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 |
|---|---|---|---|---|---|
| C0027651 | Neoplasms | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0242379 | Malignant neoplasm of lung | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0002170 | Alopecia | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0006142 | Malignant neoplasm of breast | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0022661 | Kidney Failure, Chronic | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0011847 | Diabetes | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C1263846 | Attention deficit hyperactivity disorder | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0032460 | Polycystic Ovary Syndrome | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0038454 | Cerebrovascular accident | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C1561643 | Chronic Kidney Diseases | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0005587 | Depression, Bipolar | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0028754 | Obesity | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0205643 | Carcinoma, Cribriform | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0037772 | Spastic Paraplegia | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C1849115 | SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder) | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0393559 | Troyer syndrome | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0025517 | Metabolic Diseases | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0235782 | Gallbladder Carcinoma | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0034152 | Henoch-Schoenlein Purpura | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0023772 | Lipid Metabolism, Inborn Errors | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0029408 | Degenerative polyarthritis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0011849 | Diabetes Mellitus | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C3151147 | Bile Acid Synthesis Defect, Congenital, 3 | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0009319 | Colitis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0011847 | Diabetes | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
