CPO Gene - Carboxypeptidase O

A comprehensive resource on CPO gene, its function, expression, and associated diseases.

Gene Information Card

Symbol CPO
Full Name Carboxypeptidase O
Gene Type protein-coding
Chromosomal Location 2q33.1
NCBI Gene ID 130749 ncbi.nlm.nih.gov/gene/130749
Ensembl ID ENSG00000162909
UniProt ID Q8IVL8
OMIM ID 612726
HGNC ID 23279
Aliases CPO-1, MGC138290

Description

The CPO gene encodes carboxypeptidase O, a metallocarboxypeptidase that catalyzes the removal of C-terminal basic and hydrophobic amino acids from peptides. It is involved in protein digestion and peptide processing, primarily expressed in the small intestine and colon.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal cancer Altered CPO expression may affect peptide hormone processing and tumor microenvironment NCBI Gene, COSMIC
Inflammatory bowel disease Potential role in peptide metabolism and mucosal homeostasis NCBI Gene

Expression Profile

Tissue Expression
Tissue nTPM level
Small intestine 45.2 High
Colon 32.1 Medium
Stomach 18.7 Medium
Pancreas 12.3 Low
Liver 5.6 Low
Cell Line Expression
Cell Line nTPM Notes
Caco-2 52.3 Colorectal adenocarcinoma
HT-29 38.9 Colorectal adenocarcinoma
HCT 116 29.4 Colorectal carcinoma
SW480 25.1 Colorectal adenocarcinoma
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1045C>T (p.Arg349Trp) Missense <0.01% Unknown functional impact
c.1234G>A (p.Gly412Ser) Missense <0.01% Unknown functional impact
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in CPO.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in CPO.

Dominant Negative (DN)

No confirmed dominant-negative mutations reported in CPO.

Pathways

• Protein digestion and absorption (Reactome: R-HSA-8963748)
• Peptide hormone metabolism (Reactome: R-HSA-422085)

Protein Summary

Carboxypeptidase O is a secreted metallocarboxypeptidase that removes C-terminal basic and hydrophobic amino acids from peptides. It is highly expressed in the small intestine and colon, where it participates in the final stages of protein digestion and peptide processing. The enzyme requires zinc for catalytic activity and is involved in the metabolism of peptide hormones.

Related Products

Product name Cat.No. Species Gene ID
CPO Knockout HEK293 Cell Line EDJ-KQ9249 Human 130749 Details Get a Quote
CPO Knockout HeLa Cell Line EDJ-KQ58282 Human 130749 Details Get a Quote
CPO Knockout A-549 Cell Line EDJ-KQ66772 Human 130749 Details Get a Quote
CPO Knockout HCT 116 Cell Line EDJ-KQ75175 Human 130749 Details Get a Quote
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