congenital disorder of glycosylation type ii Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain. (Human Disease Ontology, DOID_0050571)
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Genes

6 genes co-occuring with the disease congenital disorder of glycosylation type ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
COG1 component of oligomeric golgi complex 1 2.38557
MAN1B1 mannosidase, alpha, class 1B, member 1 1.99364
COG4 component of oligomeric golgi complex 4 1.86552
COG8 component of oligomeric golgi complex 8 1.84545
B4GALT6 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 6 1.48033
TF transferrin 0.379256