WBSCR17 Products

Description

WBSCR17 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]

Bioinformatics

Entrez	64409 Human
Uniprot	NM_022479 Human NP_071924.1 Human Q6IS24 Human
Product By Gene ID	64409
Alternate Names	DKFZp434I2216 EC 2.4.1.41 GalNAc-T-like protein 3 GALNT16 GALNT20 GALNTL3DKFZp761D2324 Polypeptide GalNAc transferase-like protein 3 polypeptide N-acetylgalactosaminyltransferase WBSCR17 pp-GalNAc-transferase 20 pp-GaNTase-like protein 3 Protein-UDP acetylgalactosaminyltransferase-like protein 3 putative polypeptide N-acetylgalactosaminyltransferase-like protein 3 UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase-like 3 UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase-like protein 3 UDP-N-acetyl-alpha-D-galactosamine:polypeptideN-acetylgalactosaminyltransferase 16 Williams-Beuren syndrome chromosomal region 17 protein Williams-Beuren syndrome chromosome region 17