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A related pseudogene has been identified on chromosome 1

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Mutations in this gene are associated with Barrett esophagus and esophageal adenocarcinoma

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PEX16 Polyclonal Antibody, 20ul Buffer Solutions Don't settle for anything lessThe protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two