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 |
---|---|---|---|---|---|
C0011991 | Diarrhea | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0017495 | Gerstmann-Straussler-Scheinker Disease | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C4520983 | Congenital atresia of extrahepatic bile duct | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C3150651 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C2750440 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C2711227 | Steatohepatitis | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0011847 | Diabetes | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0011849 | Diabetes Mellitus | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0008350 | Cholelithiasis | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0008370 | Cholestasis | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0005398 | Cholestasis, Extrahepatic | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0025517 | Metabolic Diseases | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0002395 | Alzheimer's Disease | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0400966 | Non-alcoholic Fatty Liver Disease | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C2750441 | LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1 | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0015695 | Fatty Liver | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C0025322 | Premature Menopause | CYP8B1 | 1582 | cytochrome P450 family 8 subfamily B member 1 | Q9UNU6 |
C3151055 | ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0848558 | Hypospadias | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C1704272 | Benign Prostatic Hyperplasia | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0023903 | Liver neoplasms | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0520463 | Chronic active hepatitis | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0175701 | Aarskog syndrome | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
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Last updated: August 19, 2024