Seroatlas · Human Serome Atlas

HBE1

Hemoglobin subunit epsilon

Also known as: HBE, HBE_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
P02100
Gene
HBE1
Ensembl
ENSG00000213931
Chromosome
11
Canonical length
147 aa
Protein class
Plasma proteins, Predicted intracellular proteins

OverviewNCBI Gene

The epsilon globin gene (HBE) is normally expressed in the embryonic yolk sac: two epsilon chains together with two zeta chains (an alpha-like globin) constitute the embryonic hemoglobin Hb Gower I; two epsilon chains together with two alpha chains form the embryonic Hb Gower II. Both of these embryonic hemoglobins are normally supplanted by fetal, and later, adult hemoglobin. The five beta-like globin genes are found within a 45 kb cluster on chromosome 11 in the following order: 5'-epsilon - G-gamma - A-gamma - delta - beta-3' [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

147 residues, UniProt reviewed canonical sequence.

>P02100|HBE1
     1  MVHFTAEEKA AVTSLWSKMN VEEAGGEALG RLLVVYPWTQ RFFDSFGNLS SPSAILGNPK
    61  VKAHGKKVLT SFGDAIKNMD NLKPAFAKLS ELHCDKLHVD PENFKLLGNV MVIILATHFG
   121  KEFTPEVQAA WQKLVSAVAI ALAHKYH

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against HBE1 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)
0.28
Highest tissue expression
1.2 nTPM

Expression across tissuesHPA

Tissue

  • liver: 1.2 nTPM
  • placenta: 0.7 nTPM
  • adipose tissue: 0.6 nTPM
  • cerebral cortex: 0.6 nTPM
  • ovary: 0.6 nTPM
  • testis: 0.5 nTPM

Single-cell type

  • late spermatids: 0.3 nCPM
  • astrocytes: 0.1 nCPM
  • early spermatids: 0.1 nCPM
  • endometrial stromal cells: 0.1 nCPM
  • extravillous trophoblasts: 0.1 nCPM
  • migrating cytotrophoblasts: 0.1 nCPM

Immune cell

  • neutrophil: 0.2 nTPM
  • total PBMC: 0.1 nTPM
  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM

Brain region

  • white matter: 3.3 nTPM
  • hypothalamus: 2.8 nTPM
  • cerebral cortex: 2.7 nTPM
  • medulla oblongata: 2.2 nTPM
  • basal ganglia: 2.1 nTPM
  • pons: 1.9 nTPM

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)
1.48
gnomAD pLI
0.02
gnomAD missense Z
0.21
DepMap mean gene effect
0.12
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% 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 HBE1 as an antibody target. Whether an autoantibody or antibody against HBE1 could matter depends on whether native HBE1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

HBE1 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 HBE1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/HBE1. 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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