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 ▼ |
---|---|---|---|---|---|
C0024809 | Marijuana Abuse | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C1959584 | Cardiac Carcinoma | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0017411 | Female Genital Diseases | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0007682 | CNS disorder | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0000768 | Congenital Abnormality | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0494475 | Tonic - clonic seizures | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0003504 | Aortic Valve Insufficiency | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0007131 | Non-Small Cell Lung Carcinoma | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0008370 | Cholestasis | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0032285 | Pneumonia | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0020459 | Hyperinsulinism | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0011849 | Diabetes Mellitus | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0162557 | Liver Failure, Acute | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0153500 | Malignant neoplasm of heart | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C1704436 | Peripheral Arterial Diseases | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0268579 | Propionic acidemia | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
C0036572 | Seizures | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
C0029456 | Osteoporosis | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
C0220981 | Metabolic acidosis | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
C0001418 | Adenocarcinoma | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
C2717876 | Propionicaciduria | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
C0013336 | Dwarfism | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
C0009402 | Colorectal Carcinoma | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
C3151140 | PONTOCEREBELLAR HYPOPLASIA, TYPE 2D | PCCB | 5096 | propionyl-CoA carboxylase subunit beta | P05166 |
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Last updated: August 19, 2024