Species Human Entrez 64409 | Human Mouse Ensembl ENSG00000185274 | |
Aliases WBSCR17, GALNACT17, GALNT16, GALNT20, GALNTL3, GalNAc-T5L, Williams-Beuren syndrome chromosome region 17 External IDs MGI: 2137594 HomoloGene: 49707 GeneCards: WBSCR17 | ||
Putative polypeptide N-acetylgalactosaminyltransferase-like protein 3 is an enzyme that in humans is encoded by the WBSCR17 gene.
This 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.
References
WBSCR17 Wikipedia(Text) CC BY-SA