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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 |
|---|---|---|---|---|---|
| C0409974 | Lupus Erythematosus | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C0022658 | Kidney Diseases | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C3805278 | Extrahepatic Cholangiocarcinoma | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C0042164 | Uveitis | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C0030186 | Paget Disease Extramammary | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C0008312 | Primary biliary cirrhosis | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C0079731 | B-Cell Lymphomas | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C0036202 | Sarcoidosis | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C0017661 | IGA Glomerulonephritis | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C0268398 | Familial lichen amyloidosis | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0085215 | Ovarian Failure, Premature | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0025322 | Premature Menopause | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0027651 | Neoplasms | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C3494522 | Hypergonadotropic Ovarian Failure, X-Linked | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0002994 | Angioedema | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C4552079 | Premature Ovarian Failure 1 | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0007847 | Malignant tumor of cervix | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0302592 | Cervix carcinoma | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0376358 | Malignant neoplasm of prostate | XPNPEP2 | 7512 | X-prolyl aminopeptidase 2 | O43895 |
| C0007131 | Non-Small Cell Lung Carcinoma | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
| C0235480 | Paroxysmal atrial fibrillation | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
| C0028754 | Obesity | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
| C0152013 | Adenocarcinoma of lung (disorder) | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
| C0004238 | Atrial Fibrillation | XXYLT1 | 152002 | xyloside xylosyltransferase 1 | Q8NBI6 |
