Seroatlas · Human Serome Atlas

PIGR

Polymeric immunoglobulin receptor

Also known as: PIGR_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
P01833
Gene
PIGR
Ensembl
ENSG00000162896
Chromosome
1
Canonical length
764 aa
Protein class
Cancer-related genes, Plasma proteins, Predicted membrane proteins, Predicted secreted proteins, Transporters
Secretome location
Secreted to digestive system

OverviewNCBI Gene

This gene is a member of the immunoglobulin superfamily. The encoded poly-Ig receptor binds polymeric immunoglobulin molecules at the basolateral surface of epithelial cells; the complex is then transported across the cell to be secreted at the apical surface. A significant association was found between immunoglobulin A nephropathy and several SNPs in this gene.[provided by RefSeq, Sep 2009]

Canonical amino-acid sequenceUniProt

764 residues, UniProt reviewed canonical sequence.

>P01833|PIGR
     1  MLLFVLTCLL AVFPAISTKS PIFGPEEVNS VEGNSVSITC YYPPTSVNRH TRKYWCRQGA
    61  RGGCITLISS EGYVSSKYAG RANLTNFPEN GTFVVNIAQL SQDDSGRYKC GLGINSRGLS
   121  FDVSLEVSQG PGLLNDTKVY TVDLGRTVTI NCPFKTENAQ KRKSLYKQIG LYPVLVIDSS
   181  GYVNPNYTGR IRLDIQGTGQ LLFSVVINQL RLSDAGQYLC QAGDDSNSNK KNADLQVLKP
   241  EPELVYEDLR GSVTFHCALG PEVANVAKFL CRQSSGENCD VVVNTLGKRA PAFEGRILLN
   301  PQDKDGSFSV VITGLRKEDA GRYLCGAHSD GQLQEGSPIQ AWQLFVNEES TIPRSPTVVK
   361  GVAGGSVAVL CPYNRKESKS IKYWCLWEGA QNGRCPLLVD SEGWVKAQYE GRLSLLEEPG
   421  NGTFTVILNQ LTSRDAGFYW CLTNGDTLWR TTVEIKIIEG EPNLKVPGNV TAVLGETLKV
   481  PCHFPCKFSS YEKYWCKWNN TGCQALPSQD EGPSKAFVNC DENSRLVSLT LNLVTRADEG
   541  WYWCGVKQGH FYGETAAVYV AVEERKAAGS RDVSLAKADA APDEKVLDSG FREIENKAIQ
   601  DPRLFAEEKA VADTRDQADG SRASVDSGSS EEQGGSSRAL VSTLVPLGLV LAVGAVAVGV
   661  ARARHRKNVD RVSIRSYRTD ISMSDFENSR EFGANDNMGA SSITQETSLG GKEEFVATTE
   721  STTETKEPKK AKRSSKEEAE MAYKDFLLQS STVAAEAQDG PQEA

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PIGR 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
1
Mean surface accessibility (rSASA)
0.38
Highest tissue expression
2,479 nTPM

Expression across tissuesHPA

Tissue

  • duodenum: 2,479 nTPM
  • colon: 1,586 nTPM
  • salivary gland: 1,544 nTPM
  • rectum: 1,149 nTPM
  • small intestine: 761 nTPM
  • cervix: 514 nTPM

Single-cell type

  • colonocytes: 8,431 nCPM
  • lacrimal acinar cells: 5,520 nCPM
  • enteric transient amplifying cells: 4,471 nCPM
  • enteric stem cells: 3,465 nCPM
  • salivary acinar cells: 2,959 nCPM
  • prostatic club cells: 2,770 nCPM

Immune cell

  • memory B-cell: 0.9 nTPM
  • naive B-cell: 0.8 nTPM
  • basophil: 0.3 nTPM
  • myeloid DC: 0.3 nTPM
  • neutrophil: 0.3 nTPM
  • plasmacytoid DC: 0.2 nTPM

Brain region

  • thalamus: 3 nTPM
  • white matter: 3 nTPM
  • cerebellum: 2.8 nTPM
  • cerebral cortex: 2.8 nTPM
  • hippocampal formation: 2.7 nTPM
  • pons: 2.7 nTPM

ReferencesPubMed · IEDB

Publications for PIGR 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)
0.37
gnomAD pLI
0.81
gnomAD missense Z
1.14
DepMap mean gene effect
-0.01
DepMap dependency class
none

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

Antibody and autoantibody relevanceSeroatlas analysis

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

PIGR is annotated at the cell surface, where native PIGR 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 PIGR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/PIGR. 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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