WBSCR16 Products


Description

WBSCR16 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. [provided by RefSeq]

Bioinformatics

Entrez Human
Uniprot Human
Human
Product By Gene ID 81554
Alternate Names
  • DKFZp434D0421
  • MGC189739
  • MGC44931
  • RCC1-like G exchanging factor-like protein
  • Williams-Beuren syndrome chromosomal region 16 protein
  • Williams-Beuren syndrome chromosome region 16