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 |
|---|---|---|---|---|---|
|
Alzheimer Disease, Late Onset
|
phospholipase D family member 3
|
||||
|
Chronic Lymphocytic Leukemia
|
phospholipase C gamma 2
|
||||
|
Dermatomyositis, Childhood Type
|
phospholipase C gamma 2
|
||||
|
Squamous cell carcinoma
|
phospholipase C gamma 1
|
||||
|
Miller Dieker syndrome
|
phospholipase C gamma 1
|
||||
|
MYELODYSPLASTIC SYNDROME
|
phospholipase C gamma 1
|
||||
|
Neoplasms
|
phospholipase C gamma 1
|
||||
|
X-Linked Lymphoproliferative Disorder
|
phospholipase C gamma 1
|
||||
|
MYELODYSPLASTIC SYNDROME
|
phospholipase C epsilon 1
|
||||
|
Miller Dieker syndrome
|
phospholipase C epsilon 1
|
Displaying entries 311 - 320 of 1194 in total
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International Collaboration
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Acknowledgements
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
