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Disease Info Card
Cohen Syndrome
Information about Cohen 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 Cohen Syndrome
Most recent studies have shown that Cohen Syndrome shares some biological mechanisms with agranulocytosis, congenital-anomaly-of-face, craniofacial-abnormalities, developmental-delay-(disorder), developmental-disabilities, dwarfism, dystrophy, eye-abnormalities, hereditary-diseases, microcephaly, muscle-hypotonia, myopia, obesity, obesity-abdominal, prader-willi-syndrome, retinal-degeneration, retinal-diseases, retinitis-pigmentosa.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cohen Syndrome, and have been seen in publications frequently: Cell Adhesion, Coagulation, Cytokinesis, Dna Methylation, Excretion, Golgi Organization, Intracellular Protein Transport, Localization, Methylation, Neutrophil Activation, Pathogenesis, Protein Transport, Sporulation, Transport
Quite a number of genes have been found to play important roles in Cohen Syndrome, such as ADSL, CS, ERG, G6PC, INS, ITGAL, ITGAM, MB, MRPL28, MTSS1, PLOD1, SELL, VPS13A, VPS13B, VPS13C, VPS13D, ZFPM2. 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.