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 |
|---|---|---|---|---|---|
|
Metabolic Syndrome X
|
phosphatase and tensin homolog
|
||||
|
Metabolic Syndrome X
|
carnitine palmitoyltransferase 1A
|
||||
|
Metabolic Syndrome X
|
lipoprotein lipase
|
||||
|
Metabolic Syndrome X
|
catechol-O-methyltransferase
|
||||
|
Dementia
|
heparan sulfate proteoglycan 2
|
||||
|
Neoplasm of uncertain or unknown behavior of breast
|
inositol polyphosphate-4-phosphatase type II B
|
||||
|
Neoplasm of uncertain or unknown behavior of breast
|
phosphatase and tensin homolog
|
||||
|
Alzheimer Disease, Late Onset
|
phospholipase D family member 3
|
||||
|
Endometrial Carcinoma
|
cadherin 13
|
||||
|
Endometrial Carcinoma
|
catechol-O-methyltransferase
|
Displaying entries 351 - 360 of 1194 in total
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International Collaboration
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Acknowledgements
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
