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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 |
|---|---|---|---|---|---|
| C0002895 | Anemia, Sickle Cell | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0038379 | Strabismus | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0010964 | Dandy-Walker Syndrome | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0005283 | beta Thalassemia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0018784 | Sensorineural Hearing Loss (disorder) | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C1856251 | Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0009806 | Constipation | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0268398 | Familial lichen amyloidosis | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C2677590 | Congenital Disorder Of Glycosylation, Type In | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0009081 | Congenital clubfoot | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0015934 | Fetal Growth Retardation | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0699885 | Carcinoma of bladder | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0017168 | Gastroesophageal reflux disease | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0005695 | Bladder Neoplasm | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0235946 | Cerebral atrophy | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0265343 | Jarcho-Levin syndrome | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0036572 | Seizures | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0036439 | Scoliosis, unspecified | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C3714756 | Intellectual Disability | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0025958 | Microcephaly | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0000768 | Congenital Abnormality | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0085136 | Central Nervous System Neoplasms | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0004352 | Autistic Disorder | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
| C0029422 | Osteochondrodysplasias | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
