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 WBSCR27 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID155368
Official gene symbolWBSCR27
Full nameWilliams Beuren syndrome chromosome region 27
Aliases,MGC40131,
Gene summaryThis gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq]
LocationChromosome: 7   Locus: 7q11.23
Gene position73256855 - 73248920  Map Viewer
Gene orientationminus
Gene size7936 bp
Gene sequence
OMIM ID612546