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 ▲ |
---|---|---|---|---|---|
C0003873 | Rheumatoid Arthritis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0677886 | Epithelial ovarian cancer | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0007131 | Non-Small Cell Lung Carcinoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0014070 | Encephalomyelitis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0008370 | Cholestasis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0020619 | Hypogonadism | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0014173 | Endometrial Hyperplasia | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C2936858 | Congenital adrenal hyperplasia due to 21 hydroxylase deficiency | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C3554460 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0238033 | Carcinoma of Male Breast | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0003504 | Aortic Valve Insufficiency | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0019163 | Hepatitis B | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C1853195 | Prostate Cancer, Hereditary, 7 | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C4552100 | Lynch Syndrome | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0079744 | Diffuse Large B-Cell Lymphoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C1621958 | Glioblastoma Multiforme | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0006145 | Breast Diseases | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0036631 | Seminoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0003469 | Anxiety Disorders | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0334524 | Mixed Germ Cell Tumor | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0019196 | Hepatitis C | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0023903 | Liver neoplasms | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0271623 | Hypogonadotropic hypogonadism | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0085215 | Ovarian Failure, Premature | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C4083212 | Alopecia, Male Pattern | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
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Last updated: August 19, 2024