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 |
---|---|---|---|---|---|
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 |
C0039585 | Androgen-Insensitivity Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0023903 | Liver neoplasms | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0009324 | Ulcerative Colitis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0028945 | oligodendroglioma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C3714756 | Intellectual Disability | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0264766 | Rheumatic mitral stenosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0014173 | Endometrial Hyperplasia | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C1175175 | Severe Acute Respiratory Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0033578 | Prostatic Neoplasms | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0011854 | Diabetes Mellitus, Insulin-Dependent | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0021390 | Inflammatory Bowel Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C1332629 | Breast Fibrocystic Change, Proliferative Type | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0699791 | Stomach Carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0524620 | Metabolic Syndrome X | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0038013 | Ankylosing spondylitis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0400966 | Non-alcoholic Fatty Liver Disease | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0025517 | Metabolic Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0007222 | Cardiovascular Diseases | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0008350 | Cholelithiasis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C1860787 | DOWN SYNDROME CRITICAL REGION | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C1332986 | Childhood Osteosarcoma | 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