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 |
---|---|---|---|---|---|
C1868598 | PARIETAL FORAMINA | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0206641 | Osteochondromatosis | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0027651 | Neoplasms | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C1442903 | Exostoses | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0008479 | Chondrosarcoma | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0338451 | Frontotemporal dementia | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0027543 | Avascular necrosis of bone | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C3714756 | Intellectual Disability | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0152441 | Madelung Deformity | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0221356 | Brachycephaly | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0015302 | External exotoses | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0013336 | Dwarfism | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C4317295 | Congenital disorder of glycosylation type 1s | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0011847 | Diabetes | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C3279947 | NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0004364 | Autoimmune Diseases | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0027708 | Nephroblastoma | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0029408 | Degenerative polyarthritis | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0020676 | Hypothyroidism | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0745103 | Hyperlipoproteinemia Type IIa | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0009806 | Constipation | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0020538 | Hypertensive disease | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0005940 | Bone Diseases | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
C0036572 | Seizures | EXT2 | 2132 | exostosin glycosyltransferase 2 | Q93063 |
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Last updated: August 19, 2024