Database of mammalian genes
Home

Home Search Browse Statistics User guide FAQs Links Questions Contribute Download


Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for WBSCR16 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID81554
Official gene symbolWBSCR16
Full nameWilliams-Beuren syndrome chromosome region 16
Aliases,DKFZp434D0421,MGC189739,MGC44931,
Gene summaryThis 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. [provided by RefSeq]
LocationChromosome: 7   Locus: 7q11.23
Gene position74489699 - 74456283  Map Viewer
Gene orientationminus
Gene size33417 bp
Gene sequence