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Gene : BCL11B Homo sapiens

Name  ? BAF chromatin remodeling complex subunit BCL11B Cytological Location  14q32.2
Brief Description  BAF chromatin remodeling complex subunit BCL11B
Description  This gene encodes a C2H2-type zinc finger protein and is closely related to BCL11A, a gene whose translocation may be associated with B-cell malignancies. Although the specific function of this gene has not been determined, the encoded protein is known to be a transcriptional repressor, and is regulated by the NURD nucleosome remodeling and histone deacetylase complex. Four alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Aug 2013]
  • synonyms:
  • BCL11B,
  • hRIT1-alpha,
  • CTIP2,
  • CTIP-2,
  • RIT1,
  • uc001yga.5,
  • HGNC:13222,
  • CTIP-2,
  • ATL1-delta,
  • B-cell CLL/lymphoma 11B (zinc finger protein),
  • B cell CLL/lymphoma 11B,
  • CTIP2,
  • BCL11B, BAF complex component,
  • ATL1-alpha,
  • hRIT1-alpha,
  • NM_138576,
  • ATL1-beta,
  • ZNF856B,
  • AJ404614,
  • ATL1,
  • ZNF856B,
  • ATL1-gamma,
  • OTTHUMG00000028967,
  • IMD49
  • identifiers:
  • 64919,
  • ENSG00000127152,
  • BCL11B

Genome feature

Region: gene ? Length: 102911  
Location: 14:99169287-99272197 reverse strand Cyto location: 14q32.2

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

49 SNPs

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results