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 ▲ |
---|---|---|---|---|---|
C0020538 | Hypertensive disease | SRGN | 5552 | serglycin | P10124 |
C1449563 | Cardiomyopathy, Familial Idiopathic | SRGN | 5552 | serglycin | P10124 |
C0006840 | Candidiasis | SRGN | 5552 | serglycin | P10124 |
C1621958 | Glioblastoma Multiforme | SRGN | 5552 | serglycin | P10124 |
C2239176 | Liver carcinoma | SRGN | 5552 | serglycin | P10124 |
C0018801 | Heart failure | SRGN | 5552 | serglycin | P10124 |
C2931822 | Nasopharyngeal carcinoma | SRGN | 5552 | serglycin | P10124 |
C0278878 | Adult Glioblastoma | SRGN | 5552 | serglycin | P10124 |
C0242231 | Coronary Stenosis | SRGN | 5552 | serglycin | P10124 |
C0362046 | Prediabetes syndrome | SRGN | 5552 | serglycin | P10124 |
C1837218 | Cleft palate, isolated | SRGN | 5552 | serglycin | P10124 |
C0009402 | Colorectal Carcinoma | SRGN | 5552 | serglycin | P10124 |
C0812413 | Malignant Pleural Mesothelioma | SRGN | 5552 | serglycin | P10124 |
C0017921 | Glycogen storage disease type II | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0241005 | Creatine phosphokinase serum increased | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0751173 | Glycogen Storage Disease Type II, Infantile | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0342751 | Generalized glycogen storage disease of infants | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0026848 | Myopathy | GAA | 2548 | glucosidase alpha, acid | P10253 |
C3539168 | PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0017919 | Glycogen Storage Disease | GAA | 2548 | glucosidase alpha, acid | P10253 |
C1968741 | Glycogen Storage Disease IIIC | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0007194 | Hypertrophic Cardiomyopathy | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0268237 | Cytochrome-c Oxidase Deficiency | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0017923 | Glycogen Storage Disease Type IV | GAA | 2548 | glucosidase alpha, acid | P10253 |
C0002986 | Fabry Disease | GAA | 2548 | glucosidase alpha, acid | P10253 |
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Last updated: August 19, 2024