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 |
---|---|---|---|---|---|
C0006826 | Malignant Neoplasms | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0029456 | Osteoporosis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0376358 | Malignant neoplasm of prostate | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0014175 | Endometriosis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0242379 | Malignant neoplasm of lung | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0268285 | Adrenal hyperplasia, congenital, type 5 | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0678222 | Breast Carcinoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0027651 | Neoplasms | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0947622 | Cholecystolithiasis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0020538 | Hypertensive disease | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0684249 | Carcinoma of lung | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0018206 | granulosa cell tumor | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0006142 | Malignant neoplasm of breast | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0020621 | Hypokalemia | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0206667 | Adrenal Cortical Adenoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C1257931 | Mammary Neoplasms, Human | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0032460 | Polycystic Ovary Syndrome | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0001430 | Adenoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0007103 | Malignant neoplasm of endometrium | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0238395 | Male Pseudohermaphroditism | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0341858 | Endometriosis of uterus | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C2937421 | Prostatic Hyperplasia | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0001627 | Congenital adrenal hyperplasia | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0010054 | Coronary Arteriosclerosis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C1275126 | TNF receptor-associated periodic fever syndrome (TRAPS) | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
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Last updated: August 19, 2024