Seroatlas · Human Serome Atlas

HBM

Hemoglobin subunit mu

Also known as: HBAP2, HBK, HBM_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q6B0K9
Gene
HBM
Ensembl
ENSG00000206177
Chromosome
16
Canonical length
141 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. This gene has an ORF encoding a 141 aa polypeptide which is similar to the delta globins found in reptiles and birds. This locus was originally described as a pseudogene; however, it is currently thought to be a protein-coding gene. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

141 residues, UniProt reviewed canonical sequence.

>Q6B0K9|HBM
     1  MLSAQERAQI AQVWDLIAGH EAQFGAELLL RLFTVYPSTK VYFPHLSACQ DATQLLSHGQ
    61  RMLAAVGAAV QHVDNLRAAL SPLADLHALV LRVDPANFPL LIQCFHVVLA SHLQDEFTVQ
   121  MQAAWDKFLT GVAVVLTEKY R

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against HBM 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
Unknown
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.29
Highest tissue expression
433 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 433 nTPM
  • spleen: 17 nTPM
  • placenta: 5.9 nTPM
  • lung: 4 nTPM
  • liver: 3.1 nTPM
  • kidney: 1.5 nTPM

Single-cell type

  • erythrocytes: 1,662 nCPM
  • erythrocyte progenitors: 902 nCPM
  • late spermatids: 3 nCPM
  • differentiating spermatogonia: 2.5 nCPM
  • undifferentiated spermatogonia: 1.7 nCPM
  • hofbauer cells: 1.3 nCPM

Immune cell

  • total PBMC: 6.9 nTPM
  • NK-cell: 0.7 nTPM
  • eosinophil: 0.4 nTPM
  • plasmacytoid DC: 0.4 nTPM
  • gdT-cell: 0.2 nTPM
  • basophil: 0 nTPM

Brain region

  • cerebral cortex: 1.5 nTPM
  • basal ganglia: 1.1 nTPM
  • amygdala: 0.9 nTPM
  • choroid plexus: 0.7 nTPM
  • medulla oblongata: 0.7 nTPM
  • pons: 0.7 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)
1.69
gnomAD pLI
0.01
gnomAD missense Z
-0.37
DepMap mean gene effect
0
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 HBM as an antibody target. Whether an autoantibody or antibody against HBM could matter depends on whether native HBM is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

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

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