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
DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name ▼ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0282577 | Congenital Disorders of Glycosylation | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C0282577 | Congenital Disorders of Glycosylation | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0282577 | Congenital Disorders of Glycosylation | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0282577 | Congenital Disorders of Glycosylation | B4GALT1 | 2683 | beta-1,4-galactosyltransferase 1 | P15291 |
| C0282577 | Congenital Disorders of Glycosylation | FUT8 | 2530 | fucosyltransferase 8 | Q9BYC5 |
| C0282577 | Congenital Disorders of Glycosylation | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
| C0282577 | Congenital Disorders of Glycosylation | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0282577 | Congenital Disorders of Glycosylation | ALG11 | 440138 | ALG11 alpha-1,2-mannosyltransferase | Q2TAA5 |
| C0282577 | Congenital Disorders of Glycosylation | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0282577 | Congenital Disorders of Glycosylation | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0282577 | Congenital Disorders of Glycosylation | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0282577 | Congenital Disorders of Glycosylation | ST3GAL3 | 6487 | ST3 beta-galactoside alpha-2,3-sialyltransferase 3 | Q11203 |
| C0282577 | Congenital Disorders of Glycosylation | ALG9 | 79796 | ALG9 alpha-1,2-mannosyltransferase | Q9H6U8 |
| C0282577 | Congenital Disorders of Glycosylation | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
| C0282577 | Congenital Disorders of Glycosylation | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0282577 | Congenital Disorders of Glycosylation | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C0282577 | Congenital Disorders of Glycosylation | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0282577 | Congenital Disorders of Glycosylation | DDOST | 1650 | dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit | P39656 |
| C0282577 | Congenital Disorders of Glycosylation | AGA | 175 | aspartylglucosaminidase | P20933 |
| C0282577 | Congenital Disorders of Glycosylation | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
| C0282577 | Congenital Disorders of Glycosylation | MPI | 4351 | mannose phosphate isomerase | P34949 |
| C0282577 | Congenital Disorders of Glycosylation | PMM2 | 5373 | phosphomannomutase 2 | O15305 |
| C0282577 | Congenital Disorders of Glycosylation | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
| C0282577 | Congenital Disorders of Glycosylation | COG6 | 57511 | component of oligomeric golgi complex 6 | Q9Y2V7 |
| C0282577 | Congenital Disorders of Glycosylation | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
