Target intelligence / Profile preview

Exosomal polycystin-1-interacting protein (EPCIP)

Target
EPCIP
Molecular classification
Other (not classified as a receptor, ion channel, enzyme, transporter, transcription factor, etc.)
01

Overview

Exosomal polycystin-1-interacting protein (EPCIP) is a human protein encoded by the EPCIP gene, located on chromosome 21 at band q22.11[3]. It is expressed in brain and reproductive organs, including ovarian, testicular, prostate, pancreatic, and kidney tissues, with moderate expression in several adult organs[3]. EPCIP is known to be highly expressed in normal ovarian surface epithelial cells and not in their cancerous counterparts, and it is overexpressed in several tumor types, such as pancreatic, germ cell, and glioma tumors[3]. Although initially suggested to interact with polycystin-1 (PKD1), a protein involved in kidney development and polycystic kidney disease, the direct functional significance of EPCIP remains unclear[3][4]. It may be involved in mitochondrial dynamics—especially the detection and exocytosis of senescent mitochondria—potentially in collaboration with PKD1[4]. Interaction by text mining is noted with several other proteins, such as BNIPL (cell death), CRYBA2 (eye lens), SSX4 (transcriptional repressor), RXFP1/2 (hormone signaling), and others; however, specific biological functions or disease mechanisms are not well established for EPCIP[3]. There is currently no evidence supporting EPCIP as a therapeutic target, receptor, or druggable molecule, nor are there known drugs, biomarkers, or prominent safety issues associated with this protein[3][4].

Other names
EPCIPC21orf62C21orf120PRED81B37chromosome 21 open reading frame 62uncharacterized protein C21orf62polycystin-1-interacting protein 1
02

Biological functions

Other (specific function not well characterized; potentially involved in the detection, sequestration, and exocytosis of senescent mitochondria, and possibly interacts with polycystin-1 (PKD1))
03

Disease associations

Other (not directly linked as causal in any major disease, but is differentially regulated in several tumor types and absent in cancerous ovarian surface epithelial cells)

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