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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 |
|---|---|---|---|---|---|
| C0013537 | Eclampsia | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0013537 | Eclampsia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0013537 | Eclampsia | CALR | 811 | calreticulin | P27797 |
| C0013537 | Eclampsia | ADH5 | 128 | alcohol dehydrogenase 5 (class III), chi polypeptide | P11766 |
| C0013537 | Eclampsia | ACE | 1636 | angiotensin I converting enzyme | P12821 |
| C0013537 | Eclampsia | ANXA5 | 308 | annexin A5 | P08758 |
| C0013537 | Eclampsia | LPL | 4023 | lipoprotein lipase | P06858 |
| C0013537 | Eclampsia | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0013537 | Eclampsia | PTGS1 | 5742 | prostaglandin-endoperoxide synthase 1 | P23219 |
| C0013537 | Eclampsia | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C0013537 | Eclampsia | CD14 | 929 | CD14 molecule | P08571 |
| C0013537 | Eclampsia | SORD | 6652 | sorbitol dehydrogenase | Q00796 |
| C0013537 | Eclampsia | IL18R1 | 8809 | interleukin 18 receptor 1 | Q13478 |
| C0013537 | Eclampsia | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0013537 | Eclampsia | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
| C0013537 | Eclampsia | HSD11B2 | 3291 | hydroxysteroid 11-beta dehydrogenase 2 | P80365 |
| C0013537 | Eclampsia | KLRB1 | 3820 | killer cell lectin like receptor B1 | Q12918 |
| C0013537 | Eclampsia | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0013528 | Echolalia | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
| C0013528 | Echolalia | HGSNAT | 138050 | heparan-alpha-glucosaminide N-acetyltransferase | Q68CP4 |
| C0013528 | Echolalia | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0013502 | Echinococcosis | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
| C0013473 | Eating Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0013473 | Eating Disorders | ACOT7 | 11332 | acyl-CoA thioesterase 7 | O00154 |
| C0013473 | Eating Disorders | DBT | 1629 | dihydrolipoamide branched chain transacylase E2 | P11182 |
