BCL6B

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Description

The BCL6B (BCL6B transcription repressor) is a protein-coding gene located on chromosome 17.

B-cell CLL/lymphoma 6 member B protein is a protein that in humans is encoded by the BCL6B gene. You can find more information about this gene's location and details on the UCSC Genome Browser.

BCL6B is also known as BAZF, ZBTB28, ZNF62.

Associated Diseases

• Okt4 epitope deficiency
• common variable immunodeficiency
• combined immunodeficiency due to moesin deficiency
• agammaglobulinemia 7, autosomal recessive
• X-linked severe congenital neutropenia
• primary familial polycythemia due to EPO receptor mutation
• immunodeficiency 18
• combined immunodeficiency with skin granulomas
• reticular dysgenesis
• neutropenia, severe congenital, 2, autosomal dominant
• severe combined immunodeficiency due to CARD11 deficiency
• immunodeficiency, common variable, 4
• neutropenia, severe congenital, 1, autosomal dominant
• X-linked sideroblastic anemia 1