Seroatlas · Human Serome Atlas

BMI1

Polycomb complex protein BMI-1

Also known as: BMI1_HUMAN, PCGF4, RNF51

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

Protein identityUniProt · HPA

UniProt accession
P35226
Gene
BMI1
Ensembl
ENSG00000168283
Chromosome
10
Canonical length
326 aa
Protein class
Cancer-related genes, Human disease related genes, Predicted intracellular proteins
Subcellular location
Nucleoplasm,Nucleoli,Nuclear bodies,Cytosol

OverviewNCBI Gene

This gene encodes a ring finger protein that is major component of the polycomb group complex 1 (PRC1). This complex functions through chromatin remodeling as an essential epigenetic repressor of multiple regulatory genes involved in embryonic development and self-renewal in somatic stem cells. This protein also plays a central role in DNA damage repair. This gene is an oncogene and aberrant expression is associated with numerous cancers and is associated with resistance to certain chemotherapies. A pseudogene of this gene is found on chromosome X. Read-through transcription also exists between this gene and the upstream COMM domain containing 3 (COMMD3) gene. [provided by RefSeq, Sep 2015]

Canonical amino-acid sequenceUniProt

326 residues, UniProt reviewed canonical sequence.

>P35226|BMI1
     1  MHRTTRIKIT ELNPHLMCVL CGGYFIDATT IIECLHSFCK TCIVRYLETS KYCPICDVQV
    61  HKTRPLLNIR SDKTLQDIVY KLVPGLFKNE MKRRRDFYAA HPSADAANGS NEDRGEVADE
   121  DKRIITDDEI ISLSIEFFDQ NRLDRKVNKD KEKSKEEVND KRYLRCPAAM TVMHLRKFLR
   181  SKMDIPNTFQ IDVMYEEEPL KDYYTLMDIA YIYTWRRNGP LPLKYRVRPT CKRMKISHQR
   241  DGLTNAGELE SDSGSDKANS PAGGIPSTSS CLPSPSTPVQ SPHPQFPHIS STMNGTSNSP
   301  SGNHQSSFAN RPRKSSVNGS SATSSG

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against BMI1 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
0
Mean surface accessibility (rSASA)
0.47
Highest tissue expression
54 nTPM

Expression across tissuesHPA

Tissue

  • parathyroid gland: 54 nTPM
  • skeletal muscle: 42 nTPM
  • retina: 37 nTPM
  • spleen: 34 nTPM
  • smooth muscle: 34 nTPM
  • breast: 34 nTPM

Single-cell type

  • late spermatids: 265 nCPM
  • early spermatids: 183 nCPM
  • parietal cells: 51 nCPM
  • plasma cells: 51 nCPM
  • gastric progenitor cells: 47 nCPM
  • smooth muscle cells: 46 nCPM

Immune cell

  • basophil: 15 nTPM
  • MAIT T-cell: 7.1 nTPM
  • memory CD4 T-cell: 5.4 nTPM
  • gdT-cell: 5.2 nTPM
  • NK-cell: 5.2 nTPM
  • memory CD8 T-cell: 5 nTPM

Brain region

  • white matter: 76 nTPM
  • basal ganglia: 56 nTPM
  • medulla oblongata: 49 nTPM
  • midbrain: 47 nTPM
  • spinal cord: 46 nTPM
  • cerebellum: 46 nTPM

ReferencesPubMed · IEDB

Publications for BMI1 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)
0.35
gnomAD pLI
0.94
gnomAD missense Z
2.43
DepMap mean gene effect
0.11
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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 BMI1 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 BMI1 as an antibody target. Whether an autoantibody or antibody against BMI1 could matter depends on whether native BMI1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

BMI1 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 BMI1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/BMI1. 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...