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Overview
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Background
COPG2 (COPI Coat Complex Subunit Gamma 2) is a Protein Coding gene. Diseases associated with COPG2 include Silver-Russell Syndrome 1 and Autism. Among its related pathways are Transport to the Golgi and subsequent modification and Metabolism of proteins. Gene Ontology (GO) annotations related to this gene include binding and structural molecule activity. An important paralog of this gene is COPG1.
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