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WBSCR16 encodes an RCC1-like G-exchanging factor. Additionally we are shipping WBSCR16 Antibodies (23) and many more products for this protein.
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Using X-ray crystallography, established the structure of human Williams-Beuren Syndrome Chromosomal Region 16 (WBSCR16), and showed that WBSCR16 has seven-bladed b-propeller fold (the RCC1 (show RCC1 Proteins) fold) with unique surface features.
This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
RCC1-like G exchanging factor-like protein
, Williams-Beuren syndrome chromosomal region 16 protein
, Williams-Beuren syndrome chromosomal region 16 protein homolog