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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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SLC22A13
solute carrier family 22 member 13
Chromosome 3 · 3p22.2
NCBI Gene: 9390Ensembl: ENSG00000172940.13HGNC: HGNC:8494UniProt: Q9Y226
22PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
urate transmembrane transporter activityplasma membraneendoplasmic reticulumGolgi apparatusVertigononpapillary renal cell carcinomaneoplasmpancreatic adenocarcinoma
✦AI Summary

SLC22A13 (OAT10) is an organic anion antiporter that mediates bidirectional transport of urate, orotate, and nicotinate across cell membranes 1. In the kidney, SLC22A13 localizes to the apical membrane of proximal tubule epithelial cells where it functions as a renal urate reabsorber, transporting urate from the tubular lumen in exchange for organic anions such as lactate and glutathione 2. The transporter also localizes to the basolateral membrane of type A intercalated cells in the collecting duct, where it mediates unidirectional efflux of aspartate and glutamate 3. Transport of urate and orotate is chloride-dependent 42. SLC22A13 exhibits similar transport characteristics to URAT1 (SLC22A12) and may compensate for URAT1 dysfunction under certain conditions. Functionally, SLC22A13 can be physically coupled to monocarboxylate transporter MCT1, affecting its substrate selectivity 5. Clinically, loss-of-function variants (rs117371763, p.R377C and p.R16H) are associated with reduced serum urate levels and increased renal urate excretion, providing protection against gout 26. Reduced SLC22A13 expression correlates with advanced clinical stage and poor prognosis in clear cell renal cell carcinoma 7. As a renal urate reabsorber, SLC22A13 represents a potential pharmacological target for urate-lowering therapy, with some uricosuric drugs like losartan and lesinurad showing inhibitory effects 2.

Sources cited
1
SLC22A13 is an organic anion transporter mediating urate and nicotinate transport via anion exchange; expressed in kidney, brain, heart, and intestine
PMID: 18411268
2
SLC22A13 acts as a renal urate reabsorber in proximal tubular apical membrane; loss-of-function variants associated with lower serum urate and protection against gout; inhibited by uricosuric drugs losartan and lesinurad
PMID: 35462902
3
SLC22A13 localizes to basolateral membrane of type A intercalated cells; mediates unidirectional efflux of aspartate and glutamate
PMID: 24147638
4
SLC22A13 is physically coupled with MCT1 transporter, affecting apparent substrate selectivity and transport function
PMID: 35926947
5
Rare SLC22A13 variants p.R16H and p.R102H significantly reduce urate transport activity in functional assays
PMID: 38222853
6
SLC22A13 expression is significantly reduced in clear cell renal cell carcinoma and correlates with clinical stage and survival
PMID: 32461965
Disease Associationsⓘ20
VertigoOpen Targets
0.27Weak
nonpapillary renal cell carcinomaOpen Targets
0.06Suggestive
neoplasmOpen Targets
0.05Suggestive
pancreatic adenocarcinomaOpen Targets
0.03Suggestive
breast carcinomaOpen Targets
0.03Suggestive
kidney neoplasmOpen Targets
0.02Suggestive
goutOpen Targets
0.02Suggestive
clear cell renal carcinomaOpen Targets
0.02Suggestive
cancerOpen Targets
0.02Suggestive
hyperuricemiaOpen Targets
0.01Suggestive
IGA glomerulonephritisOpen Targets
0.01Suggestive
hypouricemia, renalOpen Targets
0.00Suggestive
acidosisOpen Targets
0.00Suggestive
carcinomaOpen Targets
0.00Suggestive
kidney cancerOpen Targets
0.00Suggestive
prostate cancerOpen Targets
0.00Suggestive
renal carcinomaOpen Targets
0.00Suggestive
HyperinsulinemiaOpen Targets
0.00Suggestive
Alzheimer diseaseOpen Targets
0.00Suggestive
Insulin resistanceOpen Targets
0.00Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
XYLBProtein interaction91%OXSR1Protein interaction84%SLC17A3Protein interaction82%SLC2A9Protein interaction60%SLC17A1Protein interaction52%NAPRTShared pathway25%
Tissue Expression6 tissues
Bone Marrow
100%
Lung
71%
Liver
59%
Ovary
35%
Brain
6%
Heart
0%
Gene Interaction Network
Click a node to explore
SLC22A13XYLBOXSR1SLC17A3SLC2A9SLC17A1NAPRT
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q9Y226
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.03LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.79 [0.62–1.03]
RankingsWhere SLC22A13 stands among ~20K protein-coding genes
  • #13,738of 20,598
    Most Researched22
  • #10,247of 17,882
    Most Constrained (LOEUF)1.03
Genes detectedSLC22A13
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Examining the Association of Rare Allelic Variants in Urate Transporters
PMID: 38222853
Dis Markers · 2024
1.00
2
The SLC Family Are Candidate Diagnostic and Prognostic Biomarkers in Clear Cell Renal Cell Carcinoma.
PMID: 32461965
Biomed Res Int · 2020
0.90
3
27-Hydroxycholesterol regulates human SLC22A12 gene expression through estrogen receptor action.
PMID: 33368618
FASEB J · 2021
0.80
4
SLC22A13 catalyses unidirectional efflux of aspartate and glutamate at the basolateral membrane of type A intercalated cells in the renal collecting duct.
PMID: 24147638
Biochem J · 2014
0.70
5
Functional coupling of organic anion transporter OAT10 (SLC22A13) and monocarboxylate transporter MCT1 (SLC16A1) influencing the transport function of OAT10.
PMID: 35926947
J Pharmacol Sci · 2022
0.60