GALNT17, polypeptide N-acetylgalactosaminyltransferase 17

GALNT17, polypeptide N-acetylgalactosaminyltransferase 17

• 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. [provided by RefSeq, Jan 2013]

• Gene Synonyms (polypeptide N-acetylgalactosaminyltransferase 17, 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, Williams-Beuren syndrome chromosome region 17, galNAc-T-like protein 3, polypeptide GalNAc transferase 3, polypeptide GalNAc transferase-like protein 3, polypeptide N-acetylgalactosaminyltransferase WBSCR17, polypeptide N-acetylgalactosaminyltransferase-like 3, pp-GaNTase-like protein 3, pp-GalNAc-transferase 20, ppGalNAc-T17, protein-UDP acetylgalactosaminyltransferase-like protein 3, putative polypeptide N-acetylgalactosaminyltransferase-like protein 3, williams-Beuren syndrome chromosomal region 17 protein, GALNACT17, GALNT16, GALNT20, GALNTL3, GalNAc-T17, GalNAc-T19, GalNAc-T5L, WBSCR17,)
• NCBI Gene ID: 64409
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q2L4S5
  UNIPROT ID#>>Q6IS24
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

polypeptide N-acetylgalactosaminyltransferase 17 interacts with:

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