Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Homo sapiens (human)
| Pathway Name | Protein Name | UniProt ID ▲ | Gene Symbol | GlyTouCan ID |
|---|---|---|---|---|
| Defective MAN1B1 causes MRT15 |
|
|||
| alectinib-resistant ALK mutants |
|
|||
| NVP-TAE684-resistant ALK mutants |
|
|||
| lorlatinib-resistant ALK mutants |
|
|||
| crizotinib-resistant ALK mutants |
|
|||
| ASP-3026-resistant ALK mutants |
|
|||
| ceritinib-resistant ALK mutants |
|
|||
| brigatinib-resistant ALK mutants |
|
|||
| Variant SLC6A14 may confer susceptibility towards obesity |
|
|||
| Synthesis of IPs in the ER lumen |
|
|||
| Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) |
|
|||
| Defective SLC6A5 causes hyperekplexia 3 (HKPX3) |
|
|||
| Nucleotide catabolism |
|
|||
| Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) |
|
|||
| Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) |
|
