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 ▼ |
---|---|---|---|---|---|
C0042384 | Vasculitis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0028754 | Obesity | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0004943 | Behcet Syndrome | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0026691 | Mucocutaneous Lymph Node Syndrome | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0008582 | Chromoblastomycosis | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
C0270850 | Idiopathic generalized epilepsy | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0021390 | Inflammatory Bowel Diseases | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0033975 | Psychotic Disorders | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0020538 | Hypertensive disease | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0021400 | Influenza | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C1691779 | Sensory hearing loss | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C1852197 | MAJOR AFFECTIVE DISORDER 1 | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0005586 | Bipolar Disorder | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0494475 | Tonic - clonic seizures | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0036341 | Schizophrenia | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0030319 | Panic Disorder | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0600139 | Prostate carcinoma | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0376358 | Malignant neoplasm of prostate | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0270853 | Juvenile Myoclonic Epilepsy | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0018802 | Congestive heart failure | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0002395 | Alzheimer's Disease | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0008370 | Cholestasis | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0011615 | Dermatitis, Atopic | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0036572 | Seizures | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
C0013595 | Eczema | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
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Last updated: August 19, 2024