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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 |
|---|---|---|---|---|---|
| C0020224 | Polyhydramnios | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0432194 | Schneckenbecken dysplasia | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0010417 | Cryptorchidism | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0265282 | Fibrochondrogenesis | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0013595 | Eczema | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0028754 | Obesity | SLC35D3 | 340146 | solute carrier family 35 member D3 | Q5M8T2 |
| C0079504 | Hermanski-Pudlak Syndrome | SLC35D3 | 340146 | solute carrier family 35 member D3 | Q5M8T2 |
| C0524620 | Metabolic Syndrome X | SLC35D3 | 340146 | solute carrier family 35 member D3 | Q5M8T2 |
| C0242994 | Hantavirus Infections | SLC35D3 | 340146 | solute carrier family 35 member D3 | Q5M8T2 |
| C0007222 | Cardiovascular Diseases | SLC35E3 | 55508 | solute carrier family 35 member E3 | Q7Z769 |
| C0014544 | Epilepsy | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0235480 | Paroxysmal atrial fibrillation | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0017636 | Glioblastoma | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0278878 | Adult Glioblastoma | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0004238 | Atrial Fibrillation | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C1621958 | Glioblastoma Multiforme | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0024117 | Chronic Obstructive Airway Disease | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0005122 | Beriberi | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0020538 | Hypertensive disease | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0023467 | Leukemia, Myelocytic, Acute | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0007766 | Intracranial Aneurysm | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0039841 | Thiamine Deficiency | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0005586 | Bipolar Disorder | SLC35F4 | 341880 | solute carrier family 35 member F4 | A4IF30 |
| C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | SLC35F4 | 341880 | solute carrier family 35 member F4 | A4IF30 |
| C0026691 | Mucocutaneous Lymph Node Syndrome | SLC35F5 | 80255 | solute carrier family 35 member F5 | Q8WV83 |
