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DisGeNET
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 ▲ |
|---|---|---|---|---|---|
| C4552100 | Lynch Syndrome | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0238339 | Hereditary pancreatitis | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0677886 | Epithelial ovarian cancer | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0031099 | Periodontitis | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0027947 | Neutropenia | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0151779 | Cutaneous Melanoma | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0026764 | Multiple Myeloma | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0014859 | Esophageal Neoplasms | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0152136 | Low Tension Glaucoma | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0848558 | Hypospadias | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C3278153 | GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0154251 | Lipid Metabolism Disorders | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0004364 | Autoimmune Diseases | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0024141 | Lupus Erythematosus, Systemic | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C1306459 | Primary malignant neoplasm | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0036341 | Schizophrenia | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C2239176 | Liver carcinoma | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C1621958 | Glioblastoma Multiforme | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0002876 | Congenital dyserythropoietic anemia | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0027651 | Neoplasms | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0600139 | Prostate carcinoma | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0376358 | Malignant neoplasm of prostate | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C1306589 | Congenital dyserythropoietic anemia, type II | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0023452 | Childhood Acute Lymphoblastic Leukemia | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0345904 | Malignant neoplasm of liver | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
