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 |
---|---|---|---|---|---|
C0002965 | Angina, Unstable | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0677886 | Epithelial ovarian cancer | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0035309 | Retinal Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C1704436 | Peripheral Arterial Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0025149 | Medulloblastoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0023434 | Chronic Lymphocytic Leukemia | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0025362 | Mental Retardation | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0595989 | Carcinoma of larynx | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0026269 | Mitral Valve Stenosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0024809 | Marijuana Abuse | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0007102 | Malignant tumor of colon | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0039685 | Tetralogy of Fallot | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0701818 | Choledocholithiasis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0015306 | Hereditary Multiple Exostoses | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0018801 | Heart failure | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0009402 | Colorectal Carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0007124 | Noninfiltrating Intraductal Carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0032460 | Polycystic Ovary Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0277528 | Traveler's diarrhea | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0919267 | ovarian neoplasm | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0010068 | Coronary heart disease | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0015674 | Chronic Fatigue Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0276496 | Familial Alzheimer Disease (FAD) | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0027533 | Neck Neoplasms | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0011581 | Depressive disorder | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
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