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 |
---|---|---|---|---|---|
C0151744 | Myocardial Ischemia | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0024143 | Lupus Nephritis | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0282577 | Congenital Disorders of Glycosylation | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C1449563 | Cardiomyopathy, Familial Idiopathic | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0031485 | Phenylketonurias | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0008925 | Cleft Palate | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0003873 | Rheumatoid Arthritis | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0011644 | Scleroderma | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0011849 | Diabetes Mellitus | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0017924 | Glycogen Storage Disease Type V | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0015695 | Fatty Liver | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0036421 | Systemic Scleroderma | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0238463 | Papillary thyroid carcinoma | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0006826 | Malignant Neoplasms | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0878544 | Cardiomyopathies | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0019158 | Hepatitis | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0024530 | Malaria | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C2239176 | Liver carcinoma | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0009402 | Colorectal Carcinoma | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0000768 | Congenital Abnormality | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0007959 | Charcot-Marie-Tooth Disease | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C0024141 | Lupus Erythematosus, Systemic | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C3808991 | NGLY1 deficiency | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
C3888018 | Congenital Hyperinsulinism | PGM1 | 5236 | phosphoglucomutase 1 | P36871 |
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Last updated: August 19, 2024