Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55867
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 22 member 11
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC22A11
Synonyms (NCBI Gene) Gene synonyms aliases
OAT4, hOAT4
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.1
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and is found mainly in the kidney and in the placent
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1354297 hsa-miR-1207-5p CLIP-seq
MIRT1354298 hsa-miR-1321 CLIP-seq
MIRT1354299 hsa-miR-22 CLIP-seq
MIRT1354300 hsa-miR-3153 CLIP-seq
MIRT1354301 hsa-miR-3160-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005452 Function Solute:inorganic anion antiporter activity IDA 15037815
GO:0005515 Function Protein binding IPI 16236806
GO:0005886 Component Plasma membrane IDA 10660625
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607097 18120 ENSG00000168065
Protein
UniProt ID Q9NSA0
Protein name Solute carrier family 22 member 11 (Organic anion transporter 4) (OAT4) (Organic anion:dicarboxylate exchanger OAT4)
Protein function Antiporter that mediates the transport of conjugated steroids and other specific organic anions at the basal membrane of syncytiotrophoblast and at the apical membrane of proximal tubule epithelial cells, in exchange for anionic compounds (PubMe
PDB 8WJH
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00083 Sugar_tr 103 526 Sugar (and other) transporter Family
Tissue specificity TISSUE SPECIFICITY: Expressed in placental trophoblasts, syncytiotrophoblast and cytotrophoblast (PubMed:10660625, PubMed:12409283, PubMed:26277985). Also located in the proximal tubules in kidneys (PubMed:10660625, PubMed:15037815, PubMed:26277985). {ECO
Sequence
Sequence length 550
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Organic anion transport
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Gout Gout N/A N/A GWAS
Oligodendroglioma Oligodendroglioma N/A N/A GWAS
Systemic lupus erythematosus Systemic lupus erythematosus N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Inhibit 40023574
Glycosuria Renal Associate 24025986
Gout Associate 24025986, 24360580, 26290326, 38222853
Hyperuricemia Associate 38222853
Lupus Erythematosus Systemic Inhibit 40023574
Non alcoholic Fatty Liver Disease Associate 36328481