SLC22A3

Gene symbol SLC22A3
Aliases -
Protein Name Solute carrier family 22 member 3
Function SLC22A3 is a metastasis suppressor in ESCC, and deregulation of SLC22A3 facilitates cell invasion and filopodia formation by reducing its direct association with α-actinin-4 (ACTN4), leading to the increased actin-binding activity of ACTN4 in normal esophageal cells.
Species Human
Editing Sites 1
Disease Esophageal Squamous Cell Carcinoma;
Description A-to-I RNA editing may decrease the stability of SLC22A3 in familial cases, deregulated SLC22A3 Is an Early Risk Factor for Progression of Familial ESCC.
RADR RADAR
REDIportal REDI portal
External links O75751(Uniport); NM_021977 (NM id); 6581 (NCBI gene id); GeneCard; GTEx
Sequence

Editing sites

Enzyme Editing type Region AA Seq Position NT Seq Position Codon Change Amino Acid Change Molecular Consequence Editing Level Tissue Editing Effect Phenotype Disease name PMID
  • ADAR2
A-to-I CDS 71 261 AAC->GAC N->D Nonsynonymous substitution Present Esophageal tissues A-to-I RNA editing may decrease the stability of SLC22A3 in familial cases. Promote the tumor progression and malignant development