Golgin A8 family member R (GOLGA8R)

Golgin A8 family member R (GOLGA8R) is a protein encoded by the GOLGA8R gene and belongs to the golgin family of proteins localized to the Golgi apparatus[2][7]. It is predicted to be involved in the organization of the Golgi and is thought to be active in cis-Golgi networks and cisterna membranes, contributing to the maintenance of Golgi structure[2][6]. There is currently no evidence that GOLGA8R is a receptor, enzyme, or therapeutic target, nor are there known drugs or mechanisms of action described for this molecule[2][7]. Mutations or variants in GOLGA8R are associated with rare conditions such as paralytic squint and hypertropia, but it is not directly linked to common therapeutic disease indications[2].

Other names

Golgin subfamily A member 8RGOLGA8R