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 |
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DisGeNET | February 14, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▲ | UniProt ID |
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Retinal Diseases
|
cytochrome P450 family 2 subfamily C member 19
|
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Retinal Diseases
|
cytochrome P450 family 2 subfamily C member 9
|
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Parkinson Disease
|
cytochrome P450 family 2 subfamily E member 1
|
||||
Non-alcoholic Fatty Liver Disease
|
cytochrome P450 family 2 subfamily E member 1
|
||||
Congenital adrenal hyperplasia
|
cytochrome P450 family 21 subfamily A member 2
|
||||
Prostate carcinoma
|
cytochrome P450 family 24 subfamily A member 1
|
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Prostatic Neoplasms
|
cytochrome P450 family 24 subfamily A member 1
|
||||
Neoplasms
|
cytochrome P450 family 24 subfamily A member 1
|
||||
Malignant neoplasm of prostate
|
cytochrome P450 family 24 subfamily A member 1
|
||||
Breast Carcinoma
|
cytochrome P450 family 7 subfamily B member 1
|
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