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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▼ |
---|---|---|---|---|---|
C0085859 | Polyglandular Type I Autoimmune Syndrome | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0027051 | Myocardial Infarction | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0010414 | Infection by Cryptococcus neoformans | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0025202 | melanoma | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0023493 | Adult T-Cell Lymphoma/Leukemia | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0007097 | Carcinoma | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0001339 | Acute pancreatitis | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0400966 | Non-alcoholic Fatty Liver Disease | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0019189 | Hepatitis, Chronic | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C1855520 | Hyperglycemia, Postprandial | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C1704321 | Nephrotic Syndrome, Minimal Change | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C1168401 | Squamous cell carcinoma of the head and neck | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0014175 | Endometriosis | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C2931187 | Nephropathic cystinosis | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C4316899 | Cystinosis | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C0268626 | Juvenile nephropathic cystinosis (disorder) | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C0015624 | Fanconi Syndrome | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C2931013 | Cystinosis, benign, nonnephropathic | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C0235946 | Cerebral atrophy | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C0085078 | Lysosomal Storage Diseases | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C0030567 | Parkinson Disease | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C0341703 | Adult Fanconi syndrome | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C1565489 | Renal Insufficiency | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C0022658 | Kidney Diseases | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
C2749685 | CYSTINOSIS, ATYPICAL NEPHROPATHIC (disorder) | CTNS | 1497 | cystinosin, lysosomal cystine transporter | O60931 |
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Last updated: August 19, 2024