H2BC17
Histone H2B type 1-O
Also known as: H2B.2, H2B/n, H2B1O_HUMAN, H2BFN, HIST1H2BO
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P23527
- Gene
- H2BC17
- Ensembl
- ENSG00000274641
- Chromosome
- 6
- Canonical length
- 126 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
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 H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]
Canonical amino-acid sequenceUniProt
126 residues, UniProt reviewed canonical sequence.
>P23527|H2BC17
1 MPDPAKSAPA PKKGSKKAVT KAQKKDGKKR KRSRKESYSI YVYKVLKQVH PDTGISSKAM
61 GIMNSFVNDI FERIAGEASR LAHYNKRSTI TSREIQTAVR LLLPGELAKH AVSEGTKAVT
121 KYTSSKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against H2BC17 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)
- 0.52
- Highest tissue expression
- 2.4 nTPM
Expression across tissuesHPA
Tissue
- thymus: 2.4 nTPM
- bone marrow: 2.3 nTPM
- spleen: 1.2 nTPM
- lung: 0.9 nTPM
- cervix: 0.7 nTPM
- choroid plexus: 0.7 nTPM
Single-cell type
- erythrocyte progenitors: 39 nCPM
- monocyte progenitors: 21 nCPM
- megakaryocyte progenitors: 18 nCPM
- platelets: 11 nCPM
- neutrophil progenitors: 9.4 nCPM
- megakaryocyte-erythroid progenitors: 3.2 nCPM
Immune cell
- neutrophil: 2.6 nTPM
- total PBMC: 2 nTPM
- eosinophil: 1.7 nTPM
- myeloid DC: 1 nTPM
- naive B-cell: 0.9 nTPM
- plasmacytoid DC: 0.7 nTPM
Brain region
- pons: 5.7 nTPM
- white matter: 5.3 nTPM
- thalamus: 4.6 nTPM
- midbrain: 4.2 nTPM
- choroid plexus: 3.6 nTPM
- medulla oblongata: 3.6 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about H2BC17.
Disease | ImmuneIEDB
Conditions an epitope on H2BC17 was assayed in.
- rheumatoid arthritis B cell
- systemic lupus erythematosus T 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)
- 1.95
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads H2BC17 as an antibody target. Whether an autoantibody or antibody against H2BC17 could matter depends on whether native H2BC17 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
H2BC17 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 H2BC17 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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