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Golgi integral membrane protein 4 (GOLIM4) is a type II transmembrane protein localized primarily to the Golgi apparatus, where it is involved in sorting and transport of proteins from the endoplasmic reticulum through the Golgi to other cellular locations. It acts as a scaffold protein facilitating the formation of secretory vesicles by interacting with other Golgi proteins such as ATP2C1 and GOLPH3. Its dysfunction is linked to rare diseases including congenital disorders of glycosylation and distal hereditary motor neuronopathies.
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