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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SLC26A11
solute carrier family 26 member 11
Chromosome 17 · 17q25.3
NCBI Gene: 284129Ensembl: ENSG00000181045.17HGNC: HGNC:14471UniProt: Q86WA9
19PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
sulfate transmembrane transportprotein bindingplasma membranelysosomal membranemucopolysaccharidosis type 3Aalcohol drinkinggenetic disordermucopolysaccharidosis type 3
✦AI Summary

SLC26A11 is a multifunctional anion transporter that operates as both an anion exchanger and chloride channel across various tissues. The protein mediates sodium-independent sulfate transport and may cooperate with SLC26A2 to facilitate DIDS-sensitive sulfate uptake in high endothelial venules endothelial cells 1. In the central nervous system, SLC26A11 is abundantly expressed in Purkinje cells of the cerebellum and functions as a voltage-gated chloride channel activated upon neuronal depolarization to membrane potentials below -20 mV 2 3. The protein plays a critical role in neuronal volume regulation, as chloride entry via SLC26A11 following sodium influx leads to cytotoxic neuronal swelling and cell death during brain injury 3. Additionally, SLC26A11 stimulates vacuolar H+-ATPase activity, suggesting involvement in cellular acid-base regulation 2. The gene is expressed in kidney, brain, and placenta, with potential roles in renal physiology that remain to be fully characterized 1 4. Clinically, SLC26A11 has been identified in gene fusions associated with chr17 myeloid leukemia and sarcomas, though the functional significance of these alterations requires further investigation 5 6.

Sources cited
1
SLC26A11 exhibits sodium-independent sulfate transport activity and may cooperate with SLC26A2 in high endothelial venules
PMID: 12626430
2
SLC26A11 is abundantly expressed in Purkinje cells and functions as a chloride channel that stimulates V H+-ATPase
PMID: 23733100
3
SLC26A11 acts as a voltage-gated chloride channel activated below -20 mV and mediates cytotoxic neuronal swelling
PMID: 25910210
4
SLC26A11 is expressed in kidney with potential roles in renal physiology
PMID: 17071331
5
RNF213-SLC26A11 gene fusion identified in chronic myeloid leukemia
PMID: 23151810
6
RNF213-SLC26A11 gene fusion found in BCOR-CCNB3 sarcoma
PMID: 35568949
Disease Associationsⓘ20
mucopolysaccharidosis type 3AOpen Targets
0.55Moderate
alcohol drinkingOpen Targets
0.25Weak
genetic disorderOpen Targets
0.15Weak
mucopolysaccharidosis type 3Open Targets
0.12Weak
attention deficit hyperactivity disorderOpen Targets
0.07Suggestive
hereditary attention deficit-hyperactivity disorderOpen Targets
0.06Suggestive
strokeOpen Targets
0.05Suggestive
attention deficit-hyperactivity disorder 8Open Targets
0.05Suggestive
Benign familial choreaOpen Targets
0.05Suggestive
intellectual disability, autosomal recessive 59Open Targets
0.05Suggestive
schizophrenia 15Open Targets
0.05Suggestive
Tourette syndromeOpen Targets
0.05Suggestive
neurodevelopmental disorder with microcephaly, hypotonia, and absent languageOpen Targets
0.05Suggestive
autismOpen Targets
0.05Suggestive
epilepsy, progressive myoclonic, 12Open Targets
0.04Suggestive
Phelan-McDermid syndromeOpen Targets
0.04Suggestive
neurodevelopmental disorder with hypotonia and gross motor and speech delayOpen Targets
0.04Suggestive
Potocki-Lupski syndromeOpen Targets
0.03Suggestive
X-linked non-syndromic intellectual disabilityOpen Targets
0.03Suggestive
X-linked dominant intellectual disability - epilepsy syndromeOpen Targets
0.03Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
SGSHProtein interaction76%SLC26A8Shared pathway60%SLC26A2Shared pathway50%SLC26A4Shared pathway50%SLC26A1Shared pathway50%SLC26A9Shared pathway43%
Tissue Expression6 tissues
Ovary
100%
Lung
74%
Bone Marrow
64%
Liver
47%
Brain
46%
Heart
21%
Gene Interaction Network
Click a node to explore
SLC26A11SGSHSLC26A8SLC26A2SLC26A4SLC26A1SLC26A9
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q86WA9
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.21LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.97 [0.79–1.21]
RankingsWhere SLC26A11 stands among ~20K protein-coding genes
  • #14,540of 20,598
    Most Researched19
  • #12,701of 17,882
    Most Constrained (LOEUF)1.21
Genes detectedSLC26A11
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
β-Elemene induced ferroptosis via TFEB-mediated GPX4 degradation in EGFR wide-type non-small cell lung cancer.
PMID: 37689240
J Adv Res · 2024
1.00
2
Slc26a11 is prominently expressed in the brain and functions as a chloride channel: expression in Purkinje cells and stimulation of V H⁺-ATPase.
PMID: 23733100
Pflugers Arch · 2013
0.90
3
The cellular mechanisms of neuronal swelling underlying cytotoxic edema.
PMID: 25910210
Cell · 2015
0.80
4
Renal physiology of SLC26 anion exchangers.
PMID: 17693766
Curr Opin Nephrol Hypertens · 2007
0.70
5
Molecular and functional characterization of SLC26A11, a sodium-independent sulfate transporter from high endothelial venules.
PMID: 12626430
FASEB J · 2003
0.60