HIST2H2BE

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Histone H2B type 2-E is a protein that in humans is encoded by the HIST2H2BE gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesH2BC21, GL105, H2B, H2B.1, H2BFQ, H2BGL105, H2BQ, histone cluster 2, H2be, histone cluster 2 H2B family member e, H2B clustered histone 21, HIST2H2BE, H2BE, H2B-GL105
Quick facts H2BC21, Available structures ...
H2BC21
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesH2BC21, GL105, H2B, H2B.1, H2BFQ, H2BGL105, H2BQ, histone cluster 2, H2be, histone cluster 2 H2B family member e, H2B clustered histone 21, HIST2H2BE, H2BE, H2B-GL105
External IDsOMIM: 601831; MGI: 2448409; HomoloGene: 128426; GeneCards: H2BC21; OMA:H2BC21 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003528

NM_001290466
NM_178202

RefSeq (protein)

NP_003519

NP_001277395
NP_835509

Location (UCSC)Chr 1: 149.88 – 149.89 MbChr 13: 21.97 – 21.97 Mb
PubMed search[3][4]
Wikidata
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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 encodes a member of the histone H2B family, and generates two transcripts through the use of the conserved stem-loop termination motif, and the polyA addition motif.[7]

Cancer

HIST2H2BE gene has been detected progressively downregulated in Human papillomavirus-positive neoplastic keratinocytes derived from uterine cervical preneoplastic lesions at different levels of malignancy.[8] For this reason, this gene is likely to be associated with tumorigenesis and may be a potential prognostic marker for uterine cervical preneoplastic lesions progression.[8]

References

Further reading

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