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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
---|---|---|---|---|---|
C0848558 | Hypospadias | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C1956346 | Coronary Artery Disease | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C3489396 | Hypogonadism, Isolated Hypogonadotropic | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C1857276 | Trichohepatoenteric Syndrome | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0015934 | Fetal Growth Retardation | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0010417 | Cryptorchidism | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0023267 | Fibroid Tumor | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0015695 | Fatty Liver | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0346647 | Malignant neoplasm of pancreas | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C1384514 | Conn Syndrome | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C2711227 | Steatohepatitis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0524620 | Metabolic Syndrome X | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0009375 | Colonic Neoplasms | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0023890 | Liver Cirrhosis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0019360 | Herpes zoster disease | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0002395 | Alzheimer's Disease | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0001624 | Adrenal Gland Neoplasms | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0020540 | Malignant Hypertension | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0021359 | Infertility | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0020428 | Hyperaldosteronism | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0002453 | Amenorrhea | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0024305 | Lymphoma, Non-Hodgkin | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0242342 | Sheehan Syndrome | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C4721532 | Lymphoma, Non-Hodgkin, Familial | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
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Last updated: August 19, 2024