Seroatlas · Human Serome Atlas

PVALB

Parvalbumin alpha

Also known as: D22S749, PRVA_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
P20472
Gene
PVALB
Ensembl
ENSG00000100362
Chromosome
22
Canonical length
110 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nucleoplasm,Nucleoli,Cell Junctions

OverviewNCBI Gene

The protein encoded by this gene is a high affinity calcium ion-binding protein that is structurally and functionally similar to calmodulin and troponin C. The encoded protein is thought to be involved in muscle relaxation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]

Canonical amino-acid sequenceUniProt

110 residues, UniProt reviewed canonical sequence.

>P20472|PVALB
     1  MSMTDLLNAE DIKKAVGAFS ATDSFDHKKF FQMVGLKKKS ADDVKKVFHM LDKDKSGFIE
    61  EDELGFILKG FSPDARDLSA KETKMLMAAG DKDGDGKIGV DEFSTLVAES

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against PVALB 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)
0.28
Highest tissue expression
1,993 nTPM

Expression across tissuesHPA

Tissue

  • parathyroid gland: 1,993 nTPM
  • cerebellum: 639 nTPM
  • retina: 346 nTPM
  • midbrain: 121 nTPM
  • cerebral cortex: 99 nTPM
  • kidney: 94 nTPM

Single-cell type

  • retinal horizontal cells: 575 nCPM
  • hofbauer cells: 89 nCPM
  • platelets: 68 nCPM
  • retinal ganglion cells: 35 nCPM
  • brain inhibitory neurons: 27 nCPM
  • bergmann glia: 13 nCPM

Immune cell

  • total PBMC: 15 nTPM
  • neutrophil: 4.6 nTPM
  • plasmacytoid DC: 0.9 nTPM
  • classical monocyte: 0.5 nTPM
  • intermediate monocyte: 0.4 nTPM
  • T-reg: 0.3 nTPM

Brain region

  • thalamus: 577 nTPM
  • cerebellum: 525 nTPM
  • medulla oblongata: 260 nTPM
  • pons: 213 nTPM
  • hypothalamus: 197 nTPM
  • midbrain: 165 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)
1.36
gnomAD pLI
0.09
gnomAD missense Z
0.04
DepMap mean gene effect
0.04
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 PVALB as an antibody target. Whether an autoantibody or antibody against PVALB could matter depends on whether native PVALB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

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

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