Disease ID | Disease name | Source of annotation with ALG1 | OMIM link | Number of associated genes | genes |
---|---|---|---|---|---|
PS212065 | CONGENITAL DISORDERS OF GLYCOSYLATION, TYPE I | ClinVar, OMIM, HUMSAVAR | link to OMIM | 25 | ALG2, ALG1, ALG13, ALG3, CAD, STT3A, SRD5A3, ALG12, ALG8, DPAGT1, DDOST, ALG6, MPI, PMM2, STT3B, DOLK, MPDU1, RFT1, PGM1, ALG9, DPM1, DPM3, ALG11, DPM2, SSR4 |
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KEGG pathway | KEGG ID | KEGG IC |
---|---|---|
N-Glycan biosynthesis | hsa00510 | 7.07 |
Metabolic pathways | hsa01100 | 2.49 |
REACTOME pathway | REACTOME ID | REACTOME IC |
---|---|---|
Defective ALG1 causes ALG1-CDG (CDG-1k) | R-HSA-4549380 | 12.98 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | R-HSA-446193 | 6.92 |
Metabolism of proteins | R-HSA-392499 | 3.41 |
Asparagine N-linked glycosylation | R-HSA-446203 | 6.1 |
Diseases of glycosylation | R-HSA-3781865 | 6.89 |
Post-translational protein modification | R-HSA-597592 | 4.54 |
Diseases associated with N-glycosylation of proteins | R-HSA-3781860 | 8.89 |
Disease | R-HSA-1643685 | 3.33 |
GO term | GO ID | GO IC |
---|---|---|
transferase activity, transferring glycosyl groups | GO:0016757 | 4.08 |
catalytic activity | GO:0003824 | 1.05 |
transferase activity | GO:0016740 | 1.95 |
GO:0019187 | 9.74 | |
transferase activity, transferring hexosyl groups | GO:0016758 | 4.43 |
GO:0004578 | 9.74 | |
mannosyltransferase activity | GO:0000030 | 6.52 |