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 ▼ |
---|---|---|---|---|---|
C0339573 | Glaucoma, Primary Open Angle | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
C0011053 | Deafness | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
C0030297 | Pancreatic Neoplasm | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
C0235974 | Pancreatic carcinoma | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
C1956346 | Coronary Artery Disease | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C1142166 | Brugada Syndrome (disorder) | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0348626 | Other specified cardiac arrhythmias | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C2673193 | Brugada Syndrome 2 | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C4551804 | Brugada Syndrome 1 | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C1399226 | Ectopic rhythm | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C2748542 | CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0018802 | Congestive heart failure | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0264893 | Nodal rhythm disorder | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0003811 | Cardiac Arrhythmia | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0428908 | Sinus Node Dysfunction (disorder) | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0038644 | Sudden infant death syndrome | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0004238 | Atrial Fibrillation | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0015695 | Fatty Liver | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0010068 | Coronary heart disease | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0010054 | Coronary Arteriosclerosis | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0029408 | Degenerative polyarthritis | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0018801 | Heart failure | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C1168401 | Squamous cell carcinoma of the head and neck | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
C0037052 | Sick Sinus Syndrome | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
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