Seroatlas · Human Serome Atlas

BOLA1

BolA-like protein 1

Also known as: BOLA1_HUMAN, CGI-143

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

Protein identityUniProt · HPA

UniProt accession
Q9Y3E2
Gene
BOLA1
Ensembl
ENSG00000178096
Chromosome
1
Canonical length
137 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

Predicted to be involved in cell redox homeostasis; intracellular iron ion homeostasis; and iron-sulfur cluster assembly. Located in mitochondrion. Part of iron-sulfur cluster assembly complex. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

137 residues, UniProt reviewed canonical sequence.

>Q9Y3E2|BOLA1
     1  MLSGRLVLGL VSMAGRVCLC QGSAGSGAIG PVEAAIRTKL EEALSPEVLE LRNESGGHAV
    61  PPGSETHFRV AVVSSRFEGL SPLQRHRLVH AALAEELGGP VHALAIQART PAQWRENSQL
   121  DTSPPCLGGN KKTLGTP

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against BOLA1 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)
0.45
Highest tissue expression
24 nTPM

Expression across tissuesHPA

Tissue

  • liver: 24 nTPM
  • kidney: 24 nTPM
  • colon: 22 nTPM
  • skeletal muscle: 21 nTPM
  • basal ganglia: 21 nTPM
  • skin: 21 nTPM

Single-cell type

  • epididymal principal cells: 65 nCPM
  • decidual stromal cells: 48 nCPM
  • esophageal basal cells: 47 nCPM
  • hepatocytes: 45 nCPM
  • enterocytes: 43 nCPM
  • prostatic club cells: 42 nCPM

Immune cell

  • plasmacytoid DC: 19 nTPM
  • naive CD4 T-cell: 19 nTPM
  • T-reg: 19 nTPM
  • naive CD8 T-cell: 18 nTPM
  • memory B-cell: 16 nTPM
  • MAIT T-cell: 15 nTPM

Brain region

  • white matter: 16 nTPM
  • cerebellum: 14 nTPM
  • thalamus: 14 nTPM
  • medulla oblongata: 13 nTPM
  • spinal cord: 13 nTPM
  • basal ganglia: 13 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)
1.78
gnomAD pLI
0.04
gnomAD missense Z
0.51
DepMap mean gene effect
-0.12
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of BOLA1 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 BOLA1 as an antibody target. Whether an autoantibody or antibody against BOLA1 could matter depends on whether native BOLA1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

BOLA1 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 BOLA1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/BOLA1. 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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