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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 |
|---|---|---|---|---|---|
| C0036341 | Schizophrenia | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0011615 | Dermatitis, Atopic | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0271568 | Laron Syndrome | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0013595 | Eczema | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0028754 | Obesity | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0018784 | Sensorineural Hearing Loss (disorder) | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0035078 | Kidney Failure | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0027651 | Neoplasms | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0010054 | Coronary Arteriosclerosis | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0004238 | Atrial Fibrillation | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0027126 | Myotonic Dystrophy | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0043119 | Werner Syndrome | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0020437 | Hypercalcemia | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0558356 | Malignant melanoma of eye | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0085682 | Hypophosphatemia | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0001175 | Acquired Immunodeficiency Syndrome | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0020538 | Hypertensive disease | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C1306459 | Primary malignant neoplasm | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0600139 | Prostate carcinoma | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0006826 | Malignant Neoplasms | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0678222 | Breast Carcinoma | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0042870 | Vitamin D Deficiency | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0027873 | Neuromyelitis Optica | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
| C0003872 | Arthritis, Psoriatic | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
