Automated description from the Alliance of Genome Resources (Release 7.4.0)
Enables acetylglucosaminyltransferase activity. Involved in neuron migration and protein O-linked mannosylation. Predicted to be active in endoplasmic reticulum membrane. Is expressed in brain and eye. Human ortholog(s) of this gene implicated in congenital muscular dystrophy-dystroglycanopathy type A8 and muscular dystrophy-dystroglycanopathy type C8. Orthologous to human POMGNT2 (protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)).
This site uses cookies.
Some cookies are essential for site operations and others help us analyze use and utility of our web site.
Please refer to our
privacy policy
for more information.