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 |
---|---|---|---|---|---|
C0029227 | Delirium, Dementia, Amnestic, Cognitive Disorders | ACHE | 43 | acetylcholinesterase (Cartwright blood group) | P22303 |
C0029227 | Delirium, Dementia, Amnestic, Cognitive Disorders | CD14 | 929 | CD14 molecule | P08571 |
C0011206 | Delirium | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C0011206 | Delirium | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0011206 | Delirium | ENO2 | 2026 | enolase 2 | P09104 |
C0011206 | Delirium | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C0011206 | Delirium | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
C0011206 | Delirium | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0011206 | Delirium | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0011206 | Delirium | LGALS3 | 3958 | galectin 3 | P17931 |
C0011206 | Delirium | ACHE | 43 | acetylcholinesterase (Cartwright blood group) | P22303 |
C0011206 | Delirium | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C0011206 | Delirium | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0011206 | Delirium | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0011206 | Delirium | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0011206 | Delirium | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C0011206 | Delirium | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
C0011195 | Dejerine-Sottas Disease (disorder) | HPSE | 10855 | heparanase | Q9Y251 |
C0011195 | Dejerine-Sottas Disease (disorder) | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C0011195 | Dejerine-Sottas Disease (disorder) | PLCE1 | 51196 | phospholipase C epsilon 1 | Q9P212 |
C0011195 | Dejerine-Sottas Disease (disorder) | CAT | 847 | catalase | P04040 |
C0011195 | Dejerine-Sottas Disease (disorder) | LPIN1 | 23175 | lipin 1 | Q14693 |
C0011195 | Dejerine-Sottas Disease (disorder) | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0011195 | Dejerine-Sottas Disease (disorder) | GPX2 | 2877 | glutathione peroxidase 2 | P18283 |
C0011195 | Dejerine-Sottas Disease (disorder) | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
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