Seroatlas · Human Serome Atlas

DEFB124

Beta-defensin 124

Also known as: DB124_HUMAN, DEFB-24

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

Protein identityUniProt · HPA

UniProt accession
Q8NES8
Gene
DEFB124
Ensembl
ENSG00000180383
Chromosome
20
Canonical length
71 aa
Protein class
Predicted secreted proteins
Secretome location
Secreted in other tissues

OverviewNCBI Gene

Defensins are cysteine-rich cationic polypeptides that are important in the host immunologic response to invading microorganisms. This antimicrobial protein is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 20q11.1. The encoded protein may serve to enhance innate immunity in the prostate. [provided by RefSeq, Nov 2014]

Canonical amino-acid sequenceUniProt

71 residues, UniProt reviewed canonical sequence.

>Q8NES8|DEFB124
     1  MTQLLLFLVA LLVLGHVPSG RSEFKRCWKG QGACQTYCTR QETYMHLCPD ASLCCLSYAL
    61  KPPPVPKHEY E

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against DEFB124 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
Secreted
Secreted
Yes
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.5
Highest tissue expression
1 nTPM

Expression across tissuesHPA

Tissue

  • testis: 1 nTPM
  • fallopian tube: 0.9 nTPM
  • cervix: 0.8 nTPM
  • epididymis: 0.8 nTPM
  • endometrium: 0.6 nTPM
  • adipose tissue: 0.4 nTPM

Single-cell type

  • fallopian tube ciliated cells: 17 nCPM
  • pericytes: 16 nCPM
  • decidual stromal cells: 12 nCPM
  • endometrial stromal cells: 11 nCPM
  • respiratory ciliated cells: 8 nCPM
  • epididymal principal cells: 5.7 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • choroid plexus: 0.5 nTPM
  • midbrain: 0.1 nTPM
  • amygdala: 0 nTPM
  • basal ganglia: 0 nTPM
  • cerebellum: 0 nTPM
  • cerebral cortex: 0 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)
1.84
gnomAD pLI
0.11
gnomAD missense Z
0.46
DepMap mean gene effect
0.09
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

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads DEFB124 as an antibody target. Whether an autoantibody or antibody against DEFB124 could matter depends on whether native DEFB124 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

DEFB124 is annotated as secreted, so native DEFB124 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.

Annotation status

The present source text does not explicitly label DEFB124 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/DEFB124. 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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