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 ▲ |
---|---|---|---|---|---|
C0008312 | Primary biliary cirrhosis | DGKQ | 1609 | diacylglycerol kinase theta | P52824 |
C0027121 | Myositis | DGKQ | 1609 | diacylglycerol kinase theta | P52824 |
C0002395 | Alzheimer's Disease | DGKQ | 1609 | diacylglycerol kinase theta | P52824 |
C0011849 | Diabetes Mellitus | DGKQ | 1609 | diacylglycerol kinase theta | P52824 |
C0011847 | Diabetes | DGKQ | 1609 | diacylglycerol kinase theta | P52824 |
C1527366 | Salaam Seizures | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0011581 | Depressive disorder | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0684276 | Hypsarrhythmia | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0238198 | Gastrointestinal Stromal Tumors | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0035220 | Respiratory Distress Syndrome, Newborn | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0027651 | Neoplasms | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0017636 | Glioblastoma | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0014457 | Eosinophilia | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0235833 | Congenital diaphragmatic hernia | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C3714756 | Intellectual Disability | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0015393 | Eye Abnormalities | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0036857 | Severe intellectual disability | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0006142 | Malignant neoplasm of breast | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0020192 | Hyaline Membrane Disease | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0025958 | Microcephaly | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0038273 | Stereotypic Movement Disorder | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0013384 | Dyskinetic syndrome | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0234533 | Generalized seizures | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
C0027051 | Myocardial Infarction | NDST1 | 3340 | N-deacetylase and N-sulfotransferase 1 | P52848 |
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