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 |
---|---|---|---|---|---|
C0006826 | Malignant Neoplasms | CNTN2 | 6900 | contactin 2 | Q02246 |
C0162678 | Neurofibromatoses | CNTN2 | 6900 | contactin 2 | Q02246 |
C0027066 | Myoclonus | CNTN2 | 6900 | contactin 2 | Q02246 |
C1332986 | Childhood Osteosarcoma | CNTN2 | 6900 | contactin 2 | Q02246 |
C1140680 | Malignant neoplasm of ovary | CNTN2 | 6900 | contactin 2 | Q02246 |
C0022408 | Arthropathy | CNTN2 | 6900 | contactin 2 | Q02246 |
C3714756 | Intellectual Disability | CNTN2 | 6900 | contactin 2 | Q02246 |
C0149793 | Amaurosis Fugax | CNTN2 | 6900 | contactin 2 | Q02246 |
C0005956 | Bone Marrow Diseases | CNTN2 | 6900 | contactin 2 | Q02246 |
C0017638 | Glioma | CNTN2 | 6900 | contactin 2 | Q02246 |
C0036341 | Schizophrenia | CNTN2 | 6900 | contactin 2 | Q02246 |
C0029463 | Osteosarcoma | CNTN2 | 6900 | contactin 2 | Q02246 |
C0699885 | Carcinoma of bladder | CNTN2 | 6900 | contactin 2 | Q02246 |
C0005695 | Bladder Neoplasm | CNTN2 | 6900 | contactin 2 | Q02246 |
C0919267 | ovarian neoplasm | CNTN2 | 6900 | contactin 2 | Q02246 |
C1332977 | Childhood Leukemia | CNTN2 | 6900 | contactin 2 | Q02246 |
C1332206 | Adult Lymphoma | CNTN2 | 6900 | contactin 2 | Q02246 |
C0003873 | Rheumatoid Arthritis | CNTN2 | 6900 | contactin 2 | Q02246 |
C0004238 | Atrial Fibrillation | CNTN2 | 6900 | contactin 2 | Q02246 |
C0751396 | Well Differentiated Oligodendroglioma | CNTN2 | 6900 | contactin 2 | Q02246 |
C0175697 | Van der Woude syndrome | CNTN2 | 6900 | contactin 2 | Q02246 |
C0393819 | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating | CNTN2 | 6900 | contactin 2 | Q02246 |
C0585442 | Osteosarcoma of bone | CNTN2 | 6900 | contactin 2 | Q02246 |
C0024054 | Lown-Ganong-Levine Syndrome | CNTN2 | 6900 | contactin 2 | Q02246 |
C0025958 | Microcephaly | CNTN2 | 6900 | contactin 2 | Q02246 |
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Last updated: August 19, 2024