HIST1H2BL

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

Histone H2B type 1-L is a protein that in humans is encoded by the HIST1H2BL gene.[5][6][7]

AliasesH2BC13, H2B/c, H2BFC, dJ97D16.4, histone cluster 1, H2bl, histone cluster 1 H2B family member l, H2B clustered histone 13, HIST1H2BL
End27,807,929 bp[1]
Quick facts H2BC13, Identifiers ...
H2BC13
Identifiers
AliasesH2BC13, H2B/c, H2BFC, dJ97D16.4, histone cluster 1, H2bl, histone cluster 1 H2B family member l, H2B clustered histone 13, HIST1H2BL
External IDsOMIM: 602800; MGI: 2448388; HomoloGene: 136771; GeneCards: H2BC13; OMA:H2BC13 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003519

NM_178198

RefSeq (protein)

NP_003510

Location (UCSC)Chr 6: 27.81 – 27.81 MbChr 13: 22.23 – 22.23 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 is intronless and encodes 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.[7]

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