Seroatlas · Human Serome Atlas

H1-3

Histone H1.3

Also known as: H1.3, H13_HUMAN, H1d, H1F3, H1s-2, HIST1H1D

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

Protein identityUniProt · HPA

UniProt accession
P16402
Gene
H1-3
Ensembl
ENSG00000124575
Chromosome
6
Canonical length
221 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

Histones are basic nuclear proteins responsible for 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 H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]

Canonical amino-acid sequenceUniProt

221 residues, UniProt reviewed canonical sequence.

>P16402|H1-3
     1  MSETAPLAPT IPAPAEKTPV KKKAKKAGAT AGKRKASGPP VSELITKAVA ASKERSGVSL
    61  AALKKALAAA GYDVEKNNSR IKLGLKSLVS KGTLVQTKGT GASGSFKLNK KAASGEGKPK
   121  AKKAGAAKPR KPAGAAKKPK KVAGAATPKK SIKKTPKKVK KPATAAGTKK VAKSAKKVKT
   181  PQPKKAAKSP AKAKAPKPKA AKPKSGKPKV TKAKKAAPKK K

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against H1-3 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)
0.63
Highest tissue expression
20 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 20 nTPM
  • choroid plexus: 7.1 nTPM
  • thymus: 5.1 nTPM
  • vagina: 4.2 nTPM
  • cervix: 3.3 nTPM
  • skin: 2.7 nTPM

Single-cell type

  • erythrocyte progenitors: 768 nCPM
  • monocyte progenitors: 381 nCPM
  • megakaryocyte progenitors: 276 nCPM
  • plasma cells: 228 nCPM
  • thymocytes: 200 nCPM
  • hematopoietic stem cells: 185 nCPM

Immune cell

  • naive B-cell: 47 nTPM
  • naive CD4 T-cell: 37 nTPM
  • plasmacytoid DC: 33 nTPM
  • memory B-cell: 32 nTPM
  • gdT-cell: 32 nTPM
  • naive CD8 T-cell: 31 nTPM

Brain region

  • cerebellum: 57 nTPM
  • white matter: 24 nTPM
  • cerebral cortex: 18 nTPM
  • pons: 18 nTPM
  • spinal cord: 16 nTPM
  • choroid plexus: 15 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about H1-3.

Disease | ImmuneIEDB

Conditions an epitope on H1-3 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)
1.71
gnomAD pLI
0.16
DepMap mean gene effect
-0.07
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

InteractionsUniProt · HPA

Protein binding partners of H1-3 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 H1-3 as an antibody target. Whether an autoantibody or antibody against H1-3 could matter depends on whether native H1-3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

H1-3 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 H1-3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/H1-3. 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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