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Disease Info Card
Glutaric Aciduria, Type 1
Information about Glutaric Aciduria, Type 1: 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 Glutaric Aciduria, Type 1
Most recent studies have shown that Glutaric Aciduria, Type 1 shares some biological mechanisms with acidemia, acidosis, atrophy, brain-diseases-metabolic, brain-diseases-metabolic-inborn, brain-injuries, dystonia-disorders, encephalopathies, inborn-errors-of-metabolism, macrocephaly, metabolic-diseases, methylmalonic-acidemia, movement-disorders, multiple-acyl-coenzyme-a-dehydrogenase-deficiency, muscle-hypotonia, nerve-degeneration, nervous-system-disorder, neurotoxicity-syndromes.
Among the many pathways, these few ones have gauged particular interests from scientists studying Glutaric Aciduria, Type 1, and have been seen in publications frequently: Brain Development, Cell Death, Cell Migration, Cell Proliferation, Chemotaxis, Electron Transport, Excretion, Fatty Acid Oxidation, Fermentation, Membrane Depolarization, Mitosis, Myelination, Pathogenesis, Renal Tubular Secretion, Response To Anoxia, Secretion, Translation, Transport, Tricarboxylic Acid Cycle, Urea Cycle
Quite a number of genes have been found to play important roles in Glutaric Aciduria, Type 1, such as ACAA2, AGA, AMY2A, C2, CAT, CSF2, GCDH, GLS2, GLUD1, GRIN1, GRIN2B, H6PD, IL2, LAMC2, NDOR1, OTC, SLC1A3, UGDH, VEGFA. 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.