BCL7A

Protein-coding gene in humans From Wikipedia, the free encyclopedia

B-cell CLL/lymphoma 7 protein family member A is a protein that in humans is encoded by the BCL7A gene located in the chromosome 12 (Cytogenetic band: 12q24.31).[5]

AliasesBCL7A, BCL7, B-cell CLL/lymphoma 7A, BCL tumor suppressor 7A, BAF complex component, BAF chromatin remodeling complex subunit SMARCJ1
End122,062,044 bp[1]
Quick facts Identifiers, Aliases ...
BCL7A
Identifiers
AliasesBCL7A, BCL7, B-cell CLL/lymphoma 7A, BCL tumor suppressor 7A, BAF complex component, BAF chromatin remodeling complex subunit SMARCJ1
External IDsOMIM: 601406; MGI: 1924295; HomoloGene: 10869; GeneCards: BCL7A; OMA:BCL7A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_020993
NM_001024808

NM_029850

RefSeq (protein)

NP_001019979
NP_066273

NP_084126

Location (UCSC)Chr 12: 122.02 – 122.06 MbChr 5: 123.48 – 123.51 Mb
PubMed search[3][4]
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Function

This gene codifies for a protein that belongs to the SWI/SNF chromatin remodelling complex, a complex that is able to modify the interactions between DNA and histones using the energy of the ATP hydrolysis. It has found recurrently mutated in lymphomas[6] and silenced by promoter hypermetylation in haematological malignancies.[7][8]

See also

References

Further reading

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