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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SLC7A13
solute carrier family 7 member 13
Chromosome 8 · 8q21.3
NCBI Gene: 157724Ensembl: ENSG00000164893.9HGNC: HGNC:23092UniProt: Q8TCU3
10PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
plasma membraneamino acid transmembrane transportL-amino acid transmembrane transporter activityaspartate transmembrane transportovarian neoplasmmathematical abilitygram-positive bacterial infectionsAbnormality of the gastrointestinal tract
✦AI Summary

SLC7A13 (solute carrier family 7 member 13), also known as AGT1, encodes a light-chain subunit that associates with SLC3A1/rBAT to form a functional heterodimeric cystine transporter 1. This complex mediates exchange transport of anionic and neutral amino acids, particularly L-cystine, across the apical plasma membrane of renal epithelial cells in the S3 segment (late proximal tubules), exchanging luminal cystine for cytosolic glutamate or aspartate 1. While initially proposed as a cystinuria candidate gene, SLC7A13 mutations do not appear to be causative in most patients without SLC3A1/SLC7A9 mutations 23, though potential modulatory roles remain unexplored 3. Beyond renal physiology, SLC7A13 has emerged as clinically significant in cancer biology. Gene amplification and overexpression occur in ~20-50% of breast cancers and associate with worse survival in luminal subtypes 4. SLC7A13 overexpression promotes cystine uptake and glutathione biosynthesis, reducing oxidative stress and ferroptosis-induced cell death 4. The cryo-EM structure reveals a dimer-of-heterodimers architecture with a substrate-binding pocket suitable for therapeutic targeting 4. SLC7A13 is also identified as part of differentially expressed gene networks in polycystic kidney disease and represents a therapeutic target in hepatocellular carcinoma via ferroptosis induction 56.

Sources cited
1
SLC7A13/AGT1 forms a heterodimer with rBAT/SLC3A1 in the S3 segment of renal proximal tubules and mediates cystine, aspartate, and glutamate transport
PMID: 26739563
2
SLC7A13 is amplified and overexpressed in ~20-50% of breast cancers, associates with worse survival in luminal subtypes, and promotes cystine uptake and GSH biosynthesis to prevent ferroptosis
PMID: 40916662
3
SLC7A13 mutations are not a relevant cause of cystinuria in patients negative for SLC3A1 and SLC7A9 mutations
PMID: 30342472
4
SLC7A13 variants in heterozygous states show no correlation with cystinuria lithiasis phenotypes in patients, though homozygous pathogenic variants cannot be excluded
PMID: 38138969
5
SLC7A13 is identified as a differentially expressed gene in polycystic kidney disease associated with ciliogenesis-related signaling pathways
PMID: 34469896
6
SLC7A13 inhibition in the SLC7A13/GSH/GPX4 pathway induces ferroptosis in hepatocellular carcinoma cells
PMID: 41586895
Disease Associationsⓘ20
ovarian neoplasmOpen Targets
0.27Weak
mathematical abilityOpen Targets
0.17Weak
gram-positive bacterial infectionsOpen Targets
0.13Weak
Abnormality of the gastrointestinal tractOpen Targets
0.11Weak
cystinuriaOpen Targets
0.09Suggestive
clear cell renal carcinomaOpen Targets
0.07Suggestive
goutOpen Targets
0.05Suggestive
papillary renal cell carcinomaOpen Targets
0.04Suggestive
COVID-19Open Targets
0.04Suggestive
breast carcinomaOpen Targets
0.04Suggestive
severe acute respiratory syndromeOpen Targets
0.03Suggestive
hidradenitisOpen Targets
0.02Suggestive
kidney oncocytomaOpen Targets
0.02Suggestive
chromophobe renal cell carcinomaOpen Targets
0.02Suggestive
breast cancerOpen Targets
0.02Suggestive
primary hyperoxaluria type 1Open Targets
0.01Suggestive
colorectal cancerOpen Targets
0.01Suggestive
coronary artery diseaseOpen Targets
0.01Suggestive
glioblastomaOpen Targets
0.00Suggestive
nonpapillary renal cell carcinomaOpen Targets
0.00Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
SLC7A3Protein interaction76%SLC3A1Protein interaction68%SLC38A11Shared pathway40%SLC38A8Shared pathway40%SLC38A10Shared pathway40%SLC7A9Shared pathway33%
Tissue Expression6 tissues
Brain
100%
Liver
80%
Lung
0%
Bone Marrow
0%
Heart
0%
Ovary
0%
Gene Interaction Network
Click a node to explore
SLC7A13SLC7A3SLC3A1SLC38A11SLC38A8SLC38A10SLC7A9
PROTEIN STRUCTURE
Preparing viewer…
PDB8WK6 · 2.64 Å · EM
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
1.27LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.95 [0.71–1.27]
RankingsWhere SLC7A13 stands among ~20K protein-coding genes
  • #17,176of 20,598
    Most Researched10
  • #13,427of 17,882
    Most Constrained (LOEUF)1.27
Genes detectedSLC7A13
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Oncogenic role of the SLC7A13-SLC3A1 cystine transporter in human luminal breast cancer and its cryo-EM structure.
PMID: 40916662
Protein Cell · 2026
1.00
2
The genetics of cystinuria - an update and critical reevaluation.
PMID: 38240263
Curr Opin Nephrol Hypertens · 2024
0.90
3
Channels, transporters and receptors for cadmium and cadmium complexes in eukaryotic cells: myths and facts.
PMID: 30701379
Biometals · 2019
0.80
4
Exploring the Contribution of the Transporter AGT1/rBAT in Cystinuria Progression: Insights from Mouse Models and a Retrospective Cohort Study.
PMID: 38138969
Int J Mol Sci · 2023
0.70
5
Novel cystine transporter in renal proximal tubule identified as a missing partner of cystinuria-related plasma membrane protein rBAT/SLC3A1.
PMID: 26739563
Proc Natl Acad Sci U S A · 2016
0.60