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 ▼ |
---|---|---|---|---|---|
C1854181 | FIBROMATOSIS, GINGIVAL, 2 | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C3536714 | Renal dysplasia | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0011334 | Dental caries | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0020542 | Pulmonary Hypertension | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0029463 | Osteosarcoma | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0155626 | Acute myocardial infarction | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0476089 | Endometrial Carcinoma | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0031099 | Periodontitis | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0206655 | Alveolar rhabdomyosarcoma | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0023267 | Fibroid Tumor | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0342750 | Glycogen storage disease type Id | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C1956346 | Coronary Artery Disease | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0243026 | Sepsis | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C1306459 | Primary malignant neoplasm | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0154251 | Lipid Metabolism Disorders | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C4721610 | Carcinoma, Ovarian Epithelial | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C1140680 | Malignant neoplasm of ovary | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0007103 | Malignant neoplasm of endometrium | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0004997 | Benign Ovarian Neoplasm | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0175709 | Centronuclear myopathy | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0011581 | Depressive disorder | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0030567 | Parkinson Disease | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0024623 | Malignant neoplasm of stomach | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0585442 | Osteosarcoma of bone | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
C0007137 | Squamous cell carcinoma | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
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