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 |
---|---|---|---|---|---|
C2931826 | Potassium aggravated myotonia | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0155626 | Acute myocardial infarction | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0027651 | Neoplasms | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0007134 | Renal Cell Carcinoma | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0006826 | Malignant Neoplasms | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0027051 | Myocardial Infarction | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0030360 | Papillon-Lefevre Disease | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0011854 | Diabetes Mellitus, Insulin-Dependent | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0020456 | Hyperglycemia | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0678222 | Breast Carcinoma | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0021400 | Influenza | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0085580 | Essential Hypertension | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C1134719 | Invasive Ductal Breast Carcinoma | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0029408 | Degenerative polyarthritis | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
C0023467 | Leukemia, Myelocytic, Acute | PGS1 | 9489 | phosphatidylglycerophosphate synthase 1 | Q32NB8 |
C3714756 | Intellectual Disability | PIGB | 9488 | phosphatidylinositol glycan anchor biosynthesis class B | Q92521 |
C0036572 | Seizures | PIGB | 9488 | phosphatidylinositol glycan anchor biosynthesis class B | Q92521 |
C0270921 | Axonal neuropathy | PIGB | 9488 | phosphatidylinositol glycan anchor biosynthesis class B | Q92521 |
C0008925 | Cleft Palate | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
C0002736 | Amyotrophic Lateral Sclerosis | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
C0037299 | Skin Ulcer | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
C0039685 | Tetralogy of Fallot | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
C0004352 | Autistic Disorder | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
C0221356 | Brachycephaly | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
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Last updated: August 19, 2024