DisGeNET
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.
| Database | Last Updated |
|---|---|
| DisGeNET | February 14, 2024 |
| Disease ID ▲ | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
|
MYELODYSPLASTIC SYNDROME
|
phospholipase C epsilon 1
|
||||
|
MYELODYSPLASTIC SYNDROME
|
glutathione peroxidase 3
|
||||
|
MYELODYSPLASTIC SYNDROME
|
phospholipase A2 receptor 1
|
||||
|
HYDATIDIFORM MOLE, RECURRENT, 1
|
heparanase 2 (inactive)
|
||||
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
insulin receptor
|
||||
|
Lymphoma, Diffuse
|
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase
|
||||
|
Head and Neck Carcinoma
|
glutathione peroxidase 3
|
||||
|
Head and Neck Carcinoma
|
heparanase
|
||||
|
Head and Neck Carcinoma
|
sterol O-acyltransferase 1
|
||||
|
Head and Neck Carcinoma
|
cytochrome P450 family 1 subfamily A member 1
|
Displaying entries 1161 - 1170 of 1194 in total
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Acknowledgements
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
