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Disease Info Card
Purine Metabolism Disorder
Information about Purine Metabolism Disorder: 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 Purine Metabolism Disorder
Most recent studies have shown that Purine Metabolism Disorder shares some biological mechanisms with adenosine-deaminase-deficiency, adenylosuccinate-lyase-deficiency-(disorder), arthritis, gout, hereditary-diseases, hereditary-xanthinuria, hyperuricemia, immunologic-deficiency-syndromes, inborn-errors-of-metabolism, kidney-calculi, kidney-diseases, lesch-nyhan-syndrome, lithiasis, metabolic-diseases, muscle-spasticity, nervousness, urolithiasis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Purine Metabolism Disorder, and have been seen in publications frequently: Cell Proliferation, Excretion, Myelination, Ossification, Pathogenesis, Synaptic Transmission, Urea Cycle
Quite a number of genes have been found to play important roles in Purine Metabolism Disorder, such as ADA, ADSL, APRT, BRAP, HPRT1, IMPA1, INS, NT5E, PNP, PPY, PRPS1, PRPS1L1, RAPGEF5, TH, XDH. 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 Purine Metabolism Disorder
This information is being compiled and will come in a future update
| Cell Proliferation | Excretion | Myelination |
| Ossification | Pathogenesis | Synaptic Transmission |
| Urea Cycle |