Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|---|---|---|
| C1332979 | Childhood Lymphoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0020456 | Hyperglycemia | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0025267 | Multiple Endocrine Neoplasia Type 1 | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0007787 | Transient Ischemic Attack | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0340305 | Inferior Wall Myocardial Infarction | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1332206 | Adult Lymphoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0027051 | Myocardial Infarction | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C2239176 | Liver carcinoma | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0878544 | Cardiomyopathies | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C1868683 | B-CELL MALIGNANCY, LOW-GRADE | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0949857 | Mitochondrial Respiratory Chain Deficiencies | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0010674 | Cystic Fibrosis | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0018784 | Sensorineural Hearing Loss (disorder) | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0025521 | Inborn Errors of Metabolism | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0268263 | Multiple Sulfatase Deficiency Disease | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0023522 | Leukodystrophy, Metachromatic | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0086651 | Mucopolysaccharidosis, MPS-IV-A | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0085078 | Lysosomal Storage Diseases | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C1720864 | Sulfatidosis, Juvenile, Austin Type | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0006142 | Malignant neoplasm of breast | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0235946 | Cerebral atrophy | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0086647 | Mucopolysaccharidosis Type IIIA | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0086795 | Pfaundler-Hurler Syndrome | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0079588 | Ichthyosis, X-Linked | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0025958 | Microcephaly | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
