SLC22A11
Solute carrier family 22 member 11
Also known as: OAT4, S22AB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NSA0
- Gene
- SLC22A11
- Ensembl
- ENSG00000168065
- Chromosome
- 11
- Canonical length
- 550 aa
- Protein class
- FDA approved drug targets, Metabolic proteins, Plasma proteins, Predicted membrane proteins, Transporters
OverviewNCBI 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 placenta, where it may act to prevent potentially harmful organic anions from reaching the fetus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
Canonical amino-acid sequenceUniProt
550 residues, UniProt reviewed canonical sequence.
>Q9NSA0|SLC22A11
1 MAFSKLLEQA GGVGLFQTLQ VLTFILPCLM IPSQMLLENF SAAIPGHRCW THMLDNGSAV
61 STNMTPKALL TISIPPGPNQ GPHQCRRFRQ PQWQLLDPNA TATSWSEADT EPCVDGWVYD
121 RSVFTSTIVA KWDLVCSSQG LKPLSQSIFM SGILVGSFIW GLLSYRFGRK PMLSWCCLQL
181 AVAGTSTIFA PTFVIYCGLR FVAAFGMAGI FLSSLTLMVE WTTTSRRAVT MTVVGCAFSA
241 GQAALGGLAF ALRDWRTLQL AASVPFFAIS LISWWLPESA RWLIIKGKPD QALQELRKVA
301 RINGHKEAKN LTIEVLMSSV KEEVASAKEP RSVLDLFCVP VLRWRSCAML VVNFSLLISY
361 YGLVFDLQSL GRDIFLLQAL FGAVDFLGRA TTALLLSFLG RRTIQAGSQA MAGLAILANM
421 LVPQDLQTLR VVFAVLGKGC FGISLTCLTI YKAELFPTPV RMTADGILHT VGRLGAMMGP
481 LILMSRQALP LLPPLLYGVI SIASSLVVLF FLPETQGLPL PDTIQDLESQ KSTAAQGNRQ
541 EAVTVESTSLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC22A11 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 12
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 36 nTPM
Expression across tissuesHPA
Tissue
- kidney: 36 nTPM
- placenta: 31 nTPM
- epididymis: 10 nTPM
- liver: 0.3 nTPM
- adrenal gland: 0.1 nTPM
- choroid plexus: 0.1 nTPM
Single-cell type
- syncytiotrophoblasts: 2,300 nCPM
- cytotrophoblasts: 836 nCPM
- migrating cytotrophoblasts: 368 nCPM
- epididymal principal cells: 101 nCPM
- proximal tubule cells: 85 nCPM
- epididymal efferent duct absorptive cells: 44 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 0.2 nTPM
- basal ganglia: 0.1 nTPM
- cerebral cortex: 0.1 nTPM
- choroid plexus: 0.1 nTPM
- hippocampal formation: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.02
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- organic anion transmembrane transporter activity
- prostaglandin transmembrane transporter activity
- sodium-independent organic anion transmembrane transporter activity
- solute:inorganic anion antiporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC22A11 as an antibody target. Whether an autoantibody or antibody against SLC22A11 could matter depends on whether native SLC22A11 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC22A11 is annotated at the cell surface, where native SLC22A11 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label SLC22A11 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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