BRWD3


Description

The BRWD3 (bromodomain and WD repeat domain containing 3) is a protein-coding gene located on chromosome X.

BRWD3 (Bromodomain and WD repeat-containing protein 3) is a human protein encoded by the BRWD3 gene. It contains a bromodomain and several WD repeats, suggesting a role in chromatin modification and transcription. Mutations in BRWD3 can lead to mental retardation or permanent paralysis X-linked type 93, also known as mental retardation X-linked with macrocephaly. Additionally, BRWD3 is linked to translocations in B-cell chronic lymphocytic leukemia.

BRWD3 is involved in regulating cell morphology and cytoskeletal organization. It is essential for controlling cell shape.

BRWD3 is also known as BRODL, MRX93, XLID93.

Associated Diseases


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