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Disease Info Card
Deficiency Of Fructokinase
Information about Deficiency Of Fructokinase: 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 Deficiency Of Fructokinase
Most recent studies have shown that Deficiency Of Fructokinase shares some biological mechanisms with abdominal-bloating, anemia-sickle-cell, chronic-cholecystitis, diabetes-mellitus, diffuse-scleroderma, drug-induced-liver-injury, fructose-16-diphosphatase-deficiency, fructose-metabolism-disorder, hepatitis-a, hereditary-fructose-intolerance-syndrome, hypoglycemia, infective-disorder, liver-cirrhosis, liver-diseases, metabolic-diseases, pentosuria, pyoderma, rheumatism.
Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of Fructokinase, and have been seen in publications frequently: Blood Coagulation, Coagulation, Entner-doudoroff Pathway, Excretion, Pathogenesis, Transport
Quite a number of genes have been found to play important roles in Deficiency Of Fructokinase, such as ESR1, EXOSC10, G6PC, GPI, GSTP1, INS, KHK, MVD, PMP2, RPLP2, SERPINA1, SORD. 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 Deficiency Of Fructokinase
This information is being compiled and will come in a future update
| Blood Coagulation | Coagulation | Entner doudoroff Pathway |
| Excretion | Pathogenesis | Transport |