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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 |
|---|---|---|---|---|---|
| C0038356 | Stomach Neoplasms | MGAT5 | 4249 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase | Q09328 |
| C0020459 | Hyperinsulinism | MGAT5 | 4249 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase | Q09328 |
| C1621958 | Glioblastoma Multiforme | MGAT5 | 4249 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase | Q09328 |
| C0699791 | Stomach Carcinoma | MGAT5 | 4249 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase | Q09328 |
| C0017636 | Glioblastoma | MGAT5 | 4249 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase | Q09328 |
| C0700095 | Central neuroblastoma | MGAT5B | 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B | Q3V5L5 |
| C1136382 | Sclerocystic Ovaries | MGAT5B | 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B | Q3V5L5 |
| C0027819 | Neuroblastoma | MGAT5B | 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B | Q3V5L5 |
| C0006826 | Malignant Neoplasms | MGAT5B | 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B | Q3V5L5 |
| C0153633 | Malignant neoplasm of brain | MGAT5B | 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B | Q3V5L5 |
| C2239176 | Liver carcinoma | MGAT5B | 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B | Q3V5L5 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | MGAT5B | 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B | Q3V5L5 |
| C0016788 | Fucosidase Deficiency Disease | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C1527336 | Sjogren's Syndrome | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0036572 | Seizures | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0086795 | Pfaundler-Hurler Syndrome | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0006142 | Malignant neoplasm of breast | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0040136 | Thyroid Neoplasm | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0006826 | Malignant Neoplasms | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0020676 | Hypothyroidism | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C1306459 | Primary malignant neoplasm | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C1384666 | hearing impairment | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0162819 | Skin Diseases, Vascular | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0235946 | Cerebral atrophy | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
| C0027533 | Neck Neoplasms | FUCA1 | 2517 | alpha-L-fucosidase 1 | P04066 |
