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 |
---|---|---|---|---|---|
C0006826 | Malignant Neoplasms | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0023895 | Liver diseases | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0278878 | Adult Glioblastoma | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0235032 | Neurotoxicity Syndromes | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0017636 | Glioblastoma | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0040021 | Thromboangiitis Obliterans | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0086565 | Liver Dysfunction | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0339143 | Thyroid associated opthalmopathies | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C1621958 | Glioblastoma Multiforme | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0700095 | Central neuroblastoma | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0004153 | Atherosclerosis | ST8SIA1 | 6489 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 | Q92185 |
C0007131 | Non-Small Cell Lung Carcinoma | LPIN3 | 64900 | lipin 3 | Q9BQK8 |
C0006826 | Malignant Neoplasms | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0948008 | Ischemic stroke | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0026769 | Multiple Sclerosis | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0011884 | Diabetic Retinopathy | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0006111 | Brain Diseases | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0002395 | Alzheimer's Disease | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0036341 | Schizophrenia | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0030567 | Parkinson Disease | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0017638 | Glioma | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C1621958 | Glioblastoma Multiforme | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0027651 | Neoplasms | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0004114 | Astrocytoma | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
C0017636 | Glioblastoma | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
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