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 |
---|---|---|---|---|---|
C0017178 | Gastrointestinal Diseases | CEACAM6 | 4680 | CEA cell adhesion molecule 6 | P40199 |
C0017168 | Gastroesophageal reflux disease | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0017168 | Gastroesophageal reflux disease | FUT3 | 2525 | fucosyltransferase 3 (Lewis blood group) | P21217 |
C0017168 | Gastroesophageal reflux disease | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
C0017168 | Gastroesophageal reflux disease | PIGA | 5277 | phosphatidylinositol glycan anchor biosynthesis class A | P37287 |
C0017168 | Gastroesophageal reflux disease | GNE | 10020 | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Q9Y223 |
C0017168 | Gastroesophageal reflux disease | DDOST | 1650 | dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit | P39656 |
C0017168 | Gastroesophageal reflux disease | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
C0017168 | Gastroesophageal reflux disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0017168 | Gastroesophageal reflux disease | FCSK | 197258 | fucose kinase | Q8N0W3 |
C0017168 | Gastroesophageal reflux disease | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0017168 | Gastroesophageal reflux disease | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0017168 | Gastroesophageal reflux disease | CALR | 811 | calreticulin | P27797 |
C0017168 | Gastroesophageal reflux disease | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0017168 | Gastroesophageal reflux disease | CHAT | 1103 | choline O-acetyltransferase | P28329 |
C0017168 | Gastroesophageal reflux disease | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0017168 | Gastroesophageal reflux disease | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
C0017168 | Gastroesophageal reflux disease | AGRN | 375790 | agrin | O00468 |
C0017168 | Gastroesophageal reflux disease | NTM | 50863 | neurotrimin | Q9P121 |
C0017168 | Gastroesophageal reflux disease | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
C0017168 | Gastroesophageal reflux disease | PTGS1 | 5742 | prostaglandin-endoperoxide synthase 1 | P23219 |
C0017168 | Gastroesophageal reflux disease | SFTPA1 | 653509 | surfactant protein A1 | Q8IWL2 |
C0017168 | Gastroesophageal reflux disease | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
C0017168 | Gastroesophageal reflux disease | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0017168 | Gastroesophageal reflux disease | MCEE | 84693 | methylmalonyl-CoA epimerase | Q96PE7 |
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