Description
Product Characteristics:
This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, adevelopmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008].
Subcellular location: Nucleus
Synonyms: Coiled coil domain containing 28B, Coiled coil domain containing protein 28B, MGC1203, MGC16441, RP4 622L5.5, CC28B_HUMAN.
Target Information: The product of this gene localizes to centrosomes and basal bodies. It interacts and colocalizes with several proteins associated with Bardet-Biedl syndrome (BBS). [provided by RefSeq, Jul 2008]