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Disease Info Card
Deficiency Of Epimerase
Information about Deficiency Of Epimerase: 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 Epimerase
Most recent studies have shown that Deficiency Of Epimerase shares some biological mechanisms with amino-acid-metabolism-inborn-errors, atresia, classical-galactosemia, escherichia-coli-infections, failure-to-thrive, galactosemias, generalized-uridine-diphosphate-galactose-4-epimerase-deficiency, hyperammonemia, hypokinesia, icterus, inborn-errors-of-metabolism, learning-disorders, liver-diseases, mastitis-metritis-agalactia-syndrome, metabolic-acidosis, pancytopenia, pregnancy-complications, premature-menopause, udpglucose-4-epimerase-deficiency-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Deficiency Of Epimerase, and have been seen in publications frequently: Glycosylation, Proteolysis
Quite a number of genes have been found to play important roles in Deficiency Of Epimerase, such as APOA1, CAT, CBLB, CRAT, GAL, GALE, GALK1, GALT, GCSAM, GLYAT, KIT, MCEE, MMAA, MMAB, PON1, TYR. 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.
Pathways Related to Deficiency Of Epimerase
This information is being compiled and will come in a future update
| Glycosylation | Proteolysis |