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H2AFB1

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Protein-coding gene in the species Homo sapiens
H2AB1
Identifiers
AliasesH2AB1, H2A.Bbd, H2A histone family member B1, H2A.B, H2A.B variant histone 1, H2AFB1, H2A.B.2
External IDsMGI: 3644980; HomoloGene: 129517; GeneCards: H2AB1; OMA:H2AB1 - orthologs
Gene location (Human)
X chromosome (human)
Chr.X chromosome (human)
X chromosome (human)Genomic location for H2AB1Genomic location for H2AB1
BandXq28Start154,884,972 bp
End154,885,558 bp
Gene location (Mouse)
X chromosome (mouse)
Chr.X chromosome (mouse)
X chromosome (mouse)Genomic location for H2AB1Genomic location for H2AB1
BandX|X E1Start115,590,875 bp
End115,591,222 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • testicle

  • apex of heart

  • right testis

  • left testis

  • ganglionic eminence

  • blood

  • duodenum

  • muscle of thigh

  • olfactory zone of nasal mucosa

  • bone marrow
Top expressed in
  • spleen

  • thymus

  • dentate gyrus of hippocampal formation granule cell

  • lung
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

474382

624153

Ensembl

ENSG00000274183

ENSMUSG00000082482

UniProt

P0C5Y9

S4R1M3

RefSeq (mRNA)

NM_001017990

NM_001281530

RefSeq (protein)

NP_001017990

NP_001268459

Location (UCSC)Chr X: 154.88 – 154.89 MbChr X: 115.59 – 115.59 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Histone H2A-Bbd type 1 also known as H2A Barr body-deficient is a histone protein variant that in humans is encoded by the H2AFB1 gene (H2A histone family, member B1).

Function

Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a member of the histone H2A family. This gene is part of a region that is repeated three times on chromosome X, once in intron 22 of the F8 gene and twice closer to the Xq telomere. This record represents the most centromeric copy which is in intron 22 of the F8 gene.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000274183Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000082482Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: H2A histone family".

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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