H2AFB1

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

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).[5]

AliasesH2AB1, H2A.Bbd, H2A histone family member B1, H2A.B, H2A.B variant histone 1, H2AFB1, H2A.B.2
End154,885,558 bp[1]
Quick facts H2AB1, Identifiers ...
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
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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[3][4]
Wikidata
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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.[5]

References

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