IMP
Process View
Homo sapiens
10 genes annotated in human
congenital disorder of glycosylation type ii
DOID:0050571
A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain.
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In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "congenital disorder of glycosylation type ii"
| Name | Description | Probability | Func Analog Organism | |
|---|---|---|---|---|
| COG4 | component of oligomeric golgi complex 4 | 0.992 | ||
| COG3 | component of oligomeric golgi complex 3 | 0.907 | ||
| COG7 | component of oligomeric golgi complex 7 | 0.257 | ||
| COG1 | component of oligomeric golgi complex 1 | 0.124 | ||
| SCFD1 | sec1 family domain containing 1 | 0.061 | ||
| COG2 | component of oligomeric golgi complex 2 | 0.022 | ||
| STX5 | syntaxin 5 | 0.017 | ||
| SSR1 | signal sequence receptor, alpha | 0.016 | ||
| COG6 | component of oligomeric golgi complex 6 | 0.015 | ||
| SEPT2 | septin 2 | 0.013 | ||
| COG8 | component of oligomeric golgi complex 8 | 0.005 | ||
| COG5 | component of oligomeric golgi complex 5 | 0.003 | ||
| MOGS | mannosyl-oligosaccharide glucosidase | 0.002 | ||
| SLC35C1 | solute carrier family 35, member C1 | 0.002 | ||
| B4GALT1 | UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 | 0.001 | ||
| MGAT2 | mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase | 0.001 | ||
| SLC35A1 | solute carrier family 35 (CMP-sialic acid transporter), member A1 | 0.000 |