SLC22A9
Organic anion transporter 7
Also known as: FLJ23666, OAT4, OAT7, S22A9_HUMAN, UST3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IVM8
- Gene
- SLC22A9
- Ensembl
- ENSG00000149742
- Chromosome
- 11
- Canonical length
- 553 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
Enables short-chain fatty acid transmembrane transporter activity and sodium-independent organic anion transmembrane transporter activity. Involved in hormone transport; short-chain fatty acid transmembrane transport; and sodium-independent organic anion transport. Located in basolateral plasma membrane. Implicated in Lynch syndrome and mismatch repair cancer syndrome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
553 residues, UniProt reviewed canonical sequence.
>Q8IVM8|SLC22A9
1 MAFQDLLGHA GDLWRFQILQ TVFLSIFAVA TYLHFMLENF TAFIPGHRCW VHILDNDTVS
61 DNDTGALSQD ALLRISIPLD SNMRPEKCRR FVHPQWQLLH LNGTFPNTSD ADMEPCVDGW
121 VYDRISFSST IVTEWDLVCD SQSLTSVAKF VFMAGMMVGG ILGGHLSDRF GRRFVLRWCY
181 LQVAIVGTCA ALAPTFLIYC SLRFLSGIAA MSLITNTIML IAEWATHRFQ AMGITLGMCP
241 SGIAFMTLAG LAFAIRDWHI LQLVVSVPYF VIFLTSSWLL ESARWLIINN KPEEGLKELR
301 KAAHRSGMKN ARDTLTLEIL KSTMKKELEA AQKKKPSLCE MLHMPNICKR ISLLSFTRFA
361 NFMAYFGLNL HVQHLGNNVF LLQTLFGAVI LLANCVAPWA LKYMNRRASQ MLLMFLLAIC
421 LLAIIFVPQE MQTLREVLAT LGLGASALAN TLAFAHGNEV IPTIIRARAM GINATFANIA
481 GALAPLMMIL SVYSPPLPWI IYGVFPFISG FAFLLLPETR NKPLFDTIQD EKNERKDPRE
541 PKQEDPRVEV TQFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC22A9 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)
- 0.26
- Highest tissue expression
- 43 nTPM
Expression across tissuesHPA
Tissue
- liver: 43 nTPM
- skeletal muscle: 1.4 nTPM
- cerebral cortex: 0.9 nTPM
- amygdala: 0.4 nTPM
- gallbladder: 0.3 nTPM
- bone marrow: 0.2 nTPM
Single-cell type
- hepatocytes: 33 nCPM
- adipocytes: 6.6 nCPM
- brain excitatory neurons: 6.5 nCPM
- epididymal efferent duct absorptive cells: 2.8 nCPM
- epicardial cells: 2.3 nCPM
- brain inhibitory neurons: 2.1 nCPM
Immune cell
- basophil: 0.8 nTPM
- neutrophil: 0.3 nTPM
- eosinophil: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- memory B-cell: 0.1 nTPM
- naive B-cell: 0.1 nTPM
Brain region
- cerebral cortex: 6.3 nTPM
- white matter: 3.5 nTPM
- amygdala: 3.4 nTPM
- basal ganglia: 3.4 nTPM
- hypothalamus: 2.3 nTPM
- hippocampal formation: 2.1 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)
- 1.61
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.24
- DepMap mean gene effect
- -0.21
- 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
- hormone transport
- organic anion transport
- sodium-independent organic anion transport
- short-chain fatty acid transmembrane transport
Molecular functions
- organic anion transmembrane transporter activity
- short-chain fatty acid transmembrane transporter activity
- sodium-independent organic anion transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC22A9 as an antibody target. Whether an autoantibody or antibody against SLC22A9 could matter depends on whether native SLC22A9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC22A9 is annotated at the cell surface, where native SLC22A9 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 SLC22A9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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