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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for WBSCR17 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID64409
Official gene symbolWBSCR17
Full nameWilliams-Beuren syndrome chromosome region 17
Aliases,DKFZp434I2216,DKFZp761D2324,GALNT16,GALNT20,GALNTL3,
Gene summaryThis gene encodes an N-acetylgalactosaminyltransferase, which has 97% sequence identity to the mouse protein. This gene 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 position70597789 - 71178584  Map Viewer
Gene orientationplus
Gene size580796 bp
Gene sequence