SLC67A1
Solute carrier family 67 member A1
Also known as: BWR1A, BWSCR1A, IMPT1, ITM, ORCTL2, S67A1_HUMAN, SLC22A18, SLC22A1L, TSSC5
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96BI1
- Gene
- SLC67A1
- Ensembl
- ENSG00000110628
- Chromosome
- 11
- Canonical length
- 424 aa
- Protein class
- Disease related genes, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted membrane proteins, Transporters
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Several alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Oct 2015]
Canonical amino-acid sequenceUniProt
424 residues, UniProt reviewed canonical sequence.
>Q96BI1|SLC67A1
1 MQGARAPRDQ GRSPGRMSAL GRSSVILLTY VLAATELTCL FMQFSIVPYL SRKLGLDSIA
61 FGYLQTTFGV LQLLGGPVFG RFADQRGARA ALTLSFLAAL ALYLLLAAAS SPALPGVYLL
121 FASRLPGALM HTLPAAQMVI TDLSAPEERP AALGRLGLCF GVGVILGSLL GGTLVSAYGI
181 QCPAILAALA TLLGAVLSFT CIPASTKGAK TDAQAPLPGG PRASVFDLKA IASLLRLPDV
241 PRIFLVKVAS NCPTGLFMVM FSIISMDFFQ LEAAQAGYLM SFFGLLQMVT QGLVIGQLSS
301 HFSEEVLLRA SVLVFIVVGL AMAWMSSVFH FCLLVPGLVF SLCTLNVVTD SMLIKAVSTS
361 DTGTMLGLCA SVQPLLRTLG PTVGGLLYRS FGVPVFGHVQ VAINTLVLLV LWRKPMPQRK
421 DKVRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC67A1 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
- 10
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 81 nTPM
Expression across tissuesHPA
Tissue
- liver: 81 nTPM
- small intestine: 48 nTPM
- duodenum: 42 nTPM
- colon: 38 nTPM
- kidney: 33 nTPM
- heart muscle: 18 nTPM
Single-cell type
- late spermatids: 685 nCPM
- enterocytes: 541 nCPM
- colonocytes: 199 nCPM
- syncytiotrophoblasts: 142 nCPM
- early spermatids: 141 nCPM
- hepatocytes: 100 nCPM
Immune cell
- neutrophil: 42 nTPM
- basophil: 32 nTPM
- classical monocyte: 29 nTPM
- intermediate monocyte: 28 nTPM
- eosinophil: 28 nTPM
- non-classical monocyte: 23 nTPM
Brain region
- cerebral cortex: 5.4 nTPM
- hypothalamus: 4.6 nTPM
- thalamus: 4.4 nTPM
- white matter: 4.1 nTPM
- choroid plexus: 4 nTPM
- medulla oblongata: 3.3 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SLC67A1.
Disease | AllUniProt
Conditions SLC67A1 is implicated in, by any mechanism.
- Lung cancer (LNCR) MIM:211980
- Rhabdomyosarcoma, embryonal, 1 (RMSE1) MIM:268210
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)
- 1.16
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- organic cation transport
- xenobiotic detoxification by transmembrane export across the plasma membrane
- xenobiotic transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SLC67A1 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 SLC67A1 as an antibody target. Whether an autoantibody or antibody against SLC67A1 could matter depends on whether native SLC67A1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC67A1 is annotated at the cell surface, where native SLC67A1 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 SLC67A1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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