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 |
---|---|---|---|---|---|
C0079744 | Diffuse Large B-Cell Lymphoma | CD22 | 933 | CD22 molecule | P20273 |
C0017636 | Glioblastoma | CD22 | 933 | CD22 molecule | P20273 |
C0042384 | Vasculitis | CD22 | 933 | CD22 molecule | P20273 |
C2239176 | Liver carcinoma | CD22 | 933 | CD22 molecule | P20273 |
C0343084 | Capillary Leak Syndrome | CD22 | 933 | CD22 molecule | P20273 |
C0279593 | Adult B Acute Lymphoblastic Leukemia | CD22 | 933 | CD22 molecule | P20273 |
C0023467 | Leukemia, Myelocytic, Acute | CD22 | 933 | CD22 molecule | P20273 |
C0079740 | High Grade Lymphoma (neoplasm) | CD22 | 933 | CD22 molecule | P20273 |
C0006413 | Burkitt Lymphoma | CD22 | 933 | CD22 molecule | P20273 |
C0855095 | Small Lymphocytic Lymphoma | CD22 | 933 | CD22 molecule | P20273 |
C0030805 | Bullous pemphigoid | CD22 | 933 | CD22 molecule | P20273 |
C1332201 | Adult Diffuse Large B-Cell Lymphoma | CD22 | 933 | CD22 molecule | P20273 |
C0009782 | Connective Tissue Diseases | CD22 | 933 | CD22 molecule | P20273 |
C0684249 | Carcinoma of lung | CD22 | 933 | CD22 molecule | P20273 |
C0079773 | Lymphoma, T-Cell, Cutaneous | CD22 | 933 | CD22 molecule | P20273 |
C0678222 | Breast Carcinoma | CD22 | 933 | CD22 molecule | P20273 |
C0024419 | Waldenstrom Macroglobulinemia | CD22 | 933 | CD22 molecule | P20273 |
C3179455 | Niemann-Pick Disease, Type C1 | CD22 | 933 | CD22 molecule | P20273 |
C0004936 | Mental disorders | CD22 | 933 | CD22 molecule | P20273 |
C0242379 | Malignant neoplasm of lung | CD22 | 933 | CD22 molecule | P20273 |
C0024314 | Lymphoproliferative Disorders | CD22 | 933 | CD22 molecule | P20273 |
C0020951 | Immune Complex Diseases | CD22 | 933 | CD22 molecule | P20273 |
C0026650 | Movement Disorders | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
C0000768 | Congenital Abnormality | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
C0014877 | Esotropia | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
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Last updated: August 19, 2024