, dyskinetic-syndrome, ear-inflammation, fibrosis, hereditary-diseases, infective-disorder, infertility, lung-diseases, male-infertility, otitis-media, pneumonia, respiratory-tract-infections, sinusitis, situs-inversus.

Among the many pathways, these few ones have gauged particular interests from scientists studying Kartagener Syndrome, and have been seen in publications frequently: Cell Activation, Cell Differentiation, Cell Motility, Chemotaxis, Excretion, Fertilization, Hypersensitivity, Insemination, Intraflagellar Transport, Ion Transport, Keratinization, Localization, Neutrophil Chemotaxis, Pathogenesis, Phagocytosis, Secretion, Sperm Motility, Spermatogenesis, Transport, Transposition

Quite a number of genes have been found to play important roles in Kartagener Syndrome, such as AK7, CCDC103, CFTR, COL18A1, DNAAF1, DNAH11, DNAH5, DNAH9, DNAI1, DNASE1, FEV, FOXJ1, IL13, NME8, NOS2, OXSM, PCBD1, RPGR, RSPH9. 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.