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Disease Info Card
Xerocytosis
Information about Xerocytosis: 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 Xerocytosis
Most recent studies have shown that Xerocytosis shares some biological mechanisms with anemia, anemia-hemolytic, anemia-hemolytic-congenital, anemia-hemolytic-congenital-nonspherocytic, anemia-sickle-cell, cholangiocarcinoma, dehydration, edema, elliptocytosis-hereditary, fetal-diseases, hematological-disease, hemolysis-(disorder), hemolytic-disorder, hereditary-diseases, hereditary-spherocytosis, hereditary-stomatocytosis, hydrops-fetalis, pseudohyperkalaemia, stomatocytic-anemia, thalassemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Xerocytosis, and have been seen in publications frequently: Aging, Cation Transport, Cell Development, Gas Transport, Hypersensitivity, Ion Transport, Localization, Locomotion, Proteolysis, Senescence, Transport
Quite a number of genes have been found to play important roles in Xerocytosis, such as ALB, ANK1, DHPS, EPB41, EPB42, GAPDH, GUSB, HPX, LYN, MSC, MTSS1, PIEZO1, SLC4A1, SPTA1, SPTB, STOM, UBL4A. 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.
Pathways Related to Xerocytosis
This information is being compiled and will come in a future update
| Aging | Cation Transport | Cell Development |
| Gas Transport | Hypersensitivity | Ion Transport |
| Localization | Locomotion | Proteolysis |
| Senescence | Transport |