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WBSCR17 encodes an N-acetylgalactosaminyltransferase.
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GWA study identified maternal genetic effects not previously identified in ASD (show ARSD Antibodies) at a locus in WBSCR17.
a subset of O-glycosylation produced by WBSCR17 controls dynamic membrane trafficking, probably between the cell surface and the late endosomes through macropinocytosis
This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking.
UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase-like 3
, UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase-like protein 3
, UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 16
, galNAc-T-like protein 3
, polypeptide GalNAc transferase-like protein 3
, polypeptide N-acetylgalactosaminyltransferase WBSCR17
, pp-GaNTase-like protein 3
, pp-GalNAc-transferase 20
, protein-UDP acetylgalactosaminyltransferase-like protein 3
, putative polypeptide N-acetylgalactosaminyltransferase-like protein 3
, williams-Beuren syndrome chromosomal region 17 protein
, UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase
, polypeptide N-acetylgalactosaminyltransferase-like 3
, williams-Beuren syndrome chromosomal region 17 protein homolog