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Disease Info Card
Deficiency Of Glycerol Kinase
Information about Deficiency Of Glycerol Kinase: 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 Deficiency Of Glycerol Kinase
Most recent studies have shown that Deficiency Of Glycerol Kinase shares some biological mechanisms with acidemia, adrenal-gland-hypofunction, congenital-absence-of-adrenal-gland, congenital-hypoplasia-of-adrenal-gland, developmental-delay-(disorder), dystrophy, genetic-diseases-x-linked, growth-disorders, hypoglycemia, hypogonadism, hypogonadotropic-hypogonadism, hypoplasia, inborn-errors-of-metabolism, muscle-hypotonia, muscular-dystrophy, muscular-dystrophy-duchenne, myopathy, ocular-albinism-type-ii, sex-chromosome-aberrations.
Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of Glycerol Kinase, and have been seen in publications frequently: Diuresis, Dna Amplification, Electron Transport, Excretion, Eye Pigmentation, Fatty Acid Oxidation, Glucocorticoid Secretion, Gluconeogenesis, Glucose Homeostasis, Glycerol Transport, Glycolysis, Hypersensitivity, Interphase, Pathogenesis, Pigmentation, Rna Processing, Secretion, Transport
Quite a number of genes have been found to play important roles in Deficiency Of Glycerol Kinase, such as C7, CDKN1A, CXCL10, DMD, GCK, GK, IGF1, IL1RAPL1, INS, MYOD1, MYOG, NR0B1, NSG1, OTC, POMC, PPARA, PTER, TCEAL1, TG. 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.