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 |
---|---|---|---|---|---|
C0005684 | Malignant neoplasm of urinary bladder | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C2711227 | Steatohepatitis | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C1561643 | Chronic Kidney Diseases | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0007222 | Cardiovascular Diseases | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0007097 | Carcinoma | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0011849 | Diabetes Mellitus | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0011847 | Diabetes | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0017636 | Glioblastoma | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0025202 | melanoma | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0268398 | Familial lichen amyloidosis | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0026769 | Multiple Sclerosis | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0020456 | Hyperglycemia | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0009319 | Colitis | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0015695 | Fatty Liver | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0400966 | Non-alcoholic Fatty Liver Disease | CERS2 | 29956 | ceramide synthase 2 | Q96G23 |
C0018802 | Congestive heart failure | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C0027819 | Neuroblastoma | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C0017638 | Glioma | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C0010346 | Crohn Disease | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C0497327 | Dementia | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C0751779 | Action Myoclonus-Renal Failure Syndrome | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C0010068 | Coronary heart disease | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C0013069 | Double Outlet Right Ventricle | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C3151221 | CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6 | CERS1 | 10715 | ceramide synthase 1 | P27544 |
C4015619 | EPILEPSY, PROGRESSIVE MYOCLONIC, 8 | CERS1 | 10715 | ceramide synthase 1 | P27544 |
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