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 |
|---|---|---|---|---|---|
| C1834582 | MYELOPROLIFERATIVE SYNDROME, TRANSIENT | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0036341 | Schizophrenia | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0011615 | Dermatitis, Atopic | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0271568 | Laron Syndrome | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0013595 | Eczema | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0028754 | Obesity | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0018784 | Sensorineural Hearing Loss (disorder) | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0035078 | Kidney Failure | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0027651 | Neoplasms | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0010054 | Coronary Arteriosclerosis | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0004238 | Atrial Fibrillation | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0027126 | Myotonic Dystrophy | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0043119 | Werner Syndrome | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0030297 | Pancreatic Neoplasm | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
| C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
| C0235974 | Pancreatic carcinoma | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
| C0026691 | Mucocutaneous Lymph Node Syndrome | SLC35F5 | 80255 | solute carrier family 35 member F5 | Q8WV83 |
| C0027651 | Neoplasms | SLC35F5 | 80255 | solute carrier family 35 member F5 | Q8WV83 |
| C0005586 | Bipolar Disorder | SLC35F4 | 341880 | solute carrier family 35 member F4 | A4IF30 |
| C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | SLC35F4 | 341880 | solute carrier family 35 member F4 | A4IF30 |
| C0024117 | Chronic Obstructive Airway Disease | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0005122 | Beriberi | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0020538 | Hypertensive disease | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0023467 | Leukemia, Myelocytic, Acute | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
