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 |
---|---|---|---|---|---|
C0043119 | Werner Syndrome | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0036220 | Kaposi Sarcoma | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0018801 | Heart failure | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C3150651 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0152018 | Esophageal carcinoma | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0699885 | Carcinoma of bladder | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0278878 | Adult Glioblastoma | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0400966 | Non-alcoholic Fatty Liver Disease | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C2750440 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C1335302 | Pancreatic Ductal Adenocarcinoma | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0019158 | Hepatitis | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C1956346 | Coronary Artery Disease | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0041296 | Tuberculosis | SIRT6 | 51548 | sirtuin 6 | Q8N6T7 |
C0342853 | Sialuria | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0023530 | Leukopenia | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0023891 | Liver Cirrhosis, Alcoholic | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C2711227 | Steatohepatitis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0033860 | Psoriasis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C1561643 | Chronic Kidney Diseases | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0020455 | Hypergammaglobulinemia | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0028754 | Obesity | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0400966 | Non-alcoholic Fatty Liver Disease | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0011603 | Dermatitis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0019158 | Hepatitis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0019163 | Hepatitis B | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024