ST3 beta-galactoside alpha-2,3-sialyltransferase 5, also known as ST3GAL5, is a human gene.cite web | title = Entrez Gene: ST3GAL5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5| url =| accessdate = ]

section_title =
summary_text = Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene.cite web | title = Entrez Gene: ST3GAL5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5| url =| accessdate = ]


Further reading

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