Seroatlas · Human Serome Atlas

CCL4

C-C motif chemokine 4

Also known as: Act-2, AT744.1, CCL4_HUMAN, LAG1, MIP-1-beta, SCYA4

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

Protein identityUniProt · HPA

UniProt accession
P13236
Gene
CCL4
Ensembl
ENSG00000275302
Chromosome
17
Canonical length
92 aa
Protein class
Cancer-related genes, Predicted secreted proteins
Secretome location
Secreted to blood
Quaternary structure
Homodimer

OverviewNCBI Gene

The protein encoded by this gene is a mitogen-inducible monokine and is one of the major HIV-suppressive factors produced by CD8+ T-cells. The encoded protein is secreted and has chemokinetic and inflammatory functions. [provided by RefSeq, Dec 2012]

Canonical amino-acid sequenceUniProt

92 residues, UniProt reviewed canonical sequence.

>P13236|CCL4
     1  MKLCVTVLSL LMLVAAFCSP ALSAPMGSDP PTACCFSYTA RKLPRNFVVD YYETSSLCSQ
    61  PAVVFQTKRS KQVCADPSES WVQEYVYDLE LN

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CCL4 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)
0.45
Highest tissue expression
182 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 182 nTPM
  • liver: 79 nTPM
  • spleen: 78 nTPM
  • urinary bladder: 52 nTPM
  • lung: 44 nTPM
  • gallbladder: 42 nTPM

Single-cell type

  • nk-cells: 414 nCPM
  • t-cells: 186 nCPM
  • macrophages: 101 nCPM
  • monocytes: 87 nCPM
  • hofbauer cells: 85 nCPM
  • neutrophils: 62 nCPM

Immune cell

  • gdT-cell: 416 nTPM
  • memory CD8 T-cell: 241 nTPM
  • naive CD8 T-cell: 182 nTPM
  • total PBMC: 139 nTPM
  • eosinophil: 136 nTPM
  • MAIT T-cell: 102 nTPM

Brain region

  • choroid plexus: 5.3 nTPM
  • cerebellum: 3.9 nTPM
  • white matter: 3.8 nTPM
  • medulla oblongata: 3.5 nTPM
  • cerebral cortex: 3.4 nTPM
  • pons: 2.7 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about CCL4.

Disease | ImmuneIEDB

Conditions an epitope on CCL4 was assayed in.

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)
1.37
gnomAD pLI
0.24
gnomAD missense Z
-0.64
DepMap mean gene effect
-0.08
DepMap dependency class
selective

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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CCL4 as an antibody target. Whether an autoantibody or antibody against CCL4 could matter depends on whether native CCL4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CCL4 is annotated as secreted, so native CCL4 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 CCL4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CCL4. 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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