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Endosomal transmembrane epsin interactor 3 (ENTREP3)

Target
ENTREP3
Molecular classification
Other (protein coding; does not match classic families like GPCRs, transporters, or ion channels), Possible adaptor protein (based on homology to epsin family’s endocytic adaptors)
01

Overview

Endosomal transmembrane epsin interactor 3 is a protein encoded by the ENTREP3 gene[4][5]. It is described as a potential binding partner of a WW domain-containing protein involved in apoptosis and tumor suppression[4]. Its sequence and domain structure suggest possible analogy to the epsin family of endocytic adaptor proteins involved in protein trafficking, signaling, and potentially cell migration and invasion—although direct function and clinical relevance for ENTREP3 itself remain poorly characterized. Disease associations include some neoplasms and cancer phenotypes, but evidence is largely indirect or inferred from related proteins. Alternative splicing leads to multiple transcript variants[4]. No direct drug interactions or targeted therapeutics have been reported for this protein. \nIf you require more structured details or want to confirm specific disease or functional aspects (e.g., direct evidence for endocytosis or adaptor roles), more functional genomics or proteomics data may be necessary. Current public sources provide limited molecular characterization, largely associating the protein with potential protein-protein interactions and as a member of a family with disease relevance[4][3][6].

Other names
FAM189BC1orf2GC01M155261GC01M155307GC01M155371GC01M155420GC01M155488GC01M156440GC01M157760GC01M158824GC01M159913GC01M161107GC01M163975GC01M165115GC01M166340
02

Biological functions

Protein-protein interaction (described as binding partner for proteins involved in apoptosis and tumor suppression)May have roles in endocytosis or membrane traffic, given analogy to epsin adaptors, but direct evidence for ENTREP3 is lacking
03

Disease associations

Cancer (indirectly implicated based on analogy to other epsin family adaptors, which are upregulated in some cancers and affect migration/invasion)Spinal canal intradural extramedullary neoplasm (based on database association)Voyeurism (reported in GeneCards as an association, likely from phenome-wide studies, though poorly characterized)

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