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Disease Info Card
Hartnup Disease
Information about Hartnup Disease: 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 Hartnup Disease
Most recent studies have shown that Hartnup Disease shares some biological mechanisms with amino-acid-metabolism-inborn-errors, aminoaciduria, ataxia, cerebellar-ataxia, cystinuria, dermatologic-disorders, exanthema, fanconi-syndrome, galactosemias, homocystinuria, inborn-errors-of-metabolism, kidney-diseases, malabsorption-syndrome, maple-syrup-urine-disease, metabolic-diseases, pellagra, phenylketonurias, photosensitivity-disorders, renal-aminoacidurias.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hartnup Disease, and have been seen in publications frequently: Aging, Amino Acid Homeostasis, Amino Acid Transport, Brain Development, Endocytosis, Excretion, Exocytosis, Glycolysis, Histidine Transport, Intestinal Absorption, Lactation, Neutral Amino Acid Transport, Pathogenesis, Peptide Transport, Pinocytosis, Reflex, Response To Food, Transpiration, Transport, Water Transport
Quite a number of genes have been found to play important roles in Hartnup Disease, such as ACE, ACE2, AGTR1, ATM, FGF3, MTOR, PAH, PHC2, SGK1, SLC15A1, SLC1A5, SLC33A1, SLC36A1, SLC6A19, SLC6A20, SLC6A9. 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.