H2AC6
Histone H2A type 1-C
Also known as: H2A1C_HUMAN, H2AFL, HIST1H2AC
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q93077
- Gene
- H2AC6
- Ensembl
- ENSG00000180573
- Chromosome
- 6
- Canonical length
- 130 aa
- Protein class
- Cancer-related genes, 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. 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
130 residues, UniProt reviewed canonical sequence.
>Q93077|H2AC6
1 MSGRGKQGGK ARAKAKSRSS RAGLQFPVGR VHRLLRKGNY AERVGAGAPV YLAAVLEYLT
61 AEILELAGNA ARDNKKTRII PRHLQLAIRN DEELNKLLGR VTIAQGGVLP NIQAVLLPKK
121 TESHHKAKGKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against H2AC6 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)
- 0.48
- Highest tissue expression
- 34 nTPM
Expression across tissuesHPA
Tissue
- liver: 34 nTPM
- vagina: 23 nTPM
- esophagus: 22 nTPM
- cervix: 22 nTPM
- lung: 21 nTPM
- kidney: 20 nTPM
Single-cell type
- platelets: 6,283 nCPM
- esophageal apical cells: 841 nCPM
- basal prostatic cells: 616 nCPM
- neutrophils: 547 nCPM
- prostatic club cells: 496 nCPM
- prostatic hillock cells: 412 nCPM
Immune cell
- neutrophil: 1,567 nTPM
- total PBMC: 664 nTPM
- basophil: 443 nTPM
- eosinophil: 326 nTPM
- naive B-cell: 110 nTPM
- plasmacytoid DC: 80 nTPM
Brain region
- white matter: 203 nTPM
- spinal cord: 174 nTPM
- hypothalamus: 155 nTPM
- basal ganglia: 145 nTPM
- medulla oblongata: 145 nTPM
- cerebellum: 144 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about H2AC6.
Disease | ImmuneIEDB
Conditions an epitope on H2AC6 was assayed in.
- systemic lupus erythematosus 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)
- 1.03
- gnomAD pLI
- 0.6
- DepMap mean gene effect
- -0.7
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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 H2AC6 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 H2AC6 as an antibody target. Whether an autoantibody or antibody against H2AC6 could matter depends on whether native H2AC6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
H2AC6 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 H2AC6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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