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 KLocalizationUniProt · 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.
- systemic scleroderma B cell
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
- chromosome condensation
- negative regulation of DNA recombination
- negative regulation of transcription by RNA polymerase II
- nucleosome assembly
- regulation of mRNA splicing, via spliceosome
Molecular functions
- chromatin DNA binding
- double-stranded DNA binding
- nucleosomal DNA binding
- RNA binding
- structural constituent of chromatin
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.
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