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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 |
|---|---|---|---|---|---|
| C0034013 | Precocious Puberty | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0028738 | Nystagmus | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0019196 | Hepatitis C | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0019163 | Hepatitis B | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0036857 | Severe intellectual disability | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0015310 | Exotropia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0022353 | Neonatal Jaundice | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| 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 |
| C1970344 | Congenital Disorder Of Glycosylation, Type IIF | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C4552000 | Episodic Kinesigenic Dyskinesia 1 | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
