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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 |
|---|---|---|---|---|---|
| C0014544 | Epilepsy | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0019061 | Hemolytic-Uremic Syndrome | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0678222 | Breast Carcinoma | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0206624 | Hepatoblastoma | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0032460 | Polycystic Ovary Syndrome | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0023467 | Leukemia, Myelocytic, Acute | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C1834582 | MYELOPROLIFERATIVE SYNDROME, TRANSIENT | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| 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 |
| C0238052 | Xanthomatosis, Cerebrotendinous | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
| C0024523 | Malabsorption Syndrome | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
| C0302164 | Tuberous xanthoma | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
| C0600139 | Prostate carcinoma | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
| C0524851 | Neurodegenerative Disorders | CYP27A1 | 1593 | cytochrome P450 family 27 subfamily A member 1 | Q02318 |
