Seroatlas · Human Serome Atlas

PF4V1

Platelet factor 4 variant

Also known as: CXCL4L1, CXCL4V1, PF4V_HUMAN, SCYB4V1

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

Protein identityUniProt · HPA

UniProt accession
P10720
Gene
PF4V1
Ensembl
ENSG00000109272
Chromosome
4
Canonical length
104 aa
Protein class
Plasma proteins, Predicted secreted proteins
Secretome location
Secreted to blood
Quaternary structure
Homotetramer

OverviewNCBI Gene

The protein encoded by this gene is a chemokine that is highly similar to platelet factor 4. The encoded protein displays a strong antiangiogenic function and is regulated by chemokine (C-X-C motif) receptor 3. This protein also impairs tumor growth and can protect against blood-retinal barrier breakdown in diabetes patients. [provided by RefSeq, Nov 2015]

Canonical amino-acid sequenceUniProt

104 residues, UniProt reviewed canonical sequence.

>P10720|PF4V1
     1  MSSAARSRLT RATRQEMLFL ALLLLPVVVA FARAEAEEDG DLQCLCVKTT SQVRPRHITS
    61  LEVIKAGPHC PTAQLIATLK NGRKICLDLQ ALLYKKIIKE HLES

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PF4V1 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)
0.47
Highest tissue expression
2.7 nTPM

Expression across tissuesHPA

Tissue

  • spleen: 2.7 nTPM
  • duodenum: 1.6 nTPM
  • bone marrow: 1.1 nTPM
  • seminal vesicle: 1 nTPM
  • small intestine: 0.9 nTPM
  • kidney: 0.7 nTPM

Single-cell type

  • platelets: 2,137 nCPM
  • megakaryocytes: 544 nCPM
  • cholangiocytes: 19 nCPM
  • respiratory secretory cells: 17 nCPM
  • neuroendocrine cells: 17 nCPM
  • conjunctival goblet cells: 15 nCPM

Immune cell

  • basophil: 13 nTPM
  • total PBMC: 9.9 nTPM
  • neutrophil: 9.2 nTPM
  • plasmacytoid DC: 0.2 nTPM
  • classical monocyte: 0.1 nTPM
  • naive B-cell: 0.1 nTPM

Brain region

  • cerebral cortex: 0.7 nTPM
  • basal ganglia: 0.4 nTPM
  • hypothalamus: 0.3 nTPM
  • pons: 0.3 nTPM
  • thalamus: 0.3 nTPM
  • choroid plexus: 0.2 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)
1.91
gnomAD pLI
0
gnomAD missense Z
0.05
DepMap mean gene effect
0
DepMap dependency class
none

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 PF4V1 as an antibody target. Whether an autoantibody or antibody against PF4V1 could matter depends on whether native PF4V1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

PF4V1 is annotated as secreted, so native PF4V1 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 PF4V1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/PF4V1. 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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