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Disease Info Card
Propionic Acidemia
Information about Propionic Acidemia: 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 Propionic Acidemia
Most recent studies have shown that Propionic Acidemia shares some biological mechanisms with acidemia, acidosis, citrullinemia, comatose, hyperammonemia, hyperglycinemia, inborn-errors-of-metabolism, isovaleryl-coa-dehydrogenase-deficiency, ketosis, maple-syrup-urine-disease, mastitis-metritis-agalactia-syndrome, metabolic-acidosis, metabolic-diseases, methylmalonic-acidemia, muscle-hypotonia, nonketotic-hyperglycinemia, phenylketonurias, vomiting.
Among the many pathways, these few ones have gauged particular interests from scientists studying Propionic Acidemia, and have been seen in publications frequently: Aerobic Respiration, Amino Acid Transport, Anaerobic Respiration, Brain Development, Cell Death, Electron Transport, Excretion, Fatty Acid Oxidation, Histone Acetylation, Hyperphosphorylation, Localization, Myelination, Oxidative Phosphorylation, Pathogenesis, Protein Phosphorylation, Rumination, Translation, Transport, Tricarboxylic Acid Cycle, Urea Cycle
Quite a number of genes have been found to play important roles in Propionic Acidemia, such as ACAA1, ACAA2, AMY2A, BLOC1S6, BTD, C2, CSF2, ECHDC1, EPB42, HMGCL, INS, LAMC2, MMD, OTC, PCCA, PCCB, PRH1, QPCT. 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.