Target intelligence / Profile preview

Solute carrier family 22 member 23 (SLC22A23)

Target
SLC22A23
Molecular classification
Transporter, Solute carrier (SLC) family
01

Overview

Solute carrier family 22 member 23 (SLC22A23) is a transmembrane protein belonging to the organic ion transporter family, specifically the solute carrier (SLC) superfamily. SLC22A23 is considered an orphan transporter, meaning its endogenous substrate(s) and exact functional role remain uncharacterized. Genome-wide association studies have linked variants in SLC22A23 to drug-induced QT interval prolongation and susceptibility to intestinal inflammation such as ulcerative colitis. Its expression in heart tissue and implication in cardiac development suggest a role in modulating cardiac electrophysiology by regulating the movement of bioactive molecules. SLC22A23 may also impact gastrointestinal inflammatory diseases by altering the bioavailability or clearance of metabolic substrates relevant to inflammation.

Other names
C6orf85FLJ221743110004L20RikDKFZP434F011Nritpsolute carrier family 22, member 23S22AN_HUMAN
02

Biological functions

Transport of organic ions across cell membranes (potentially includes drugs, environmental toxins, and endogenous metabolites)Cardiac electrophysiology modulation (inferred from cardiac expression and GWAS links to QT prolongation)Possible influence on intestinal inflammatory processes
03

Disease associations

Cardiac arrhythmias (e.g., drug-induced QT prolongation)Inflammatory bowel disease (e.g., ulcerative colitis)Intestinal inflammation
04

Safety considerations

Potential for involvement in drug-induced cardiac arrhythmia (QT prolongation), based on genetic association studies
05

Biomarkers

SLC22A23 gene variants (e.g., SNP rs17309827-T) have been associated with drug-induced QT prolongation and risk for ulcerative colitis

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