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	81554 Human
Uniprot	AAH07823 Human AAH07823.1 Human
Product By Gene ID	81554
Alternate Names	Williams-Beuren syndrome chromosomal region 16 protein MGC44931 MGC189739 DKFZp434D0421 RCC1-like G exchanging factor-like protein Williams-Beuren syndrome chromosome region 16

Diseases related to WBSCR16

Discover more about diseases related to WBSCR16.

Haploinsufficiency
Williams Syndrome
Developmental Disabilities

Bioinformatics Tool for WBSCR16

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