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 |
---|---|---|---|---|---|
Colorectal Carcinoma
|
cytochrome P450 family 2 subfamily B member 6
|
||||
Retinal Diseases
|
cytochrome P450 family 2 subfamily C member 19
|
||||
Retinal Diseases
|
cytochrome P450 family 2 subfamily C member 9
|
||||
Parkinson Disease
|
cytochrome P450 family 2 subfamily E member 1
|
||||
Non-alcoholic Fatty Liver Disease
|
cytochrome P450 family 2 subfamily E member 1
|
||||
Adrenal Gland Hyperfunction
|
cytochrome P450 family 11 subfamily B member 1
|
||||
Adrenal Cortical Adenoma
|
cytochrome P450 family 11 subfamily B member 1
|
||||
Adrenal Gland Hyperfunction
|
cytochrome P450 family 11 subfamily B member 2
|
||||
Adrenal Cortical Adenoma
|
cytochrome P450 family 11 subfamily B member 2
|
||||
Hyperandrogenism
|
cytochrome P450 family 17 subfamily A member 1
|
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