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 |
|---|---|---|---|---|---|
|
Neuroblastoma
|
TNF receptor superfamily member 10c
|
||||
|
Neuroblastoma
|
fragile histidine triad diadenosine triphosphatase
|
||||
|
Neuroblastoma
|
solute carrier family 2 member 3
|
||||
|
Neurofibromatosis 2
|
prostaglandin D2 synthase
|
||||
|
Obesity
|
paraoxonase 1
|
||||
|
Obesity, Morbid
|
mesoderm specific transcript
|
||||
|
Oculocerebrorenal Syndrome
|
OCRL inositol polyphosphate-5-phosphatase
|
||||
|
oligodendroglioma
|
UDP glycosyltransferase 8
|
||||
|
Oligospermia
|
mesoderm specific transcript
|
||||
|
Degenerative polyarthritis
|
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
|
Displaying entries 551 - 560 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
