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.
Source | Last Updated |
---|---|
DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID ▲ | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0524620 | Metabolic Syndrome X | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0684249 | Carcinoma of lung | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0026769 | Multiple Sclerosis | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0302280 | Adrenogenital Syndrome | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0003872 | Arthritis, Psoriatic | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0017661 | IGA Glomerulonephritis | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C2239176 | Liver carcinoma | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0268542 | Ornithine carbamoyltransferase deficiency | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0553723 | Squamous cell carcinoma of skin | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0034013 | Precocious Puberty | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0023806 | Lipomucopolysaccharidosis | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0001430 | Adenoma | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0206667 | Adrenal Cortical Adenoma | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0376338 | Diagnosis, Psychiatric | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0041408 | Turner Syndrome | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0004943 | Behcet Syndrome | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0020437 | Hypercalcemia | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0751967 | Multiple Sclerosis, Relapsing-Remitting | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0006142 | Malignant neoplasm of breast | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C1337013 | Differentiated Thyroid Gland Carcinoma | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0151468 | Thyroid Gland Follicular Adenoma | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0007114 | Malignant neoplasm of skin | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C1306459 | Primary malignant neoplasm | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0042170 | Uveomeningoencephalitic Syndrome | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
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
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024