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Disease Info Card
Nonketotic Hyperglycinemia
Information about Nonketotic Hyperglycinemia: 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 Nonketotic Hyperglycinemia
Most recent studies have shown that Nonketotic Hyperglycinemia shares some biological mechanisms with apnea, brain-diseases, brain-diseases-metabolic, encephalopathies, epilepsies-myoclonic, epilepsy, hyperglycemia, hyperglycinemia, inborn-errors-of-metabolism, infantile-spasms, ketosis, lethargy, metabolic-diseases, muscle-hypotonia, myoclonus, nervousness, phenylketonurias, propionic-acidemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Nonketotic Hyperglycinemia, and have been seen in publications frequently: Brain Development, Conjugation, Electron Transport, Electron Transport Chain, Excretion, Fatty Acid Oxidation, Gluconeogenesis, Glycine Transport, Glycosylation, Localization, Myelination, Neurogenesis, Pathogenesis, Reflex, Secretion, Serotonin Uptake, Synaptic Transmission, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Nonketotic Hyperglycinemia, such as AMT, CSF2, DEFA1, DLD, ECHDC1, ELANE, GCLC, GCSH, GLDC, GYPC, LAMC2, MYBPH, OCA2, SLC6A9, SUOX, UGCG. 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.