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 |
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