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 |
---|---|---|---|---|---|
C0013537 | Eclampsia | ANXA5 | 308 | annexin A5 | P08758 |
C0013537 | Eclampsia | LPL | 4023 | lipoprotein lipase | P06858 |
C0013537 | Eclampsia | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
C0013537 | Eclampsia | PTGS1 | 5742 | prostaglandin-endoperoxide synthase 1 | P23219 |
C0013537 | Eclampsia | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
C0013537 | Eclampsia | CD14 | 929 | CD14 molecule | P08571 |
C0013537 | Eclampsia | SORD | 6652 | sorbitol dehydrogenase | Q00796 |
C0013537 | Eclampsia | IL18R1 | 8809 | interleukin 18 receptor 1 | Q13478 |
C0013537 | Eclampsia | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0013537 | Eclampsia | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
C0013537 | Eclampsia | HSD11B2 | 3291 | hydroxysteroid 11-beta dehydrogenase 2 | P80365 |
C0013537 | Eclampsia | KLRB1 | 3820 | killer cell lectin like receptor B1 | Q12918 |
C0013537 | Eclampsia | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0013528 | Echolalia | SLC35C1 | 55343 | solute carrier family 35 member C1 | Q96A29 |
C0013528 | Echolalia | HGSNAT | 138050 | heparan-alpha-glucosaminide N-acetyltransferase | Q68CP4 |
C0013528 | Echolalia | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
C0152069 | Echinococcus multilocularis infection | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0152069 | Echinococcus multilocularis infection | KLRK1 | 22914 | killer cell lectin like receptor K1 | P26718 |
C0152069 | Echinococcus multilocularis infection | MICA | 100507436 | MHC class I polypeptide-related sequence A | Q29983 |
C0013502 | Echinococcosis | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0334347 | Eccrine spiradenoma | LYZ | 4069 | lysozyme | P61626 |
C1266065 | Eccrine porocarcinoma | CEACAM5 | 1048 | CEA cell adhesion molecule 5 | P06731 |
C0346026 | Eccrine mixed tumor of skin | CEACAM5 | 1048 | CEA cell adhesion molecule 5 | P06731 |
C0013473 | Eating Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0013473 | Eating Disorders | ACOT7 | 11332 | acyl-CoA thioesterase 7 | O00154 |
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