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Synapse differentiation-inducing gene protein 1-like (SYNDIG1L) is a human transmembrane protein encoded by the SYNDIG1L gene, also known as TMEM90A, Capucin, and other aliases[8][6]. SYNDIG1L is predicted to be located in cellular membranes and the Golgi apparatus, similar to other dispanin family members. Its biological function is not fully characterized; however, it is closely related to SYNDIG1, which regulates AMPA receptor content and is involved in synapse maturation and development in the brain[1]. Currently, there is no direct evidence linking SYNDIG1L itself as a therapeutic target or receptor for drugs, nor are there established interacting drugs, biomarkers, or safety concerns associated with this protein[8]. Diseases genetically associated with SYNDIG1L include osteogenesis imperfecta and ovary sarcoma[8].
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