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Disease Info Card
Acanthocytosis
Information about Acanthocytosis: 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 Acanthocytosis
Most recent studies have shown that Acanthocytosis shares some biological mechanisms with abetalipoproteinemia, anemia, anemia-hemolytic, atrophy, blood-group-deletion-syndrome, chorea, chorea-acanthocytosis-syndrome, dyskinetic-syndrome, hematological-disease, hemolysis-(disorder), huntington-disease, liver-cirrhosis, liver-cirrhosis-alcoholic, liver-diseases, movement-disorders, muscular-atrophy, myopathy, nervous-system-disorder, retinitis-pigmentosa.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acanthocytosis, and have been seen in publications frequently: Aging, Anion Transport, Cation Transport, Cell Activation, Chemotaxis, Coagulation, Cytokinesis, Intestinal Absorption, Mitochondrial Depolarization, Muscle Atrophy, Pathogenesis, Phagocytosis, Pigmentation, Proteolysis, Reflex, Secretion, Sporulation, Sulfate Transport, Translation, Transport
Quite a number of genes have been found to play important roles in Acanthocytosis, such as APOB, CHKA, CHKB, CSF2, CYBB, HOXA10, HP, HTT, MT1B, MTTP, PANK2, PNLIP, VPS13A, XK. 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.