Seroatlas · Human Serome Atlas

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  DKVR

LocalizationUniProt · 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.

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

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.

Canonical record: https://seroatlas.com/gene/SLC67A1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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