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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 |
|---|---|---|---|---|---|
| C0699790 | Colon Carcinoma | ST6GALNAC1 | 55808 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 | Q9NSC7 |
| C1140680 | Malignant neoplasm of ovary | ST6GALNAC1 | 55808 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 | Q9NSC7 |
| C1269683 | Major Depressive Disorder | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0023066 | Laryngospasm | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0002736 | Amyotrophic Lateral Sclerosis | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0025202 | melanoma | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0029410 | Osteoarthritis of hip | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0151779 | Cutaneous Melanoma | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0003467 | Anxiety | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0011581 | Depressive disorder | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0036341 | Schizophrenia | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0041696 | Unipolar Depression | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0409959 | Osteoarthritis, Knee | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0005586 | Bipolar Disorder | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C0029408 | Degenerative polyarthritis | GLT8D1 | 55830 | glycosyltransferase 8 domain containing 1 | Q68CQ7 |
| C3553571 | Carbohydrate deficient glycoprotein syndrome type 2k | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0575158 | Kyphoscoliosis deformity of spine | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0241005 | Creatine phosphokinase serum increased | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0011989 | Camurati-Engelmann Syndrome | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C1306459 | Primary malignant neoplasm | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0002452 | Amelogenesis Imperfecta | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C2239176 | Liver carcinoma | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0013336 | Dwarfism | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0000768 | Congenital Abnormality | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0027859 | Acoustic Neuroma | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
