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 |
---|---|---|---|---|---|
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 |
C0027651 | Neoplasms | SLC35F5 | 80255 | solute carrier family 35 member F5 | Q8WV83 |
C0030297 | Pancreatic Neoplasm | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
C0235974 | Pancreatic carcinoma | SLC35F6 | 54978 | solute carrier family 35 member F6 | Q8N357 |
C0011570 | Mental Depression | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
C0600139 | Prostate carcinoma | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
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Last updated: August 19, 2024