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 ▼ |
---|---|---|---|---|---|
C0086565 | Liver Dysfunction | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0600139 | Prostate carcinoma | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0005695 | Bladder Neoplasm | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0028754 | Obesity | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0023890 | Liver Cirrhosis | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0011991 | Diarrhea | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0085580 | Essential Hypertension | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0007137 | Squamous cell carcinoma | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0027051 | Myocardial Infarction | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0023467 | Leukemia, Myelocytic, Acute | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0220668 | Congenital contractural arachnodactyly | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0035220 | Respiratory Distress Syndrome, Newborn | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0241910 | Autoimmune Chronic Hepatitis | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0014544 | Epilepsy | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0011847 | Diabetes | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0085859 | Polyglandular Type I Autoimmune Syndrome | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0039590 | Testicular Neoplasms | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0162566 | Porphyria Cutanea Tarda | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0206698 | Cholangiocarcinoma | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0037997 | Splenic Diseases | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0007097 | Carcinoma | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0002395 | Alzheimer's Disease | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0003469 | Anxiety Disorders | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C3714636 | Pneumonitis | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0037315 | Sleep Apnea Syndromes | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
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Last updated: August 19, 2024