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 |
---|---|---|---|---|---|
C0220981 | Metabolic acidosis | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0677886 | Epithelial ovarian cancer | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C2239176 | Liver carcinoma | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0029456 | Osteoporosis | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0023890 | Liver Cirrhosis | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0019693 | HIV Infections | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C1857276 | Trichohepatoenteric Syndrome | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
C0677886 | Epithelial ovarian cancer | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C1846142 | HOYERAAL-HREIDARSSON SYNDROME | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0007134 | Renal Cell Carcinoma | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0263628 | Tumoral calcinosis | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C1854310 | Hypotrichosis simplex | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0007097 | Carcinoma | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C4721610 | Carcinoma, Ovarian Epithelial | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0014175 | Endometriosis | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0011849 | Diabetes Mellitus | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C4692564 | TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1 | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0265354 | CHARGE Syndrome | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0085681 | Hyperphosphatemia (disorder) | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0152013 | Adenocarcinoma of lung (disorder) | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0025517 | Metabolic Diseases | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C1876187 | TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0553730 | Calcium pyrophosphate deposition disease | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0010054 | Coronary Arteriosclerosis | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
C0029410 | Osteoarthritis of hip | GALNT3 | 2591 | polypeptide N-acetylgalactosaminyltransferase 3 | Q14435 |
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Last updated: August 19, 2024