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DisGeNET
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 ▼ |
|---|---|---|---|---|---|
| C0235974 | Pancreatic carcinoma | B3GALT5 | 10317 | beta-1,3-galactosyltransferase 5 | Q9Y2C3 |
| C2239176 | Liver carcinoma | B3GALT5 | 10317 | beta-1,3-galactosyltransferase 5 | Q9Y2C3 |
| C0346647 | Malignant neoplasm of pancreas | B3GALT5 | 10317 | beta-1,3-galactosyltransferase 5 | Q9Y2C3 |
| C0023467 | Leukemia, Myelocytic, Acute | B3GALT5 | 10317 | beta-1,3-galactosyltransferase 5 | Q9Y2C3 |
| C0007102 | Malignant tumor of colon | B3GALT5 | 10317 | beta-1,3-galactosyltransferase 5 | Q9Y2C3 |
| C0699790 | Colon Carcinoma | B3GALT5 | 10317 | beta-1,3-galactosyltransferase 5 | Q9Y2C3 |
| C0001418 | Adenocarcinoma | B3GALT5 | 10317 | beta-1,3-galactosyltransferase 5 | Q9Y2C3 |
| C0010346 | Crohn Disease | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0038013 | Ankylosing spondylitis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0006826 | Malignant Neoplasms | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0004238 | Atrial Fibrillation | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0235480 | Paroxysmal atrial fibrillation | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0269102 | Endometrioma | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0029408 | Degenerative polyarthritis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0014175 | Endometriosis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| 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 |
| C0019569 | Hirschsprung Disease | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0014877 | Esotropia | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0023449 | Acute lymphocytic leukemia | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0027066 | Myoclonus | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
