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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 |
|---|---|---|---|---|---|
| C0026697 | Mucolipidoses | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C0023283 | Leishmaniasis, Cutaneous | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C1276035 | Pena-Shokeir syndrome type I | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C0038356 | Stomach Neoplasms | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C0007137 | Squamous cell carcinoma | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C0282687 | Hemorrhagic Fever, Ebola | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C2239176 | Liver carcinoma | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C1708349 | Hereditary Diffuse Gastric Cancer | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C0086543 | Cataract | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
| C3463824 | MYELODYSPLASTIC SYNDROME | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0270824 | Visual seizure | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0342708 | Gamma aminobutyric acid transaminase deficiency | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C1510586 | Autism Spectrum Disorders | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0014544 | Epilepsy | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0238111 | Lennox-Gastaut syndrome | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0037769 | West Syndrome | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0242422 | Parkinsonian Disorders | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0006826 | Malignant Neoplasms | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0282513 | Primary Progressive Aphasia (disorder) | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0004352 | Autistic Disorder | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0751494 | Convulsive Seizures | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C1306459 | Primary malignant neoplasm | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0751495 | Seizures, Focal | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0036572 | Seizures | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0376545 | Hematologic Neoplasms | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
