Seroatlas · Human Serome Atlas

H2AC20

Histone H2A type 2-C

Also known as: H2A, H2A/q, H2A2C_HUMAN, H2AFQ, HIST2H2AC

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

Protein identityUniProt · HPA

UniProt accession
Q16777
Gene
H2AC20
Ensembl
ENSG00000184260
Chromosome
1
Canonical length
129 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nucleoplasm

OverviewNCBI Gene

Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. [provided by RefSeq, Aug 2015]

Canonical amino-acid sequenceUniProt

129 residues, UniProt reviewed canonical sequence.

>Q16777|H2AC20
     1  MSGRGKQGGK ARAKAKSRSS RAGLQFPVGR VHRLLRKGNY AERVGAGAPV YMAAVLEYLT
    61  AEILELAGNA ARDNKKTRII PRHLQLAIRN DEELNKLLGK VTIAQGGVLP NIQAVLLPKK
   121  TESHKAKSK

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against H2AC20 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)
0.49
Highest tissue expression
24 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 24 nTPM
  • spleen: 5.6 nTPM
  • lung: 4.7 nTPM
  • skin: 4.7 nTPM
  • ovary: 4.4 nTPM
  • cervix: 4.1 nTPM

Single-cell type

  • erythrocyte progenitors: 335 nCPM
  • monocyte progenitors: 209 nCPM
  • megakaryocyte progenitors: 159 nCPM
  • plasma cells: 95 nCPM
  • neutrophil progenitors: 94 nCPM
  • tuft cells: 92 nCPM

Immune cell

  • neutrophil: 99 nTPM
  • basophil: 47 nTPM
  • classical monocyte: 34 nTPM
  • naive B-cell: 33 nTPM
  • non-classical monocyte: 26 nTPM
  • plasmacytoid DC: 25 nTPM

Brain region

  • hypothalamus: 163 nTPM
  • cerebellum: 153 nTPM
  • medulla oblongata: 147 nTPM
  • basal ganglia: 145 nTPM
  • choroid plexus: 142 nTPM
  • white matter: 142 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about H2AC20.

Disease | ImmuneIEDB

Conditions an epitope on H2AC20 was assayed in.

Disease | AutoantibodyPubMed

Conditions in which antibodies against H2AC20 are reported. Each links to that disease's full target list.

ReferencesPubMed · IEDB

Publications for H2AC20 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.

Reference: B cellIEDB

1 publication

Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. IEDB — curated epitope assays from the Immune Epitope Database (Vita et al., Nucleic Acids Research 2019). Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.

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)
1.59
gnomAD pLI
0.19
DepMap mean gene effect
-0.87
DepMap dependency class
common

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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

InteractionsUniProt · HPA

Protein binding partners of H2AC20 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 H2AC20 as an antibody target. Whether an autoantibody or antibody against H2AC20 could matter depends on whether native H2AC20 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

H2AC20 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 H2AC20 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/H2AC20. 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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