XB-FEAT-6032436: Difference between revisions
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= | =galnt17= | ||
This is the community wiki page for the gene '' | This is the community wiki page for the gene ''galnt17'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
05/08/2017 | |||
Human symbol has changed for genepage ID: 6032436 From wbscr17 to galnt17 | |||
Human symbol has changed for Entrez Gene: 64409. From WBSCR17 to GALNT17 | |||
Human name has changed for Entrez Gene: 64409. From Williams-Beuren syndrome chromosome region 17 to polypeptide N-acetylgalactosaminyltransferase 17 | |||
=summary= | |||
In humans, 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] | |||
Latest revision as of 08:53, 15 May 2017
galnt17
This is the community wiki page for the gene galnt17 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
05/08/2017
Human symbol has changed for genepage ID: 6032436 From wbscr17 to galnt17
Human symbol has changed for Entrez Gene: 64409. From WBSCR17 to GALNT17
Human name has changed for Entrez Gene: 64409. From Williams-Beuren syndrome chromosome region 17 to polypeptide N-acetylgalactosaminyltransferase 17
summary
In humans, 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]