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 ▼ |
---|---|---|---|---|---|
C0007102 | Malignant tumor of colon | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C0006826 | Malignant Neoplasms | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C0699790 | Colon Carcinoma | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C0025202 | melanoma | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C0009402 | Colorectal Carcinoma | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C1306459 | Primary malignant neoplasm | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C1140680 | Malignant neoplasm of ovary | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C4721610 | Carcinoma, Ovarian Epithelial | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C0677886 | Epithelial ovarian cancer | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C2239176 | Liver carcinoma | GCNT3 | 9245 | glucosaminyl (N-acetyl) transferase 3, mucin type | O95395 |
C3887645 | Job Syndrome | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0029422 | Osteochondrodysplasias | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0021051 | Immunologic Deficiency Syndromes | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0036572 | Seizures | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0013595 | Eczema | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0018784 | Sensorineural Hearing Loss (disorder) | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C2936739 | Hyper-Immunoglobulin E Syndrome, Autosomal Dominant | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0085110 | Severe Combined Immunodeficiency | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0024299 | Lymphoma | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0282577 | Congenital Disorders of Glycosylation | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0010674 | Cystic Fibrosis | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0017168 | Gastroesophageal reflux disease | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0243026 | Sepsis | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0004096 | Asthma | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
C0017662 | Glomerulonephritis, Membranoproliferative | PGM3 | 5238 | phosphoglucomutase 3 | O95394 |
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Last updated: August 19, 2024