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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SLC28A2
solute carrier family 28 member 2
Chromosome 15 · 15q21.1
NCBI Gene: 9153Ensembl: ENSG00000137860.13HGNC: HGNC:11002UniProt: O43868
40PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
neurotransmitter transmembrane transporter activitypurine nucleobase transmembrane transporter activitynucleoside:sodium symporter activitypurine nucleoside transmembrane transporter activitykidney failurebenign neoplasm of eyeBarrett's esophagusesophageal adenocarcinoma
✦AI Summary

SLC28A2 (concentrative nucleoside transporter 2, CNT2) is a sodium-dependent, purine-selective transporter that mediates cellular uptake of purine nucleosides and uridine 1. The transporter exhibits N1/cif subtype characteristics, selectively recognizing purine nucleosides while showing preference for inosine, ribavirin, and uridine as substrates 234. SLC28A2 plays a critical role in purine nucleoside salvage pathways across tissues including kidney, intestine, and liver, contributing to nucleotide biosynthesis and regulating organic compound transport in specialized tissues 1. Genetic variants in SLC28A2 have significant clinical implications. Promoter polymorphisms, particularly rs2413775 (-146T>A), enhance transcriptional activity through altered hepatic nuclear factor 1 binding, potentially affecting nucleoside analog pharmacokinetics 5. In gout etiology, rs2271437 and rs16941238 variants associate with serum uric acid levels and hyperuricemia susceptibility in Han Chinese populations 6. Additionally, SLC28A2 rs11854484 genotypes predict clinically significant anemia in hepatitis C patients receiving protease inhibitor-ribavirin therapy 7. High SLC28A2 expression correlates with poor responses to neoadjuvant chemoradiotherapy in rectal cancer and serves as an independent prognostic marker for disease-specific survival 8. These findings establish SLC28A2 as both a nucleoside salvage facilitator and a genetic determinant of drug response and disease susceptibility.

Sources cited
1
SLC28A2 is a sodium-dependent, purine-nucleoside preferring concentrative transporter that mediates nucleoside salvage pathways
PMID: 12856181
2
SLC28A2 exhibits sodium-dependent purine-selective transport characteristics of the N1/cif subtype
PMID: 10087507
3
SLC28A2 plays critical role in uptake and salvage of purine nucleosides
PMID: 9435697
4
SLC28A2 functional variants show ethnic differences and variable substrate uptake capacity for inosine, ribavirin, and uridine
PMID: 17700367
5
SLC28A2 promoter variant rs2413775 (-146T>A) increases transcriptional activity through altered HNF1 transcription factor binding
PMID: 19098160
6
SLC28A2 variants rs16941238 and rs2271437 associate with serum uric acid levels, hyperuricemia, and gout susceptibility
PMID: 30679935
7
SLC28A2 rs11854484 TT genotype independently predicts clinically significant anemia in hepatitis C patients receiving protease inhibitor-ribavirin therapy
PMID: 26071337
8
High SLC28A2 expression correlates with poor neoadjuvant chemoradiotherapy response and is an independent prognostic factor for rectal cancer survival
PMID: 36244249
Disease Associationsⓘ20
kidney failureOpen Targets
0.24Weak
benign neoplasm of eyeOpen Targets
0.10Suggestive
Barrett's esophagusOpen Targets
0.07Suggestive
esophageal adenocarcinomaOpen Targets
0.04Suggestive
chronic kidney diseaseOpen Targets
0.04Suggestive
Crohn's diseaseOpen Targets
0.04Suggestive
Abnormality of the skeletal systemOpen Targets
0.03Suggestive
actinic keratosisOpen Targets
0.03Suggestive
colorectal cancerOpen Targets
0.03Suggestive
rectum cancerOpen Targets
0.02Suggestive
leukemiaOpen Targets
0.02Suggestive
goutOpen Targets
0.02Suggestive
myocardial infarctionOpen Targets
0.01Suggestive
colorectal carcinomaOpen Targets
0.01Suggestive
hyperuricemiaOpen Targets
0.01Suggestive
diabetes mellitusOpen Targets
0.01Suggestive
neoplasmOpen Targets
0.01Suggestive
gastric non-cardia carcinomaOpen Targets
0.01Suggestive
Miyoshi myopathyOpen Targets
0.01Suggestive
clear cell renal carcinomaOpen Targets
0.01Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
SLC22A1Protein interaction82%GATMProtein interaction79%SLC30A4Protein interaction79%SLC29A2Protein interaction78%SLC29A1Protein interaction77%DUOX1Protein interaction73%
Tissue Expression6 tissues
Brain
100%
Ovary
98%
Liver
75%
Lung
41%
Heart
19%
Bone Marrow
0%
Gene Interaction Network
Click a node to explore
SLC28A2SLC22A1GATMSLC30A4SLC29A2SLC29A1DUOX1
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt O43868
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.18LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.92 [0.72–1.18]
RankingsWhere SLC28A2 stands among ~20K protein-coding genes
  • #10,236of 20,598
    Most Researched40
  • #12,331of 17,882
    Most Constrained (LOEUF)1.18
Genes detectedSLC28A2
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Common variants in the
PMID: 30679935
Hereditas · 2019
1.00
2
Identification and characterization of proximal promoter polymorphisms in the human concentrative nucleoside transporter 2 (SLC28A2).
PMID: 19098160
J Pharmacol Exp Ther · 2009
0.90
3
Identification and functional analysis of variants in the human concentrative nucleoside transporter 2, hCNT2 (SLC28A2) in Chinese, Malays and Indians.
PMID: 17700367
Pharmacogenet Genomics · 2007
0.80
4
High SLC28A2 expression endows an inferior survival for rectal cancer patients managed by neoadjuvant CCRT.
PMID: 36244249
Pathol Res Pract · 2022
0.70
5
Role of ITPA and SLC28A2 genes in the prediction of anaemia associated with protease inhibitor plus ribavirin and peginterferon in hepatitis C treatment.
PMID: 26071337
J Clin Virol · 2015
0.60