SLC22A1
Solute carrier family 22 member 1
Also known as: 1-Oct, S22A1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15245
- Gene
- SLC22A1
- Ensembl
- ENSG00000175003
- Chromosome
- 6
- Canonical length
- 554 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants encoding two different isoforms have been found for this gene, but only the longer variant encodes a functional transporter. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
554 residues, UniProt reviewed canonical sequence.
>O15245|SLC22A1
1 MPTVDDILEQ VGESGWFQKQ AFLILCLLSA AFAPICVGIV FLGFTPDHHC QSPGVAELSQ
61 RCGWSPAEEL NYTVPGLGPA GEAFLGQCRR YEVDWNQSAL SCVDPLASLA TNRSHLPLGP
121 CQDGWVYDTP GSSIVTEFNL VCADSWKLDL FQSCLNAGFL FGSLGVGYFA DRFGRKLCLL
181 GTVLVNAVSG VLMAFSPNYM SMLLFRLLQG LVSKGNWMAG YTLITEFVGS GSRRTVAIMY
241 QMAFTVGLVA LTGLAYALPH WRWLQLAVSL PTFLFLLYYW CVPESPRWLL SQKRNTEAIK
301 IMDHIAQKNG KLPPADLKML SLEEDVTEKL SPSFADLFRT PRLRKRTFIL MYLWFTDSVL
361 YQGLILHMGA TSGNLYLDFL YSALVEIPGA FIALITIDRV GRIYPMAMSN LLAGAACLVM
421 IFISPDLHWL NIIIMCVGRM GITIAIQMIC LVNAELYPTF VRNLGVMVCS SLCDIGGIIT
481 PFIVFRLREV WQALPLILFA VLGLLAAGVT LLLPETKGVA LPETMKDAEN LGRKAKPKEN
541 TIYLKVQTSE PSGTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC22A1 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
- 596 nTPM
Expression across tissuesHPA
Tissue
- liver: 596 nTPM
- spleen: 1.4 nTPM
- skeletal muscle: 0.9 nTPM
- kidney: 0.8 nTPM
- thyroid gland: 0.7 nTPM
- gallbladder: 0.6 nTPM
Single-cell type
- hepatocytes: 1,218 nCPM
- neutrophils: 118 nCPM
- cholangiocytes: 65 nCPM
- endometrial secretory cells: 17 nCPM
- endometrial luminal cells: 16 nCPM
- epididymal clear cells: 14 nCPM
Immune cell
- neutrophil: 3.5 nTPM
- gdT-cell: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- memory CD8 T-cell: 0.1 nTPM
- naive B-cell: 0.1 nTPM
- plasmacytoid DC: 0.1 nTPM
Brain region
- cerebral cortex: 3.3 nTPM
- hippocampal formation: 2.4 nTPM
- amygdala: 1.9 nTPM
- pons: 1.9 nTPM
- choroid plexus: 1.8 nTPM
- basal ganglia: 1.7 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)
- 1.67
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.09
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
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
- acetylcholine transport
- cellular detoxification
- dopamine transport
- dopamine uptake
- epinephrine transport
- establishment or maintenance of transmembrane electrochemical gradient
- metanephric proximal tubule development
- monoamine transport
- neurotransmitter transport
- norepinephrine transport
- organic cation transport
- prostaglandin transport
- purine-containing compound transmembrane transport
- putrescine transport
- quaternary ammonium group transport
- serotonin transport
- serotonin uptake
- spermidine transport
- thiamine transmembrane transport
- thiamine transport
- transport across blood-brain barrier
- xenobiotic metabolic process
- xenobiotic transport
- xenobiotic transport across blood-brain barrier
- O-acyl-L-carnitine transmembrane transport
Molecular functions
- (R)-carnitine transmembrane transporter activity
- acetylcholine transmembrane transporter activity
- dopamine:sodium symporter activity
- identical protein binding
- monoamine transmembrane transporter activity
- neurotransmitter transmembrane transporter activity
- norepinephrine:sodium symporter activity
- organic anion transmembrane transporter activity
- organic cation transmembrane transporter activity
- prostaglandin transmembrane transporter activity
- putrescine transmembrane transporter activity
- pyrimidine nucleoside transmembrane transporter activity
- quaternary ammonium group transmembrane transporter activity
- spermidine transmembrane transporter activity
- thiamine transmembrane transporter activity
- toxin transmembrane transporter activity
- xenobiotic transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SLC22A1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC22A1 as an antibody target. Whether an autoantibody or antibody against SLC22A1 could matter depends on whether native SLC22A1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC22A1 is annotated at the cell surface, where native SLC22A1 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 SLC22A1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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