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 |
---|---|---|---|---|---|
C0030319 | Panic Disorder | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0010232 | Cowpox | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C1621958 | Glioblastoma Multiforme | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0039483 | Giant Cell Arteritis | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0013146 | Drug abuse | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0079731 | B-Cell Lymphomas | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0018801 | Heart failure | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0025289 | Meningitis | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0006142 | Malignant neoplasm of breast | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0008479 | Chondrosarcoma | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0278878 | Adult Glioblastoma | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0026896 | Myasthenia Gravis | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0340569 | Internal Carotid Artery Stenosis | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0006826 | Malignant Neoplasms | CDS1 | 1040 | CDP-diacylglycerol synthase 1 | Q92903 |
C0009451 | Communicating Hydrocephalus | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C0686353 | Muscular Dystrophies, Limb-Girdle | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C3553330 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7 | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C0026848 | Myopathy | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C4015095 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C0010038 | Corneal Opacity | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C0266544 | Microcornea | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C0020256 | Congenital Hydrocephalus | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C0265221 | Walker-Warburg congenital muscular dystrophy | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C4284790 | Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
C0015393 | Eye Abnormalities | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
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