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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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SLC22A9
solute carrier family 22 member 9
Chromosome 11 · 11q12.3
NCBI Gene: 114571Ensembl: ENSG00000149742.11HGNC: HGNC:16261UniProt: Q8IVM8
29PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingsecondary active transmembrane transporter activityshort-chain fatty acid transmembrane transporter activitytransmembrane transporter activityAbnormal erythrocyte morphologychronic intestinal vascular insufficiencyovarian neoplasmmale reproductive organ cancer
✦AI Summary

SLC22A9 encodes organic anion transporter 7 (OAT7), a sodium-independent hepatic membrane transporter with high specificity for sulfated conjugates of xenobiotics and steroid hormones, particularly estrone 3-sulfate and dehydroepiandrosterone sulfate 1. The transporter is uniquely activated by short-chain fatty acids including propionate, butyrate, and valerate, and may operate an exchange mechanism between sulfated organic components and short-chain fatty acids at the hepatocyte sinusoidal membrane 1. OAT7 transports the statin pravastatin and may contribute to its hepatic disposition when other organic anion transporting polypeptides are compromised 1. Recent studies have identified SLC22A9 as a transporter for the thyroid hormone analog TRIAC, with uptake inhibited by the known substrate estrone-3-sulfate 2. The transporter exhibits substantial inter-individual variability in hepatic expression (28-fold mRNA, 15-fold protein), primarily regulated by hepatic nuclear factor 4-alpha (HNF4α) 1. Genome-wide association studies have linked SLC22A9 variants to total thyroid hormone levels and renal urate handling, suggesting broader physiological roles beyond xenobiotic transport 34. However, variants do not appear to significantly impact osteoporosis risk in Europeans 5.

Sources cited
1
OAT7 is a sodium-independent transporter with specificity for sulfated conjugates, transports pravastatin, activated by short-chain fatty acids, and shows variable hepatic expression regulated by HNF4α
PMID: 26239079
2
SLC22A9 transports TRIAC with uptake inhibited by estrone-3-sulfate
PMID: 38801167
3
GWAS identified association between SLC22A9 variants and total thyroid hormone levels
PMID: 30824882
4
SLC22A9 variants associated with renal urate handling in Chinese men with gout
PMID: 35264217
5
SLC22A9 variants do not significantly impact osteoporosis risk in Europeans
PMID: 33013684
Disease Associationsⓘ20
Abnormal erythrocyte morphologyOpen Targets
0.28Weak
chronic intestinal vascular insufficiencyOpen Targets
0.27Weak
ovarian neoplasmOpen Targets
0.24Weak
male reproductive organ cancerOpen Targets
0.23Weak
ovarian dysfunctionOpen Targets
0.05Suggestive
glycoprotein storage diseaseOpen Targets
0.05Suggestive
central nervous system cancerOpen Targets
0.05Suggestive
neuronal ceroid lipofuscinosis 1Open Targets
0.04Suggestive
hemoglobin H diseaseOpen Targets
0.04Suggestive
Hemoglobin C - beta-thalassemiaOpen Targets
0.04Suggestive
hemoglobin C-beta-thalassemia syndromeOpen Targets
0.04Suggestive
combined immunodeficiency due to OX40 deficiencyOpen Targets
0.04Suggestive
coronary artery calcificationOpen Targets
0.04Suggestive
Abnormality of the skeletal systemOpen Targets
0.04Suggestive
familial isolated congenital aspleniaOpen Targets
0.04Suggestive
Hyperlipoproteinemia type 1Open Targets
0.04Suggestive
dominant beta-thalassemiaOpen Targets
0.04Suggestive
Felty's syndromeOpen Targets
0.04Suggestive
osteoporosisOpen Targets
0.04Suggestive
erythroleukemia, familial, susceptibility toOpen Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
SLC47A2Protein interaction77%SLCO2B1Protein interaction77%SLC47A1Protein interaction77%SLC2A9Protein interaction74%ABCC4Protein interaction72%SLCO1A2Protein interaction63%
Tissue Expression6 tissues
Liver
100%
Brain
2%
Bone Marrow
0%
Lung
0%
Ovary
0%
Heart
0%
Gene Interaction Network
Click a node to explore
SLC22A9SLC47A2SLCO2B1SLC47A1SLC2A9ABCC4SLCO1A2
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q8IVM8
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.46LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF1.16 [0.94–1.46]
RankingsWhere SLC22A9 stands among ~20K protein-coding genes
  • #12,233of 20,598
    Most Researched29
  • #14,938of 17,882
    Most Constrained (LOEUF)1.46
Genes detectedSLC22A9
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Identification of Human TRIAC Transmembrane Transporters.
PMID: 38801167
Thyroid · 2024
1.00
2
Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population.
PMID: 30824882
J Hum Genet · 2019
0.90
3
The Membrane Transporter OAT7 (SLC22A9) Is Not a Susceptibility Factor for Osteoporosis in Europeans.
PMID: 33013684
Front Endocrinol (Lausanne) · 2020
0.80
4
Rifampin Regulation of Drug Transporters Gene Expression and the Association of MicroRNAs in Human Hepatocytes.
PMID: 27199754
Front Pharmacol · 2016
0.70
5
The clinical and genetic spectrum of paediatric speech and language disorders.
PMID: 39412438
Brain · 2025
0.60