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 |
|---|---|---|---|---|---|
| C0017574 | Gingivitis | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
| C0017574 | Gingivitis | SELE | 6401 | selectin E | P16581 |
| C0017574 | Gingivitis | FCN2 | 2220 | ficolin 2 | Q15485 |
| C0017574 | Gingivitis | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C0017574 | Gingivitis | OCRL | 4952 | OCRL inositol polyphosphate-5-phosphatase | Q01968 |
| C0017574 | Gingivitis | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0017572 | Gingival Recession | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C0017572 | Gingival Recession | LCT | 3938 | lactase | P09848 |
| C0017567 | Gingival Hypertrophy | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0017551 | Gilbert Disease (disorder) | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0017551 | Gilbert Disease (disorder) | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0017551 | Gilbert Disease (disorder) | G6PD | 2539 | glucose-6-phosphate dehydrogenase | P11413 |
| C0017551 | Gilbert Disease (disorder) | UGT1A7 | 54577 | UDP glucuronosyltransferase family 1 member A7 | Q9HAW7 |
| C0017551 | Gilbert Disease (disorder) | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0017551 | Gilbert Disease (disorder) | UGT1A10 | 54575 | UDP glucuronosyltransferase family 1 member A10 | Q9HAW8 |
| C0017551 | Gilbert Disease (disorder) | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
| C0017551 | Gilbert Disease (disorder) | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
| C0017551 | Gilbert Disease (disorder) | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
| C0017551 | Gilbert Disease (disorder) | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
| C0017551 | Gilbert Disease (disorder) | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0017551 | Gilbert Disease (disorder) | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0017551 | Gilbert Disease (disorder) | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0017551 | Gilbert Disease (disorder) | SELP | 6403 | selectin P | P16109 |
| C0017551 | Gilbert Disease (disorder) | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0017551 | Gilbert Disease (disorder) | PRKAA2 | 5563 | protein kinase AMP-activated catalytic subunit alpha 2 | P54646 |
