Seroatlas · Human Serome Atlas

SPN

Leukosialin

Also known as: CD43, GPL115, LEU-22, LEUK_HUMAN, LSN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P16150
Gene
SPN
Ensembl
ENSG00000197471
Chromosome
16
Canonical length
400 aa
Protein class
CD markers, Predicted membrane proteins
Subcellular location
Plasma membrane

OverviewNCBI Gene

This gene encodes a highly sialylated glycoprotein that functions in antigen-specific activation of T cells, and is found on the surface of thymocytes, T lymphocytes, monocytes, granulocytes, and some B lymphocytes. It contains a mucin-like extracellular domain, a transmembrane region and a carboxy-terminal intracellular region. The extracellular domain has a high proportion of serine and threonine residues, allowing extensive O-glycosylation, and has one potential N-glycosylation site, while the carboxy-terminal region has potential phosphorylation sites that may mediate transduction of activation signals. Different glycoforms of this protein have been described. In stimulated immune cells, proteolytic cleavage of the extracellular domain occurs in some cell types, releasing a soluble extracellular fragment. Defects in expression of this gene are associated with Wiskott-Aldrich syndrome. [provided by RefSeq, Sep 2017]

Canonical amino-acid sequenceUniProt

400 residues, UniProt reviewed canonical sequence.

>P16150|SPN
     1  MATLLLLLGV LVVSPDALGS TTAVQTPTSG EPLVSTSEPL SSKMYTTSIT SDPKADSTGD
    61  QTSALPPSTS INEGSPLWTS IGASTGSPLP EPTTYQEVSI KMSSVPQETP HATSHPAVPI
   121  TANSLGSHTV TGGTITTNSP ETSSRTSGAP VTTAASSLET SRGTSGPPLT MATVSLETSK
   181  GTSGPPVTMA TDSLETSTGT TGPPVTMTTG SLEPSSGASG PQVSSVKLST MMSPTTSTNA
   241  STVPFRNPDE NSRGMLPVAV LVALLAVIVL VALLLLWRRR QKRRTGALVL SRGGKRNGVV
   301  DAWAGPAQVP EEGAVTVTVG GSGGDKGSGF PDGEGSSRRP TLTTFFGRRK SRQGSLAMEE
   361  LKSGSGPSLK GEEEPLVASE DGAVDAPAPD EPEGGDGAAP

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against SPN 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
Intracellular
Secreted
No
Transmembrane segments
1
Mean surface accessibility (rSASA)
0.71
Highest tissue expression
68 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 68 nTPM
  • thymus: 48 nTPM
  • lung: 27 nTPM
  • lymph node: 25 nTPM
  • tonsil: 22 nTPM
  • spleen: 18 nTPM

Single-cell type

  • megakaryocyte progenitors: 9.8 nCPM
  • megakaryocyte-erythroid progenitors: 7.3 nCPM
  • erythrocyte progenitors: 5.8 nCPM
  • thymocytes: 4.2 nCPM
  • neutrophil progenitors: 2.7 nCPM
  • nk-cells: 2.7 nCPM

Immune cell

  • non-classical monocyte: 219 nTPM
  • gdT-cell: 96 nTPM
  • intermediate monocyte: 96 nTPM
  • NK-cell: 69 nTPM
  • memory CD8 T-cell: 65 nTPM
  • total PBMC: 52 nTPM

Brain region

  • white matter: 12 nTPM
  • medulla oblongata: 11 nTPM
  • thalamus: 8.9 nTPM
  • pons: 8.4 nTPM
  • spinal cord: 7.4 nTPM
  • hypothalamus: 6.3 nTPM

ReferencesPubMed · IEDB

Publications for SPN from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.

Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.

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)
1.94
gnomAD pLI
0.01
gnomAD missense Z
-0.09
DepMap mean gene effect
-0.03
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

  • Leukosialin

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of SPN 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 SPN as an antibody target. Whether an autoantibody or antibody against SPN could matter depends on whether native SPN is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

SPN is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.

Annotation status

The present source text does not explicitly label SPN as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/SPN. 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).

Loading the interactive Seroatlas protein explorer...