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 ▼ |
---|---|---|---|---|---|
C0034152 | Henoch-Schoenlein Purpura | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0023772 | Lipid Metabolism, Inborn Errors | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0029408 | Degenerative polyarthritis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0011849 | Diabetes Mellitus | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C3151147 | Bile Acid Synthesis Defect, Congenital, 3 | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0009319 | Colitis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0011847 | Diabetes | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0205644 | Carcinoma, Granular Cell | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0037773 | Spastic Paraplegia, Hereditary | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0028738 | Nystagmus | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0009324 | Ulcerative Colitis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0023895 | Liver diseases | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0008372 | Intrahepatic Cholestasis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0009402 | Colorectal Carcinoma | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0009714 | Hepatic Fibrosis, Congenital | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0086565 | Liver Dysfunction | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C2931356 | Spastic paraplegia type 5A, recessive | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0027651 | Neoplasms | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C1306459 | Primary malignant neoplasm | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0006826 | Malignant Neoplasms | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0376358 | Malignant neoplasm of prostate | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0005779 | Blood Coagulation Disorders | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C2711227 | Steatohepatitis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
C0026769 | Multiple Sclerosis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
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Last updated: August 19, 2024