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 |
---|---|---|---|---|---|
C0242422 | Parkinsonian Disorders | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0242422 | Parkinsonian Disorders | DPEP1 | 1800 | dipeptidase 1 | P16444 |
C0242422 | Parkinsonian Disorders | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
C0242422 | Parkinsonian Disorders | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
C0242422 | Parkinsonian Disorders | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
C0242422 | Parkinsonian Disorders | LGALS1 | 3956 | galectin 1 | P09382 |
C0242422 | Parkinsonian Disorders | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0242422 | Parkinsonian Disorders | ACHE | 43 | acetylcholinesterase (Cartwright blood group) | P22303 |
C0242422 | Parkinsonian Disorders | PRNP | 5621 | prion protein | P04156 |
C0242422 | Parkinsonian Disorders | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
C0242422 | Parkinsonian Disorders | SYNJ1 | 8867 | synaptojanin 1 | O43426 |
C0242422 | Parkinsonian Disorders | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0242422 | Parkinsonian Disorders | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0242422 | Parkinsonian Disorders | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
C0242422 | Parkinsonian Disorders | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
C0242422 | Parkinsonian Disorders | GAD2 | 2572 | glutamate decarboxylase 2 | Q05329 |
C0242422 | Parkinsonian Disorders | GFRA1 | 2674 | GDNF family receptor alpha 1 | P56159 |
C0242422 | Parkinsonian Disorders | PAFAH1B1 | 5048 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 | P43034 |
C0242422 | Parkinsonian Disorders | PPT1 | 5538 | palmitoyl-protein thioesterase 1 | P50897 |
C0242422 | Parkinsonian Disorders | PRNP | 5621 | prion protein | F7VJQ1 |
C0242422 | Parkinsonian Disorders | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0242422 | Parkinsonian Disorders | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0242429 | Sore Throat | GALNS | 2588 | galactosamine (N-acetyl)-6-sulfatase | P34059 |
C0242429 | Sore Throat | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0242459 | Simple Pulmonary Eosinophilia | PARP9 | 83666 | poly(ADP-ribose) polymerase family member 9 | Q8IXQ6 |
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