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 ▲ |
|---|---|---|---|---|---|
| C0002395 | Alzheimer's Disease | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
| C1140680 | Malignant neoplasm of ovary | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
| C0010068 | Coronary heart disease | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
| C0040580 | Tracheal Diseases | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
| C0040580 | Tracheal Diseases | DPEP3 | 64180 | dipeptidase 3 | Q9H4B8 |
| C0010068 | Coronary heart disease | DPEP3 | 64180 | dipeptidase 3 | Q9H4B8 |
| C0027651 | Neoplasms | ST6GALNAC4 | 27090 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 | Q9H4F1 |
| C0206682 | Follicular thyroid carcinoma | ST6GALNAC4 | 27090 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 | Q9H4F1 |
| C0018378 | Guillain-Barre Syndrome | ST6GALNAC4 | 27090 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4 | Q9H4F1 |
| C0032460 | Polycystic Ovary Syndrome | FBXO44 | 93611 | F-box protein 44 | Q9H4M3 |
| C1136382 | Sclerocystic Ovaries | FBXO44 | 93611 | F-box protein 44 | Q9H4M3 |
| C0033578 | Prostatic Neoplasms | FBXO44 | 93611 | F-box protein 44 | Q9H4M3 |
| C0376358 | Malignant neoplasm of prostate | FBXO44 | 93611 | F-box protein 44 | Q9H4M3 |
| C4015597 | MYASTHENIC SYNDROME, CONGENITAL, 14 | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0009363 | Congenital ocular coloboma (disorder) | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C3665347 | Visual Impairment | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0027651 | Neoplasms | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0751882 | Myasthenic Syndromes, Congenital | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0684276 | Hypsarrhythmia | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C1306459 | Primary malignant neoplasm | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0026848 | Myopathy | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0266551 | Congenital coloboma of iris | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0241005 | Creatine phosphokinase serum increased | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0751883 | Congenital Myasthenic Syndromes, Postsynaptic | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0282577 | Congenital Disorders of Glycosylation | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
