BCL-6 corepressor

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

BCL-6 corepressor is a protein that in humans is encoded by the BCOR gene.[5][6]

AliasesBCOR, ANOP2, MAA2, MCOPS2, BCL6 corepressor
External IDsOMIM: 300485; MGI: 1918708; GeneCards: BCOR
PDBOrtholog search: PDBe RCSB
Quick facts BCOR, Identifiers ...
BCOR
Identifiers
AliasesBCOR, ANOP2, MAA2, MCOPS2, BCL6 corepressor
External IDsOMIM: 300485; MGI: 1918708; GeneCards: BCOR
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001168321
NM_029510
NM_175044
NM_175045
NM_175046

RefSeq (protein)

NP_001116855
NP_001116856
NP_001116857
NP_060215

NP_001161793
NP_083786
NP_778209
NP_778210
NP_778211

Location (UCSC)Chr X: 40.05 – 40.18 MbChr X: 11.9 – 12.03 Mb
PubMed search[3][4]
Wikidata
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Function

The protein encoded by this gene was identified as an interacting corepressor of BCL6, a POZ/zinc finger transcription repressor that is required for germinal center formation and may influence apoptosis. This protein selectively interacts with the POZ domain of BCL6, but not with eight other POZ proteins. Specific class I and II histone deacetylases (HDACs) have been shown to interact with this protein, which suggests a possible link between the two classes of HDACs. At least four alternatively spliced transcript variants, which encode different isoforms, have been reported for this gene.[6]

Clinical significance

Mutations in the BCOR gene cause a form of syndromic microphthalmia (small eye) called MCOPS2. This syndrome incorporates microphthalmia, congenital cataracts, cardiac defects, dental defects and skeletal anomalies. Mutations in this gene have also been found associated to acute myeloid leukemia.[7]

Interactions

BCOR has been shown to interact with MLLT3[8] and BCL6.[5]

References

Further reading

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