H2AC13 Gene

Name H2A clustered histone 13
Description 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 small histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015]
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Histone H2AC13 is one of the replication‐dependent core histone variants that, as an integral component of the nucleosome, contributes not only to chromatin compaction but also to the regulation of gene expression, cellular differentiation, and DNA repair. In several studies, H2A isoforms interacting with key repair proteins, such as MGMT, have been shown to enhance DNA repair activity and thereby promote genomic stability."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In the context of carcinogenesis, altered expression of H2A variants is frequently observed; increased levels of H2A isoforms (for example, those akin to H2AC13) correlate with dedifferentiation and the maintenance of an undifferentiated state in hepatocytes, suggesting a role in tumor progression and cell fate determination."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Furthermore, detailed mutagenesis and functional studies have demonstrated that while the N-terminal tail acetylation of major H2A variants may be nonessential for cell viability, it contributes to the establishment of a critical charge patch that governs nucleosome stability and interactions with chromatin remodelers."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": " Beyond its canonical role in organizing DNA, H2A isoforms have been implicated in nonchromatin functions; for instance, several reports indicate that the C-terminal regions of these proteins can bind bacterial lipopolysaccharide with high specificity and affinity—this interaction in turn can modulate immune cell activation and inflammatory signaling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": " In addition, environmental stresses such as exposure to polycyclic aromatic hydrocarbons result in altered abundance of H2A variants, highlighting their involvement in cellular stress responses."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": " Finally, the observation that transcripts encoding these histone variants remain stably expressed during key developmental transitions further underscores their function as dynamic regulators of chromatin architecture and gene expression programs."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": "\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Suryakant K Niture, Catalin E Doneanu, Chinavenmeni S Velu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Proteomic analysis of human O6-methylguanine-DNA methyltransferase by affinity chromatography and tandem mass spectrometry."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2005.09.177"}], "href": "https://doi.org/10.1016/j.bbrc.2005.09.177"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16226712"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16226712"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Monica Tyagi, Bharat Khade, Shafqat A Khan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Expression of histone variant, H2A.1 is associated with the undifferentiated state of hepatocyte."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Exp Biol Med (Maywood) (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1177/1535370214531869"}], "href": "https://doi.org/10.1177/1535370214531869"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24764240"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24764240"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Monica Tyagi, Divya Reddy, Sanjay Gupta "}, {"type": "b", "children": [{"type": "t", "text": "Genomic characterization and dynamic methylation of promoter facilitates transcriptional regulation of H2A variants, H2A.1 and H2A.2 in various pathophysiological states of hepatocyte."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Biochem Cell Biol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biocel.2017.01.019"}], "href": "https://doi.org/10.1016/j.biocel.2017.01.019"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28163185"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28163185"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Qinghu Ren, Martin A Gorovsky "}, {"type": "b", "children": [{"type": "t", "text": "The nonessential H2A N-terminal tail can function as an essential charge patch on the H2A.Z variant N-terminal tail."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.23.8.2778-2789.2003"}], "href": "https://doi.org/10.1128/MCB.23.8.2778-2789.2003"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12665578"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12665578"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Luis A Augusto, Paulette Decottignies, Monique Synguelakis, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Histones: a novel class of lipopolysaccharide-binding molecules."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochemistry (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1021/bi0268394"}], "href": "https://doi.org/10.1021/bi0268394"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12667084"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12667084"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Louisa Ada Hooven, William M Baird "}, {"type": "b", "children": [{"type": "t", "text": "Proteomic analysis of MCF-7 cells treated with benzo[a]pyrene, dibenzo[a,l]pyrene, coal tar extract, and diesel exhaust extract."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Toxicology (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.tox.2008.03.019"}], "href": "https://doi.org/10.1016/j.tox.2008.03.019"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18495319"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18495319"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Christian Vigneault, Isabelle Gilbert, Marc-André Sirard, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Using the histone H2a transcript as an endogenous standard to study relative transcript abundance during bovine early development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Reprod Dev (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/mrd.20665"}], "href": "https://doi.org/10.1002/mrd.20665"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17133602"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17133602"}]}]}]}
NCBI Gene ID 8329
API
Download Associations
Predicted Functions View H2AC13's ARCHS4 Predicted Functions.
Co-expressed Genes View H2AC13's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View H2AC13's ARCHS4 Predicted Functions.

Functional Associations

H2AC13 has 1,000 functional associations with biological entities spanning 5 categories (disease, phenotype or trait, chemical, functional term, phrase or reference, cell line, cell type or tissue, gene, protein or microRNA) extracted from 8 datasets.

Click the + buttons to view associations for H2AC13 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles tissue samples with high or low expression of H2AC13 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
CM4AI KOLF21J CRISPRi Gene Perturbation Atlas gene perturbations changing expression of H2AC13 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset.
DISEASES Experimental Gene-Disease Association Evidence Scores 2025 diseases associated with H2AC13 gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 diseases co-occuring with H2AC13 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
GTEx Tissue Gene Expression Profiles 2023 tissues with high or low expression of H2AC13 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.
LINCS L1000 CMAP Chemical Perturbation Consensus Signatures small molecule perturbations changing expression of H2AC13 gene from the LINCS L1000 CMAP Chemical Perturbations Consensus Signatures dataset.
PFOCR Pathway Figure Associations 2024 pathways involving H2AC13 protein from the Wikipathways PFOCR 2024 dataset.
Rummagene Transcription Factor Associations 2026 transcription factors regulating expression of H2AC13 gene from the Rummagene Transcription Factor Associations 2026 dataset.