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 |
---|---|---|---|---|---|
C0036875 | Disorders of Sex Development | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0031117 | Peripheral Neuropathy | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0013080 | Down Syndrome | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0004775 | Bartter Disease | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0001418 | Adenocarcinoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0282160 | Aplasia Cutis Congenita | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0007104 | Female Breast Carcinoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0079731 | B-Cell Lymphomas | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0023895 | Liver diseases | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0949691 | Spondylarthropathies | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0020594 | Hypoactive Sexual Desire Disorder | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0010068 | Coronary heart disease | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C1332979 | Childhood Lymphoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0740457 | Malignant neoplasm of kidney | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0848676 | Subfertility, Male | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0235974 | Pancreatic carcinoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0206650 | Fibroadenoma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0027051 | Myocardial Infarction | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0007102 | Malignant tumor of colon | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0702166 | Acne | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0017638 | Glioma | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0026769 | Multiple Sclerosis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C4721610 | Carcinoma, Ovarian Epithelial | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0949690 | Spondylarthritis | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0020635 | Hypopituitarism | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
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Last updated: August 19, 2024