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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 ▼ |
|---|---|---|---|---|---|
| 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 |
| C0026769 | Multiple Sclerosis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0004364 | Autoimmune Diseases | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0020538 | Hypertensive disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0008312 | Primary biliary cirrhosis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0001403 | Addison Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C4049006 | Selective immunoglobulin A deficiency | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0011849 | Diabetes Mellitus | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0008313 | Cholangitis, Sclerosing | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0010346 | Crohn Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0948008 | Ischemic stroke | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0027051 | Myocardial Infarction | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0524620 | Metabolic Syndrome X | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0023892 | Biliary cirrhosis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0002171 | Alopecia Areata | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
