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Disease Info Card
Deficiency Of Galactokinase
Information about Deficiency Of Galactokinase: 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 Galactokinase
Most recent studies have shown that Deficiency Of Galactokinase shares some biological mechanisms with blind-vision, cancer-patients-and-suicide-and-depression, cataract, classical-galactosemia, diabetes-mellitus, diseases-in-twins, disorder-of-galactose-metabolism, galactosemias, homocystinuria, inborn-errors-of-metabolism, influenza, lens-opacities, metabolic-diseases, phenylketonurias, pneumonia, salmonella-infections, sarcoma, tuberculosis, udpglucose-4-epimerase-deficiency-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of Galactokinase, and have been seen in publications frequently: Aging, Cell Growth, Dna Repair, Dna Replication, Excretion, Fermentation, Gluconeogenesis, Glycosylation, Hypersensitivity, Localization, Metaphase, Methylation, Regulation Of Gene Expression, Sos Response, Transcription Antitermination, Translation, Translational Initiation, Transport, Transposition, Virulence
Quite a number of genes have been found to play important roles in Deficiency Of Galactokinase, such as A4GALT, B3GALNT1, EXOSC10, GAL, GALE, GALK1, GALM, GALT, GCSAM, GLB1, IGHM, NUCKS1, PMEL, PRF1, PRM1, PSMD1, RHO, RPLP1, TK1, TKT. 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.