Compare GO annotations related to Congenital disorder of glycosylation, type Ic using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0042281dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase activity S000005528IMPYeastSGD_REF:S000070115|PMID:10336995
Molecular FunctionGO:0046527glucosyltransferase activity Q9Y672IDAHumanPMID:10359825
Molecular FunctionGO:0016758transferase activity, transferring hexosyl groups S000005528IMPYeastSGD_REF:S000055554|PMID:8877369
Cellular ComponentGO:0005783endoplasmic reticulum S000005528IMPYeastSGD_REF:S000055554|PMID:8877369
Biological ProcessGO:0009060aerobic respiration S000005528IMPYeastSGD_REF:S000081264|PMID:15794922
Biological ProcessGO:0006490oligosaccharide-lipid intermediate assembly S000005528IMPYeastSGD_REF:S000070115|PMID:10336995
Biological ProcessGO:0006486protein amino acid glycosylation S000005528IMPYeastSGD_REF:S000055554|PMID:8877369
Biological ProcessGO:0006487protein amino acid N-linked glycosylation Q9Y672IGIHumanPMID:10359825
Biological ProcessGO:0006487protein amino acid N-linked glycosylation Q9Y672IGIHumanPMID:11106564