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Genes search result for Homo sapiens
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2 records found for search term Galnt2
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1321743GALNT2polypeptide N-acetylgalactosaminyltransferase 2This gene encodes a member of the glycosyltransferase 2 protein family. Members of this family initiate mucin-type O-glycoslation of peptides in the Golgi apparatus. The encoded protein may be involved in O-linked glycosylation of the immunoglobulin A1 hinge region. This gene may influence triglycer1230057789230282122Human265symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1342451GALNT17polypeptide N-acetylgalactosaminyltransferase 17This 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. [77113214471713599Human63old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]