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 |
---|---|---|---|---|---|
C0006826 | Malignant Neoplasms | PIGS | 94005 | phosphatidylinositol glycan anchor biosynthesis class S | Q96S52 |
C0024790 | Paroxysmal nocturnal hemoglobinuria | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0002878 | Anemia, Hemolytic | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0036439 | Scoliosis, unspecified | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C3665347 | Visual Impairment | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0011991 | Diarrhea | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0020438 | Hypercalciuria | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0221356 | Brachycephaly | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0231528 | Myalgia | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0042109 | Urticaria | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C3809356 | MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3 | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0027709 | Nephrocalcinosis | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0678222 | Breast Carcinoma | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0014544 | Epilepsy | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0020630 | Hypophosphatasia | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0006142 | Malignant neoplasm of breast | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0036572 | Seizures | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0014877 | Esotropia | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0013274 | Patent ductus arteriosus | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0086774 | Cold paroxysmal hemoglobinuria | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C3809369 | PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0029456 | Osteoporosis | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0000768 | Congenital Abnormality | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0028738 | Nystagmus | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
C0019050 | Hemoglobinuria, Paroxysmal | PIGT | 51604 | phosphatidylinositol glycan anchor biosynthesis class T | Q969N2 |
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Last updated: August 19, 2024